Professor Michael Gill
Fellow Emeritus, Psychiatry
Professor Emeritus, Trinity Inst. of Neurosciences (TCIN)
Professor Emeritus, Molecular Medicine Ireland

Ruderfer, D.M. and Ripke, S. and McQuillin, A. and Boocock, J. and Stahl, E.A. and Pavlides, J.M.W. and Mullins, N. and Charney, A.W. and Ori, A.P.S. and Loohuis, L.M.O. and Domenici, E. and Di Florio, A. and Papiol, S. and Kalman, J.L. and Trubetskoy, V. and Adolfsson, R. and Agartz, I. and Agerbo, E. and Akil, H. and Albani, D. and Albus, M. and Alda, M. and Alexander, M. and Alliey-Rodriguez, N. and Als, T.D. and Amin, F. and Anjorin, A. and Arranz, M.J. and Awasthi, S. and Bacanu, S.A. and Badner, J.A. and Baekvad-Hansen, M. and Bakker, S. and Band, G. and Barchas, J.D. and Barroso, I. and Bass, N. and Bauer, M. and Baune, B.T. and Begemann, M. and Bellenguez, C. and Belliveau, R.A. and Bellivier, F. and Bender, S. and Bene, J. and Bergen, S.E. and Berrettini, W.H. and Bevilacqua, E. and Biernacka, J.M. and Bigdeli, T.B. and Black, D.W. and Blackburn, H. and Blackwell, J.M. and Blackwood, D.H.R. and Pedersen, C.B. and Boehnke, M. and Boks, M. and Borglum, A.D. and Bramon, E. and Breen, G. and Brown, M.A. and Bruggeman, R. and Buccola, N.G. and Buckner, R.L. and Budde, M. and Bulik-Sullivan, B. and Bumpstead, S.J. and Bunney, W. and Burmeister, M. and Buxbaum, J.D. and Bybjerg-Grauholm, J. and Byerley, W. and Cahn, W. and Cai, G. and Cairns, M.J. and Campion, D. and Cantor, R.M. and Carr, V.J. and Carrera, N. and Casas, J.P. and Casas, M. and Catts, S.V. and Cervantes, P. and Chambert, K.D. and Chan, R.C.K. and Chen, E.Y.H. and Chen, R.Y.L. and Cheng, W. and Cheung, E.F.C. and Chong, S.A. and Clarke, T.-K. and Cloninger, C.R. and Cohen, D. and Cohen, N. and Coleman, J.R.I. and Collier, D.A. and Cormican, P. and Coryell, W. and Craddock, N. and Craig, D.W. and Crespo-Facorro, B. and Crowley, J.J. and Cruceanu, C. and Curtis, D. and Czerski, P.M. and Dale, A.M. and Daly, M.J. and Dannlowski, U. and Darvasi, A. and Davidson, M. and Davis, K.L. and de Leeuw, C.A. and Degenhardt, F. and Del Favero, J. and DeLisi, L.E. and Deloukas, P. and Demontis, D. and DePaulo, J.R. and di Forti, M. and Dikeos, D. and Dinan, T. and Djurovic, S. and Dobbyn, A.L. and Donnelly, P. and Donohoe, G. and Drapeau, E. and Dronov, S. and Duan, J. and Dudbridge, F. and Duncanson, A. and Edenberg, H. and Edkins, S. and Ehrenreich, H. and Eichhammer, P. and Elvsashagen, T. and Eriksson, J. and Escott-Price, V. and Esko, T. and Essioux, L. and Etain, B. and Fan, C.C. and Farh, K.-H. and Farrell, M.S. and Flickinger, M. and Foroud, T.M. and Forty, L. and Frank, J. and Franke, L. and Fraser, C. and Freedman, R. and Freeman, C. and Freimer, N.B. and Friedman, J.I. and Fromer, M. and Frye, M.A. and Fullerton, J.M. and Gade, K. and Garnham, J. and Gaspar, H.A. and Gejman, P.V. and Genovese, G. and Georgieva, L. and Giambartolomei, C. and Giannoulatou, E. and Giegling, I. and Gill, M. and Gillman, M. and Pedersen, M.G. and Giusti-Rodriguez, P. and Godard, S. and Goes, F. and Goldstein, J.I. and Gopal, S. and Gordon, S.D. and Gordon-Smith, K. and Gratten, J. and Gray, E. and Green, E.K. and Green, M.J. and Greenwood, T.A. and Grigoroiu-Serbanescu, M. and Grove, J. and Guan, W. and Gurling, H. and Parra, J.G. and Gwilliam, R. and de Haan, L. and Hall, J. and Hall, M.-H. and Hammer, C. and Hammond, N. and Hamshere, M.L. and Hansen, M. and Hansen, T. and Haroutunian, V. and Hartmann, A.M. and Hauser, J. and Hautzinger, M. and Heilbronner, U. and Hellenthal, G. and Henskens, F.A. and Herms, S. and Hipolito, M. and Hirschhorn, J.N. and Hoffmann, P. and Hollegaard, M.V. and Hougaard, D.M. and Huang, H. and Huckin, Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes, Cell, 173, (7), 2018, p1705-1715.e16 Journal Article, 2018 DOI TARA - Full Text

Peyrot, W.J. and Van der Auwera, S. and Milaneschi, Y. and Dolan, C.V. and Madden, P.A.F. and Sullivan, P.F. and Strohmaier, J. and Ripke, S. and Rietschel, M. and Nivard, M.G. and Mullins, N. and Montgomery, G.W. and Henders, A.K. and Heat, A.C. and Fisher, H.L. and Dunn, E.C. and Byrne, E.M. and Air, T.A. and Wray, N.R. and Ripke, S. and Mattheisen, M. and Trzaskowski, M. and Byrne, E.M. and Abdellaoui, A. and Adams, M.J. and Agerbo, E. and Air, T.M. and Andlauer, T.F.M. and Bacanu, S.-A. and BÊkvad-Hansen, M. and Beekman, A.T.F. and Bigdeli, T.B. and Binder, E.B. and Blackwood, D.H.R. and Bryois, J. and ButtenschÞn, H.N. and Bybjerg-Grauholm, J. and Cai, N. and Castelao, E. and Christensen, J.H. and Clarke, T.-K. and Coleman, J.R.I. and Colodro-Conde, L. and Couvy-Duchesne, B. and Craddock, N. and Crawford, G.E. and Davies, G. and Deary, I.J. and Degenhardt, F. and Derks, E.M. and Direk, N. and Dolan, C.V. and Dunn, E.C. and Eley, T.C. and Escott-Price, V. and Farnush and Kiadeh, F.H. and Finucane, H.K. and Forstner, A.J. and Frank, J. and Gaspar, H.A. and Gill, M. and Goes, F.S. and Gordon, S.D. and Grove, J. and Hall, L.S. and Hansen, C.S. and Hansen, T.F. and Herms, S. and Hicki, I.B. and Hoffmann, P. and Homuth, G. and Horn, C. and Hottenga, J.-J. and Hougaard, D.M. and Ising, M. and Jansen, R. and Jorgenson, E. and Knowles, J.A. and Kohane, I.S. and Kraft, J. and Kretzschmar, W.W. and Krogh, J. and Kutalik, Z. and Li, Y. and Lind, P.A. and MacIntyre, D.J. and MacKinnon, D.F. and Maier, R.M. and Maier, W. and Marchini, J. and Mbarek, H. and McGrath, P. and McGuffin, P. and Medland, S.E. and Mehta, D. and Middeldorp, C.M. and Mihailov, E. and Milaneschi, Y. and Milani, L. and Mondimore, F.M. and Montgomery, G.W. and Mostafavi, S. and Mullins, N. and Nauck, M. and Ng, B. and Nivard, M.G. and Nyholt, D.R. and O'Reilly, P.F. and Oskarsson, H. and Owen, M.J. and Painter, J.N. and Pedersen, C.B. and Pedersen, M.G. and Peterson, R.E. and Pettersson, E. and Peyrot, W.J. and Pistis, G. and Posthuma, D. and Quiroz, J.A. and Qvist, P. and Rice, J.P. and Riley, B.P. and Rivera, M. and Mirza, S.S. and Schoevers, R. and Schulte, E.C. and Shen, L. and Shi, J. and Shyn, S.I. and Sigurdsson, E. and Sinnamon, G.C.B. and Smit, J.H. and Smith, D.J. and Stefansson, H. and Steinberg, S. and Streit, F. and Strohmaier, J. and Tansey, K.E. and Teismann, H. and Teumer, A. and Thompson, W. and Thomson, P.A. and Thorgeirsson, T.E. and Traylor, M. and Treutlein, J. and Trubetskoy, V. and Uitterlinden, A.G. and Umbricht, D. and Van der Auwera, S. and van Hemert, A.M. and Viktorin, A. and Visscher, P.M. and Wang, Y. and Webb, B.T. and Weinsheimer, S.M. and Wellmann, J. and Willemsen, G. and Witt, S.H. and Wu, Y. and Xi, H.S. and Yang, J. and Zhang, F. and Arolt, V. and Baune, B.T. and Berger, K. and Boomsma, D.I. and Cichon, S. and Dannlowski, U. and de Geus, E.J.C. and DePaulo, J.R. and Domenici, E. and Domschke, K. and Esko, T. and Grabe, H.J. and Hamilton, S.P. and Hayward, C. and Heath, A.C. and Kendler, K.S. and Kloiber, S. and Lewis, G. and Li, Q.S. and Lucae, S. and Madden, P.A.F. and Magnusson, P.K. and Martin, N.G. and McIntosh, A.M. and Metspalu, A. and Mors, O. and Mortensen, P.B. and MÌller-Myhsok, B. and Nordentoft, M. and Nöthen, M.M. and O'Donovan, M.C. and Paciga, S.A. and Pedersen, N.L. and Penninx, B.W.J.H. and Perlis, R.H. and Porteous, D.J. and Potash, J.B. and Preisig, M. and Rietschel, M. and Schaefer, C. and Schulze, T.G. and Smoller, J.W. and Stefansson, K. and Ti, Does Childhood Trauma Moderate Polygenic Risk for Depression? A Meta-analysis of 5765 Subjects From the Psychiatric Genomics Consortium, Biological Psychiatry, 84, (2), 2018, p138-147 Journal Article, 2018 DOI

Blokland, G.A.M. and del Re, E.C. and Mesholam-Gately, R.I. and Jovicich, J. and Trampush, J.W. and Keshavan, M.S. and DeLisi, L.E. and Walters, J.T.R. and Turner, J.A. and Malhotra, A.K. and Lencz, T. and Shenton, M.E. and Voineskos, A.N. and Rujescu, D. and Giegling, I. and Kahn, R.S. and Roffman, J.L. and Holt, D.J. and Ehrlich, S. and Kikinis, Z. and Dazzan, P. and Murray, R.M. and Di Forti, M. and Lee, J. and Sim, K. and Lam, M. and Wolthusen, R.P.F. and de Zwarte, S.M.C. and Walton, E. and Cosgrove, D. and Kelly, S. and Maleki, N. and Osiecki, L. and Picchioni, M.M. and Bramon, E. and Russo, M. and David, A.S. and Mondelli, V. and Reinders, A.A.T.S. and Falcone, M.A. and Hartmann, A.M. and Konte, B. and Morris, D.W. and Gill, M. and Corvin, A.P. and Cahn, W. and Ho, N.F. and Liu, J.J. and Keefe, R.S.E. and Gollub, R.L. and Manoach, D.S. and Calhoun, V.D. and Schulz, S.C. and Sponheim, S.R. and Goff, D.C. and Buka, S.L. and Cherkerzian, S. and Thermenos, H.W. and Kubicki, M. and Nestor, P.G. and Dickie, E.W. and Vassos, E. and Ciufolini, S. and Reis Marques, T. and Crossley, N.A. and Purcell, S.M. and Smoller, J.W. and van Haren, N.E.M. and Toulopoulou, T. and Donohoe, G. and Goldstein, J.M. and Seidman, L.J. and McCarley, R.W. and Petryshen, T.L., The Genetics of Endophenotypes of Neurofunction to Understand Schizophrenia (GENUS) consortium: A collaborative cognitive and neuroimaging genetics project, Schizophrenia Research, 195, 2018, p306-317 Journal Article, 2018 DOI TARA - Full Text

Donohoe, G. and Holland, J. and Mothersill, D. and McCarthy-Jones, S. and Cosgrove, D. and Harold, D. and Richards, A. and Mantripragada, K. and Owen, M.J. and O'Donovan, M.C. and Wtccc2 and Gill, M. and Corvin, A. and Morris, D.W., Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation, Psychological Medicine, 2018, p1-10 Journal Article, 2018 DOI

Davies, G. and Lam, M. and Harris, S.E. and Trampush, J.W. and Luciano, M. and Hill, W.D. and Hagenaars, S.P. and Ritchie, S.J. and Marioni, R.E. and Fawns-Ritchie, C. and Liewald, D.C.M. and Okely, J.A. and Ahola-Olli, A.V. and Barnes, C.L.K. and Bertram, L. and Bis, J.C. and Burdick, K.E. and Christoforou, A. and Derosse, P. and Djurovic, S. and Espeseth, T. and Giakoumaki, S. and Giddaluru, S. and Gustavson, D.E. and Hayward, C. and Hofer, E. and Ikram, M.A. and Karlsson, R. and Knowles, E. and Lahti, J. and Leber, M. and Li, S. and Mather, K.A. and Melle, I. and Morris, D. and Oldmeadow, C. and Palviainen, T. and Payton, A. and Pazoki, R. and Petrovic, K. and Reynolds, C.A. and Sargurupremraj, M. and Scholz, M. and Smith, J.A. and Smith, A.V. and Terzikhan, N. and Thalamuthu, A. and Trompet, S. and Van Der Lee, S.J. and Ware, E.B. and Windham, B.G. and Wright, M.J. and Yang, J. and Yu, J. and Ames, D. and Amin, N. and Amouyel, P. and Andreassen, O.A. and Armstrong, N.J. and Assareh, A.A. and Attia, J.R. and Attix, D. and Avramopoulos, D. and Bennett, D.A. and Böhmer, A.C. and Boyle, P.A. and Brodaty, H. and Campbell, H. and Cannon, T.D. and Cirulli, E.T. and Congdon, E. and Conley, E.D. and Corley, J. and Cox, S.R. and Dale, A.M. and Dehghan, A. and Dick, D. and Dickinson, D. and Eriksson, J.G. and Evangelou, E. and Faul, J.D. and Ford, I. and Freimer, N.A. and Gao, H. and Giegling, I. and Gillespie, N.A. and Gordon, S.D. and Gottesman, R.F. and Griswold, M.E. and Gudnason, V. and Harris, T.B. and Hartmann, A.M. and Hatzimanolis, A. and Heiss, G. and Holliday, E.G. and Joshi, P.K. and KÃ"hönen, M. and Kardia, S.L.R. and Karlsson, I. and Kleineidam, L. and Knopman, D.S. and Kochan, N.A. and Konte, B. and Kwok, J.B. and Le Hellard, S. and Lee, T. and LehtimÃ"ki, T. and Li, S.-C. and Liu, T. and Koini, M. and London, E. and Longstreth, W.T. and Lopez, O.L. and Loukola, A. and Luck, T. and Lundervold, A.J. and Lundquist, A. and LyytikÃ"inen, L.-P. and Martin, N.G. and Montgomery, G.W. and Murray, A.D. and Need, A.C. and Noordam, R. and Nyberg, L. and Ollier, W. and Papenberg, G. and Pattie, A. and Polasek, O. and Poldrack, R.A. and Psaty, B.M. and Reppermund, S. and Riedel-Heller, S.G. and Rose, R.J. and Rotter, J.I. and Roussos, P. and Rovio, S.P. and Saba, Y. and Sabb, F.W. and Sachdev, P.S. and Satizabal, C.L. and Schmid, M. and Scott, R.J. and Scult, M.A. and Simino, J. and Slagboom, P.E. and Smyrnis, N. and Soumaré, A. and Stefanis, N.C. and Stott, D.J. and Straub, R.E. and Sundet, K. and Taylor, A.M. and Taylor, K.D. and Tzoulaki, I. and Tzourio, C. and Uitterlinden, A. and Vitart, V. and Voineskos, A.N. and Kaprio, J. and Wagner, M. and Wagner, H. and Weinhold, L. and Wen, K.H. and Widen, E. and Yang, Q. and Zhao, W. and Adams, H.H.H. and Arking, D.E. and Bilder, R.M. and Bitsios, P. and Boerwinkle, E. and Chiba-Falek, O. and Corvin, A. and De Jager, P.L. and Debette, S. and Donohoe, G. and Elliott, P. and Fitzpatrick, A.L. and Gill, M. and Glahn, D.C. and HÃ"gg, S. and Hansell, N.K. and Hariri, A.R. and Ikram, M.K. and Jukema, J.W. and Vuoksimaa, E. and Keller, M.C. and Kremen, W.S. and Launer, L. and Lindenberger, U. and Palotie, A. and Pedersen, N.L. and Pendleton, N. and Porteous, D.J. and RÃ"ikkönen, K. and Raitakari, O.T. and Ramirez, A. and Reinvang, I. and Rudan, I., Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function, Nature Communications, 9, (1), 2018, p2098- Journal Article, 2018 TARA - Full Text DOI

Walton, E. and Hibar, D.P. and Van Erp, T.G.M. and Potkin, S.G. and Roiz-Santiañez, R. and Crespo-Facorro, B. and Suarez-Pinilla, P. and Van Haren, N.E.M. and De Zwarte, S.M.C. and Kahn, R.S. and Cahn, W. and Doan, N.T. and Jorgensen, K.N. and Gurholt, T.P. and Agartz, I. and Andreassen, O.A. and Westlye, L.T. and Melle, I. and Berg, A.O. and Morch-Johnsen, L. and FÊrden, A. and Flyckt, L. and Fatouros-Bergman, H. and Jönsson, E.G. and Hashimoto, R. and Yamamori, H. and Fukunaga, M. and Jahanshad, N. and De Rossi, P. and Piras, F. and Banaj, N. and Spalletta, G. and Gur, R.E. and Gur, R.C. and Wolf, D.H. and Satterthwaite, T.D. and Beard, L.M. and Sommer, I.E. and Koops, S. and Gruber, O. and Richter, A. and KrÀmer, B. and Kelly, S. and Donohoe, G. and McDonald, C. and Cannon, D.M. and Corvin, A. and Gill, M. and Di Giorgio, A. and Bertolino, A. and Lawrie, S. and Nickson, T. and Whalley, H.C. and Neilson, E. and Calhoun, V.D. and Thompson, P.M. and Turner, J.A. and Ehrlich, S., Prefrontal cortical thinning links to negative symptoms in schizophrenia via the ENIGMA consortium, Psychological Medicine, 48, (1), 2018, p82-94 Journal Article, 2018 DOI TARA - Full Text

Kelly, S. and Jahanshad, N. and Zalesky, A. and Kochunov, P. and Agartz, I. and Alloza, C. and Andreassen, O.A. and Arango, C. and Banaj, N. and Bouix, S. and Bousman, C.A. and Brouwer, R.M. and Bruggemann, J. and Bustillo, J. and Cahn, W. and Calhoun, V. and Cannon, D. and Carr, V. and Catts, S. and Chen, J. and Chen, J.-X. and Chen, X. and Chiapponi, C. and Cho, K.K. and Ciullo, V. and Corvin, A.S. and Crespo-Facorro, B. and Cropley, V. and De Rossi, P. and Diaz-Caneja, C.M. and Dickie, E.W. and Ehrlich, S. and Fan, F.-M. and Faskowitz, J. and Fatouros-Bergman, H. and Flyckt, L. and Ford, J.M. and Fouche, J.-P. and Fukunaga, M. and Gill, M. and Glahn, D.C. and Gollub, R. and Goudzwaard, E.D. and Guo, H. and Gur, R.E. and Gur, R.C. and Gurholt, T.P. and Hashimoto, R. and Hatton, S.N. and Henskens, F.A. and Hibar, D.P. and Hickie, I.B. and Hong, L.E. and Horacek, J. and Howells, F.M. and Hulshoff Pol, H.E. and Hyde, C.L. and Isaev, D. and Jablensky, A. and Jansen, P.R. and Janssen, J. and Jönsson, E.G. and Jung, L.A. and Kahn, R.S. and Kikinis, Z. and Liu, K. and Klauser, P. and Knöchel, C. and Kubicki, M. and Lagopoulos, J. and Langen, C. and Lawrie, S. and Lenroot, R.K. and Lim, K.O. and Lopez-Jaramillo, C. and Lyall, A. and Magnotta, V. and Mandl, R.C.W. and Mathalon, D.H. and McCarley, R.W. and McCarthy-Jones, S. and McDonald, C. and McEwen, S. and McIntosh, A. and Melicher, T. and Mesholam-Gately, R.I. and Michie, P.T. and Mowry, B. and Mueller, B.A. and Newell, D.T. and O'Donnell, P. and Oertel-Knöchel, V. and Oestreich, L. and Paciga, S.A. and Pantelis, C. and Pasternak, O. and Pearlson, G. and Pellicano, G.R. and Pereira, A. and Pineda Zapata, J. and Piras, F. and Potkin, S.G. and Preda, A. and Rasser, P.E. and Roalf, D.R. and Roiz, R. and Roos, A. and Rotenberg, D. and Satterthwaite, T.D. and Savadjiev, P. and Schall, U. and Scott, R.J. and Seal, M.L. and Seidman, L.J. and Shannon Weickert, C. and Whelan, C.D. and Shenton, M.E. and Kwon, J.S. and Spalletta, G. and Spaniel, F. and Sprooten, E. and StÀblein, M. and Stein, D.J. and Sundram, S. and Tan, Y. and Tan, S. and Tang, S. and Temmingh, H.S. and Westlye, L.T. and TÞnnesen, S. and Tordesillas-Gutierrez, D. and Doan, N.T. and Vaidya, J. and Van Haren, N.E.M. and Vargas, C.D. and Vecchio, D. and Velakoulis, D. and Voineskos, A. and Voyvodic, J.Q. and Wang, Z. and Wan, P. and Wei, D. and Weickert, T.W. and Whalley, H. and White, T. and Whitford, T.J. and Wojcik, J.D. and Xiang, H. and Xie, Z. and Yamamori, H. and Yang, F. and Yao, N. and Zhang, G. and Zhao, J. and Van Erp, T.G.M. and Turner, J. and Thompson, P.M. and Donohoe, G., Widespread white matter microstructural differences in schizophrenia across 4322 individuals: Results from the ENIGMA Schizophrenia DTI Working Group, Molecular Psychiatry, 23, (5), 2018, p1261-1269 Journal Article, 2018 TARA - Full Text DOI

Savage, J.E. and Jansen, P.R. and Stringer, S. and Watanabe, K. and Bryois, J. and De Leeuw, C.A. and Nagel, M. and Awasthi, S. and Barr, P.B. and Coleman, J.R.I. and Grasby, K.L. and Hammerschlag, A.R. and Kaminski, J.A. and Karlsson, R. and Krapohl, E. and Lam, M. and Nygaard, M. and Reynolds, C.A. and Trampush, J.W. and Young, H. and Zabaneh, D. and HÀgg, S. and Hansell, N.K. and Karlsson, I.K. and Linnarsson, S. and Montgomery, G.W. and Muñoz-Manchado, A.B. and Quinlan, E.B. and Schumann, G. and Skene, N.G. and Webb, B.T. and White, T. and Arking, D.E. and Avramopoulos, D. and Bilder, R.M. and Bitsios, P. and Burdick, K.E. and Cannon, T.D. and Chiba-Falek, O. and Christoforou, A. and Cirulli, E.T. and Congdon, E. and Corvin, A. and Davies, G. and Deary, I.J. and Derosse, P. and Dickinson, D. and Djurovic, S. and Donohoe, G. and Conley, E.D. and Eriksson, J.G. and Espeseth, T. and Freimer, N.A. and Giakoumaki, S. and Giegling, I. and Gill, M. and Glahn, D.C. and Hariri, A.R. and Hatzimanolis, A. and Keller, M.C. and Knowles, E. and Koltai, D. and Konte, B. and Lahti, J. and Le Hellard, S. and Lencz, T. and Liewald, D.C. and London, E. and Lundervold, A.J. and Malhotra, A.K. and Melle, I. and Morris, D. and Need, A.C. and Ollier, W. and Palotie, A. and Payton, A. and Pendleton, N. and Poldrack, R.A. and RÀikkönen, K. and Reinvang, I. and Roussos, P. and Rujescu, D. and Sabb, F.W. and Scult, M.A. and Smeland, O.B. and Smyrnis, N. and Starr, J.M. and Steen, V.M. and Stefanis, N.C. and Straub, R.E. and Sundet, K. and Tiemeier, H. and Voineskos, A.N. and Weinberger, D.R. and Widen, E. and Yu, J. and Abecasis, G. and Andreassen, O.A. and Breen, G. and Christiansen, L. and Debrabant, B. and Dick, D.M. and Heinz, A. and Hjerling-Leffler, J. and Ikram, M.A. and Kendler, K.S. and Martin, N.G. and Medland, S.E. and Pedersen, N.L. and Plomin, R. and Polderman, T.J.C. and Ripke, S. and Van Der Sluis, S. and Sullivan, P.F. and Vrieze, S.I. and Wright, M.J. and Posthuma, D., Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence, Nature Genetics, 50, (7), 2018, p912-919 Journal Article, 2018 DOI

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Bigdeli, T.B. and Ripke, S. and Peterson, R.E. and Trzaskowski, M. and Bacanu, S.-A. and Abdellaoui, A. and Andlauer, T.F.M. and Beekman, A.T.F. and Berger, K. and Blackwood, D.H.R. and Boomsma, D.I. and Breen, G. and ButtenschÃ"n, H.N. and Byrne, E.M. and Cichon, S. and Clarke, T.-K. and Couvy-Duchesne, B. and Craddock, N. and De Geus, E.J.C. and Degenhardt, F. and Dunn, E.C. and Edwards, A.C. and Fanous, A.H. and Forstner, A.J. and Frank, J. and Gill, M. and Gordon, S.D. and Grabe, H.J. and Hamilton, S.P. and Hardiman, O. and Hayward, C. and Heath, A.C. and Henders, A.K. and Herms, S. and Hickie, I.B. and Hoffmann, P. and Homuth, G. and Hottenga, J.-J. and Ising, M. and Jansen, R. and Kloiber, S. and Knowles, J.A. and Lang, M. and Li, Q.S. and Lucae, S. and MacIntyre, D.J. and Madden, P.A.F. and Martin, N.G. and McGrath, P.J. and McGuffin, P. and McIntosh, A.M. and Medland, S.E. and Mehta, D. and Middeldorp, C.M. and Milaneschi, Y. and Montgomery, G.W. and Mors, O. and MÃ"ller-Myhsok, B. and Nauck, M. and Nyholt, D.R. and Nöthen, M.M. and Owen, M.J. and Penninx, B.W.J.H. and Pergadia, M.L. and Perlis, R.H. and Peyrot, W.J. and Porteous, D.J. and Potash, J.B. and Rice, J.P. and Rietschel, M. and Riley, B.P. and Rivera, M. and Schoevers, R. and Schulze, T.G. and Shi, J. and Shyn, S.I. and Smit, J.H. and Smoller, J.W. and Streit, F. and Strohmaier, J. and Teumer, A. and Treutlein, J. and Van Der Auwera, S. and Van Grootheest, G. and Van Hemert, A.M. and Völzke, H. and Webb, B.T. and Weissman, M.M. and Wellmann, J. and Willemsen, G. and Witt, S.H. and Levinson, D.F. and Lewis, C.M. and Wray, N.R. and Flint, J. and Sullivan, P.F. and Kendler, K.S., Genetic effects influencing risk for major depressive disorder in China and Europe, Translational Psychiatry, 7, (3), 2017, pe1074- Journal Article, 2017 DOI TARA - Full Text

McCarthy-Jones S, Smailes D, Corvin A, Gill M, Morris D.W, Dinan T.G, Murphy K.C, Anthony O′Neill F, Waddington J.L, Australian Schizophrenia Research Ban, Donohoe G, Dudley R, Occurrence and co-occurrence of hallucinations by modality in schizophrenia-spectrum disorders, Psychiatry Research, 252, 2017, p154 - 160 Journal Article, 2017 DOI URL

Weiner DJ, Wigdor EM, Ripke S, Walters RK, Kosmicki JA, Grove J, Samocha KE, Goldstein JI, Okbay A, Bybjerg-Grauholm J, Werge T, Hougaard DM, Taylor J, iPSYCH-Broad Autism Group, Psychiatric Genomics Consortium Autism Group, Skuse D, Devlin B, Anney R, Sanders SJ, Bishop S, Mortensen PB, Børglum AD, Smith GD, Daly MJ, Robinson EB., Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders., Nature genetics, 49, (7), 2017, p978-985 Journal Article, 2017 DOI

Fabbri C, Hosak L, Mössner R, Giegling I, Mandelli L, Bellivier F, Claes S, Collier D.A, Corrales A, Delisi L.E, Gallo C, Gill M, Kennedy J.L, Leboyer M, Lisoway A, Maier W, Marquez M, Massat I, Mors O, Muglia P, Nöthen M.M, O†Donovan M.C, Ospina-Duque J, Propping P, Shi Y, St Clair D, Thibaut F, Cichon S, Mendlewicz J, Rujescu D, Serretti A, Consensus paper of the WFSBP Task Force on Genetics: Genetics, epigenetics and gene expression markers of major depressive disorder and antidepressant response, World Journal of Biological Psychiatry, 18, (1), 2017, p5 - 28 Journal Article, 2017 URL DOI

Rivera, M. and Locke, A.E. and Corre, T. and Czamara, D. and Wolf, C. and Ching-Lopez, A. and Milaneschi, Y. and Kloiber, S. and Cohen-Woods, S. and Rucker, J. and Aitchison, K.J. and Bergmann, S. and Boomsma, D.I. and Craddock, N. and Gill, M. and Holsboer, F. and Hottenga, J.-J. and Korszun, A. and Kutalik, Z. and Lucae, S. and Maier, W. and Mors, O. and Muller-Myhsok, B. and Owen, M.J. and Penninx, B.W.J.H. and Preisig, M. and Rice, J. and Rietschel, M. and Tozzi, F. and Uher, R. and Vollenweider, P. and Waeber, G. and Willemsen, G. and Craig, I.W. and Farmer, A.E. and Lewis, C.M. and Breen, G. and McGuffin, P., Interaction between the FTO gene, body mass index and depression: Meta-analysis of 13701 individuals, British Journal of Psychiatry, 211, (2), 2017, p70-76 Journal Article, 2017 DOI

Naaijen, J. and Bralten, J. and Poelmans, G. and Glennon, J.C. and Franke, B. and Buitelaar, J.K. and Faraone, S. and Asherson, P. and Banaschewski, T. and Buitelaar, J. and Franke, B. and P Ebstein, R. and Gill, M. and Miranda, A. and Oades, R.D. and Roeyers, H. and Rothenberger, A. and Sergeant, J. and Sonuga-Barke, E. and Anney, R. and Mulas, F. and Steinhausen, H.-C., Glutamatergic and GABAergic gene sets in attention-deficit/hyperactivity disorder: Association to overlapping traits in ADHD and autism, Translational Psychiatry, 7, (1), 2017, pe999- Journal Article, 2017 TARA - Full Text DOI

Cosgrove, D. and Harold, D. and Mothersill, O. and Anney, R. and Hill, M.J. and Bray, N.J. and Blokland, G. and Petryshen, T. and Richards, A. and Mantripragada, K. and Owen, M. and O'Donovan, M.C. and Gill, M. and Corvin, A. and Morris, D.W. and Donohoe, G., MiR-137-derived polygenic risk: Effects on cognitive performance in patients with schizophrenia and controls, Translational Psychiatry, 7, (1), 2017, pe1012- Journal Article, 2017 DOI TARA - Full Text

Hawi Z, Bellgrove M, Kirley A, Barry E, Heron E, Fitzgerald M, Gill M, Linkage disequilibrium mapping of multi markers in 11 noradrenergic and SNAP-25 genes: evidence of linkage and association with SLC6A2, ADRA1A, ADRA1B, ADRA2B, DBH and SNAP-25 with ADHD, Americal Journal of Medical Genetics, 2017 Journal Article, 2017

Bralten J, Franke B, Waldman I, Roommelse N, Hartman C, Asherson P, Banaschewski T, Ebstein R, Gill M, Miranda A, Oades R, Roeyers H, Rothenberger A, Sergeant J, Oosterlaan J, Sonuga-Barke E, Steinhausen H, Faraone S, Buitelaar J, Arias-Vasquez A. , Genetics pathways for ADHD show association to hyperactive/impulsive symptoms. , Biological Psychiatry, 2017 Journal Article, 2017

Walton, E., Hibar, D.P., van Erp, T.G.M., (...), Malmqvist, A., Hedberg, M. , Positive symptoms associate with cortical thinning in the superior temporal gyrus via the ENIGMA Schizophrenia consortium, Acta Psychiatrica Scandinavica, 135, (5), 2017, p439-447 Journal Article, 2017 DOI

Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium., Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia., Molecular autism, 8, 2017, p21 Journal Article, 2017 TARA - Full Text DOI

Giegling I, Hosak L, Mössner R, Serretti A, Bellivier F, Claes S, Collier D.A, Corrales A, DeLisi L.E, Gallo C, Gill M, Kennedy J.L, Leboyer M, Maier W, Marquez M, Massat I, Mors O, Muglia P, Nöthen M.M, Ospina-Duque J, Owen M.J, Propping P, Shi Y, St Clair D, Thibaut F, Cichon S, Mendlewicz J, O'Donovan M.C, Rujescu D, Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics, WFSBP Consensus Paper , 2017, p492-505 Journal Article, 2017 DOI URL

Whitton L, Cosgrove D, Clarkson C, Harold D, Kendall K, Richards A, Mantripragada K, Owen M.J, O'Donovan M.C, Walters J, Hartmann A, Konte B, Rujescu D, Gill M, Corvin A, Rea S, Donohoe G, Morris D.W, Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression, American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 171, (8), 2016, p1170 - 1179 Journal Article, 2016 DOI URL

Tozzi L., Carballedo A., Wetterling F., McCarthy H., O'Keane V., Gill M., Morris D., Fahey C., Meaney J., Frodl T., Single Nucleotide Polymorphism of the FKBP5 Gene and Childhood Maltreatment as Predictors of Structural Changes in Brain Areas Involved in Emotional Processing in Depression., Neuropsychopharmacology, 41, 2016, p487-497 Journal Article, 2016 DOI

Mothersill O, Tangney N, Morris D.W, McCarthy H, Frodl T, Gill M, Corvin A, Donohoe G, Further evidence of alerted default network connectivity and association with theory of mind ability in schizophrenia, Schizophrenia Research, 2016 Journal Article, 2016 DOI TARA - Full Text URL

Merikangas, A.K., Segurado, R., Kelleher, E., Hogan, D., Delaney, C., Gill, M., Gallagher, L., Corvin, A.P., and Heron, E.A., Parental age, birth order and neurodevelopmental disorders, 2016 Journal Article, 2016 DOI

Thapar A, Martin J, Mick E, Arias Vásquez A, Langley K, Scherer S.W, Schachar R, Crosbie J, Williams N, Franke B, Elia J, Glessner J, Hakonarson H, Owen M.J, Faraone S.V, O'Donovan M.C, Holmans P, Freitag C.M, Gill M, Psych M.R.C, Anney R, Kent L, Middleton F, Zhang-James Y, Liu L, Meyer J, Nguyen T.T, Romanos J, Romanos M, Seitz C, Renner T.J, Walitza S, Warnke A, Palmason H, Buitelaar J, Franke B, Rommelse N, Hawi Z, Sergeant J, Steinhausen H.-C, Roeyers H, Biederman J, Zaharieva I, Lionel A.C, Marshall C.R, Todorov A, Smalley S.L, Loo S, Nelson S, Shtir C, Asherson P, Psych M.R.C, Kuntsi J, Reif A, Lesch K.-P, McGough J, Psychiatric gene discoveries shape evidence on ADHD's biology, Molecular Psychiatry, 21, (9), 2016, p1202 - 1207 Journal Article, 2016 URL DOI

Hawi Z, Cummins T.D.R, Tong J, Arcos-Burgos M, Zhao Q, Matthews N, Newman D.P, Johnson B, Vance A, Heussler H.S, Levy F, Easteal S, Wray N.R, Kenny E, Morris D, Kent L, Gill M, Bellgrove M.A, Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study, Molecular Psychiatry , 2016, p1-5 Journal Article, 2016 URL DOI

Mooney M.A, McWeeney S.K, Faraone S.V, Hinney A, Hebebrand J, Faraone S.V, Romanos M, Warnke A, Reif A, Walitza S, Roeyers H, Franke B, Buitelaar J.K, Lesch K.-P, Kent L, Vasquez A.A, Thapar A, Martin J, O†Donovan M.C, Owen M.J, Williams N, Holmans P, Langley K, Freitag C, Lambregts-Rommelse N, Anney R.J.L, Mulligan A, Rothenberger A, Steinhausen H.-C, Gill M, Asherson P, Nguyen T.T, Biederman J, Doyle A.E, Romanos J, Rivero O, Palmason H, Meyer J, Renner T.J, Albayrak à - Volckmar A.-L, Dempfle A, Cichon S, Hoffmann P, Cichon S, Hoffmann P, Nöthen M.M, Schreiber S, Möbus S, Wichmann H.-E, Herpertz-Dahlmann B, Sinzig J, Lehmkuhl G, Romanos M, Schimmelmann B.G, Nigg J.T, Wilmot B, Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach, American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 171, (6), 2016, p815 - 826 Journal Article, 2016 URL DOI

Roessner V, Banaschewski T, Becker A, Buse J, Wanderer S, Buitelaar J.K, Sergeant J.A, Sonuga-Barke E.J, Gill M, Manor I, Miranda A, Mulas F, Oades R.D, Roeyers H, Steinhausen H.-C, Faraone S.V, Asherson P, Rothenberger A, Familiality of Co-existing ADHD and Tic Disorders: Evidence from a Large Sibling Study., Frontiers in Psychology, 7, (JUL), 2016, p1060- Journal Article, 2016 DOI TARA - Full Text URL

McCarty H. Stanley J, Piech R, Skokauskas N, Mulligan A, Donohoe G, Mullins D, Kelly J, Johnson K, Fagan A, Gill M, Meaney J, Frodl T, Childhood-Diagnosed ADHD, Symptom Progression, and Reversal Learning in Adulthood, Journal of Attention Disorders, 2016 Journal Article, 2016 DOI

Tulio Guadalupe, Samuel R Mathias, GM Theo, Christopher D Whelan, Marcel P Zwiers, Yoshinari Abe, Lucija Abramovic, Ingrid Agartz, Ole A Andreassen, Alejandro Arias-Vásquez, Benjamin S Aribisala, Nicola J Armstrong, Volker Arolt, Eric Artiges, Rosa Ayesa-Arriola, Vatche G Baboyan, Tobias Banaschewski, Gareth Barker, Mark E Bastin, Bernhard T Baune, John Blangero, Arun LW Bokde, Premika SW Boedhoe, Anushree Bose, Silvia Brem, Henry Brodaty, Uli Bromberg, Samantha Brooks, Christian Büchel, Jan Buitelaar, Vince D Calhoun, Dara M Cannon, Anna Cattrell, Yuqi Cheng, Patricia J Conrod, Annette Conzelmann, Aiden Corvin, Benedicto Crespo-Facorro, Fabrice Crivello, Udo Dannlowski, Greig I De Zubicaray, Sonja MC De Zwarte, Ian J Deary, Sylvane Desrivières, Nhat Trung Doan, Gary Donohoe, Erlend S Dørum, Stefan Ehrlich, Thomas Espeseth, Guillén Fernández, Herta Flor, Jean-Paul Fouche, Vincent Frouin, Masaki Fukunaga, Jürgen Gallinat, Hugh Garavan, Michael Gill, Andrea Gonzalez Suarez, Penny Gowland, Hans J Grabe, Dominik Grotegerd, Oliver Gruber, Saskia Hagenaars, Ryota Hashimoto, Tobias U Hauser, Andreas Heinz, Derrek P Hibar, Pieter J Hoekstra, Martine Hoogman, Fleur M Howells, Hao Hu, Hilleke E Hulshoff Pol, Chaim Huyser, Bernd Ittermann, Neda Jahanshad, Erik G Jönsson, Sarah Jurk, Rene S Kahn, Sinead Kelly, Bernd Kraemer, Harald Kugel, Jun Soo Kwon, Herve Lemaitre, Klaus-Peter Lesch, Christine Lochner, Michelle Luciano, Andre F Marquand, Nicholas G Martin, Ignacio Martínez-Zalacaín, Jean-Luc Martinot, David Mataix-Cols, Karen Mather, Colm Mcdonald, Katie L Mcmahon, Sarah E Medland, José M Menchón, Derek W Morris, Omar Mothersill, Susana Munoz Maniega, Benson Mwangi, Takashi Nakamae, Tomohiro Nakao, Janardhanan C Narayanaswaamy, Frauke Nees, Jan E Nordvik, A Marten H Onnink, Nils Opel, Roel Ophoff, Marie-Laure Paillère Martinot, Dimitri Papadopoulos Orfanos, Paul Pauli, Tomá Paus, Luise Poustka, Janardhan Yc Reddy, Miguel E Renteria, Roberto Roiz-Santiáñez, Annerine Roos, Natalie A Royle, Perminder Sachdev, Pascual Sánchez-Juan, Lianne Schmaal, Gunter Schumann, Elena Shumskaya, Michael N Smolka, Jair C Soares, Carles Soriano-Mas, Dan J Stein, Lachlan T Strike, Roberto Toro, Jessica A Turner, Nathalie Tzourio-Mazoyer, Anne Uhlmann, Maria Valdés Hernández, Odile A Van den Heuvel, Dennis Van Der Meer, Neeltje EM Van Haren, Dick J Veltman, Ganesan Venkatasubramanian, Nora C Vetter, Daniella Vuletic, Susanne Walitza, Henrik Walter, Esther Walton, Zhen Wang, Joanna Wardlaw, Wei Wen, Lars T Westlye, Robert Whelan, Katharina Wittfeld, Thomas Wolfers, Human subcortical brain asymmetries in 15,847 people worldwide reveal effects of age and sex, Brain imaging and behavior, 2016, p1 - 18 Journal Article, 2016 TARA - Full Text DOI URL

Tropea D, Mortimer N, Bellini S, Molinos I, Sanfeliu A, Shovlin S, McAllister D, Gill M, Mitchell K, Corvin A, Expression of nuclear Methyl-CpG binding protein 2 (Mecp2) is dependent on neuronal stimulation and application of Insulin-like growth factor 1, Neuroscience Letters, 621, 2016, p111 - 116 Journal Article, 2016 URL DOI

Ferentinos P, Koukounari A, Power R, Rivera M, Uher R, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Ising M, Maier W, Mors O, Rietschel M, Preisig M, Binder EB, Aitchison KJ, Mendlewicz J, Souery D, Hauser J, Henigsberg N, Breen G, Craig IW, Farmer AE, Müller-Myhsok B, McGuffin P, Lewis CM, Familiality and SNP heritability of age at onset and episodicity in major depressive disorder., Psychological medicine, 2015, p1-11 Journal Article, 2015 DOI TARA - Full Text

Wetterling, F., McCarthy, H., Tozzi, L., Skokauskas, N., O'Doherty J. P., Mulligan, A., Meaney, J., Fagan, A. J., Gill, M., Frodl, T., Impaired Reward Processing in the Human Prefrontal Cortex Distinguishes Between Persistent and Remittent Attention Deficit Hyperactivity Disorder, HUMAN BRAIN MAPPING, 36, (1), 2015, p4648-4663 Journal Article, 2015 DOI URL

Hung CF, Breen G, Czamara D, Corre T, Wolf C, Kloiber S, Bergmann S, Craddock N, Gill M, Holsboer F, Jones L, Jones I, Korszun A, Kutalik Z, Lucae S, Maier W, Mors O, Owen MJ, Rice J, Rietschel M, Uher R, Vollenweider P, Waeber G, Craig IW, Farmer AE, Lewis CM, Müller-Myhsok B, Preisig M, McGuffin P, Rivera M, A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder., BMC medicine, 13, 2015, p86 Journal Article, 2015 TARA - Full Text DOI

Booij L, Szyf M, Carballedo A, Frey E.-M, Morris D, Dymov S, Vaisheva F, Ly V, Fahey C, Meaney J, Gill M, Frodl T, DNA methylation of the serotonin transporter gene in peripheral cells and stress-related changes in hippocampal volume: A study in depressed patients and healthy controls, PLoS ONE, 10, (3), 2015, p011906- Journal Article, 2015 URL DOI TARA - Full Text

Escott-Price V, Sims R, Bannister C, Harold D, Vronskaya M, Majounie E, Badarinarayan N, Morgan K, Passmore P, Holmes C, Powell J, Brayne C, Gill M, Mead S, Goate A, Cruchaga C, Lambert J.-C, Van Duijn C, Maier W, Ramirez A, Holmans P, Jones L, Hardy J, Seshadri S, Schellenberg G.D, Amouyel P, Williams J, Common polygenic variation enhances risk prediction for Alzheimer's disease, Brain, 138, (12), 2015, p3673 - 3684 Journal Article, 2015 DOI URL

Trampush J.W, Lencz T, Knowles E, Davies G, Guha S, Pe'er I, Liewald D.C, Starr J.M, Djurovic S, Melle I, Sundet K, Christoforou A, Reinvang I, Mukherjee S, Derosse P, Lundervold A, Steen V.M, John M, Espeseth T, Räikkönen K, Widen E, Palotie A, Eriksson J.G, Giegling I, Konte B, Ikeda M, Roussos P, Giakoumaki S, Burdick K.E, Payton A, Ollier W, Horan M, Scult M, Dickinson D, Straub R.E, Donohoe G, Morris D, Corvin A, Gill M, Hariri A, Weinberger D.R, Pendleton N, Iwata N, Darvasi A, Bitsios P, Rujescu D, Lahti J, Le Hellard S, Keller M.C, Andreassen O.A, Deary I.J, Glahn D.C, Malhotra A.K, Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment, American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 168, (5), 2015, p363 - 373 Journal Article, 2015 DOI URL

Murray C, Cosgrove D, Corvin A, Gill M, Morris D.W, Donohoe G, Greater number of older siblings is associated with decreased theory of mind ability in psychosis, Schizophrenia Research, 165, (2-3), 2015, p247 - 248 Journal Article, 2015 URL DOI

Merikangas AK, Segurado R, Heron EA, Anney RJ, Paterson AD, Cook EH, Pinto D, Scherer SW, Szatmari P, Gill M, Corvin AP, Gallagher L, The phenotypic manifestations of rare genic CNVs in autism spectrum disorder., Molecular psychiatry, 20, (11), 2015, 1366-72 Journal Article, 2015 DOI TARA - Full Text

Tong J, McKinley L.-A, Cummins T.D.R, Johnson B, Matthews N, Vance A, Heussler H, Gill M, Kent L, Bellgrove M.A, Hawi Z, Identification and functional characterisation of a novel dopamine beta hydroxylase gene variant associated with attention deficit hyperactivity disorder, World Journal of Biological Psychiatry, 16, (8), 2015, p610 - 618 Journal Article, 2015 URL DOI

Hong Lee, S., Byrne, E.M., Hultman, C.M., Kähler, A., Vinkhuyzen, A.A., Ripke, S., Andreassen, O.A., Frisell, T., Gusev, A., Hu, X., Karlsson, R., Mantzioris, V.X., McGrath, J.J., Mehta, D., Stahl, E.A., Zhao, Q., Kendler, K.S., Sullivan, P.F., Price, A.L., O'Donovan, M., Okada, Y., Mowry, B.J., Raychaudhuri, S., Wray, N.R., Agartz, I., Amin, F., Azevedo, M.H., Bass, N., Black, D.W., Blackwood, D.H.R., Bruggeman, R., Buccola, N.G., Choudhury, K., Cloninger, C.R., Corvin, A., Craddock, N., Daly, M.J., Datta, S., Donohoe, G.J., Duan, J., Dudbridge, F., Fanous, A., Freedman, R., Freimer, N.B., Friedl, M., Gill, M., Gurling, H., Haan, L.D., Hamshere, M.L., Hartmann, A.M., Holmans, P.A., Kahn, R.S., Keller, M.C., Kenny, E., Kirov, G.K., Krabbendam, L., Krasucki, R., Lawrence, J., Lencz, T., Levinson, D.F., Lieberman, J.A., Lin, D.-Y., Linszen, D.H., Magnusson, P.K.E., Maier, W., Malhotra, A.K., Mattheisen, M., Mattingsdal, M., McCarroll, S.A., Medeiros, H., Melle, I., Milanova, V., Myin-Germeys, I., Neale, B.M., Ophoff, R.A., Owen, M.J., Pimm, J., Purcell, S.M., Puri, V., Quested, D.J., Rossin, L., Ruderfer, D., Sanders, A.R., Shi, J., Sklar, P., St Clair, D., Scott Stroup, T., Van Os, J., Visscher, P.M., Wiersma, D., Zammit, S., Byerley, W., Cahn, W., Cantor, R.M., Cichon, S., Cormican, P., Curtis, D., Djurovic, S., Escott-Price, V., Gejman, P.V., Georgieva, L., Giegling, I., Hansen, T.F., Ingason, Andrés, Kim, Y., Konte, B., Lee, P.H., McIntosh, A., McQuillin, A., Morris, D.W., Nöthen, M.M., O'Dushlaine, C., Olincy, A., Olsen, L., Pato, C.N., Pato, M.T., Pickard, B.S., Posthuma, D., Rasmussen, H.B., Rietschel, M., Rujescu, D., Schulze, T.G., Silverman, J.M., Thirumalai, S., Werge, T., Louis Bridges, S., Choi, H.K., Coenen, M.J.H., De Vries, N., Dieud, P., Greenberg, J.D., Huizinga, T.W.J., Padyukov, L., Siminovitch, K.A., Tak, P.P., Worthington, J., De Jager, P.L., Denny, J.C., Gregersen, P.K., Klareskog, L., Mariette, X., Plenge, R.M., Van Laar, M., Van Riel, P., New data and an old puzzle: The negative association between schizophrenia and rheumatoid arthritis, International Journal of Epidemiology, 44, (5), 2015, p1706-1721 Journal Article, 2015 TARA - Full Text DOI

Martin J, Cooper M, Hamshere ML, Pocklington A, Scherer SW, Kent L, Gill M, Owen MJ, Williams N, O'Donovan MC, Thapar A, Holmans P, Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants., Journal of the American Academy of Child and Adolescent Psychiatry, 53, (7), 2014, p761-70.e26 Journal Article, 2014 TARA - Full Text DOI

Kenny EM, Cormican P, Furlong S, Heron E, Kenny G, Fahey C, Kelleher E, Ennis S, Tropea D, Anney R, Corvin AP, Donohoe G, Gallagher L, Gill M, Morris DW, Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders., Molecular psychiatry, 19, 2014, p872-879 Journal Article, 2014 TARA - Full Text DOI

Mullins N, Perroud N, Uher R, Butler AW, Cohen-Woods S, Rivera M, Malki K, Euesden J, Power RA, Tansey KE, Jones L, Jones I, Craddock N, Owen MJ, Korszun A, Gill M, Mors O, Preisig M, Maier W, Rietschel M, Rice JP, Müller-Myhsok B, Binder EB, Lucae S, Ising M, Craig IW, Farmer AE, McGuffin P, Breen G, Lewis CM, Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study., American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 165B, (5), 2014, p428-37 Journal Article, 2014 TARA - Full Text DOI

Webb B, Oord E, Knight J, Breen G, Brewster S, Tozzi F, Craddock N, Gill M, Korzun A, Maier W, Middleton L, Mors O, Owen M, Perry J, Preisig M, Rice J, Rietschel M, Jones L, Farmer A, Muglia P, McGuffin P., Genome-wide linkage analysis of waves 1 and 2 of the Depression Network Study , 2014 Journal Article, 2014

Gill M, Anney R, Mulligan A, Overlap between ADHD and Autism-Clinical and Genetic Evidence, Current Reviews in Psychiatry, 10, 2014, p143 - 155 Review Article, 2014 DOI

Fahey C, Byrne S, McLaughlin R, Kenna K, Shatunov A, Donohoe G, Gill M, Al-Chalabi A, Bradley DG, Hardiman O, Corvin AP, Morris DW, Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample., Neurobiology of aging, 35, (6), 2014, p1510.e1-1510.e5 Journal Article, 2014 DOI TARA - Full Text

Ferentinos, P., Rivera, M., Ising, M., (...), McGuffin, P., Lewis, C.M. , Investigating the genetic variation underlying episodicity in major depressive disorder: Suggestive evidence for a bipolar contribution, Journal of Affective Disorders, 155, (1), 2014, p81-89 Journal Article, 2014 TARA - Full Text DOI

Lencz T, Knowles E, Davies G, Guha S, Liewald DC, Starr JM, Djurovic S, Melle I, Sundet K, Christoforou A, Reinvang I, Mukherjee S, DeRosse P, Lundervold A, Steen VM, John M, Espeseth T, Räikkönen K, Widen E, Palotie A, Eriksson JG, Giegling I, Konte B, Ikeda M, Roussos P, Giakoumaki S, Burdick KE, Payton A, Ollier W, Horan M, Donohoe G, Morris D, Corvin A, Gill M, Pendleton N, Iwata N, Darvasi A, Bitsios P, Rujescu D, Lahti J, Hellard SL, Keller MC, Andreassen OA, Deary IJ, Glahn DC, Malhotra AK, Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT)., Molecular psychiatry, 19, (2), 2014, p168-74 Journal Article, 2014 DOI TARA - Full Text

Mothersill O, Morris DW, Kelly S, Rose EJ, Bokde A, Reilly R, Gill M, Corvin AP, Donohoe G, Altered medial prefrontal activity during dynamic face processing in schizophrenia spectrum patients, Schizophrenia research, 157, 2014, p225 - 230 Journal Article, 2014 DOI

Rose EJ, Morris DW, Fahey C, Cannon D, McDonald C, Scanlon C, Kelly S, Gill M, Corvin A, Donohoe G., The miR-137 schizophrenia susceptibility variant rs1625579 does not predict variability in brain volume in a sample of schizophrenic patients and healthy individuals., Am J Med Genet B Neuropsychiatr Genet., 26, 2014, p1209-17 Journal Article, 2014 TARA - Full Text DOI

Merikangas AK, Segurado R, Heron EA, Anney RJ, Paterson AD, Cook EH, Pinto D, Scherer SW, Szatmari P, Gill M, Corvin AP, Gallagher L., The phenotypic manifestations of rare genic CNVs in autism spectrum disorder., Molecular Psychiatry, 2014, p1-7 Journal Article, 2014 DOI TARA - Full Text

Schizophrenia Working Group of the Psychiatric Genomics Consortium , Biological insights from 108 schizophrenia-associated genetic loci., Nature, 511, (7510), 2014, p421-7 Journal Article, 2014 TARA - Full Text DOI

Morris DW, Pearson RD, Cormican P, Kenny EM, O'Dushlaine CT, Perreault LP, Giannoulatou E, Tropea D, Maher BS, Wormley B, Kelleher E, Fahey C, Molinos I, Bellini S, Pirinen M, Strange A, Freeman C, Thiselton DL, Elves RL, Regan R, Ennis S, Dinan TG, McDonald C, Murphy KC, O'Callaghan E, Waddington JL, Walsh D, O'Donovan M, Grozeva D, Craddock N, Stone J, Scolnick E, Purcell S, Sklar P, Coe B, Eichler EE, Ophoff R, Buizer J, Szatkiewicz J, Hultman C, Sullivan P, Gurling H, McQuillin A, St Clair D, Rees E, Kirov G, Walters J, Blackwood D, Johnstone M, Donohoe G, O'Neill FA, Kendler KS, Gill M, Riley BP, Spencer CC, Corvin A, An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis., Human molecular genetics, 23, (12), 2014, p3316-26 Journal Article, 2014 DOI TARA - Full Text

Hung CF, Rivera M, Craddock N, Owen MJ, Gill M, Korszun A, Maier W, Mors O, Preisig M, Rice JP, Rietschel M, Jones L, Middleton L, Aitchison KJ, Davis OS, Breen G, Lewis C, Farmer A, McGuffin P, Relationship between obesity and the risk of clinically significant depression: Mendelian randomisation study., The British journal of psychiatry : the journal of mental science, 205, (1), 2014, p24-8 Journal Article, 2014 TARA - Full Text DOI

Proitsi P, Lupton MK, Velayudhan L, Newhouse S, Fogh I, Tsolaki M, Daniilidou M, Pritchard M, Kloszewska I, Soininen H, Mecocci P, Vellas B, Williams J, Stewart R, Sham P, Lovestone S, Powell JF, Genetic predisposition to increased blood cholesterol and triglyceride lipid levels and risk of Alzheimer disease: a mendelian randomization analysis., PLoS medicine, 11, (9), 2014, pe1001713 Journal Article, 2014 DOI TARA - Full Text

O'Donoghue T, Morris DW, Fahey C, Da Costa A, Moore S, Cummings E, Leicht G, Karch S, Hoerold D, Tropea D, Foxe JJ, Gill M, Corvin A, Donohoe G, Effects of ZNF804A on auditory P300 response in schizophrenia., Translational psychiatry, 4, 2014, pe345 Journal Article, 2014 DOI TARA - Full Text

Rose EJ, Hargreaves A, Morris D, Fahey C, Tropea D, Cummings E, Caltagirone C, Bossù P, Chiapponi C, Piras F, Spalletta G, Gill M, Corvin A, Donohoe G, Effects of a novel schizophrenia risk variant rs7914558 at CNNM2 on brain structure and attributional style., The British journal of psychiatry : the journal of mental science, 204, (2), 2014, p115-121 Journal Article, 2014 TARA - Full Text DOI

Escott-Price V, Bellenguez C, Wang LS, Choi SH, Harold D, Jones L, Holmans P, Gerrish A, Vedernikov A, Richards A, DeStefano AL, Lambert JC, Ibrahim-Verbaas CA, Naj AC, Sims R, Jun G, Bis JC, Beecham GW, Grenier-Boley B, Russo G, Thornton-Wells TA, Denning N, Smith AV, Chouraki V, Thomas C, Ikram MA, Zelenika D, Vardarajan BN, Kamatani Y, Lin CF, Schmidt H, Kunkle B, Dunstan ML, Vronskaya M, Johnson AD, Ruiz A, Bihoreau MT, Reitz C, Pasquier F, Hollingworth P, Hanon O, Fitzpatrick AL, Buxbaum JD, Campion D, Crane PK, Baldwin C, Becker T, Gudnason V, Cruchaga C, Craig D, Amin N, Berr C, Lopez OL, De Jager PL, Deramecourt V, Johnston JA, Evans D, Lovestone S, Letenneur L, Hernández I, Rubinsztein DC, Eiriksdottir G, Sleegers K, Goate AM, Fiévet N, Huentelman MJ, Gill M, Brown K, Kamboh MI, Keller L, Barberger-Gateau P, McGuinness B, Larson EB, Myers AJ, Dufouil C, Todd S, Wallon D, Love S, Rogaeva E, Gallacher J, George-Hyslop PS, Clarimon J, Lleo A, Bayer A, Tsuang DW, Yu L, Tsolaki M, Bossù P, Spalletta G, Proitsi P, Collinge J, Sorbi S, Garcia FS, Fox NC, Hardy J, Naranjo MC, Bosco P, Clarke R, Brayne C, Galimberti D, Scarpini E, Bonuccelli U, Mancuso M, Siciliano G, Moebus S, Mecocci P, Zompo MD, Maier W, Hampel H, Pilotto A, Frank-García A, Panza F, Solfrizzi V, Caffarra P, Nacmias B, Perry W, Mayhaus M, Lannfelt L, Hakonarson H, Pichler S, Carrasquillo MM, Ingelsson M, Beekly D, Alvarez V, Zou F, Valladares O, Younkin SG, Coto E, Hamilton-Nelson KL, Gu W, Razquin C, Pastor P, Mateo I, Owen MJ, Faber KM, Jonsson PV, Combarros O, O'Donovan MC, Cantwell LB, Soininen H, Blacker D, Mead S, Mosley TH, Bennett DA, Harris TB, Fratiglioni L, Holmes C, de Bruijn RF, Passmore P, Montine TJ, Bettens K, Rotter JI, Brice A, Morgan K, Foroud TM, Kukull WA, Hannequin D, Powell JF, Nalls MA, Ritchie K, Lunetta KL, Kauwe JS, Boerwinkle E, Riemenschneider M, Boada M, Hiltunen M, Martin ER, Schmidt R, Rujescu D, Dartigues JF, Mayeux R, Tzourio C, Hofman A, Nöthen MM, Graff C, Psaty BM, Haines JL, Lathrop M, Pericak-Vance MA, Launer LJ, Van Broeckhoven C, Farrer LA, van Duijn CM, Ramirez A, Seshadri S, Schellenberg GD, Amouyel P, Williams J, Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease., PloS one, 9, (6), 2014, pe94661 Journal Article, 2014 DOI TARA - Full Text

Kelly,Sinéad S., Morris,Derek W. D.W., Mothersill,Omar O., Rose,Emma Jane E.J., Fahey,Ciara A. C.A., O'Brien,Carol H. C.H., O'Hanlon,Erik E., Gill,Michael M., Corvin,Aiden P. A.P., Donohoe,Gary J. G.J., Genome-wide schizophrenia variant at MIR137 does not impact white matter microstructure in healthy participants, Neuroscience Letters, 574, 2014, p6-10 Journal Article, 2014 TARA - Full Text DOI

Frodl T, Carballedo A, Frey EM, O'Keane V, Skokauskas N, Morris D, Gill M, Hughes MM, Harkin A, Connor T, Expression of glucocorticoid inducible genes is associated with reductions in cornu ammonis and dentate gyrus volumes in patients with major depressive disorder., Development and psychopathology, 26, (4 Pt 2), 2014, p1209-17 Journal Article, 2014 TARA - Full Text DOI

Gentil G P, Gill M, Murray R, Vallada H, Caracteristicas Clinicas da Esquizofrenia Familiar: estudo em uma populacao brasileira., 2014 Journal Article, 2014

Rees E, Walters JT, Chambert KD, O'Dushlaine C, Szatkiewicz J, Richards AL, Georgieva L, Mahoney-Davies G, Legge SE, Moran JL, Genovese G, Levinson D, Morris DW, Cormican P, Kendler KS, O'Neill FA, Riley B, Gill M, Corvin A, Sklar P, Hultman C, Pato C, Pato M, Sullivan PF, Gejman PV, McCarroll SA, O'Donovan MC, Owen MJ, Kirov G, CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1., Human molecular genetics, 23, (6), 2014, 1669-1676 Journal Article, 2014 DOI TARA - Full Text

Rees E, Kirov G, Sanders A, Walters JT, Chambert KD, Shi J, Szatkiewicz J, O'Dushlaine C, Richards AL, Green EK, Jones I, Davies G, Legge SE, Moran JL, Pato C, Pato M, Genovese G, Levinson D, Duan J, Moy W, Göring HH, Morris D, Cormican P, Kendler KS, O'Neill FA, Riley B, Gill M, Corvin A, Craddock N, Sklar P, Hultman C, Sullivan PF, Gejman PV, McCarroll SA, O'Donovan MC, Owen MJ, Evidence that duplications of 22q11.2 protect against schizophrenia., Molecular psychiatry, 19, (1), 2014, p37-40 Journal Article, 2014 DOI TARA - Full Text

Nicodemus KK, Hargreaves A, Morris D, Anney R, Gill M, Corvin A, Donohoe G, Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway., JAMA psychiatry, 71, (7), 2014, p778-85 Journal Article, 2014 DOI TARA - Full Text

De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, Biscaldi M, Bolton PF, Brownfeld JM, Cai J, Campbell NG, Carracedo A, Chahrour MH, Chiocchetti AG, Coon H, Crawford EL, Curran SR, Dawson G, Duketis E, Fernandez BA, Gallagher L, Geller E, Guter SJ, Hill RS, Ionita-Laza J, Jimenz Gonzalez P, Kilpinen H, Klauck SM, Kolevzon A, Lee I, Lei I, Lei J, Lehtimäki T, Lin CF, Ma'ayan A, Marshall CR, McInnes AL, Neale B, Owen MJ, Ozaki N, Parellada M, Parr JR, Purcell S, Puura K, Rajagopalan D, Rehnström K, Reichenberg A, Sabo A, Sachse M, Sanders SJ, Schafer C, Schulte-Rüther M, Skuse D, Stevens C, Szatmari P, Tammimies K, Valladares O, Voran A, Li-San W, Weiss LA, Willsey AJ, Yu TW, Yuen RK, Cook EH, Freitag CM, Gill M, Hultman CM, Lehner T, Palotie A, Schellenberg GD, Sklar P, State MW, Sutcliffe JS, Walsh CA, Scherer SW, Zwick ME, Barett JC, Cutler DJ, Roeder K, Devlin B, Daly MJ, Buxbaum JD, Synaptic, transcriptional and chromatin genes disrupted in autism., Nature, 515, (7526), 2014, p209-15 Journal Article, 2014 TARA - Full Text DOI

Mothersill O, Morris DW, Kelly S, Rose EJ, Fahey C, O'Brien C, Lyne R, Reilly R, Gill M, Corvin AP, Donohoe G, Effects of MIR137 on fronto-amygdala functional connectivity., NeuroImage, 90, 2014, p189-95 Journal Article, 2014 TARA - Full Text DOI

Li, M., Luo, X.-J., Rietschel, M., (...), Wright, M.J., Su, B., Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility, Molecular Psychiatry, 19, (4), 2014, p452-461 Journal Article, 2014 DOI TARA - Full Text

McCarthy, S.E., Gillis, J., Kramer, M., (...), McCombie, W.R., Corvin, A. , De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability, Molecular Psychiatry, 19, 2014, p652-658 Journal Article, 2014 DOI TARA - Full Text

Pinto, D., Delaby, E., Merico, D., (...), Betancur, C., Scherer, StephenW. , Convergence of genes and cellular pathways dysregulated in autism spectrum disorders, American Journal of Human Genetics, 94, (5), 2014, p677-694 Journal Article, 2014 DOI TARA - Full Text

Heron, E.A., Cormican, P., Donohoe, G., O'Neill, F.A., Kendler, K.S., Riley, B.P., Gill, M., Corvin, A.P., Morris, D.W., No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset, Schizophrenia Research, 154, (1-3), 2014, p79-82 Journal Article, 2014 DOI TARA - Full Text

Frodl T, Skokauskas N, Frey EM, Morris D, Gill M, Carballedo A, BDNF Val66Met genotype interacts with childhood adversity and influences the formation of hippocampal subfields., Human brain mapping, 35, (12), 2014, p5776-83 Journal Article, 2014 TARA - Full Text DOI

Hadley, D., Wu, Z.-L., Kao, C., (...), Betancur, C., Scherer, S.W. , The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism, Nature Communications, 5, 2014, p4074- Journal Article, 2014 DOI

Guha S, Rees E, Darvasi A, Ivanov D, Ikeda M, Bergen SE, Magnusson PK, Cormican P, Morris D, Gill M, Cichon S, Rosenfeld JA, Lee A, Gregersen PK, Kane JM, Malhotra AK, Rietschel M, Nöthen MM, Degenhardt F, Priebe L, Breuer R, Strohmaier J, Psych D, Ruderfer DM, Moran JL, Chambert KD, Sanders AR, Shi J, Kendler K, Riley B, O'Neill T, Walsh D, Malhotra D, Corvin A, Purcell S, Sklar P, Iwata N, Hultman CM, Sullivan PF, Sebat J, McCarthy S, Gejman PV, Levinson DF, Owen MJ, O'Donovan MC, Lencz T, Kirov G, Implication of a Rare Deletion at Distal 16p11.2 in Schizophrenia., JAMA Psychiatry, 70, (3), 2013, p253-60 Journal Article, 2013 DOI TARA - Full Text

Schosser, A., Butler, A.W., Uher, R., Ng, M.Y., Cohen-Woods, S., Craddock, N., Owen, M.J., Korszun, A., Gill, M., Rice, J., Hauser, J., Henigsberg, N., Maier, W., Mors, O., Placentino, A., Rietschel, M., Souery, D., Preisig, M., Craig, I.W., Farmer, A.E., Lewis, C.M., McGuffin, P., Genome-wide association study of co-occurring anxiety in major depression, World Journal of Biological Psychiatry, 14, (8), 2013, p611-621 Journal Article, 2013 DOI

Hargreaves, A., Anney, R., O'Dushlaine, C.a, Nicodemus, K.K.a, Gill, M., Corvin, A., Morris, D., Donohoe, G, The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis, Psychological Medicine, 44, (10), 2013, p2177-2187 Journal Article, 2013 TARA - Full Text DOI

Cummings E, Donohoe G, Hargreaves A, Moore S, Fahey C, Dinan TG, McDonald C, O'Callaghan E, O'Neill FA, Waddington JL, Murphy KC, Morris DW, Gill M, Corvin A. , Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137., Neuroscience Letters, 532, 2013, p33-38 Journal Article, 2013 DOI

Hawi Z, Matthews N, Wagner J, Wallace RH, Butler TJ, Vance A, Kent L, Gill M, Bellgrove MA, DNA variation in the SNAP25 gene confers risk to ADHD and is associated with reduced expression in prefrontal cortex., PloS one, 8, (4), 2013, pe60274 Journal Article, 2013 TARA - Full Text DOI

Ripke S, O'Dushlaine C, Chambert K, Moran JL, Kähler AK, Akterin S, Bergen SE, Collins AL, Crowley JJ, Fromer M, Kim Y, Lee SH, Magnusson PK, Sanchez N, Stahl EA, Williams S, Wray NR, Xia K, Bettella F, Borglum AD, Bulik-Sullivan BK, Cormican P, Craddock N, de Leeuw C, Durmishi N, Gill M, Golimbet V, Hamshere ML, Holmans P, Hougaard DM, Kendler KS, Lin K, Morris DW, Mors O, Mortensen PB, Neale BM, O'Neill FA, Owen MJ, Milovancevic MP, Posthuma D, Powell J, Richards AL, Riley BP, Ruderfer D, Rujescu D, Sigurdsson E, Silagadze T, Smit AB, Stefansson H, Steinberg S, Suvisaari J, Tosato S, Verhage M, Walters JT, Levinson DF, Gejman PV, Kendler KS, Laurent C, Mowry BJ, O'Donovan MC, Owen MJ, Pulver AE, Riley BP, Schwab SG, Wildenauer DB, Dudbridge F, Holmans P, Shi J, Albus M, Alexander M, Campion D, Cohen D, Dikeos D, Duan J, Eichhammer P, Godard S, Hansen M, Lerer FB, Liang KY, Maier W, Mallet J, Nertney DA, Nestadt G, Norton N, O'Neill FA, Papadimitriou GN, Ribble R, Sanders AR, Silverman JM, Walsh D, Williams NM, Wormley B, Arranz MJ, Bakker S, Bender S, Bramon E, Collier D, Crespo-Facorro B, Hall J, Iyegbe C, Jablensky A, Kahn RS, Kalaydjieva L, Lawrie S, Lewis CM, Lin K, Linszen DH, Mata I, McIntosh A, Murray RM, Ophoff RA, Powell J, Rujescu D, Van Os J, Walshe M, Weisbrod M, Wiersma D, Donnelly P, Barroso I, Blackwell JM, Bramon E, Brown MA, Casas JP, Corvin AP, Deloukas P, Duncanson A, Jankowski J, Markus HS, Mathew CG, Palmer CN, Plomin R, Rautanen A, Sawcer SJ, Trembath RC, Viswanathan AC, Wood NW, Spencer CC, Band G, Bellenguez C, Freeman C, Hellenthal G, Giannoulatou E, Pirinen M, Pearson RD, Strange A, Su Z, Vukcevic D, Donnelly P, Langford C, Hunt SE, Edkins S, Gwilliam R, Blackburn H, Bumpstead SJ, Dronov S, Gillman M, Gray E, Hammond N, Jayakumar A, McCann OT, Liddle J, Potter SC, Ravindrarajah R, Ricketts M, Tashakkori-Ghanbaria A, Waller MJ, Weston P, Widaa S, Whittaker P, Barroso I, Deloukas P, Mathew CG, Blackwell JM, Brown MA, Corvin AP, McCarthy MI, Spencer CC, Bramon E, Corvin AP, O'Donovan MC, Stefansson K, Scolnick E, Purcell S, McCarroll SA, Sklar P, Hultman CM, Sullivan PF, Genome-wide association analysis identifies 13 new risk loci for schizophrenia., Nature genetics, 45, (10), 2013, p1150-9 Journal Article, 2013 TARA - Full Text DOI

Johnson KA, Barry E, Lambert D, Fitzgerald M, McNicholas F, Kirley A, Gill M, Bellgrove MA, Hawi Z, Methylphenidate side effect profile is influenced by genetic variation in the attention-deficit/hyperactivity disorder-associated CES1 gene., Journal of child and adolescent psychopharmacology, 23, (10), 2013, p655 - 665 Journal Article, 2013 URL URL DOI

Power RA, Cohen-Woods S, Ng MY, Butler AW, Craddock N, Korszun A, Jones L, Jones I, Gill M, Rice JP, Maier W, Zobel A, Mors O, Placentino A, Rietschel M, Aitchison KJ, Tozzi F, Muglia P, Breen G, Farmer AE, McGuffin P, Lewis CM, Uher R, Genome-wide association analysis accounting for environmental factors through propensity-score matching: application to stressful live events in major depressive disorder., American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 162B, (6), 2013, p521-9 Journal Article, 2013 DOI

Paton K, Hammond P, Barry E, Fitzgerald M, McNicholas F, Kirley A, Robertson IH, Bellgrove MA, Gill M, & Johnson KA., Methylphenidate improves some but not all measures of ATTENTION, as measured by the TEA-Ch in medication-naïve children with ADHD, Child Neuropsychology, 20, (3), 2013, p303 - 318 Journal Article, 2013 DOI TARA - Full Text URL URL

Hawi Z, Matthews N, Barry E, Kirley A, Wagner J, Wallace RH, Heussler HS, Vance A, Gill M, Bellgrove MA., A high density linkage disequilibrium mapping in 14 noradrenergic genes: evidence of association between SLC6A2, ADRA1B and ADHD., Psychopharmacology (Berl), 225, (4), 2013, p895-902 Journal Article, 2013 DOI

Vorstman JA, Anney RJ, Derks EM, Gallagher L, Gill M, de Jonge MV, van Engeland H, Kahn RS, Ophoff RA, No evidence that common genetic risk variation is shared between schizophrenia and autism., American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 162, (1), 2013, p55-60 Journal Article, 2013 DOI

Cummings E, Donohoe G, Hargreaves A, Moore S, Fahey C, Dinan TG, McDonald C, O'Callaghan E, O'Neill FA, Waddington JL, Murphy KC, Morris DW, Gill M, Corvin A, Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137., Neuroscience Letters, 532, 2013, p33-38 Journal Article, 2013 DOI

Rucker JJ, Breen G, Pinto D, Pedroso I, Lewis CM, Cohen-Woods S, Uher R, Schosser A, Rivera M, Aitchison KJ, Craddock N, Owen MJ, Jones L, Jones I, Korszun A, Muglia P, Barnes MR, Preisig M, Mors O, Gill M, Maier W, Rice J, Rietschel M, Holsboer F, Farmer AE, Craig IW, Scherer SW, McGuffin P., Genome-wide association analysis of copy number variation in recurrent depressive disorder., Molecular Psychiatry, 18, (2), 2013, p183-189 Journal Article, 2013 DOI

Kuntsi J, Frazier-Wood AC, Banaschewski T, Gill M, Miranda A, Oades RD, Roeyers H, Rothenberger A, Steinhausen HC, van der Meere JJ, Faraone SV, Asherson P, Rijsdijk F. , Genetic analysis of reaction time variability: room for improvement?, Psychological Medicine, 43, (6), 2013, p1323-1333 Journal Article, 2013 DOI

Donohoe G, Walters J, Hargreaves A, Rose EJ, Morris DW, Fahey C, Bellini S, Cummins E, Giegling I, Hartmann AM, Möller HJ, Muglia P, Owen MJ, Gill M, O'Donovan MC, Tropea D, Rujescu D, Corvin A, Neuropsychological Effects Of The CSMD1 Genome-Wide Associated Schizophrenia Risk Variant rs10503253, Genes Brain Behaviour, 12, (2), 2013, p203-9 Journal Article, 2013 DOI

Robertson DA, Hargreaves A, Kelleher EB, Morris D, Gill M, Corvin A, Donohoe G, Social dysfunction in schizophrenia: An investigation of the GAF scale's sensitivity to deficits in social cognition., Schizophrenia research, 146, (1-3), 2013, p363-365 Journal Article, 2013 TARA - Full Text DOI

Hamshere ML, Walters JT, Smith R, Richards AL, Green E, Grozeva D, Jones I, Forty L. Jones L. Gordon-Smith K, Riley B, O'Neill T, Kendler KS, Sklar P, Purcell S, Kranz J, The Schizophrenia Psychiatric Genome-wide Association Study Consortium (PGC), Well Trust Case Control Consortium +(WTCCC+), Welcome Trust Case Control Consortium 2 9WTCCC2), Morris D, Gill M, Holmans P, Craddock N, Corvin A, Owen MJ, O'Donovan MC, Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC. , Molecular Psychiatry, 18, (2), 2013, p708-12 Journal Article, 2013 DOI

Hamshere, ML, Stergiakouli, E, Langley, K, Martin, J, Holmans, P, Kent, L, Owen, MJ, Gill, M, Thapar, A, O'Donovan, M, Craddock, N, Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia, BRITISH JOURNAL OF PSYCHIATRY, 203, (2), 2013, p107-111 Journal Article, 2013 DOI

Carballedo A, Morris D, Zill P, Fahey C, Reinhold E, Meisenzahl E, Bondy B, Gill M, Möller HJ, Frodl T., Brain-derived neurotrophic factor Val66Met polymorphism and early life adversity affect hippocampal volume, Am J. Med Genet B Neuropsychiatric Genetics, 162B, (2), 2013, p183-90 Journal Article, 2013 DOI

Walters JT, Rujescu D, Franke B, Giegling I, Vásquez AA, Hargreaves A, Russo G, Morris DW, Hoogman M, Da Costa A, Moskvina V, Fernández G, Gill M, Corvin A, O'Donovan MC, Donohoe G, Owen MJ, The role of the major histocompatibility complex region in cognition and brain structure: a schizophrenia GWAS follow-up., The American journal of psychiatry, 170, (8), 2013, p877-85 Journal Article, 2013 DOI

McCarthy H, Skokauskas N, Mulligan A, Donohoe G, Mullins D, Kelly J, Johnson K, Fagan A, Gill M, Meaney J, Frodl T, Attention network hypoconnectivity with default and affective network hyperconnectivity in adults diagnosed with attention-deficit/hyperactivity disorder in childhood., JAMA psychiatry, 70, (12), 2013, p1329-37 Journal Article, 2013 DOI

Quinn EM, Cormican P, Kenny EM, Hill M, Anney R, Gill M, Corvin AP, Morris DW, Development of Strategies for SNP Detection in RNA-Seq Data: Application to Lymphoblastoid Cell Lines and Evaluation Using 1000 Genomes Data., PloS one, 8, (3), 2013, pe58815 Journal Article, 2013 TARA - Full Text DOI

Mota, N.R., Bau, C.H.D., Banaschewski, T., (...), Faraone, S.V., Asherson, P. , Association between DRD2/DRD4 interaction and conduct disorder: a potential developmental pathway to alcohol dependence., American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 162, (2), 2013, p546-549 Journal Article, 2013 DOI

Donohoe G, Walters J, Hargreaves A, Rose EJ, Morris DW, Fahey C, Bellini S, Cummins E, Giegling I, Hartmann AM, Möller HJ, Muglia P, Owen MJ, Gill M, O'Donovan MC, Tropea D, Rujescu D, Corvin A, Neuropsychological Effects Of The CSMD1 Genome-Wide Associated Schizophrenia Risk Variant rs10503253., Genes, Brain, and Behavior, 12, (12), 2013, p203- 209 Journal Article, 2013 DOI

Bralten, J., Franke, B., Waldman, I., Rommelse, N., Hartman, C., Asherson, P., Banaschewski, T., Ebstein, R.P., Gill, M., Miranda, A., Oades, R.D., Roeyers, H., Rothenberger, A., Sergeant, J.A., Oosterlaan, J., Sonuga-Barke, E., Steinhausen, H.-C., Faraone, S.V., Buitelaar, J.K., Arias-Vásquez, A., Candidate genetic pathways for attention-deficit/hyperactivity disorder (ADHD) show association to hyperactive/impulsive symptoms in children with ADHD, Journal of the American Academy of Child and Adolescent Psychiatry, 52, (11), 2013, p1204-1212.e1 Journal Article, 2013 DOI

Lee, S.H., Ripke, S., Neale, B.M., (...), Kendler, K.S., Wray, N.R., Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs, Nature Genetics , 45, (9), 2013, p984-994 Journal Article, 2013 TARA - Full Text URL

The Genetic Architecture of Autism and Related Conditions in, editor(s)M Fitzgerald , Recent Advances in Autism Spectrum Disorders - Volume I, InTech, 2013, pp299 - 320, [Gil M, Kenny G, Anney R] Book Chapter, 2013 URL DOI

Corvin AP, Molinos I, Little G, Donohoe G, Gill M, Morris DW, Tropea D, Insulin-like growth factor 1 (IGF1) and its active peptide (1-3)IGF1 enhance the expression of synaptic markers in neuronal circuits through different cellular mechanisms., Neuroscience letters, 520, (1), 2012, p51-56 Journal Article, 2012 DOI

Derks EM, Vorstman JA, Ripke S, Kahn RS, Schizophrenia Psychiatric Genomic Consortium, Ophoff RA, Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis., PloS one, 7, (6), 2012, pe37852 Journal Article, 2012 TARA - Full Text DOI

Donohoe G, Duignan A, Hargreaves A, Morris DW, Rose E, Robertson D, Cummings E, Moore S, Gill M, Corvin A, Social cognition in bipolar disorder versus schizophrenia: comparability in mental state decoding deficits., Bipolar Disorders, 14, (7), 2012, p743-748 Journal Article, 2012 DOI

Stein JL, Medland SE, Vasquez AA, Hibar DP, Senstad RE, Winkler AM, Toro R, Appel K, Bartecek R, Bergmann Ø, Bernard M, Brown AA, Cannon DM, Chakravarty MM, Christoforou A, Domin M, Grimm O, Hollinshead M, Holmes AJ, Homuth G, Hottenga JJ, Langan C, Lopez LM, Hansell NK, Hwang KS, Kim S, Laje G, Lee PH, Liu X, Loth E, Lourdusamy A, Mattingsdal M, Mohnke S, Maniega SM, Nho K, Nugent AC, O'Brien C, Papmeyer M, Pütz B, Ramasamy A, Rasmussen J, Rijpkema M, Risacher SL, Roddey JC, Rose EJ, Ryten M, Shen L, Sprooten E, Strengman E, Teumer A, Trabzuni D, Turner J, van Eijk K, van Erp TG, van Tol MJ, Wittfeld K, Wolf C, Woudstra S, Aleman A, Alhusaini S, Almasy L, Binder EB, Brohawn DG, Cantor RM, Carless MA, Corvin A, Czisch M, Curran JE, Davies G, de Almeida MA, Delanty N, Depondt C, Duggirala R, Dyer TD, Erk S, Fagerness J, Fox PT, Freimer NB, Gill M, Göring HH, Hagler DJ, Hoehn D, Holsboer F, Hoogman M, Hosten N, Jahanshad N, Johnson MP, Kasperaviciute D, Kent JW, Kochunov P, Lancaster JL, Lawrie SM, Liewald DC, Mandl R, Matarin M, Mattheisen M, Meisenzahl E, Melle I, Moses EK, Mühleisen TW, Nauck M, Nöthen MM, Olvera RL, Pandolfo M, Pike GB, Puls R, Reinvang I, Rentería ME, Rietschel M, Roffman JL, Royle NA, Rujescu D, Savitz J, Schnack HG, Schnell K, Seiferth N, Smith C, Steen VM, Valdés Hernández MC, Van den Heuvel M, van der Wee NJ, Van Haren NE, Veltman JA, Völzke H, Walker R, Westlye LT, Whelan CD, Agartz I, Boomsma DI, Cavalleri GL, Dale AM, Djurovic S, Drevets WC, Hagoort P, Hall J, Heinz A, Jack CR, Foroud TM, Le Hellard S, Macciardi F, Montgomery GW, Poline JB, Porteous DJ, Sisodiya SM, Starr JM, Sussmann J, Toga AW, Veltman DJ, Walter H, Weiner MW, Bis JC, Ikram MA, Smith AV, Gudnason V, Tzourio C, Vernooij MW, Launer LJ, DeCarli C, Seshadri S, Andreassen OA, Apostolova LG, Bastin ME, Blangero J, Brunner HG, Buckner RL, Cichon S, Coppola G, de Zubicaray GI, Deary IJ, Donohoe G, de Geus EJ, Espeseth T, Fernández G, Glahn DC, Grabe HJ, Hardy J, Hulshoff Pol HE, Jenkinson M, Kahn RS, McDonald C, McIntosh AM, McMahon FJ, McMahon KL, Meyer-Lindenberg A, Morris DW, Müller-Myhsok B, Nichols TE, Ophoff RA, Paus T, Pausova Z, Penninx BW, Potkin SG, Sämann PG, Saykin AJ, Schumann G, Smoller JW, Wardlaw JM, Weale ME, Martin NG, Franke B, Wright MJ, Thompson PM, Identification of common variants associated with human hippocampal and intracranial volumes., Nature genetics, 44, (5), 2012, p552-561 Journal Article, 2012 TARA - Full Text DOI

Bermingham R, Carballedo A, Lisiecka D, Fagan A, Morris D, Fahey C, Donohoe G, Meaney J, Gill M, Frodl T, Effect of genetic variant in BICCI on functional and structural brain changes in depression, Neuropsychopharmacology, 37, (13), 2012, p2855-2862 Journal Article, 2012 DOI TARA - Full Text

Skokauskas N, Doody B, Gallagher L, Lawlor M, Moran T, Fitzgerald M, Gill M, Problem-based learning in child and adolescent psychiatry at Trinity College, Dublin, Ireland., Academic psychiatry : the journal of the American Association of Directors of Psychiatric Residency Training and the Association for Academic Psychiatry, 36, (4), 2012, p335-9 Journal Article, 2012 DOI

Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, Corsello C, Crawford EL, de Jonge M, Delorme R, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Gilbert J, Gillberg C, Glessner JT, Green A, Green J, Guter SJ, Heron EA, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Jacob S, Kenny GP, Kim C, Kolevzon A, Kustanovich V, Lajonchere CM, Lamb JA, Law-Smith M, Leboyer M, Le Couteur A, Leventhal BL, Liu XQ, Lombard F, Lord C, Lotspeich L, Lund SC, Magalhaes TR, Mantoulan C, McDougle CJ, Melhem NM, Merikangas A, Minshew NJ, Mirza GK, Munson J, Noakes C, Nygren G, Papanikolaou K, Pagnamenta AT, Parrini B, Paton T, Pickles A, Posey DJ, Poustka F, Ragoussis J, Regan R, Roberts W, Roeder K, Roge B, Rutter ML, Schlitt S, Shah N, Sheffield VC, Soorya L, Sousa I, Stoppioni V, Sykes N, Tancredi R, Thompson AP, Thomson S, Tryfon A, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Vorstman JA, Wallace S, Wing K, Wittemeyer K, Wood S, Zurawiecki D, Zwaigenbaum L, Bailey AJ, Battaglia A, Cantor RM, Coon H, Cuccaro ML, Dawson G, Ennis S, Freitag CM, Geschwind DH, Haines JL, Klauck SM, McMahon WM, Maestrini E, Miller J, Monaco AP, Nelson SF, Nurnberger JI, Oliveira G, Parr JR, Pericak-Vance MA, Piven J, Schellenberg GD, Scherer SW, Vicente AM, Wassink TH, Wijsman EM, Betancur C, Buxbaum JD, Cook EH, Gallagher L, Gill M, Hallmayer J, Paterson AD, Sutcliffe JS, Szatmari P, Vieland VJ, Hakonarson H, Devlin B, Individual common variants exert weak effects on the risk for autism spectrum disorderspi., Human molecular genetics, 21, (21), 2012, p4781-92 Journal Article, 2012 TARA - Full Text DOI

O'Donoghue T, Morris DW, Fahey C, Costa AD, Foxe JJ, Hoerold D, Tropea D, Gill M, Corvin A, Donohoe G, A NOS1 variant implicated in cognitive performance influences evoked neural responses during a hight density EEG study of early visual perception. , Human Brain Mapping, 33, (5), 2012, p1202-1211 Journal Article, 2012 TARA - Full Text DOI

Hollingworth P, Sweet R, Sims R, Harold D, Russo G, Abraham R, Stretton A, Jones N, Gerrish A, Chapman J, Ivanov D, Moskvina V, Lovestone S, Priotsi P, Lupton M, Brayne C, Gill M, Lawlor B, Lynch A, Craig D, McGuinness B, Johnston J, Holmes C, Livingston G, Bass NJ, Gurling H, McQuillin A; the GERAD Consortium; the National Institute on Aging Late-Onset Alzheimer's Disease Family Study Group, Holmans P, Jones L, Devlin B, Klei L, Barmada MM, Demirci FY, Dekosky ST, Lopez OL, Passmore P, Owen MJ, O'Donovan MC, Mayeux R, Kamboh MI, Williams J, Genome-wide association study of Alzheimer's disease with psychotic symptoms., Molecular Psychiatry, 17, (12), 2012, p1316 - 1327 Journal Article, 2012 DOI TARA - Full Text

Stergiakouli E, Hamshere M, Holmans P, Langley K, Zaharieva I, Hawi Z, Kent L, Gill M, Williams N, Owen MJ, O'Donovan M, Thapar A., Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD. , American Journal of Psychiatry, 169, 2012, p169 - 194 Journal Article, 2012 DOI TARA - Full Text

Rose EJ, Morris DW, Fahey C, Robertson IH, Greene C, O'Doherty J, Newell FN, Garavan H, McGrath J, Bokde A, Tropea D, Gill M, Corvin AP, Donohoe G., The effect of the neurogranin schizophrenia risk variant rs12807809 on brain structure and function., Twin Research and Human Genetics, 15, (3), 2012, p296 - 303 Journal Article, 2012 DOI TARA - Full Text

Strange A, Riley BP, Spencer CA, Morris DW, Pirinen M, O'Dushlaine CT, Su Z, Maher BS, Freeman C, Cormican P, Bellenguez C, Kenny EM, Band G, Wormley B, Donohoe G, Dilthey A, Moutsianas L,Quinn E, Edkins S, Judge R, Coleman K, Hunt S, Tropea D, Roche S, Cummings L, Kelleher E, McKeon P, Dinan T, McDonald C, Murphy KC, O'Callaghan E, O'Neill FA, Waddington JL, Walsh D, Giannoulatou E, Langford C, Deloukas P, Gray E, Dronov S, Potter S, Pearson R, Vukcevic D, Tashakkori-Ghanbaria A, Blackwell JM,15, Bramon E, Brown MA, Casas JP, Duncanson A, Jankowski J, Markus HS, Mathew CG, Palmer CNA, Plomin RP, Rautanen A, Sawcer SJ, Trembath RC, Viswanathan AC, Wood NW, Stone J, Scolnick E, Purcell S, Sklar P, SGENE+ Consortium, Ripke S, Walters J, Owen MJ, O'Donovan MC, Schizophrenia Working Group of the Psychiatric GWAS Consortium, Peltonen L, McVean G, Kendler KS, Gill M, Donnelly P, Corvin A for Irish Schizophrenia Genomics Consortium and the Wellcome Trust Case Control Consortium 2, Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia., Biological Psychiatry, 72, (8), 2012, p620-628 Journal Article, 2012 DOI TARA - Full Text

McGrath J, Johnson K, Ecker C, O'Hanlon E, Gill M, Gallagher L, Garavan H, Atypical visuospatial processing in autism: insights from functional connectivity analysis., Autism research : official journal of the International Society for Autism Research, 5, (5), 2012, p314-30 Journal Article, 2012 DOI

Proitsi P, Lupton MK, Reeves SJ, Hamilton G, Archer N, Martin BM, Lyegbe C, Hollingworth P, Lawlor B, Gill M, Brayne C, Rubinsztein DC, Owen MJ, Williams J, Lovestone S, Powell JF. , Association of serotonin and dopamine gene pathways with behavioural subphenotypes in dementia. , Neurobiology of Aging, 33, (4), 2012, p791-803 Journal Article, 2012 TARA - Full Text

Emma J. Rose, Ciara Greene, Sinead Kelly, Derek W. Morris, Ian H. Robertson, Ciara Fahey, Sarah Jacobson, John O'Doherty, Fiona N. Newell, Jane McGrath, Arun Bodke, Hugh Garavan, Thomas Frodl, Michael Gill, Aiden P. Corvin, Gary Donohoe, The NOS1 variant rs6490121 is associated with variation in prefrontal function and gray matter density in healthy individuals, NeuroImage, 60, (1), 2012, p614-622 Journal Article, 2012 TARA - Full Text

Toplak, M.E., Sorge, G.B., Flora, D.B., Chen, W., Banaschewski, T., Buitelaar, J., Ebstein, R., Eisenberg, J., Franke, B., Gill, M., Miranda, A., Oades, R.D., Roeyers, H., Rothenberger, A., Sergeant, J., Sonuga-Barke, E., Steinhausen, H.-C., Thompson, M., Tannock, R., Asherson, P., Faraone, S.V., The hierarchical factor model of ADHD: Invariant across age and national groupings?, Journal of Child Psychology and Psychiatry and Allied Disciplines, 53, (3), 2012, p292-303 Journal Article, 2012 DOI TARA - Full Text

Collins AL, Kim Y, Sklar P, International Schizophrenia Consortium, O'Donovan MC, Sullivan PF, Hypothesis-driven candidate genes for schizophrenia compared to genome-wide association results., Psychological Medicine, 42, 2012, p607 - 616 Journal Article, 2012 URL

Richards AL, Jones L, Moskvina V, Kirov G, Gejman PV, Levinson DF, Sanders AR, Molecular Genetics of Schizophrenia Collaboration (MGS), International Schizophrenia Consortium (ISC), Purcell S, Visscher PM, Craddock N, Owen MJ, Holmans P, O'Donovan MC, Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain., Molecular psychiatry, 17, (2), 2012, p193-201 Journal Article, 2012 URL

Williams NM, Franke B, Mick E, Anney RJ, Freitag CM, Gill M, Thapar A, O'Donovan MC, Owen MJ, Holmans P, Kent L, Middleton F, Zhang-James Y, Liu L, Meyer J, Nguyen TT, Romanos J, Romanos M, Seitz C, Renner TJ, Walitza S, Warnke A, Palmason H, Buitelaar J, Rommelse N, Vasquez AA, Hawi Z, Langley K, Sergeant J, Steinhausen HC, Roeyers H, Biederman J, Zaharieva I, Hakonarson H, Elia J, Lionel AC, Crosbie J, Marshall CR, Schachar R, Scherer SW, Todorov A, Smalley SL, Loo S, Nelson S, Shtir C, Asherson P, Reif A, Lesch KP, Faraone SV, Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3., The American journal of psychiatry, 169, (2), 2012, p195-204 Journal Article, 2012 DOI TARA - Full Text

Stein JL, Medland SE, Vasquez AA, Hibar DP, Senstad RE, Winkler AM, Toro R, Appel K, Bartecek R, Bergmann O, Bernard M, Brown AA, Cannon DM, Chakravarty MM, Christoforou A, Domin M, Grimm O, Hollinshead M, Holmes AJ, Homuth G, Hottenga JJ, Langan C, Lopez LM, Hansell NK, Hwang KS, Kim S, Laje G, Lee PH, Liu X, Loth E, Lourdusamy A, Mattingsdal M, Mohnke S, Maniega SM, Nho K, Nugent AC, O'Brien C, Papmeyer M, Pütz B, Ramasamy A, Rasmussen J, Rijpkema M, Risacher SL, Roddey JC, Rose EJ, Ryten M, Shen L, Sprooten E, Strengman E, Teumer A, Trabzuni D, Turner J, van Eijk K, van Erp TG, van Tol MJ, Wittfeld K, Wolf C, Woudstra S, Aleman A, Alhusaini S, Almasy L, Binder EB, Brohawn DG, Cantor RM, Carless MA, Corvin A, Czisch M, Curran JE, Davies G, de Almeida MA, Delanty N, Depondt C, Duggirala R, Dyer TD, Erk S, Fagerness J, Fox PT, Freimer NB, Gill M, Göring HH, Hagler DJ, Hoehn D, Holsboer F, Hoogman M, Hosten N, Jahanshad N, Johnson MP, Kasperaviciute D, Kent JW Jr, Kochunov P, Lancaster JL, Lawrie SM, Liewald DC, Mandl R, Matarin M, Mattheisen M, Meisenzahl E, Melle I, Moses EK, Mühleisen TW, Nauck M, Nöthen MM, Olvera RL, Pandolfo M, Pike GB, Puls R, Reinvang I, Rentería ME, Rietschel M, Roffman JL, Royle NA, Rujescu D, Savitz J, Schnack HG, Schnell K, Seiferth N, Smith C, Steen VM, Valdés Hernández MC, Van den Heuvel M, van der Wee NJ, Van Haren NE, Veltman JA, Völzke H, Walker R, Westlye LT, Whelan CD, Agartz I, Boomsma DI, Cavalleri GL, Dale AM, Djurovic S, Drevets WC, Hagoort P, Hall J, Heinz A, Jack CR Jr, Foroud TM, Le Hellard S, Macciardi F, Montgomery GW, Poline JB, Porteous DJ, Sisodiya SM, Starr JM, Sussmann J, Toga AW, Veltman DJ, Walter H, Weiner MW; the Alzheimer's Disease Neuroimaging Initiative (ADNI); EPIGEN Consortium; IMAGEN Consortium; Saguenay Youth Study Group (SYS), Bis JC, Ikram MA, Smith AV, Gudnason V, Tzourio C, Vernooij MW, Launer LJ, Decarli C, Seshadri S; Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium; the Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) Consortium, Andreassen OA, Apostolova LG, Bastin ME, Blangero J, Brunner HG, Buckner RL, Cichon S, Coppola G, de Zubicaray GI, Deary IJ, Donohoe G, de Geus EJ, Espeseth T, Fernández G, Glahn DC, Grabe HJ, Hardy J, Hulshoff Pol HE, Jenkinson M, Kahn RS, McDonald C, McIntosh AM, McMahon FJ, McMahon KL, Meyer-Lindenberg A, Morris DW, Müller-Myhsok B, Nichols TE, Ophoff RA, Paus T, Pausova Z, Penninx BW, Potkin SG, Sämann PG, Saykin AJ, Schumann G, Smoller JW, Wardlaw JM, Weale ME, Martin NG, Franke B, Wright MJ, Thompson PM. , Identification of common variants associated with human hippocampal and intracranial volumes, Nature Genetics, 44, (5), 2012, p552-561 Journal Article, 2012 TARA - Full Text DOI

Banaschewski T, Jennen-Steinmetz C, Brandeis D, Buitelaar JK, Kuntsi J, Poustka L, Sergeant JA, Sonuga-Barke EJ, Frazier-Wood AC, Albrecht B, Chen W, Uebel H, Schlotz W, van der Meere JJ, Gill M, Manor I, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Steinhausen HC, Faraone SV, Asherson P, Neuropsychological correlates of emotional lability in children with ADHD., Journal of child psychology and psychiatry, and allied disciplines, 53, (11), 2012, p1139-48 Journal Article, 2012 DOI TARA - Full Text

Corvin A, Donohoe G, Hargreaves A, Gallagher L, Gill M., The Cognitive Genetics of Neuropsychiatric Disorders. , Current Topics in Behavioral Neurosciences, 12, 2012, p579-613 Journal Article, 2012 DOI

Delaney C, McGrane J, Cummings E, Morris DW, Tropea D, Gill M, Corvin A, Donohoe G, Preserved cognitive function is associated with suicidal ideation and single suicide attempts in schizophrenia., Schizophrenia research, 140, (1-3), 2012, p232-6 Journal Article, 2012 DOI

Power RA, Wingenbach T, Cohen-Woods S, Uher R, Ng MY, Butler AW, Ising M, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Maier W,Zobel A, Mors O, Placentino A, Rietschel M, Lucae S, Holsboer F, Binder EB, Keers R, Tozzi F, Muglia P, Breen G, Craig IW, Müller-Myhsok B, Kennedy JL,Strauss J, Vincent JB, Lewis CM, Farmer AE, McGuffin P, Estimating the heritability of reporting stressful life events captured by common genetic variants., Psychological Medicine, 43, (9), 2012, p1965-71 Journal Article, 2012 DOI

Skokauskas N, Gallagher L, Frodl T, Gill M. , Assessing Problem based learning in Child and Adolescent Psychiatry at the Trinity College Dublin Ireland, Oman Medical Journal, 27, (2), 2012, p168 - 169 Journal Article, 2012 TARA - Full Text

Vorstman JA, Anney RJ, Derks EM, Gallagher L, Gill M, de Jonge MV, van Engeland H, Kahn RS, Ophoff RA; the Autism Genome Project, the International Schizophrenia Consortium. , No evidence that common genetic risk variation is shared between schizophrenia and autism, Am J. Med Genet B Neuropsychiatric Genetics, 162B, (1), 2012, p55-60 Journal Article, 2012 DOI

Jablensky A, Angelicheva D, Donohoe GJ, Cruickshank M, Azmanov DN, Morris DW, McRae A, Weickert CS, Carter KW, Chandler D, Alexandrov B, Usheva A, Morar B, Verbrugghe PL, Filipovska A, Rackham O, Bishop AR, Rasmussen KO, Dragovic M, Cooper M, Phillips M, Badcock J, Bramon-Bosch E, Almeida OP, Flicker L, Gill M, Corvin A, Macgregor S, Kalaydjieva L, Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia., Molecular psychiatry, 17, (12), 2012, p1328-1339 Journal Article, 2012 DOI

Gill M, Developmental psychopathology: The role of structural variation in the genome., Dev Psychopathology, 24, (4), 2012, p1319 - 1324 Journal Article, 2012 DOI

Steinberg S, de Jong S, Mattheisen M, Costas J, Demontis D, Jamain S, Pietiläinen OP, Lin K, Papiol S, Huttenlocher J, Sigurdsson E, Vassos E, Giegling I, Breuer R, Fraser G, Walker N, Melle I, Djurovic S, Agartz I, Tuulio-Henriksson A, Suvisaari J, Lönnqvist J, Paunio T, Olsen L, Hansen T, Ingason A, Pirinen M, Strengman E; GROUP, Hougaard DM, Orntoft T, Didriksen M, Hollegaard MV, Nordentoft M, Abramova L, Kaleda V, Arrojo M, Sanjuán J, Arango C, Etain B, Bellivier F, Méary A, Schürhoff F, Szoke A, Ribolsi M, Magni V, Siracusano A, Sperling S, Rossner M, Christiansen C, Kiemeney LA, Franke B, van den Berg LH, Veldink J, Curran S, Bolton P, Poot M, Staal W, Rehnstrom K, Kilpinen H, Freitag CM, Meyer J, Magnusson P, Saemundsen E, Martsenkovsky I, Bikshaieva I, Martsenkovska I, Vashchenko O, Raleva M, Paketchieva K, Stefanovski B, Durmishi N, Pejovic Milovancevic M, Lecic Tosevski D, Silagadze T, Naneishvili N, Mikeladze N, Surguladze S, Vincent JB, Farmer A, Mitchell PB, Wright A, Schofield PR, Fullerton JM, Montgomery GW, Martin NG, Rubino IA, van Winkel R, Kenis G, De Hert M, Réthelyi JM, Bitter I, Terenius L, Jönsson EG, Bakker S, van Os J, Jablensky A, Leboyer M, Bramon E, Powell J, Murray R, Corvin A, Gill M, Morris D, O'Neill FA, Kendler K, Riley B; Wellcome Trust Case Control Consortium 2, Craddock N, Owen MJ, O'Donovan MC, Thorsteinsdottir U, Kong A, Ehrenreich H, Carracedo A, Golimbet V, Andreassen OA, Børglum AD, Mors O, Mortensen PB, Werge T, Ophoff RA, Nöthen MM, Rietschel M, Cichon S, Ruggeri M, Tosato S, Palotie A, St Clair D, Rujescu D, Collier DA, Stefansson H, Stefansson K. , Common variant at 16p11.2 conferring risk of psychosis, Molecular Psychiatry, 19, (1), 2012, p108-14 Journal Article, 2012 DOI TARA - Full Text

Lips ES, Cornelisse LN, Toonen RF, Min JL, Hultman CM, Holmans PA, O'Donovan MC, Purcell SM, Smit AB, Verhage M, Sullivan PF, Visscher PM, Posthuma D, Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia., Molecular Psychiatry, 17, (10), 2012, p996-1006 Journal Article, 2012 TARA - Full Text DOI

Gilks WP, Hill M, Gill M, Donohoe G, Corvin AP, Morris DW, Functional investigation of a schizophrenia GWAS signal at the CDC42 gene., World Journal of Biological Psychiatry, 13, (7), 2012, p550-554 Journal Article, 2012 DOI

Keller MC, Simonson MA, Ripke S, Neale BM, Gejman PV, Howrigan DP, Lee SH, Lencz T, Levinson DF, Sullivan PF, Runs of homozygosity implicate autozygosity as a schizophrenia risk factor., PLoS genetics, 8, (4), 2012, pe1002656 Journal Article, 2012 TARA - Full Text DOI

Rose EJ, Morris DW, Fahey C, Robertson IH, Greene C, O'Doherty J, Newell FN, Garavan H, McGrath J, Bokde A, Tropea D, Gill M, Corvin AP, Donohoe G, The effect of the neurogranin schizophrenia risk variant rs12807809 on brain structure and function., Twin research and human genetics : the official journal of the International Society for Twin Studies, 15, (3), 2012, p296-303 Journal Article, 2012 DOI

Badner JA, Koller D, Foroud T, Edenberg H, Nurnberger JI, Zandi PP, Willour VL, McMahon FJ, Potash JB, Hamshere M, Grozeva D, Green E, Kirov G, Jones I, Jones L, Craddock N, Morris D, Segurado R, Gill M, Sadovnick D, Remick R, Keck P, Kelsoe J, Ayub M, MacLean A, Blackwood D, Liu CY, Gershon ES, McMahon W, Lyon GJ, Robinson R, Ross J, Byerley W, Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms., Molecular psychiatry, 17, (8), 2012, p818-26 Journal Article, 2012 DOI

Sakrikar D, Mazei-Robison M, Mergy M, Richtand N, Han Q, Hamilton P, Bowton E, Galli A, Veenestra-Vanderweele J, Gill M, Blakely R. , ADHD-Derived Coding Variation in the Dopamine Transporter Disrupts Microdomain Targeting and Trafficking Regulation., The Journal of Neuroscience, 32, (16), 2012, p5385 - 5397 Journal Article, 2012 TARA - Full Text DOI

Power RA R, Keers R, Ng M, Butler A, Uher R, Cohen-Woods S, Ising M, Craddock N, Owen M, Korszun A, Jones L, Jones I, Gill M, Rice J, Hauser J, Henigsbert N, Maier W, Mors O, Dissecting the genetic heterogeneith of depression through age at onset, Am J Medical Genetics B Neuropsychiatric Genetics, 159B, (7), 2012, p859 - 868 Journal Article, 2012 DOI

Badner JA, Koller D, Foroud T, Edenberg H, Numberger JI, Sandi PP, Willour VL, McMahon FJ, Potash JB, Hamshere M, Grozeva D, Green E, Kirov G, Jones I, Jones L, Craddock N, Morris D, Segurado R, Gill M, Sadovnick D, Remick R, Keck P, Kelso J, Ayub M, et al. , Geonome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms, Molecular Psychiatry, 17, (8), 2011, p818-26 Journal Article, 2011 URL TARA - Full Text

Casey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bolton PF, Bourgeron T, Brennan S, Cali P, Correia C, Corsello C, Coutanche M, Dawson G, de Jonge M, Delorme R, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Foley S, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Green J, Guter SJ, Hakonarson H, Holt R, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Lamb JA, Leboyer M, Le Couteur A, Leventhal BL, Lord C, Lund SC, Maestrini E, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Merikangas A, Miller J, Minopoli F, Mirza GK, Munson J, Nelson SF, Nygren G, Oliveira G, Pagnamenta AT, Papanikolaou K, Parr JR, Parrini B, Pickles A, Pinto D, Piven J, Posey DJ, Poustka A, Poustka F, Ragoussis J, Roge B, Rutter ML, Sequeira AF, Soorya L, Sousa I, Sykes N, Stoppioni V, Tancredi R, Tauber M, Thompson AP, Thomson S, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Vorstman JA, Wallace S, Wang K, Wassink TH, White K, Wing K, Wittemeyer K, Yaspan BL, Zwaigenbaum L, Betancur C, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Geschwind DH, Haines JL, Hallmayer J, Monaco AP, Nurnberger JI Jr, Pericak-Vance MA, Schellenberg GD, Scherer SW, Sutcliffe JS, Szatmari P, Vieland VJ, Wijsman EM, Green A, Gill M, Gallagher L, Vicente A, Ennis S, A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. , Human Genetics, 131, (4), 2011, p565-579 Journal Article, 2011 TARA - Full Text DOI

Annette E. Rünker, Colm O'Tuathaigh, Mark Dunleavy,Derek W. Morris, Graham E. Little, Aiden P. Corvin,Michael Gill, David C. Henshall, John L. Waddington, Kevin J. Mitchell, Mutation of Semaphorin-6A Disrupts Limbic and Cortical Connectivity and Models Neurodevelopmental Psychopathology, PLoS ONE , 6, (11, ), 2011, pe26488 Journal Article, 2011 TARA - Full Text

Muller UC, Asherson P, Banaschewski T, Buitelaar JK, Epstein RP, Eisenberg J, Gill M, Manor I, Miranda A, Oades RD, Roeyers J, Rothenberger A, Sergeant JA, sonuga-Barke EJ, Thompson M, Faraone SV, Steinhausen HC. , The impact of study design and diagnostic approach in a large multi-centre ADHD study: Part 2: Dimensional measures of psychopathology and intelligence. , BMC Psychaitry, 11, (1), 2011 Journal Article, 2011

The Schizophrenia Psychiatric Genome-wide Assocaition Study (GWAS) Corsortium., Genome-wide association study identifies five new schizophrenia, Nature Genetics, 43, (10), 2011, p969 - 976 Journal Article, 2011

Sonuga-Barke EJ, Kumsta R, Schlotz W, Lasky-Su J, Marco R, Miranda A, Mulas F, Oades RD, Banaschewski T, Mueller U, Andreou P, Christiansen H, Gabriels I, Uebel H, Kuntsi J, Franke B, Buitelaar J, Ebstein R, Gill M, Anney R, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Asherson P, Faraone SV, A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings., Biological psychiatry, 70, (3), 2011, p230-6 Journal Article, 2011 DOI TARA - Full Text

Chen X, Lee G, Maher B. Fanous A, Chen J, Shao Z, Guo A, Van den Ord E, Sullivan F, Shi J, Levinson D, Gejman P, Sanders A, duan J, Owen M, Craddock N, O'Donovan M, Blackman J, Lewis D, Kirov G, Qin W, Schwab S, Wildenauer D et al., GWA Study data-mining and independent replication identify cardiomyopathy associated 5 (CMYA5) as a risk gene for schizophrenia.(2010) , Molecular Psychiatry, 16, 2011, p1117-1129 Journal Article, 2011 TARA - Full Text DOI

Wood AC, Rijsdijk F, Johnson KA, Andreou P, Albrecht B, Arias-Vasquez A, Buitelaar JK, McLoughlin G, Rommelse NNJ, Sergeant JA, Sonuga-Barke EJS, Uebel H, Van Der Meere JJ et al.(, The relationship between ADHD and key cognitive phenotypes is not mediated by shared familial effects with IQ, Psychological Medicine, 41, (4), 2011, p861 - 871 Journal Article, 2011 TARA - Full Text

Rivera M, Cohen-Woods S, Kapur K, Breen G, Ng MY, Butler AW, Craddock N, Gill M, Korszun A, Maier W, Mors O, Owen MJ, Preisig M, Bergmann S, Tozzi F, Rice J, Rietschel M, Rucker J, Schosser A, Aitchison KJ, Uher R, Craig IW, Lewis CM, Farmer AE, McGuffin P. , Depressive disorder moderates the effect of the FTO gene on body mass index. , Molecular Psychiatry, 17, (6), 2011, p604-611 Journal Article, 2011 DOI

G, Webb B T, Butler A, Vanden Oord E, Tozzi F, Craddock N, Gill M, Korszun A, Maier W, Middleton L, Mors O, Owen M, Cohen-Woods S, Perry J, Galwey N, Upmanyu R, Craig I, Lewis C, Ng M, Brewster S, Preisig M, Rietschel M, Jones L, Knight J, Rice J, Muglia P, Farmer A, McGuffin P. , A genome-wide significant linkage for severe depression on chromosome 3: the depression network study, American Journal of Psychiatry, 168, (8), 2011, p840 - 847 Journal Article, 2011 DOI

Williams HJ, Norton N, Dwyer S, Moskvina V, Nikolov I, Carroll L, Georgieva L, Williams NM, Morris DW, Quinn EM, Giegling I, Ikeda M, Wood J, Lencz T, Hultman C, Lichtenstein P, Thiselton D, Maher BS; Molecular Genetics of Schizophrenia Collaboration (MGS) International Schizophrenia Consortium (ISC), SGENE-plus, GROUP, Malhotra AK, Riley B, Kendler KS, Gill M, Sullivan P, Sklar P, Purcell S, Nimgaonkar VL, Kirov G, Holmans P, Corvin A, Rujescu D, Craddock N, Owen MJ, O'Donovan MC, Fine mapping of ZNF804A and genomime-wide significant evidence for it's involvement in Schizophrenia and bipolar disorder. , Molecular Psychiatry, 16, (4), 2011, p429-441 Journal Article, 2011 DOI TARA - Full Text

Segurado R, Bellgrove A, Mancone F, Gill M, Hawi Z, Epistasis between neurochemical gene polymorphisms and risk for ADHD, European Journal of Human Genetics, 19, (5), 2011, p577-582 Journal Article, 2011 DOI TARA - Full Text

Dagdan E, Morris D, Campbell M, Hill M, Rothermundt M, Kastner F, Hofoff C, Von Eiff, Krakowitzky P, Gill M, McKeon P, Roche S, Functional Assessment of a Promoter Polymorphism in S100B, a putative Risk Variant for Bipolar Disorder, Neuropsychiatric Genetics, 156, (6), 2011, p691 - 699 Journal Article, 2011 DOI

Hargreaves A, Morris DW, Rose E, Fahey C, Moore S, Cummings E, Tropea D, Gill M, Corvin A, Donohoe G, ZNF804A and social cognition in patients with schizophrenia and healthy controls., Molecular psychiatry, 17, (2), 2011, p118 - 119 Journal Article, 2011 DOI

Gerrish A, Russo G, Richards A, Moskvina V, Ivanov D, Harold D, Sims R, Abraham R, Hollingworth P, Chapman J, Hamshere M, Pahwa JS, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Johnston JA, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Hardy J, Mead S, Fox N, Rossor M, Collinge J, Maier W, Jessen F, Kölsch H, Heun R, Schürmann B, Bussche HV, Heuser I, Kornhuber J, Wiltfang J, Dichgans M, Frölich L, Hampel H, Hüll M, Rujescu D, Goate AM, Kauwe JS, Cruchaga C, Nowotny P, Morris JC, Mayo K, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Davies G, Harris SE, Starr JM, Deary IJ, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R, Mühleisen TW, Nöthen MM, Moebus S, Jöckel KH, Klopp N, Wichmann HE, Carrasquillo MM, Pankratz VS, Younkin SG, Jones L, Holmans PA, O'Donovan MC, Owen MJ, Williams J, The Role of Variation at AßPP, PSEN1, PSEN2, and MAPT in Late Onset Alzheimer's Disease., Journal of Alzheimer's disease : JAD, 28, (2), 2011, p377-387 Journal Article, 2011 TARA - Full Text DOI

Heron Elizabeth A, O'Dushlane C, Segurado R, Gallagher L, Gill M., Exploration of empirical Bayes hierarchical modeling for the analysis of genome-wide association study data., Oxford Journal Mathematics & Physical Sciences Biostatistics, 12, (3), 2011, p445-461 Journal Article, 2011 TARA - Full Text

Schosser A, Butler A, Ising M, Perroud N, Sher R, Ng M, Cohen-Woods S, Craddock N, Owen M, Korszun A, Jones L, Jones I, Gill M, Rice J, Maier W, et al, Genomewide Association Scan of Suicidal Thoughts and Behaviour in Major Depression, PLOS One, 6, (7), 2011, pE20690 Journal Article, 2011 DOI TARA - Full Text

Anney RJ, Kenny EM, O'Dushlaine C, Yaspan BL, Parkhomenka E, Buxbaum JD, Sutcliffe J, Gill M, Gallagher L; Autism Genome Project, Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders., Eur J Human Genetics, 19, (10), 2011, p1082 - 1089 Journal Article, 2011 TARA - Full Text DOI

Psychiatric GWAS Consortium Bipolar Disorder Working Group, Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4, Nature Genetics, 43, 2011, p977 - 983 Journal Article, 2011 DOI TARA - Full Text

Sklar P, Ripke S, Scott LJ, Andreassen OA, Cichon S, Craddock N, Edenberg HJ, Nurnberger JI, Rietschel M, Blackwood D, Corvin A, Flickinger M, Guan W, Mattingsdal M, McQuillin A, Kwan P, Wienker TF, Daly M, Dudbridge F, Holmans PA, Lin D, Burmeister M, Greenwood TA, Hamshere ML, Muglia P, Smith EN, Zandi PP, Nievergelt CM, McKinney R, Shilling PD, Schork NJ, Bloss CS, Foroud T, Koller DL, Gershon ES, Liu C, Badner JA, Scheftner WA, Lawson WB, Nwulia EA, Hipolito M, Coryell W, Rice J, Byerley W, McMahon FJ, Schulze TG, Berrettini W, Lohoff FW, Potash JB, Mahon PB, McInnis MG, Zöllner S, Zhang P, Craig DW, Szelinger S, Barrett TB, Breuer R, Meier S, Strohmaier J, Witt SH, Tozzi F, Farmer A, McGuffin P, Strauss J, Xu W, Kennedy JL, Vincent JB, Matthews K, Day R, Ferreira MA, O'Dushlaine C, Perlis R, Raychaudhuri S, Ruderfer D, Hyoun PL, Smoller JW, Li J, Absher D, Thompson RC, Meng FG, Schatzberg AF, Bunney WE, Barchas JD, Jones EG, Watson SJ, Myers RM, Akil H, Boehnke M, Chambert K, Moran J, Scolnick E, Djurovic S, Melle I, Morken G, Gill M, Morris D, Quinn E, Mühleisen TW, Degenhardt FA, Mattheisen M, Schumacher J, Maier W, Steffens M, Propping P, Nöthen MM, Anjorin A, Bass N, Gurling H, Kandaswamy R, Lawrence J, McGhee K, McIntosh A, McLean AW, Muir WJ, Pickard BS, Breen G, St Clair D, Caesar S, Gordon-Smith K, Jones L, Fraser C, Green EK, Grozeva D, Jones IR, Kirov G, Moskvina V, Nikolov I, O'Donovan MC, Owen MJ, Collier DA, Elkin A, Williamson R, Young AH, Ferrier IN, Stefansson K, Stefansson H, Thornorgeirsson T, Steinberg S, Gustafsson O, Bergen SE, Nimgaonkar V, Hultman C, Landén M, Lichtenstein P, Sullivan P, Schalling M, Osby U, Backlund L, Frisén L, Langstrom N, Jamain S, Leboyer M, Etain B, Bellivier F, Petursson H, Sigur Sson E, Müller-Mysok B, Lucae S, Schwarz M, Schofield PR, Martin N, Montgomery GW, Lathrop M, Oskarsson H, Bauer M, Wright A, Mitchell PB, Hautzinger M, Reif A, Kelsoe JR, Purcell SM, Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4., Nature Genetics, 43, (10), 2011, p977-83 Journal Article, 2011 DOI

Donohoe G, Walters J, Morris DW, Da Costa A, Rose E, Hargreaves A, Maher K, Hayes E, Giegling I, Hartmann AM, Möller HJ, Muglia P, Moskvina V, Owen MJ, O'Donovan MC, Gill M, Corvin A, Rujescu D, A neuropsychological investigation of the genome wide associated schizophrenia risk variant NRGN rs12807809, Schizophrenia Research, 125, (2-3), 2011, p304-306 Journal Article, 2011 DOI

Hollingsworth P, Harold D, Sims R, Gerrish A, Lambert JC, Carrasquillo MM, Abraham R, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Jones N, Stretton A, Thomas C, Richards A, Ivanov D et al., Common Variants at ABCA7, MS4A6A/MS4A4E, EPHA1/CD33 and CD2AP are associated with Alzheimer's disease, Nature Genetics, 43, (5), 2011, p429-436 Journal Article, 2011 TARA - Full Text DOI

Mulligan A, Anney R, Butler L, O'Regan M, Richardson T, Tulewicz EM, Fitzgerald M, Gill M., Home environment: association with hyperactivity/impulsivity in children with ADHD and their non-ADHD siblings, Child: care, health and development, 39, (2), 2011, p202-212 Journal Article, 2011 TARA - Full Text DOI

O'Dushlaine C, Kenny E, Heron E, Donohoe G, Gill M, Morris D, Consortium IS, Corvin A, Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility., Molecular Psychiatry, 16, (3), 2011, p286-292 Journal Article, 2011 DOI TARA - Full Text

Fliers EA, Vasques AA, Poelmans G, rommeise N, Altink M, Buschgens C, Asherson P, Banaschewski T, Ebstein R, Gill M, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Faraone SV, Buitelaar JK, Franke B., Genome-wide association study of motor coordination problems in ADHD indentifies genes for brain and muscle function. , World Journal of Biological Psychaitry, 13, (3), 2011, 211-222 Journal Article, 2011 DOI

Vacic V, McCarthy S, Malhotra D, Murray F, Chou HH, Peoples A, Makarov V, Yoon S, Bhandari A, Corominas R, Iakoucheva LM, Krastoshevsky O, Krause V, Larach-Walters V, Welsh DK, Craig D, Kelsoe JR, Gershon ES, Leal SM, Dell Aquila M, Morris DW, Gill M, Corvin A, Insel PA, McClellan J, King MC, Karayiorgou M, Levy DL, DeLisi LE, Sebat J, Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia., Nature, 471, (7339), 2011, p499-503 Journal Article, 2011 DOI TARA - Full Text

Runker AE, O'Tuathaight C, Dunleavy M, Morris DW, Little GE, Corvin AP, Gill M, Henshall DC, Waddington JL, Mitchell KJ. , Mutation of Semaphorin-6A Disrupts Limbic and Cortical Connectivity and Models Neurodevelopmental Psychpathology, PLoS ONE , 6, 2011, pe26488 Journal Article, 2011 TARA - Full Text DOI

W Braet, KA Johnson, CT Tobin, R Acheson, C McDonnell, Z Hawi, E Barry, A Mulligan, M Gill, MA Bellgrove, IH Robertson, H Garavan, fMRI activation during response inhibition and error processing: the role of the DAT1 gene in typically developing adolescents and those diagnosed with ADHD, Neuropsychologia, 49, (7), 2011, p1641-1650 Journal Article, 2011 DOI TARA - Full Text

Muller U, Asherson P, Bnaschewski T, Buitelaar J, Epstein R, Eisenberg J, Gill M, Manor I, Miranda A, Oades R, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Thompson M, Faraone S, Steinhausen H. , The impact of study design and diagnostic approach in a larege multi-centre ADHD study. Part 1: ADHD Symptom patterns., BMC Psychiatry, 11, 2011, p54 Journal Article, 2011 DOI TARA - Full Text

Sims R, Dwyer S, Harold D, Gerrish A, Hollingworth P, Chapman J, Jones N, Abraham R, Ivanov D, Pahwa J, Moskvina V, Dowzell K, Thomas C, Stretton A, Livestone S, Powell J et al. , No Evidence that Extended Tracts of Homozygosity are Associated with Alzheimber's Disease., Neuropsychiatric Genetics, 156B, (7), 2011, p764-71 Journal Article, 2011 URL

Hill MJ, Kenny E, Roche S, Morris DW, Corvin A, Hawi Z, Gill M, Anney RJ, Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: evidence of cis-acting variation and tissue specific regulation., Psychiatric genetics, 21, (6), 2011, p281-286 Journal Article, 2011 DOI

Proitsi P, Hamilton G, Tsolaki M, Lupton M, Daniilidou M, Hollingworth P, Archer N, Foy C, Stylios F, McGuinness B, Todd S, Lawlor B, Gill M, Brayne C, Rubinsztein DC, Owen M, Williams J, Craig D, Passmore P, Lovestone S, Powell JF, A Multiple Indicators Multiple Causes (MIMIC) model of Behavioural and Psychological Symptoms in Dementia (BPSD)., Neurobiology of Aging, 32, (3), 2011, p434-442 Journal Article, 2011 DOI TARA - Full Text

Malhotra D, McCarthy S, Michaelson JJ, Vacic V, Burdick KE, Yoon S, Cichon S, Corvin A, Gary S, Gershon ES, Gill M, Karayiorgou M, Kelsoe JR, Krastoshevsky O, Krause V, Leibenluft E, Levy DL, Makarov V, Bhandari A, Malhotra AK, McMahon FJ, Nöthen MM, Potash JB, Rietschel M, Schulze TG, Sebat J, High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia, Neuron, 72, (6), 2011, p951 - 963 Journal Article, 2011 TARA - Full Text DOI

Kenny EM, Cormican P, Gilks WP, Gates AS, O'Dushlaine CT, Pinto C, Corvin AP, Gill M, Morris DW, Multiplex Target Enrichment Using DNA Indexing for Ultra-High Throughput SNP Detection., DNA research : an international journal for rapid publication of reports on genes and genomes, 18, (1), 2011, p31-38 Journal Article, 2011 TARA - Full Text DOI

Bridges M, Heron E, O'Dushlaine, Segurado R, The International Schizophrenia Consortium (ISC), Morris DW, Corvin A, Gill M, Pinto C. , Genetic Classification of Populations using Supervised Learning., PLos One, 6, (5), 2011, pe14802 Journal Article, 2011 DOI TARA - Full Text

Ripke S, Sanders AR, Kendler KS, Levinson DF, Sklar P, Holmans PA, Lin DY, Duan J, Ophoff RA, Andreassen OA, Scolnick E, Cichon S, St Clair D, Corvin A, Gurling H, Werge T, Rujescu D, Blackwood DH, Pato CN, Malhotra AK, Purcell S, Dudbridge F, Neale BM, Rossin L, Visscher PM, Posthuma D, Ruderfer DM, Fanous A, Stefansson H, Steinberg S, Mowry BJ, Golimbet V, De Hert M, Jönsson EG, Bitter I, Pietiläinen OP, Collier DA, Tosato S, Agartz I, Albus M, Alexander M, Amdur RL, Amin F, Bass N, Bergen SE, Black DW, Børglum AD, Brown MA, Bruggeman R, Buccola NG, Byerley WF, Cahn W, Cantor RM, Carr VJ, Catts SV, Choudhury K, Cloninger CR, Cormican P, Craddock N, Danoy PA, Datta S, de Haan L, Demontis D, Dikeos D, Djurovic S, Donnelly P, Donohoe G, Duong L, Dwyer S, Fink-Jensen A, Freedman R, Freimer NB, Friedl M, Georgieva L, Giegling I, Gill M, Glenthøj B, Godard S, Hamshere M, Hansen M, Hansen T, Hartmann AM, Henskens FA, Hougaard DM, Hultman CM, Ingason A, Jablensky AV, Jakobsen KD, Jay M, Jürgens G, Kahn RS, Keller MC, Kenis G, Kenny E, Kim Y, Kirov GK, Konnerth H, Konte B, Krabbendam L, Krasucki R, Lasseter VK, Laurent C, Lawrence J, Lencz T, Lerer FB, Liang KY, Lichtenstein P, Lieberman JA, Linszen DH, Lönnqvist J, Loughland CM, Maclean AW, Maher BS, Maier W, Mallet J, Malloy P, Mattheisen M, Mattingsdal M, McGhee KA, McGrath JJ, McIntosh A, McLean DE, McQuillin A, Melle I, Michie PT, Milanova V, Morris DW, Mors O, Mortensen PB, Moskvina V, Muglia P, Myin-Germeys I, Nertney DA, Nestadt G, Nielsen J, Nikolov I, Nordentoft M, Norton N, Nöthen MM, O'Dushlaine CT, Olincy A, Olsen L, O'Neill FA, Orntoft TF, Owen MJ, Pantelis C, Papadimitriou G, Pato MT, Peltonen L, Petursson H, Pickard B, Pimm J, Pulver AE, Puri V, Quested D, Quinn EM, Rasmussen HB, Réthelyi JM, Ribble R, Rietschel M, Riley BP, Ruggeri M, Schall U, Schulze TG, Schwab SG, Scott RJ, Shi J, Sigurdsson E, Silverman JM, Spencer CC, Stefansson K, Strange A, Strengman E, Stroup TS, Suvisaari J, Terenius L, Thirumalai S, Thygesen JH, Timm S, Toncheva D, van den Oord E, van Os J, van Winkel R, Veldink J, Walsh D, Wang AG, Wiersma D, Wildenauer DB, Williams HJ, Williams NM, Wormley B, Zammit S, Sullivan PF, O'Donovan MC, Daly MJ, Gejman PV, Genome-wide association study identifies five new schizophrenia loci., Nature genetics, 43, (10), 2011, p969-976 Journal Article, 2011 TARA - Full Text DOI

Tansey K, Hill M, Cochrane L, Gill M, Anney R, Gallagher L, Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for Autism. , Molecular Autism, 2, (3), 2011 Journal Article, 2011 DOI URL TARA - Full Text

Aebi M, Muller U, Asherson P, Banaschewski T, Buitelaar J, Ebstein R, Eisenberg J, Gill M, Manor I, Miranda A, Oades R, Roeyers H, Tothenberger A, Sergeant J, Sonuga-Barke E, Thompson M, Taylor E, Faraone S, Steinhausen H. , Predictability and construct validity of oppositional defiant disorder in children and adolescents with ADHD combined type. , Psychological Medicine, 40, 2010, p2089-2100 Journal Article, 2010 TARA - Full Text

Neale BM, Medland S, Ripke S, Anney RJ, Asherson P, Buitelaar J, Franke B, Gill M, Kent L, Holmans P, Middleton F, Thapar A, Lesch KP, Faraone SV, Daly M, Nguyen TT, Schäfer H, Steinhausen HC, Reif A, Renner TJ, Romanos M, Romanos J, Warnke A, Walitza S, Freitag C, Meyer J, Palmason H, Rothenberger A, Hawi Z, Sergeant J, Roeyers H, Mick E, Biederman J, Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder., Journal of the American Academy of Child and Adolescent Psychiatry, 49, (9), 2010, p906-920 Journal Article, 2010 DOI

M. Aebi, U. C. Müller, P. Asherson, T. Banaschewski, J. Buitelaar, R. Ebstein, J. Eisenberg, M. Gill, I. Manor, A. Miranda, R. D. Oades, H. Roeyers, A. Rothenberger, J. Sergeant E. Sonuga-Barke, M. Thompson, E. Taylor, S. V. Faraone and H.-C. Steinhausen, Predictability of oppositional defiant disorder and symptom dimensions in children and adolescents with ADHD combined type, Psychological Medicine, 10, (12), 2010, p2089-2100 Journal Article, 2010 TARA - Full Text

Anney R, Lkei L, Pinto D, Pagnamenta A, Regan R, Conroy J, Magalhaes T, Correia C, Abrahams B, Almeida J, GBacchelli E, Bailey A, Baird G, Battaglia A, Berney T, Bolshakova N, Bolte S , A Genomeside scan for common risk variants nominates phospholipase D and polysialytransferase proteins for a role in autism, Human Molecular Genetics, 2010 Journal Article, 2010

Sobanski E, Banaschewski T, Asherson P, Buitelaar J, Chen W, Franke B, Holtmann M, Krumm B, Sergeant J, Sonuga-Barke E, Stringaris A, Taylor E, Anney R, Ebstein RP, Gill M, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Steinhausen HC, Faraone SV, Emotional lability in children and adolescents with attention deficit/hyperactivity disorder (ADHD): clinical correlates and familial prevalence., Journal of child psychology and psychiatry, and allied disciplines, 51, (8), 2010, p915-912 Journal Article, 2010 DOI

Quinn EM, Hill M, Anney R, Gill M, Corvin AP, Morris DW, Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression., Bipolar disorders, 12, (4), 2010, p440-445 Journal Article, 2010 DOI

O'Dushlaine CT, Morris DW, Moskvina V, Kirov G, International Schizophrenia Consortium, Gill M, Corvin A, Wilson JF, Cavalleri GL. , Population structure and genome-wide patters of variation in Ireland and Britain. , European Journal of Human Genetics, 18, (11), 2010, p1248-1254 Journal Article, 2010 DOI TARA - Full Text

Pinto, D, Pagnamenta, AT, Klei, L, Anney, R, Merico, D, Regan, R, Conroy, J, Magalhaes, TR, Correia, C, Abrahams, BS, Almeida, J, Bacchelli, E, Bader, GD, Bailey, AJ, Baird, G, Battaglia, A, Berney, T, Bolshakova, N, Bolte, S, Bolton, PF, Bourgeron, T, Brennan, S, Brian, J, Bryson, SE, Carson, AR, Casallo, G, Casey, J, Chung, BHY, Cochrane, L, Corsello, C, Crawford, EL, Crossett, A, Cytrynbaum, C, Dawson, G, de Jonge, M, Delorme, R, Drmic, I, Duketis, E, Duque, F, Estes, A, Farrar, P, Fernandez, BA, Folstein, SE, Fombonne, E, Freitag, CM, Gilbert, J, Gillberg, C, Glessner, JT, Goldberg, J, Green, A, Green, J, Guter, SJ, Hakonarson, H, Heron, EA, Hill, M, Holt, R, Howe, JL, Hughes, G, Hus, V, Igliozzi, R, Kim, C, Klauck, SM, Kolevzon, A, Korvatska, O, Kustanovich, V, Lajonchere, CM, Lamb, JA, Laskawiec, M, Leboyer, M, Le Couteur, A, Leventhal, BL, Lionel, AC, Liu, XQ, Lord, C, Lotspeich, L, Lund, SC, Maestrini, E, Mahoney, W, Mantoulan, C, Marshall, CR, McConachie, H, McDougle, CJ, McGrath, J, McMahon, WM, Merikangas, A, Migita, O, Minshew, NJ, Mirza, GK, Munson, J, Nelson, SF, Noakes, C, Noor, A, Nygren, G, Oliveira, G, Papanikolaou, K, Parr, JR, Parrini, B, Paton, T, Pickles, A, Pilorge, M, Piven, J, Ponting, CP, Posey, DJ, Poustka, A, Poustka, F, Prasad, A, Ragoussis, J, Renshaw, K, Rickaby, J, Roberts, W, Roeder, K, Roge, B, Rutter, ML, Bierut, LJ, Rice, JP, Salt, J, Sansom, K, Sato, D, Segurado, R, Sequeira, AF, Senman, L, Shah, N, Sheffield, VC, Soorya, L, Sousa, I, Stein, O, Sykes, N, Stoppioni, V, Strawbridge, C, Tancredi, R, Tansey, K, Thiruvahindrapduram, B, Thompson, AP, Thomson, S, Tryfon, A, Tsiantis, J, Van Engeland, H, Vincent, JB, Volkmar, F, Wallace, S, Wang, K, Wang, ZZ, Wassink, TH, Webber, C, Weksberg, R, Wing, K, Wittemeyer, K, Wood, S, Wu, J, Yaspan, BL, Zurawiecki, D, Zwaigenbaum, L, Buxbaum, JD, Cantor, RM, Cook, EH, Coon, H, Cuccaro, ML, Devlin, B, Ennis, S, Gallagher, L, Geschwind, DH, Gill, M, Haines, JL, Hallmayer, J, Miller, J, Monaco, AP, Nurnberger, JI, Paterson, AD, Pericak-Vance, MA, Schellenberg, GD, Szatmari, P, Vicente, AM, Vieland, VJ, Wijsman, EM, Scherer, SW, Sutcliffe, JS, Betancur, C, Functional impact of global rare copy number variation in autism spectrum disorders, NATURE, 466, 2010, p368-372 Journal Article, 2010 TARA - Full Text

Nwachukwu I, Crumlish N, Heron EA, Gill M, The Irish Mental Health Act 2001: Impact on involuntary admissions in a community mental health service in Dublin, The Psychiatrist, 34, 2010, p436-440 Journal Article, 2010 DOI

Haq F, Behan C, McGlade N, Mulkerrin U, O'Callaghan E, Kinsella A, Corvin A, Donohoe G, Gill M. , The clinical and demographic factors that influence attitudes to antipsychotic medication among people with schizophrenia and schizoaffective disorder, Irish Journal of Psychological Medicine, 2010 Journal Article, 2010

Hill M, Anney RJ, Gill M, Hawi Z, Functional analysis of intron 8 and 3' UTR variable number of tandem repeats of SLC6A3: differential activity of intron 8 variants., Pharmacogenomics Journal, 10, (5), 2010, p442-447 Journal Article, 2010 DOI

Butler AW, Breen G, Tozzi F, Craddock N, Gill M, Korszun A, Maier W, Middleton L, Mors O, Owen M, Perry J, Preisig M, Rice J, Rietschel M, Jones L, Farmer A, Lewis C, McGuffin P., A Genomewide Linkage Study in Suicidality in Major Depressive Disorder Confirms Evidence for Linkage to 2p12, American Journal of Medical Genetics Neuropsychaitric Genetics, 2010 Journal Article, 2010

Kuntsi J, Wood A.C. Rijsdijk F, Johnson K.A. Andreou P, Albrecht B, Arias-Vansquez A, Buitelaar J.K. Mcloughlin G, Rommelse N.N.J. Sergeant J.A. Sonuga-Barke E.J.S. Uebel H, Van Der Meere J.J.. Banaschewski T, Gill M. et al., Separation of cognitive impairments in attention-deficit/hyperactivity disorder into 2 familial factors., Archives of General Psychiatry, 67, (11), 2010, p1159-1167 Journal Article, 2010 DOI TARA - Full Text

Spalletta G, Morris DW, Angelucci F, Rubino IA, Spoletini I, Bria P, Martinotti G, Siracusano A, Bonaviri G, Bernadini S, Caltagirone C, Bossu P, Donohoe G, Gill M, Corvin AP. , BDNF Val66 Met polymorphism is associated with aggressive behaviour in schizophrenia. , European Psychiatry, 25, (6), 2010, p311-313 Journal Article, 2010 DOI

J. Park, M. Willmott, G. Vetuz, C. Toye, A. Kirley, Z. Hawi, K.J. Brookes, M. Gill, L. Kent, Evidence that genetic variation in the oxytocin receptor (OXTR) gene influences social cognition in ADHD, Progress in Neuro-Psychopharmacology and Biological Psychiatry, 34, (4), 2010, p697-702 Journal Article, 2010 TARA - Full Text

Greene CM, Robertson IH, Gill M, Bellgrove MA., Dopaminergic genotype influences spatial bias in healthy adults. , Neuropsychologia, 48, (9), 2010, p2458-2464 Journal Article, 2010 DOI

Nijmeijer JS, Arias-Vásquez A, Rommelse NN, Altink ME, Anney RJ, Asherson P, Banaschewski T, Buschgens CJ, Fliers EA, Gill M, Minderaa RB, Poustka L, Sergeant JA, Buitelaar JK, Franke B, Ebstein RP, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sonuga-Barke EJ, Steinhausen HC, Faraone SV, Hartman CA, Hoekstra PJ, Identifying Loci for the Overlap Between Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Using a Genome-wide QTL Linkage Approach., Journal of the American Academy of Child and Adolescent Psychiatry, 49, (7), 2010, p675-685 Journal Article, 2010 DOI

Moskvina V, Smith M, Ivanov D, Blackwood D, St. Clair D, Hultman C, Toncheva D, Gill M, Corvin A, O'Dushlaine C, Morris DW, Wray N, Sullivan P, Pato C, Pato M, Sklar Pm Purcell S, Holmans P, O'Donovan M, Owen M, Kirov, G, International Schizophrenia Consortium. , Genetic Differences between five european populations. , Human Heredity, 70, 2010, p141 - 149 Journal Article, 2010 DOI

Sobanski E, Banaschewski T, Asherson P, Buitelaar J, Chem W, Frank B, Holtmann M, Bertram K, Sergeant J, Sonuga-Barke E, Stringaris A, Taylor E, Anney R, Ebstein R, Gill M, Ana M, Mulas F, Oades R, Roeyers H, Rothenberger A, Steinhausen H, Faraone S. , Emotional liability in children and adolescents with Attention Deficit Hyperactivity Disorder (ADHD) clinical correlates and familial prevalence, Journal of Child Psychology and Psychiatry, 51, (8), 2010, p915-923 Journal Article, 2010

Johnson, K.A., Dáibhis, A., Tobin, C.T., Acheson, R., Watchorn, A., Mulligan, A., Barry, E., J.L. Bradshaw, M. Gill, Robertson, I.H., Right-sided spatial difficulties in ADHD demonstrated in continuous movement control, Neuropsychologia, 48, (5), 2010, p1255-1264 Journal Article, 2010 DOI

Brooks KJ, Hawi Z, Park J, Scott S, Gill M, Kent L, Polymorphisms of the steroid sulfatase (STS) gene are associated with attention deficit hyperactivity disorder and influence brain tissue mRNA expression., American Journal of Medical Genetics, Neuropsychiatric Genetics, 2010, p1417 - 1423 Journal Article, 2010

Gill, M., Donohoe, G., Corvin, A, What have the genomics ever done for the psychoses?, Psychological Medicine, 40, (4), 2010, p529-540 Journal Article, 2010 TARA - Full Text

Walters J, Corvin A, Williams H, Dragovic M, Quinn E, Judge R, Smith D, Norton N, Giegline I, Hartmann A, Moller HJ, Muglia P, Moskvina V, O'Donoghue T, Morar B, Cooper M, Chandler D, Jablensky A, Gill M, Owen MJ, Kaladjieva L, Morris D, O'Donovan MC, Rujescu D, Donohoe G., Variation in memory function associated with the psychosis susceptibility gene ZNF804A. , Archives of General Psychiatry, 67, (7), 2010, p692 - 700 Journal Article, 2010 URL

Hawi, Z, Kent, L, Hill, M, Anney, RJ, Brookes, KJ, Barry, E, Franke, B, Banaschewski, T, Buitelaar, J, Ebstein, R, Miranda, A, Oades, RD, Roeyers, H, Rothenberger, A, Sergeant, J, Sonuga-Barke, E, Steinhausen, HC, Faraone, SV, Asherson, P, Gill, M, ADHD and DAT1: Further evidence of paternal over-transmission of risk alleles and haplotype., American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 153, (1), 2010, p97-102 Journal Article, 2010 DOI

Cummings E, Donohoe G, Morris DW, Gill M, Corvin A. , Clinical symptomatology and the psychosis risk gene, ZNF804A, Schizophrenia Research, 122, (1-3), 2010, p273-275 Journal Article, 2010 TARA - Full Text

Raychaudhuri S, Korn JM, McCarroll SA, International Schizophrenia Consortium, Altshuler D, Sklar P, Purcell S, Daly MJ, Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function., PLoS genetics, 6, (9, e1001097), 2010 Journal Article, 2010 DOI TARA - Full Text

Cochrane LE, Tansey KE, Gill M, Gallagher L, Anney RJ, Lack of association between markers in the ITGA3, ITGAV, ITGA6 and ITGB3 and autism in an Irish sample., Autism research : official journal of the International Society for Autism Research, 3, (6), 2010, p342 - 344 Journal Article, 2010 DOI

Psychiatric Genetics in, Wright, Stern, Phelan , Core Psychiatry, Elsevier Saunders, 2010, [Corvin A, Gill M.] Book Chapter, 2010

Correia CT, Coutinho AM, Sequeira AF Sousa IG, Almeida JP, Abreu RL, Lobo C, Miguel TS, Conroy J, Cochrane L, Gallagher L, Gill M, Ennis S, Oliveira GG, Vincente AM. , Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TRKB signalling in autism. , Genes Brain Behavior, 9, (7), 2010, p841-848 Journal Article, 2010 DOI

Law Smith, M.J. , Montagne, B., Perrett, D.I., Gill, M., Gallagher, L. , Detecting subtle facial emotion recognition deficits in high-functioning Autism using dynamic stimuli of varying intensities, Neuropsychologia, 48, (9), 2010, p2777-2781 Journal Article, 2010 DOI

Donohoe G, Frodl T, Morris D, Spoletini I, Cannon DM, Cherubini A, Caltagirone C, Bossù P, McDonald C, Gill M, Corvin AP, Spalletta G, Reduced Occipital and Prefrontal Brain Volumes in Dysbindin-Associated Schizophrenia, Neuropsychopharmacology, 35, (2), 2010, p368 - 373 Journal Article, 2010 DOI

Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Carson AR, Casallo G, Casey J, Chu S, Cochrane L, Corsello C, Crawford EL, Crossett A, Dawson G, de Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Goldberg J, Green A, Green J, Guter SJ, Hakonarson H, Heron EA, Hill M, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere CM, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lionel AC, Liu XQ, Lord C, Lotspeich L, Lund SC, Maestrini E, Mahoney W, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Melhem NM, Merikangas A, Migita O, Minshew NJ, Mirza GK, Munson J, Nelson SF, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr JR, Parrini B, Paton T, Pickles A, Piven J, Posey DJ, Poustka A, Poustka F, Prasad A, Ragoussis J, Renshaw K, Rickaby J, Roberts W, Roeder K, Roge B, Rutter ML, Bierut LJ, Rice JP, Salt J, Sansom K, Sato D, Segurado R, Senman L, Shah N, Sheffield VC, Soorya L, Sousa I, Stoppioni V, Strawbridge C, Tancredi R, Tansey K, Thiruvahindrapduram B, Thompson AP, Thomson S, Tryfon A, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Wallace S, Wang K, Wang Z, Wassink TH, Wing K, Wittemeyer K, Wood S, Yaspan BL, Zurawiecki D, Zwaigenbaum L, Betancur C, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Gallagher L, Geschwind DH, Gill M, Haines JL, Miller J, Monaco AP, Nurnberger JI, Paterson AD, Pericak-Vance MA, Schellenberg GD, Scherer SW, Sutcliffe JS, Szatmari P, Vicente AM, Vieland VJ, Wijsman EM, Devlin B, Ennis S, Hallmayer J, A genomewide scan for common alleles affecting risk for autism., Human molecular genetics, 19, (20), 2010, p4072-4082 Journal Article, 2010 TARA - Full Text DOI

Carroll LS, Williams NM, Moskvina V, Russell E, Norton N, Williams HJ, Peirce T, Georgieva , Dwyer S, Grozeva D, Greene E, Farmer A, McGuffin P, Morris DW, corvin A, Gill M, Rujescu D, Sham P, Holmans P, Jones I, Kirov G, Craddock N. O'Donovan MC, Owen MJ. , Evidence for rate and common genetic risk variants for schizophrenia at a protein kinase C, alpha, Molecular Psychiatry, 15, (11), 2010, p1101-1111 Journal Article, 2010 DOI

Smith MJ, Montagne B, Perrett DI, Gill M, Gallagher L. , Detecting subtle facial emotional recognition deficits in high functioning Autism using dynamic stimuli of varying intensities. , Neuropsychologia, 48, (9), 2010, p2777-2781 Journal Article, 2010 DOI

Chen X, Lee G, Maher BS, Fanous AH, Chen J, Zhao Z, Guo A, van den Oord E, Sullivan PF, Shi J, Levinson DF, Gejman PV, Sanders A, Duan J, Owen MJ, Craddock NJ, O'Donovan MC, Blackman J, Lewis D, Kirov GK, Qin W, Schwab S, Wildenauer D, Chowdari K, Nimgaonkar V, Straub RE, Weinberger DR, O'Neill FA, Walsh D, Bronstein M, Darvasi A, Lencz T, Malhotra AK, Rujescu D, Giegling I, Werge T, Hansen T, Ingason A, Nöethen MM, Rietschel M, Cichon S, Djurovic S, Andreassen OA, Cantor RM, Ophoff R, Corvin A, Morris DW, Gill M, Pato CN, Pato MT, Macedo A, Gurling HM, McQuillin A, Pimm J, Hultman C, Lichtenstein P, Sklar P, Purcell SM, Scolnick E, St Clair D, Blackwood DH, Kendler KS, GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia., Molecular Psychiatry, 153B, (8), 2010, p1417 - 1424 Journal Article, 2010 TARA - Full Text DOI

Gilks WP, Allott EH, Donohoe G, Cummings E, Consortium IS, Gill M, Corvin AP, Morris DW, Replicated genetic evidence supports a role for HOMER2 in schizophrenia., Neuroscience Letters, 468, (3), 2010, p229 - 233 Journal Article, 2010 DOI

Murtagh A, Hurley AL, Kinsella A, Corvin A, Donohoe G, Gill M, O'Callaghan E, Murphy KC. , The Letter-Number Sequencing Test and its association with potential to work among people with psychotic illness , European Psychiatry, 25, (2), 2010, p101-104 Journal Article, 2010 DOI

Nwachukwu I, Crumlish N, Heron E, Gill M., Irish Mental Health Act2001 impact on involuntary admissions in a community mental health service in Dublin, The Psychiatrist, 34, 2010, p436 - 440 Journal Article, 2010

Lupton MK, Stahl D, Archer N, Foy C, Poppe M, Lovestone S, Hollingworth P, Williams J, Owen MJ, Dowzell K, Abraham R, Sims R, Brayne C, Rubinsztein D, Gill M, Lawlor B, Lynch A, Powell JF, Education, occupation and retirement age effects on the age of onset of Alzheimer's disease., International Journal of Geriatric Psychiatry, 25, (1), 2010, p30-36 Journal Article, 2010 DOI

Tansey KE, Brookes KJ, Hill MJ, Cochrane LE, Gill M, Skuse D, Correia C, Vicente A, Kent L, Gallagher L, Anney RJ, Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studies., Neuroscience Letters, 474, (3), 2010, p163-167 Journal Article, 2010 DOI

Gary Donohoe, Emma Rose, Thomas Frodl, Derek Morris, Ilaria Spoletini, Fulvia Adriano, Sergio Bernardini, CarloCaltagirone, Paola Bossù, Michael Gill, Aiden P. Corvin and Gianfranco Spalletta, ZNF804A risk allele is associated with relatively intact gray matter volume in patients with schizophrenia, NeuroImage, 54, (3), 2010, p2132-2137 Journal Article, 2010 TARA - Full Text

Bellgrove, M.A., Johnson, K.A., Barry, E., Mulligan, A., Hawi, Z., Gill, M., Robertson, I.H., Chambers, C.D, Dopaminergic haplotype predicts spatial inattention in children with ADHD, Archives of General Psychiatry, 66, (10), 2009, p1135 - 1142 Journal Article, 2009 URL

O'Dushlaine C., Kenny E., Heron E.A., Segurado R., Gill M,, Morris D.W., Corvin A. , The SNP ratio test: pathway analysis of genome-wide association datasets., Bioinformatics, 25, (20), 2009, p2762 - 2763 Journal Article, 2009 DOI TARA - Full Text

Christopher Doyle, Keeley Brookes, Jennifer Simpson, Joanne Park, Sarah Scott, David R. Coghill, Ziarah Hawi, Aiveen Kirley, Michael Gill and Lindsey Kent, Replication of an Association of a Promoter Polymorphism of the Dopamine Transporter Gene and Attention Deficit Hyperactivity Disorder, Neuroscience Letters, 462, 2009, p179 - 181 Journal Article, 2009 TARA - Full Text DOI

International Schizophrenia Consortium, Common polygenic variation contributes to risk of schizophrenia and bipolar disorder., Nature, 460, (7256), 2009, p748-752 Journal Article, 2009 DOI

Curran TA, Gawley E, Casey P, Gill M, Crumlish N, Depression, Suicidality and Alcohol Abuse among Medical and Business Students, Irish Medical Journal, 102, (8), 2009, p249 - 251 Journal Article, 2009 URL

Weiss LA, Arking DE, The Gene Discovery project of Johns Hopkins & the Austism Consortium, A genome-wide linkage and association scan reveals novel loci for autism. , Nature, 461, (7265), 2009, p802 - 808 Journal Article, 2009 TARA - Full Text

McCarthy SE, Makarov V, Kirov G, Addinton AM, McClellan J, Yoon S, Perkins DO, Dickel DE Kusenda M, Kratoshevsky O, Krause V, Kumar RA Grozveva D, Malhotra D et al. , Microduplications of 16p11.2 are associated with schizophrenia, Nature Genetics, 41, (11), 2009, p1223-1227 Journal Article, 2009 TARA - Full Text

Raychaudhuri S, Plenge RM, Rossin EJ, Ng AC; International Schizophrenia Consortium, Purcell SM, Sklar P, Scolnick EM, Xavier RJ, Altshuler D, Daly MJ, Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions., PLoS Genetics, 5, (6), 2009, pe1000534- Journal Article, 2009 TARA - Full Text

Donohoe G, Hayden J, McGlade N, O'Gráda C, Burke T, Barry S, Behan C, Dinan TG, O'Callaghan E, Gill M, Corvin AP, Is "clinical" insight the same as "cognitive" insight in schizophrenia?, Journal of the International Neuropsychological Society : JINS, 15, (3), 2009, p471-5 Journal Article, 2009 DOI TARA - Full Text

Greene CM, Bellgrove MA, Gill M, Robertson IH, Noradrenergic genotype predicts lapses in sustained attention, Neuropsychologia, 47, (2), 2009, p591 - 594 Journal Article, 2009 DOI

Marco R, Miranda A, Schlotz W, Melia A, Mulligan A, JMuller U, Andreou P, Butler L, Christiansen H, Gabriels I, Medad S, Albrecht B, Uebel J, Asherson P, Banaschewski T, Gill M, Kuntsi J, Mulas F, Oades R, Roeyers H, Steinhausen HC, Rothenberger A, Faraone SV, Sonuga-Barke EJ, Delay and reward choice in ADHD: An Experimental test of the role of delay aversion., Neuropsychology, 23, (3), 2009, p367 - 380 Journal Article, 2009 URL

Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, Powell J, Proitsi P, Lupton MK, Brayne C, Rubinsztein DC, Gill M, Lawlor B, Lynch A, Morgan K, Brown KS, Passmore PA, Craig D, McGuinness B, Todd S, Holmes C, Mann D, Smith AD, Love S, Kehoe PG, Hardy J, Mead S, Fox N, Rossor M, Collinge J, Maier W, Jessen F, Schürmann B, van den Bussche H, Heuser I, Kornhuber J, Wiltfang J, Dichgans M, Frölich L, Hampel H, Hüll M, Rujescu D, Goate AM, Kauwe JS, Cruchaga C, Nowotny P, Morris JC, Mayo K, Sleegers K, Bettens K, Engelborghs S, De Deyn PP, Van Broeckhoven C, Livingston G, Bass NJ, Gurling H, McQuillin A, Gwilliam R, Deloukas P, Al-Chalabi A, Shaw CE, Tsolaki M, Singleton AB, Guerreiro R, Mühleisen TW, Nöthen MM, Moebus S, Jöckel KH, Klopp N, Wichmann HE, Carrasquillo MM, Pankratz VS, Younkin SG, Holmans PA, O'Donovan M, Owen MJ, Williams J, Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease., Nature Genetics, 41, (10), 2009, p1088-1093 Journal Article, 2009 DOI TARA - Full Text

Ball HA, Samaan Z, Brewster S, Craddock N, Gill M, Korszun A, Maier W, Middleton L, Mors O, Owen MJ, Perry J, Preisig M, Rice J, Rietschel M, Jones L, Jones I, Farmer AE, McGuffin P. , Depression, migraine with aura and migrane without auta: their familiality and interrelatedness. , Cephalalgia, 29, (8), 2009, p848 - 854 Journal Article, 2009 DOI

Correia C, Coutinho AM, Almeida J, Lontro R, Lobo C, Miguel TS, martins M, Gallagher L, Conroy J, Gill M, Oliveira G, Vincente AM. , Association of the alpha4 intergrin gene (ITGA4) with autism., American Journal of Medical Genetics, 2009 Journal Article, 2009 DOI

Conroy, J, Cochrane, L, Anney, RJ, Sutcliffe, JS, Carthy, P, Dunlop, A, Mullarkey, M, O'hici, B, Green, AJ, Ennis, S, Gill, M, Gallagher, L, Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32., American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 150, (4), 2009, p535-544 Journal Article, 2009 DOI

Lupton MK, Stahl D, Archer N, Foy C, Poppe M, Lovestone S, Hollingworth P, Williams J, Owen MJ, Dowzell K, Abraham R, Sims R, Brayne C, Ruginstein D, Gill M, Lawlor B, Lynch A Powell JF., Education, occupation and retirement age effects on the age of onset of Alzheimer's disease. , International Journal of Geriatric Psychiatry, 2009 Journal Article, 2009 DOI

O'Gráda C, Barry S, McGlade N, Behan C, Haq F, Hay, Does the ability to sustain attention underlie symptom severity in schizophrenia? , Schizophrenia Research, 107, (2-3), 2009, p319 - 323 Journal Article, 2009 URL DOI

O'Donovan MC, Norton N, Williams H, Peirce T, Moskvina V, Nikolov I, Hamshere M, Carroll L, Georgieva L, Dwyer S, Holmans P, Marchini JL, Spencer CC, Howie B, Leung HT, Giegling I, Hartmann AM, Möller HJ, Morris DW, Shi Y, Feng G, Hoffmann P, Propping P, Vasilescu C, Maier W, Rietschel M, Zammit S, Schumacher J, Quinn EM, Schulze TG, Iwata N, Ikeda M, Darvasi A, Shifman S, He L, Duan J, Sanders AR, Levinson DF, Adolfsson R, Osby U, Terenius L, Jönsson EG, Cichon S, Nöthen MM, Gill M, Corvin AP, Rujescu D, Gejman PV, Kirov G, Craddock N, Williams NM, Owen MJ., Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2., Molecular Psychiatry, 14, (1), 2009, p30 - 36 Journal Article, 2009 DOI URL TARA - Full Text

Donohoe G, Hayden J, McGlade N, O'Grada C, Burke T, Barry S, Behan C, DInan T, O'Callaghan E, Gill M, Corvin A. , Is 'Clinical' insight the same as 'Cognitive' insight in schizophrenia?, Journal of the International Neuropsychological Society, 15, (3), 2009, p471-475 Journal Article, 2009 DOI TARA - Full Text

Mulligan A, Anney RJ, O'Regan M, Chen W, Butler L, Fitzgerald M, Buitelaar J, Steinhausen HC, Rothenberger A, Minderaa R, Nijmeijer J, Hoekstra PJ, Oades RD, Roeyers H, Buschgens C, Christiansen H, Franke B, Gabriels I, Hartman C, Kuntsi J, Marco R, Meidad S, Müller UC, Psychogiou L, Rommelse N, Thompson M, Uebel H, Banaschewski T, Ebstein R, Eisenberg J, Manor I, Miranda A, Mulas F, Sergeant J, Sonuga-Barke E, Asherson P, Faraone SV, Gill M., Autism Symptoms in Attention-Deficit/Hyperactivity Disorder: A Familial Trait which Correlates with Conduct, Oppositional Defiant, Language and Motor Disorders., Journal of Autism and Developmental Disorders, 39, (2), 2009, p210 - 211 Journal Article, 2009 DOI DOI URL

Kirov G, Grozeva D, Norton N, Ivanov D, Mantripragada KK, Holmans P; International Schizophrenia Consortium; Wellcome Trust Case Control Consortium, Craddock N, Owen MJ, O'Donovan MC, Support for the involvement of large copy number variants in the pathogenesis of schizophrenia., Human Molecular Genetics, 18, (8), 2009, p1497 - 1503 Journal Article, 2009 DOI

Hamshere ML, Schulze TG, Schumacher J, Corvin A, Owen JM, Jamra RA, Propping Pm Maier W. Orozco y Diaz G, Mayoral F, Rivas F. Jones I, Jones L, Kirov G, Gill M, Holmans PA, Nothen MM, Cichon S, Rietschel M, Craddock N, Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis show genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31., Bipolar Disorders, 11, (6), 2009, p610 - 620 Journal Article, 2009 DOI

Donohoe G, Walters J, Morris DW, Quinn EM, Judge R, Norton N, Giegling I, Hartmann AM, Möller HJ, Muglia P, Williams H, Moskvina V, Peel R, O'Donoghue T, Owen MJ, O'Donovan MC, Gill M, Rujescu D, Corvin A, Influence of NOS1 on verbal intelligence and working memory in both patients with schizophrenia and healthy control subjects., Archives of General Psychiatry, 66, (10), 2009, p1045-54 Journal Article, 2009 TARA - Full Text DOI URL

Correia, C., Coutinho, A.M., Almeida, J., (...), Oliveira, G., Vicente, A.M. , Association of the α4 integrin subunit gene, American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 150, (8), 2009, p1147-1151 Journal Article, 2009 DOI

K Zhou, Chen W, Buitelaar J, Banaschewski T, Oades R, Franke B, Sonuga-Barke E, Ebstein R, Eisenberg J, Gill M, Manor I, Miranda A, Mulas F, Roeyers J, Rothenberger A, Sergeant J, Steinhausen H, Lasky-Su J, Taylor E, Brookes K, Xu X, Neale B, Rijsdijk F, Thompson M, Asherson P, Faraone S, Genetic Heterogeneity in ADHD: DAT1 Gene Only Affects Probands without CD., American Journal of Medical Genetics, 147B, (8), 2008, p1481 - 1487 Journal Article, 2008 DOI

Mulligan, A, Gill M, Fitzgerald M, Case of ADHD and Major Y chromosome Abnormality, Journal of Attention Disorders, 12, (1), 2008, p103 - 105 Journal Article, 2008 DOI

Ferreira MA, O'Donovan MC, Meng YA, Jones IR, Ruderfer DM, Jones L, Fan J, Kirov G, Perlis RH, Green EK, Smoller JW, Grozeva D, Stone J, Nikolov I, Chambert K, Hamshere ML, Nimgaonkar VL, Moskvina V, Thase ME, Caesar S, Sachs GS, Franklin J, Gordon-Smith K, Ardlie KG, Gabriel SB, Fraser C, Blumenstiel B, Defelice M, Breen G, Gill M, Morris DW, Elkin A, Muir WJ, McGhee KA, Williamson R, Macintyre DJ, Maclean AW, St Clair D, Robinson M, Van Beck M, Pereira AC, Kandaswamy R, McQuillin A, Collier DA, Bass NJ, Young AH, Lawrence J, Nicol Ferrier I, Anjorin A, Farmer A, Curtis D, Scolnick EM, McGuffin P, Daly MJ, Corvin AP, Holmans PA, Blackwood DH; Wellcome Trust Case Control Consortium, Gurling HM, Owen MJ, Purcell SM, Sklar P, Craddock N., Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder., Nature Genetics, 40, (9), 2008, p1056 - 1058 Journal Article, 2008 DOI TARA - Full Text

Morris DW, Murphy K, Kenny N, Purcell SM, McGhee KA, Schwaiger S, Nangle JM, Donohoe G, Clarke S, Scully P, Quinn J, Meagher D, Baldwin P, Crumlish N, O'Callaghan E, Waddington JL, Gill M, Corvin AP, Dysbindin (DTNBP1) and the BLOC-1 protein complex: main and epistatic gene effects are potential contributors to schizophrenia susceptibility, Biological Psychiatry, 63, (1), 2008, p24 - 31 Journal Article, 2008 URL DOI URL

Lynch CA, Brazil J, Cullen B, Coakley D, Gill M, Lawlor BA, Hawi Z, Apolipoprotein E promoter polymorphisms (-491A/T and -427T/C) and Alzheimer's disease: no evidence of association in the Irish population., Irish Journal of Medical Science, 177, (1), 2008, p29-33 Journal Article, 2008 DOI

Johnson, K.A., Robertson, I.H. Barry, E., Mulligan, A., Dáibhis, A., Daly, M., Watchorn, A., Gill, M., Bellgrove, M.A, Impaired conflict resolution and alerting in children with ADHD: evidence from the Attention Network Task (ANT). , Journal of Child Psychology and Psychiatry, 49, (12), 2008, p1339 - 1347 Journal Article, 2008 DOI

O'Dushlaine, C. T., Dolan, C., Weale, M. E., Stanton, A., Croke, D. T., Kalviainen, R., Eriksson, K., Kantanen, A. M., Gibson, R. A., Hosford, D., Sisodiya, S. M., Gill, M., Corvin, A. P., Morris, D. W., Delanty, N., Cavalleri, G. L., An assessment of the Irish population for large-scale genetic mapping studies involving epilepsy and other complex diseases, Eur J Hum Genet, 16, (2), 2008, p176 - 183 Journal Article, 2008 TARA - Full Text DOI

Zhou, K, Asherson, P, Sham, P, Franke, B, Anney, RJ, Buitelaar, J, Ebstein, R, Gill, M, Brookes, K, Buschgens, C, Campbell, D, Chen, W, Christiansen, H, Fliers, E, Gabriëls, I, Johansson, L, Marco, R, Mulas, F, Müller, U, Mulligan, A, Neale, BM, Rijsdijk, F, Rommelse, N, Uebel, H, Psychogiou, L, Xu, X, Banaschewski, T, Sonuga-Barke, E, Eisenberg, J, Manor, I, Miranda, A, Oades, RD, Roeyers, H, Rothenberger, A, Sergeant, J, Steinhausen, HC, Taylor, E, Thompson, M, Faraone, SV, Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings., Biological psychiatry, 64, (7), 2008, p571-6 Journal Article, 2008 TARA - Full Text DOI

Johnson, K.A., Barry, E., Bellgrove, M.A., Cox, M., Kelly, S.P., Daibhis, A., Daly, M., Keavey, M., Watchorn, M., Fitzgerald, M., McNicholas, F., Kirley, A., Robertson, I.H., Gill, M, Dissociation in response to methylphenidate on response variability in a group of medication naïve children with ADHD , Neuropsychologia, 46, (5), 2008, p1532 - 1541 Journal Article, 2008 URL DOI TARA - Full Text URL

Christiansen H, Chen W, Oades R, Asherson P, Taylor E, Lasky-Su J, Zhou K, Banaschewski T, Buitelaar J, Andreou P, Buschgens C, Campbell D, Ebstein R, Eisenberg J, fliers E, Gill M, et al. , Co-transmission of Conduct Problems with Attention Deficit Hyperactivity Disorder: familial evidence for a distinct disorder., Journal of Neural Transmission, 115, (2), 2008, p163 - 175 Journal Article, 2008 DOI

Corvin A, Donohoe G, Nangle JM, Schwaiger S, Morris D, Gill M., A dysbindin risk haplotype associated with less severe manic-type symptoms in psychosis., Neuroscience Letters, 431, (2), 2008, p146 - 149 Journal Article, 2008 URL DOI URL

Mefford J, Sharp A, Baker C, Itsara A, Jiang Z, Buysse K, Huang S, Maloney V, Crolla J, Baralle D, Collins A, Mercer C, Norga K, De Ravel T, Devriendt K, Bongers E, de Leeuw N, Reardon W, Gimelli S, Bena F, Hennekam R et al , Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes, The New England Journal of Medicine, 359, (16), 2008, p1685-1699 Journal Article, 2008 TARA - Full Text DOI

Brookes KJ, Hawi Z, Kirley A, Barry E, Gill M, Kent L. Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder. , Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder., American Journal of Medical Genetics, 147B, (8), 2008, p1531 - 1535 Journal Article, 2008 DOI

K.A. Johnson, S.P. Kelly, I.H. Robertson, E. Barry, A. Mulligan, M. Daly, D. Lambert, C. McDonnell, T.J. Connor, Z. Hawi, M. Gill and M.A. Bellgrove, Absence of the 7-repeat variant of the DRD4 VNTR is associated with drifting sustained attention in children with ADHD but not in controls, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics , 147B , (6), 2008, p927 - 937 Journal Article, 2008 DOI TARA - Full Text

Yang MS, Morris DW, Kenny E, O'Dushalaine CT, Schwaiger S, Nangle, JM, Clarke S, Scully P, Quinn J, Meagher D, Baldwin P, Crumlish N, O'Callaghan E, Waddington JL, Gill M, Corvin A, Chitinase-3-Like1 (CHI3L1) Gene and Schizophrenia: Genetic Association and a Potential functional Mechanism. , Biological Psychaitry, 64, (2), 2008, p98 - 103 Journal Article, 2008 URL URL DOI

Zhou K, Dempfle A, Acros-Burgos M, Bakker SC, Banaschewski T, Biederman J, Buitelaar J, Castellanos FX, Doyle A, Ebstein RP, Ekholm J, ForaboscoP, Franke B, Freitag C, Friedel S, Gill M, Heberbrand J, Hinney A et al., Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder. , American Journal of Medical Genetics, 147B, (8), 2008, p1392 - 1398 Journal Article, 2008 DOI

Chen Wai, Zhou K, Sham P, Franke B, Kuntsi J, Campbell D, Fleischman K, Knight J, Andreou P, Arnold R, Marieke A, Boer F, Boholst M, Buschgens C, Butler L, Christiansen H, Fliers E, Howe-forbes R, Bariels I, Heise A, Lbetzki Korn I, Marco R, Medad S, Minderaa R, Muller U, Mulligan A, et al., DSM-IV Combined type ADHD Shows Familial Association with Sibling Trait Scores: A sampling Strategy for QTL Linkage, American Journal of Medical genetics Part B (Neuropsychaitric Genetics), 147B, (8), 2008, p1450 - 1460 Journal Article, 2008 DOI

Nicola McGlade, Caragh Behan, Judy Hayden, Therese O'Donoghue, Rosie Peel, Farhan Haq, Michael Gill, Aiden Corvin, Eadbhard O'Callaghan, Gary Donohoe, Mental state decoding v. mental state reasoning as a mediator between cognitive and social function in psychosis , British Journal of Psychiatry, 193, (1), 2008, p77-78 Journal Article, 2008 TARA - Full Text DOI

Donohoe G, Behan C, Hayden J, O'Donoghue T, Peel R, Haq F, Gill M, Corvin A, O'Callaghan E. , Mental state decoding versus mental state reasoning as a mediator between cognitive and social function in psychosis., British Journal of Psychiatry, 193, (1), 2008, p77 - 78 Journal Article, 2008 TARA - Full Text DOI

O'Donovan MC, Craddock N, Norton N, Williams H, Peirce T, Moskvina V, Nikolov I, Hamshere M, Carroll L, Georgieva L, Dwyer S, Holmans P, Marchini JL, Spencer CC, Howie B, Leung HT, Hartmann AM, Möller HJ, Morris DW, Shi Y, Feng G, Hoffmann P, Propping P, Vasilescu C, Maier W, Rietschel M, Zammit S, Schumacher J, Quinn EM, Schulze TG, Williams NM, Giegling I, Iwata N, Ikeda M, Darvasi A, Shifman S, He L, Duan J, Sanders AR, Levinson DF, Gejman PV; Molecular Genetics of Schizophrenia Collaboration, Gejman PV, Sanders AR, Duan J, Levinson DF, Buccola NG, Mowry BJ, Freedman R, Amin F, Black DW, Silverman JM, Byerley WF, Cloninger CR, Cichon S, Nöthen MM, Gill M, Corvin A, Rujescu D, Kirov G, Owen MJ., Identification of loci associated with schizophrenia by genome-wide association and follow-up., Nature Genetics, 40, (9), 2008, p1053 - 1055 Journal Article, 2008 DOI URL

Donohoe G, Spoletini I, McGlade N, Behan C, Hayden J, O'Donoghue T, Peel R, Haq F, Walker C, O'Callaghan E, Spalletta G, Gill M, Corvin A , Are relational style and neuropsychological performance predictors of social attributions in chronic schizophrenia?, Psychiatric Research, 161, (1), 2008, p19-27 Journal Article, 2008 DOI URL

Donohoe G, Morris D.W., De Sanctis P, Magno E, Montesi J, Garavan H, Robertson I, Javitt D, Gill M, Corvin A, Fox J. , Early Visual Processing Deficits in Dysbindin-Associated Schizophrenia, Biological Psychiatry, 63, (5), 2008, p484 - 489 Journal Article, 2008 TARA - Full Text

Sanders J, Johnson K, Garavan H, Gill M, Gallagher L, A review of neuropsychological and neuroimaging research in autistic spectrum disorders: Attention, inhibition and cognitive flexibility., Research in Autism Spectrum Disorders, 2, (1), 2008, p1 - 16 Journal Article, 2008 DOI

Anney RJ, Kenny E, O'Dushlaine CT, Lasky-Su J, Franke B, Morris DW, Neale BM, Asherson P, Faraone SV, Gill M, Non-random error in genotype calling procedures: Implications for family-based and case-control genome-wide association studies, American Journal of Medical Genetics B Neuropsychiatric Genetics, 147B, (8), 2008, p1379 - 1386 Journal Article, 2008 TARA - Full Text

Johnson K, Robertson I, Kelly S, Silk T, Barry E, Daibhis A, Watchorn A, Keavey M, Fitzgerald M, Gallagher L, Gill M, Bellgrove M, Dissociation in performance of children with ADHD and high-functioning autism on a task of sustained attention. , Neuropsychologia, 45, (10), 2007, p2234 - 2245 Journal Article, 2007 TARA - Full Text DOI

Bellgrove MA, Barry E, Johnson KA, Cox M, Dáibhis A, Daly M, Hawi Z, Lambert D, Fitzgerald M, McNicholas F, Robertson IH, Gill M, Kirley A., Spatial attentional bias as a marker of genetic risk, symptom severity and stimulant response in ADHD. , Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 33, (10), 2007, p2536 - 2545 Journal Article, 2007 TARA - Full Text DOI URL URL

Yang M, S, Gill M, A Review of Gene Linkage, Assocaition and Expression Studies in Autism and an Assessment of Convergent Evidence, International Journal of Developmental Neuroscience, 25, (2), 2007, p69 - 85 Journal Article, 2007 DOI

Walsh E, Dagger D, Rogers C, Wade V, Gaffney C, Armstrong K, Fitzmaurice B, Gill, M, Semantic Interoperation of Services: Adaptive Simulations and Sakai, 7th Sakai Conference, The Netherlands, June 12- 14, 2007 Conference Paper, 2007

Armstrong K, Rogers C, Fitzmaurice B, Dagger D, Gill M. , The use of an Online Simulator to Teach Communications Skills in Healthcare., Education Technology Users Conference, Dublin Institute of Technology, 23rd May-25th May 20, 2007 Conference Paper, 2007

Sanders J, Gill M, Unravelling the genome: a review of molecular genetic research in schizophrenia., Irish Journal of Medical Science , 176, (1), 2007, p5 - 9 Journal Article, 2007

Donohoe G, Morris DW, Clarke S, McGhee K, Schwaiger S, Nangle JM, Garavan H, Robertson I, Gill M, Corvin A., Variance in neurocognitive performance is associated with Dysbindin-1 in schizophrenia: a preliminary study., Neuropsychologia, 45, (2), 2007, p454 - 458 Journal Article, 2007 URL URL DOI

Dagger, D., Rogers, C., Wade, V., Gaffney, C., Armstrong, K., Fitzmaurice, B., Gill, M., Walsh, E., Adaptive Simulations for Communication Skills Training in Healthcare, In Proceedings of 2nd International Workshop on Personalisation for E-Health at the 11th International Conference on User Modelling, Corfu, Greece, 25-29 June, 2007 , 2007 Conference Paper, 2007 URL

Yang M, Cochrane L, Conroy J, Hawi Z, Fitzgerald M, Gallagher L, Gill M, Protein Kinase C-Beta 1 gene variants are not associated with autism in the Irish population, Psychiatric Genetics , 17, (1), 2007, p39 - 41 Journal Article, 2007 DOI URL

Bellgrove, M.A., Chambers, C.D., Johnson, K.A., Dáibhis, A., Daly, M., Hawi, Z., Lambert, D., Gill, M., Robertson, I.H., Dopaminergic genotype biases spatial attention in healthy children, Molecular Psychiatry, 12, (8), 2007, p786 - 792 Journal Article, 2007 DOI

Corvin A, Donohoe G, McGhee K, Murphy K, Kenny N, Schwaiger S, Nangle JM, Morris D, Gill M., D-amino acid oxidase (DAO) genotype and mood symptomatology in schizophrenia., Neuroscience Letters, 426, (2), 2007, p97 - 100 Journal Article, 2007 URL URL DOI

Jones I, Hanshere M L, Nangle J M, Bennett P, Middle F, Heron J, Segurado R, Lambert D, Williams H, Corvin A, Owen J J, Jones L, Gill M Craddock N, Bipolar affective puerperal psychosis- genome-wide significant evidence for linkage to chromosome 16., American Journal of Psychiatry , 164, (7), 2007, p1 - 6 Journal Article, 2007 DOI TARA - Full Text

Fitzmaurice B, Armstrong K, Carroll V, Dagger D, Gill M., Virtual Interviews for Students Interacting Online for Psychiatry (VISIOn): a novel resource for learning clinical interview skills, Psychiatric Bulletin, 31, 2007, p218 - 220 Journal Article, 2007 DOI

Lasky-Su J, Banaschewski T, Buitelaar J, Branke B, Brookes K, Sonuga-Barke E, Ebstei4n R, Eisenberg J, Gill M, Manor I, Miranda A, Mulas F, Oades R, Roeyers H, Rothenberger A, Sergeant J, Steinhausen, H, Taylor E, Zhou K, Thompson M, Asherson P, Faraone S., Partial Replication of a DRD4 association in ADHD individuals using a statistically derived quantitative trait for ADHD in a family-based association test. , Biological Psychiatry, 62, (9), 2007, p985 - 990 Journal Article, 2007 DOI

Johnson, K.A., Robertson, I.H., Kelly, S.P., Silk, T.J., Daibhis A, Watchorn A, Keavey M, Gallagher, L., Barry, E., Cox, M., Fitzgerald, M., Gill, M., Bellgrove, M.A., Dissociation in performance of children with ADHD and autism on a task of sustained attention, Neuropsychologia, 45, (10), 2007, p2234 - 2245 Journal Article, 2007 URL TARA - Full Text DOI URL

Johnson KA,Kelly SP,Bellgrove MA,Barry E,Cox M, Gill M, Robertson IH, Response variability in Attention Deficit Hyperactivity Disorder:, Neuropsychologia, 45, (4), 2007, p630 - 638 Journal Article, 2007 DOI TARA - Full Text

Donohoe G, Morris DW, Robertson IH, McGhee KA, Murphy K, Kenny N, Clarke S, Gill M, Corvin AP., DAOA ARG30LYS and verbal memory function in schizophrenia., Molecular Psychiatry, 12, (9), 2007, p795 - 796 Journal Article, 2007 URL URL DOI

Corvin A, McGhee KA, Murphy K, Donohoe G, Nangle JM, Schwaiger S, Kenny N, Clarke S, Meagher D, Quinn J, Scully P, Baldwin P, Browne D, Walsh C, Waddington JL, Morris DW, Gill M, Evidence for association and epistasis at the DAOA/G30 and D-amino acid oxidase loci in an Irish schizophrenia sample, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 144, (7), 2007, p949 - 953 Journal Article, 2007 URL DOI URL

Avenues for the Neuro-Remediation of ADHD: lessons from clinical neurosciences in, editor(s)Bellgrove MA, Fitzgerald M, Gill M , Handbook of Attention Deficit Hyperactivity Disorder, London, Wyley, 2007, [O'Connell RG, Bellgrove MA, Robertson IH] Book Chapter, 2007

Moskvina V, Farmer a, Jones I, Brewster S, Ferrero F, Gill M, Jones L, Maier W, Mors O, Owen M, Perry J, Preisig M, Rietschel M, McGuffin P, Craddock N, Korszun A, , Sex Differences in Symptom Patterns of Recurrent Major Depression in Siblings. , Depress Anxiety, Oct 12, 2007 Journal Article, 2007

Thapar A, Langley K, Asherson P, Gill M., Gene-environment interplay in attention-deficit hyperactivity disorder and the importance of a develomental perspective, British Journal of Psychiatry, 190, 2007, p1 - 3 Journal Article, 2007 TARA - Full Text DOI

Donohoe G, Morris D, Clarke S, McGhee K, Schwaiger S, Nangle JM, Robertson I, Gill M, Corvin A. , Variance in facial recognition performance associated with BDNF in schizophrenia., American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 144B, 2007, p578 - 579 Journal Article, 2007 URL DOI URL

Waddington JL, Corvin A, Donohoe G, O'Tuathaigh C, Mitchell K, Gill M., Functional genomics and schizophrenia; endophenotypes and mutant models., Psychiatric Clinics of North America, 30, (3), 2007, p365 - 399 Journal Article, 2007 URL

Armstrong K, Rogers C, Fitzmaurice B, Dagger D, Gill M, The use of an Online Simulator to Teach Communication Skills in Healthcare, Edtech 2007, Dublin, Ireland, May, 2007 Invited Talk, 2007

Donohoe G, Clarke S, Morris D, Nangle JM, Schwaiger S, Gill M, Corvin A, Robertson IH., Are deficits in executive sub-processes simply reflecting more general cognitive decline in schizophrenia, Schizophrenia Research, 85, (1-3), 2006, p168 - 173 Journal Article, 2006 URL DOI URL

Norton N, Moskvina V, Morris DW, Bray NJ, Zammit S, Williams NM, Williams HJ, Preece AC, Dwyer SL, Wilkinson JC, Spurlock G, Kirov G, Buckland P, Waddington JL, Gill M, Corvin AP, Owen MJ, O?Donovan MC. , Evidence that interaction between Neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia., American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 141B, (1), 2006, p96 - 101 Journal Article, 2006 DOI

Hollingworth P, Hamshere M, Moskvina V, Dowzell K, Moore P, Foy C, Archer BA, Lynch A, Lovestone S, Brayne C, Rubinsztein D, Lawlor B, Gill M, Owen M, Williams J., Four Components describe behavioural symptoms in 1120 individuals with late onset Alzheimer's disease, Journal of the American Geriatrics Society, 54, (9), 2006, p1348 - 1354 Journal Article, 2006 DOI

Donohoe G, Morris D, Robertson IH, Gill M, Foxe J, Corvin A, Dysbindin and Cognition In An Irish Sample., Biological Psychiatry , 59, (8), 2006, pp623 Meeting Abstract, 2006

Brookes K.J., Neale B, Thapar A, Gill M, Langley K, Hawi Z, Xu X, Mill J, Taylor E, Franke B, Chen W, Ebstein R, Buitelaar J, Banaschewski T, Sonuga-Barke E, Eisenberg J, Manor I, Miranda A, Oades RD, Roeyers J, Rothenberger A, Sergeant J, Steinhausen H.C. Faraone S.V. Asherson P, Differential dopamine receptor D4 allele association with ADHD dependent of proband season of birth, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B, (1), 2006, p94-99 Journal Article, 2006 DOI

Bellgrove M, Mattingley J, Hawi Z, Mullins C, Kirley A, Gill M, Robertson I, Impaired temporal resolution of visual attention and DBH genotype in attention deficit hyperactivity disorder (ADHD) , Biological Psychiatry, 60, (10), 2006, p1039 - 1045 Journal Article, 2006 DOI URL

Bellgrove MA, Hawi Z, Gill M and Robertson IH , The Cognitive Genetics of Attention Deficit Hyperactivity Disorder (ADHD): Sustained attention as a Candidate Phenotype, Cortex, 42, (6), 2006, p838 - 845 Journal Article, 2006 DOI

Nangle JM, Clarke S, Morris DW, Schwaiger S, McGhee KA, Kenny N, Murphy K, Gill M, Corvin A, Donohoe G., Neurocognition and suicidal behaviour in an Irish population with major psychotic disorders., Schizophrenia Research, 85, (1-3), 2006, p196 - 200 Journal Article, 2006 URL DOI URL

Talkowski ME, Seltman H, Bassett AS, Brzustowicz LM, Chen X, Chowdari KV, Collier DA, Cordeiro Q, Corvin AP, Deshpande S, Egan MF, Ferrell RE, Gill M, Kendler KS, Kirov G, Levitt P, Lewis DA, Li T, Mirnics K, Morris DW, O?Donovan MC, Owen MJ, Sobell JL, Thelma BK, Vallada H, Weinberger DR, Williams NM, Wood J, Devlin B, and Nimgaonkar VL. , Evaluation of a Susceptibility Gene for Schizophrenia: Genotype Based Meta-Analysis of RGS4 Polymorphisms from Thirteen Independent Samples , Biological Psychiatry, 60, (2), 2006, p152 - 162 Journal Article, 2006 TARA - Full Text URL DOI URL

Bellgrove, M. A., K. Domschke, Hawi Z, Kirley A, Mullins C, Robertson IH, Gill M, The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD, Experimental Brain Research, 163, (3), 2006, p218 - 229 Journal Article, 2006 DOI

Segurado R, ConroyJ., Meally E., Fitzgerald M., Gill M,.Gallagher, L.,, Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31, American Journal of Psychiatry, 162, (11), 2005, p2182 - 2184 Journal Article, 2005 TARA - Full Text URL DOI URL

Lambert D, Middle F, Hamshere ML, Segurado R, Raybould R, Corvin A, O'Mahony E, Mulcahy T, Bort S, Bennett P, Norton N, Owen MJ, Kirov G, Lendon C, Jones L, Jones I, Holmans P, Gill M and Craddock N, Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22. , Molecular Psychiatry, 10, (9), 2005, p831 - 841 Journal Article, 2005 DOI URL

McGhee KA, Morris DW, Schwaiger S, Nangle JM, Donohoe G, Clarke S, Meagher D, QuinnJ, Scully P, Waddington JL, Gill M, Corvin A, Investigation of the apolipoprotein-L (APOL) gene family and schizophrenia using a novel DNA pooling strategy for public database SNPs , Schizophrenia Research, 76, (2-3), 2005, p231 - 238 Journal Article, 2005 URL DOI URL

McCarron M, Gill M, McCallion P, Begley C. , Health co-morbidities in ageing persons with Down Syndrome and Alzheimber's dementia., Journal of Intellectual Disability Research, 49, (7), 2005, p560 - 566 Journal Article, 2005 DOI URL

Hamshere M, Bennett P, Williams N, Segurado R, Cardno A, Norton N, Lambert D, Williams H, Kirov G, Corvin A, Holmans P, Jones L, Jones I, Gill M, O'Donovan M, Owen M, Craddock N., Genome-wide linkage scan in schizoaffective disorder: Significant evidence for linkage (LOD=3.54) at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19q13., Archives of General Psychiatry, 62, (10), 2005, p1081 - 1088 Journal Article, 2005 URL

Bellgrove MA, Hawi Z, Lowe N, Kirley, A, Robertson IH, Gill M, DRD4 gene variants and sustained attention in attention deficit hyperactivity disorder (ADHD): effects of associated alleles at the VNTR and -521 SNP., American Journal of Medical Genetics Part B (Neuropsychiatric Genetics), 136B, (1), 2005, p81 - 86 Journal Article, 2005 DOI

Bellgrove M.A., Domschke K, Hawi Z, Robertson I.H. Gill M , The COMT Met allele impairs sustained attention performance in children and adolescents with ADHD. Experimental Brain Research, Experimental Brain Research , 163, (3), 2005, p352 - 360 Journal Article, 2005 URL

Mullins C, Bellgrove M.A., Gill M, Robertson I.H., Difference in ADHD Combined and Inattentive Subtypes. , Journal of The American Academy of Child and Adolescent Psychiatry , 44, (2), 2005, p169 - 176 Journal Article, 2005 URL

Lynch C, Brazil J, Cullen B, Coakley D, Gill M. Lawlor B, Hawi Z. , Apolipoprotein E(APOE) Promotor Polymorphisims (-491A/T and -427T/C) and Alzheimers Disease: No evidence of Association in the Irish Population, Irish Journal of Medical Science, 177, (1), 2005, p29-33 Journal Article, 2005 DOI

Kent L, Green E, Hawi Z, Kirley A, Dudbridge F, Lowe N, Raybould R, Langley K, Fitzgerald M, O'Donovan M, Gill M, Thapar A, Craddock N. , Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain derived neurotrophic factor (BDNF) gene with susceptibility to ADHD, Molecular Psychiatry, 10, (10), 2005, p939 - 943 Journal Article, 2005 URL URL DOI

Clarke S, Donohoe G, Morris D, Nangle JM, Schwaiger S, McGhee K, Gill M, Garavan H, Robertson IH, Corvin A. , Evidence Of independence between antisaccade performance and working memory task performance in schizophrenia, Schizophrenia Bulletin , 31, (2), 2005, pp353 Meeting Abstract, 2005

McGuffin P, Knight J, Breen G, Brewster S, Boyd P, Craddock N, Gill M, Korszun A, Maier W, Middleton L, Mors O, Owen M, Perry J, Preisig M, Reich T, Rice J, Rietschel M, Jones L, Sham P, Farmer A, Whole genome linkage scan of recurrent depressive disorder from the depression network study , Human Molecular Genetics, 14, (22), 2005, p3337 - 3345 Journal Article, 2005 DOI URL TARA - Full Text

Sheehan K, Lowe N, Kirley A, Jullins C, Fitzgerald M. Gill M, Hawi Z, Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD , Molecular Psychiatry, 10, (10), 2005, p944 - 949 Journal Article, 2005 URL DOI URL

Tandon K, Patel M, Kinirons M, Sundberg I, Gill M, McGuffin P, Kerwin R, Aitchison K., The pharmacogenetics of response to tricuyclic antidepressants in relation to CYP2D6 genotype and phenotype and CYP2C19 genotype. , 2005 Journal Article, 2005

Bellgrove MA, Domschke K, Hawi Z, Kirley A, Mullins C, Robertson IH, Gill M, The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD, Experimental Brain Research, 163, (3), 2005, p352 - 360 Journal Article, 2005 DOI

Morris DW, Murphy K, Kenny N, Williams NM, McGhee KA, Schwaiger S, Nangle J, Donohoe G, Clarke S, Owen MJ, O'Donovan MC, Waddington JL, Gill M Corvin AP., Association analyses of the BLOC-1 genes suggest the involvement of BLOC-1 in schizophrenia etiology, American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, 138B, 2005, pp129 Meeting Abstract, 2005

Psychiatric Genetics in, editor(s)Wright, Stern , Core Psychiatry, Phelan, Elsevier Saunders, 2005, pp35-54 , [Corvin A, Gill M.] Book Chapter, 2005

Segurado, R, Conroy, J, Meally, E, Fitzgerald, M, Gill, M, Gallagher, L, Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31, AMERICAN JOURNAL OF PSYCHIATRY, 162, (11), 2005, p2182-U5 Journal Article, 2005

Hawi Z, Lowe N, Kirley A, Fitzgerald M, Gill M., Multi marker and Hallotype Analysis of SNAP-25 Gene in Attention Deficit Hyperactivity Disorder (ADHD): Weak Evidence of Association in the Irish Population., 2005 Journal Article, 2005

Hawi Z, Segurado R, Conroy J, Sheehan K, Lowe N, Kirley A, Shields D, Fitzgerald M, Gallagher L, Gill M., Preferential Transmission of Paternal Alleles at Risk Genes in Attention Deficit/Hyperactivity Disorder , American Journal of Human Genetics, 77, (6), 2005, p958 - 965 Journal Article, 2005 URL TARA - Full Text URL DOI

Psychiatric Genetics in, editor(s)Wright, Stern Phelan , Core Psychiatry, UK, Elseview Saunders, 2005, pp35 - 54, [Corvin A Gill M] Book Chapter, 2005

Bellgrove M. A., Hawi Z, Lowe N, Kirley A, Robertson I.H., Gill M, DRD4 gene variants and response inhibition in Attention Deficit Hyperactivity Disorder (ADHD): Effects of associated alleles at the VNTR and 521 SNP, American Journal of Medical Genetics, 136(1), 2005, p81 - 86 Journal Article, 2005 URL

Bellgrove M.A., Gill M., Kirley A, Robertson I.H., Dissecting the attention deficit hyperactivity disorder (ADHD) phenotype: Sustained attention, response variability and spatial attentional asymmetries in relation to dopamine transporter (DAT1) genotype, Neuropsychologia, 43, (13), 2005, p1847 - 1857 Journal Article, 2005 URL DOI

Domschke K, Sheehan K, Lowe N, Kirley A, Mullins C, O'Sullivan R, Freitag C, Becker T, Conroy J, Fitzgerald M, Gill M, Hawi Z, Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: Preferential transmission of the MAO-A 941G allele to affected children, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 134B, (1), 2005, p110 - 114 Journal Article, 2005 URL URL DOI

McQueen M, Devling B, Faraone S, Vishwajit L, Nimgaonkar P, Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q , American Journal of Human Genetics, 77, (4), 2005, p582 - 595 Journal Article, 2005 DOI TARA - Full Text

Mullins C, Bellgrove MA, Gill, M Robertson IH, Variability in time reproduction: differences in ADHD combined and inattentive subtypes, Journal of the American Academy of Child and Adolescent Psychiatry, 44, (2), 2005, p169 - 176 Journal Article, 2005 URL

Bellgrove M.A., Gill M, Hawi Z, Kirley A, Fitzgerald M. Robertson I.H. , Association between dopamine transporter (DAT1)genotype, left sided inattention, and an enhanced response to methylphenidate in attention deficit hyperactivity disorder , Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 30, (12), 2005, p2290 - 2297 Journal Article, 2005 TARA - Full Text URL DOI URL

N. Lowe, A. Kirley, C. Mullins, M. Fitzgerald, M. Gill and Z. Hawi, Multiple marker analysis at the promoter region of the DRD4 gene and ADHD: Evidence of linkage and association with the SNP -616, American journal of medical genetics, 131B, (1), 2004, p33-37 Journal Article, 2004 DOI URL

Morris DW, Nangle JM, Kiely B, Corvin A, Gill M. , The molecular basis of schizophrenia: a complex genetic disorder. , Irish Psychiatrist, 5, 2004, p134 - 137 Journal Article, 2004

Farmer A, Breen G, Brewster S, Craddock N, Gill M. Korsun A, Maier W, Middleton L, Mors O, Owen M, Perry J, Preisig M, Reitchel M, Reich T, McGuffin P. (2004), The Depression Network (DeNT) Study: Methodology and Sociodemographic characteristics of the first 470 affected sibling pairs from a large multi-site linkage genetics study, BioMed Central Psychiatry, 4, 2004, p42 Journal Article, 2004 DOI TARA - Full Text

Kirsun, V. Moskvina, S. Brewster, N. Craddock, M. Gill, W. Maier, O. mors, MJ Owen, M. Preisig, T. Reich, M. Reitchel, AE Farmer, P. McGuffin., A Familiality of Symtom Dimensions in Depression, Archives of Psychiatry, 61, (5), 2004, p468 - 474 Journal Article, 2004 URL

N. M. Williams, A. Preece, D. W. Morris, G. Spurlock, N. J. Bray, M. Stephens, N. Norton, H. Williams, M. Clement, S. Dwyer, C. Curran, J. Wilkinson, V. Moskvina, J. L. Waddington, M. Gill, A. P. Corvin, S. Zammit, G. Kirov, M. J. Owen and M. C. O'Donovan, Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1), Archives of General Psychiatry, 61, (4), 2004, p336 - 344 Journal Article, 2004 URL

N. Lowe, A. Kirley, Z. Hawi, P. Sham, H. Wickham, C. J. Kratochvil, S. D. Smith, S. Y. Lee, F. Levy, L. Kent, F. Middle, L. A. Rohde, T. Roman, E. Tahir, Y. Yazgan, P. Asherson, J. Mill, A. Thapar, A. Payton, R. D. Todd, T. Stephens, R. P. Ebstein, I. Manor, C. L. Barr, K. G. Wigg, R. J. Sinke, J. K. Buitelaar, S. L. Smalley, S. F. Nelson, J. Biederman, S. V. Faraone and M. Gill, Joint Analysis of the DRD5 Marker Concludes Association with Attention-Deficit/Hyperactivity Disorder Confined to the Predominantly Inattentive and Combined Subtypes, American Journal of Human Genetics, 74, (2), 2004, p348-356 Journal Article, 2004 TARA - Full Text DOI

Morris DW, Nangle JM, Kiely B, Corvin A, Gill M., The Molecular Basis of Schizophrenia:- a Complex Genetic Disorder:, Irish Psychiatrist, 5, 2004, p134 - 137 Journal Article, 2004

Corvin A, Nangle JM, Gill M , Schizophrenia Susceptibility Genes: Recent Discoveries and New Challenges., Irish Medical Journal , 97, (3), 2004, p70 - 71 Journal Article, 2004 URL

Nangle JM, Morris D, Gill M, SNPs explained., Irish Psychiatrist , 5, (2), 2004, p61 - 62 Journal Article, 2004

L. Gallagher, Z. Hawi, G. Kearney, M. Fitzgerald and M. Gill, No association between allelic variants of HOXA1/HOXB1 and autism, American journal of medical genetics, 124B, (1), 2004, p64 - 67 Journal Article, 2004 URL DOI URL

Morris DW, Rodgers A, McGhee KA, Schwaiger S, Scully P, Quinn J, Meagher D, Waddington JL, Gill M, Corvin AP, Confirming RGS4 as a susceptibility gene for schizophrenia., American Journal of Medical Genetics (Part B: Neuropsychiatric Genetics), 125B, (1), 2004, p50 - 53 Journal Article, 2004 DOI URL URL

Corvin AP, Morris DW, McGhee K, Schwaiger S, Scully P, Quinn J, Meagher D, Clair DS, Waddington JL, Gill M, Confirmation and refinement of an 'at-risk' haplotype for schizophrenia suggests the EST cluster, Hs.97362, as a potential susceptibility gene at the Neuregulin-1 locus., Molecular Psychiatry, 9, (2), 2004, p208 - 213 Journal Article, 2004 DOI URL URL

Kirley A, Lowe N. Mullins C, McCarron M, Daly G, Waldman I, Fitzgerald M, Gill M, Hawi Z, Phenotype studies of the DRD4 gene polymorphisms in ADHD: Assocaition with opportional defiant disorder and positive family history., American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, 131B, (1), 2004, p38 - 42 Journal Article, 2004 DOI URL

Conroy J, Meally E. Kearney G, Fitzgerald M, Gill M, Gallagher L, Serotonin transporter gene and autism: a haplotype analysis in the Irish autistic population, Molecular Psychiatry, 9, (6), 2004, p587 - 593 Journal Article, 2004 URL DOI

D. W. Morris, K. A. McGhee, S. Schwaiger, P. Scully, J. Quinn, D. Meagher, J. L. Waddington, M. Gill and A. P. Corvin, No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study, Schizophrenia research, 60, (2-3), 2003, p167-72 Journal Article, 2003 URL DOI URL

R. Segurado, S. D. Detera-Wadleigh, D. F. Levinson, C. M. Lewis, M. Gill, J. I. Nurnberger, Jr., N. Craddock, J. R. DePaulo, M. Baron, E. S. Gershon, J. Ekholm, S. Cichon, G. Turecki, S. Claes, J. R. Kelsoe, P. R. Schofield, R. F. Badenhop, J. Morissette,, Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder, American Journal of Human Genetics, 73, (1), 2003, p49-62 Journal Article, 2003 DOI TARA - Full Text

L. Gallagher, K. Becker, G. Kearney, A. Dunlop, R. Stallings, A. Green, M. Fitzgerald and M. Gill, Brief report: A case of autism associated with del(2)(q32.1q32.2) or (q32.2q32.3), Journal of Autism and Developmental Disorders, 33, (1), 2003, p105 - 108 Journal Article, 2003 DOI URL URL

Kirley A, Lowe N, Hawi Z, Mullins C, Daly G, Waldman I, McCarron M, O'Donnell D, Fitzgerald M, Gill M, Association of the 480bp DAT1 allele with methylphenidate response in a sample of Irish children with ADHD., American Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, 121B, (1), 2003, p50 - 54 Journal Article, 2003 DOI URL

Hawi Z, Lowe N, Kirley A, Gruenhage F, Nothen M, Greenwood T, Kelsoe J, Fitzgerald M, Gill M., Linkage Disequilibrium Mapping at DAT1, DRD5 and DBH narrows the Search for ADHD Susceptibility Alleles. , Molecular Psychiatry, 8, (3), 2003, p299 - 308 Journal Article, 2003 URL URL DOI URL

Kirley A, Lowe N, Hawi Z, Mullins C, Daly G, Waldman I, McCarron M, O'Donnell D, Fitzgerald M, Gill M, Association of the 480 bp DAT1 allele with methylphenidate response in a sample of Irish children with ADHD., American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 121B, (1), 2003, p50-4 Journal Article, 2003

Hawi Z, Sheehan K, Lynch A, Evans I, Lowe N, Lawlor B, Gill M., Late onset Alzheimer's disease and apoliproprotein association in the Irish population: relative risk and attributable fraction., Irish Journal of Medical Science , 172, (2), 2003, p74 - 76 Journal Article, 2003 DOI URL

Corvin A, Gill M , Psychiatric Genetics in the post genome age, British Journal of Psychiatry, 182, 2003, p95 - 96 Journal Article, 2003 TARA - Full Text URL

Hawi Z, Kirley A, Lowe N, Fitzgerald M, Gill M., Recent Genetic Advances in ADHD and diagnostice and therapeutic prospects., Expert Review in Neurotherapeutics , 3, (4), 2003, p453 - 464 Journal Article, 2003 DOI

McEvoy B, Hawi Z, Fitzgerald M, Gill M. , No Evidence of Linkage or Association Between the Norepinephrine Transporter (NET) Gene Polymorphisms and ADHD in the Irish Population., American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 114, (6), 2002, p665 - 666 Journal Article, 2002 DOI URL URL

Lawlor, B, McCarron, M, Cosgrave, M, Tyrrell, J, Gill, M, , Responding to dementia care needs in persons with Intellectual Disability., IASSID Europe Conference, Dublin, Ireland., 2002 Conference Paper, 2002

McCarron, M, Gill, M, Lawlor, B, Tyrrell, J, Cosgrave, M, Begley, C. , The Influence of Alzheimer's dementia on Time Spent Caregiving in persons with Down syndrome., IASSID Europe Conference, Dublin, Ireland., 2002 Conference Paper, 2002

McCarron M, Gill M, Lawlor B, Begley C. , Time spent caregiving for persons with the dual disability of Down syndrome and Alzheimer's dementia: Preliminary findings. , Journal of Learning Disabilities, 6, (3), 2002, p263 - 279 Journal Article, 2002 DOI

Tyrrell J, McCarron M, Cosgrave M, Gill M, Lawlor B. , A longitudinal study of 289 people with Down's syndrome: results at year three., IASSID Europe Conference, Dublin, Ireland., 2002 Conference Paper, 2002

J. Holmes, A. Payton, J. Barrett, R. Harrington, P. McGuffin, M. Owen, W. Ollier, J. Worthington, M. Gill, A. Kirley, Z. Hawi, M. Fitzgerald, P. Asherson, S. Curran, J. Mill, A. Gould, E. Taylor, L. Kent, N. Craddock and A. Thapar, Association of DRD4 in children with ADHD and comorbid conduct problems, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 114, (2), 2002, p150 - 153 Journal Article, 2002 URL DOI URL

Wickham H, Walsh C, Asherson, Gill M, Owen M, McGuffin P, Murray R, Sham P. , Familiarity of clinical characteristics in schizophrenia , Journal Psychiatry Research, 36, (5), 2002, p325 - 329 Journal Article, 2002 URL DOI

Mulligan A, Webb M, Gill M., A variant of nymphomania in association with obsessive-compulsive disorder., Irish Journal of Psychological Medicine, 19, (3), 2002 Journal Article, 2002 URL

Brophy K, Hawi Z, Kirley A, Fitzgerald M and Gill M., Synaptosomal-Associated Protein 25 (SNAP-25) and Attention Deficit Hyperactivity Disorder (ADHD): Evidence of linkage and Association in the Irish Population. , Molecular Psychiatry , 7, (8), 2002, p913 - 917 Journal Article, 2002 TARA - Full Text URL URL DOI

McCarron, M, Gill, M, Tyrrell J, Cosgrave M, Lawlor B, ApoE e4 is a risk factor for dementia and premature death: Findings from a longitudinal study on persons with Down's syndrome:, World Genetics Conference. Brussels. , 2002 Conference Paper, 2002

O'Mahony E, Corvin A, Comerford C, O'Connell R, Larsen B, Jones IR, Mc Candless F, Kirov G, Cardno A, Craddock N, and Gill M. , Sibling pairs with affective disorders: resemblance of demographic and clinical features, Psychological Medicine, 32 , (1), 2002, p55 - 61 Journal Article, 2002 URL DOI

McCarron, M, Cosgrave, M, Tyrrell, J, Gill, M, Lawlor, B, Association between Age at Onset of Dementia and Age of Menopause in Women with Down's Syndrome. , IASSID Europe Conference, Dublin, Ireland., 2002 Conference Paper, 2002

M. McCarron, M. Gill, B. Lawlor and C. Begly, A pilot study of the reliability and validity of the Caregiver Activity Survey - Intellectual Disability (CAS-ID), Journal of Intellectual Disability Research, 46, (8), 2002, p605-612 Journal Article, 2002 URL DOI

Kennedy N, Jerrard-Dunne P, Gill M, Webb M., Characteristics and treatment of asylum seekers reviewed by psychiatrists in an Irish inner city area., Irish Journal of Psychological Medicine, 19, (1), 2002, p4 - 7 Journal Article, 2002 URL

D. Lambert and M. Gill, Evaluation of parent-of-origin effect in bipolar affective disorder relating to susceptibility loci on chromosome 18, Bipolar disorders, 4, (1), 2002, p31-2 Journal Article, 2002 URL DOI

Kent L, Doerry U, Hardy E, Parmar R, Gingell K, Hawi Z, Kirley A, Lowe N, Fitzgerald M, Gill M, Craddock N., Evidence that variation at the serotonin transporter gene influences susceptibility to attention deficit hyperactivity disorder (ADHD): analysis and pooled analysis. , Molecular Psychiatry, 7, 2002, p908 - 912 Journal Article, 2002 DOI TARA - Full Text

A. Kirley, Z. Hawi, G. Daly, M. McCarron, C. Mullins, N. Millar, I. Waldman, M. Fitzgerald and M. Gill, Dopaminergic system genes in ADHD: toward a biological hypothesis, Neuropsychopharmacology, 27, (4), 2002, p607-619 Journal Article, 2002 DOI TARA - Full Text

Behavioural Genetics in the Postgenomic Era in, editor(s)Plomin R, DeFries JC, Craig IC, McGuffin P , Pharmacogenetics in the Post genomic era, Washington DC, APA Books, 2002, pp335 - 331, [M Gill] Book Chapter, 2002

P. Bennett, R. Segurado, I. Jones, S. Bort, F. McCandless, D. Lambert, J. Heron, C. Comerford, F. Middle, A. Corvin, G. Pelios, G. Kirov, B. Larsen, T. Mulcahy, N. Williams, R. O'Connell, E. O'Mahony, A. Payne, M. Owen, P. Holmans, N. Craddock and M. Gill, The Wellcome trust UK-Irish bipolar affective disorder sibling-pair genome screen: first stage report, Molecular Psychiatry, 7, (2), 2002, p189-200 Journal Article, 2002 TARA - Full Text DOI

Hawi Z, Dring M, Kirley A, Foley D, Kent K, Asherson P, Curran C, Gould A, Richards S, Thapar A, Fitzgerald M and Gill M., Serotonergic System and Attention Deficit Hyperactivity Disorder (ADHD): a potential susceptibility locus at the 5-HT1B receptor gene in 270 Trios from a multi-center sample, Molecular Psychiatry, 7, (7), 2002, p718 - 725 Journal Article, 2002 TARA - Full Text URL URL DOI

Z. Hawi, D. Foley, A. Kirley, M. McCarron, M. Fitzgerald and M. Gill, Dopa decarboxylase gene polymorphisms and attention deficit hyperactivity disorder (ADHD): no evidence for association in the Irish population, Molecular Psychiatry, 6, (4), 2001, p420 - 424 Journal Article, 2001 DOI TARA - Full Text URL URL URL

Wickham H, Walsh C, Asherson P, Taylor C, Sigmundson T, Gill M, Owen MJ, McGuffin P, Murray R, Sham P., Familiality of symptom dimensions in schizophrenia. , Schizophrenia Research, 47, (2-3), 2001, p223 - 232 Journal Article, 2001 URL DOI

McCarron, M, Gill, M, Lawlor, B, Begley, C. , A pilot study of Reliability and Validity of the Caregiving Activity Survey-Intellectual Disability (CAS-ID), 11TH IASSID International Roundtable on Aging and Intellectual Disabilities. Luxembourg. , 2001 Conference Paper, 2001

McCarron, M, Gill, M, Lawlor, B, Begley, C. , The social and economic impact of caring for persons with the dual disability of Alzheimer's dementia and Down syndrome, Transforming Healthcare Through Research, Education &Technology Research Conference. Trinity College, Dublin. Ireland. , 2001 Conference Paper, 2001

J. Tyrrell, M. Cosgrave, M. McCarron, J. McPherson, J. Calvert, A. Kelly, M. McLaughlin, M. Gill and B. A. Lawlor, Dementia in people with Down's syndrome, International journal of geriatric psychiatry, 16, (12), 2001, p1168-1174 Journal Article, 2001 DOI URL

O'Reilly J, Murphy P, Byrne M, Larkin C, Gill M, O'Callaghan E, Lane A , Dermatoglyphic fluctuating asymmetry and atypical handedness in schizophrenia , Schizophrenia Research, 50, (3), 2001, p159 - 168 Journal Article, 2001 DOI

Kirley, A., Hawi, Z.Dr., McCarron, M., (...), Fitzgerald, M., Gill, M., A review of attention deficit hyperactivity disorder and dopamine system candidate, American Journal of Medical Genetics - Neuropsychiatric Genetics, 105, (7), 2001, p634 Journal Article, 2001

Kent L, Green E, Holmes J, Thapar A, Gill M, Hawi Z, Fitzgerald M, Asherson P, Curran S, Mills J, Payton A, Craddock N. , No Association Between CHRNA7 Microsatellite Markers and Attention-Deficit Hyperactivity Disorder, Neuropsychiatric Genetics, 105, (8), 2001, p686 - 689 Journal Article, 2001 DOI URL

L. Kent, F. Middle, Z. Hawi, M. Fitzgerald M. Gill, C. Feehan and N. Craddock, Nicotinic acetylcholine receptor alpha4 subunit gene polymorphism and attention deficit hyperactivity disorder, Psychiatric genetics, 11, (1), 2001, p37 - 40 Journal Article, 2001 URL URL DOI URL

N. Lowe, Z. Hawi, M. Fitzgerald and M. Gill, No evidence of linkage or association between ADHD and DXS7 locus in Irish population, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 105, (4), 2001, p394 - 395 Journal Article, 2001 URL URL DOI

A. Corvin, E. O'Mahony, M. O'Regan, C. Comerford, R. O'Connell, N. Craddock and M. Gill, Cigarette smoking and psychotic symptoms in bipolar affective disorder, The British Journal of Psychiatry , 179, 2001, p35-38 Journal Article, 2001 TARA - Full Text URL

Neuropsychiatric Genetics in, editor(s)Lawlor , Revision Psychiatry, MedMedia , 2001, [Corvin A, Gill M. ] Book Chapter, 2001

Gallagher, L. , Kearney, G., Fitzgerald, M., Gill, M. , Three cases of autism associated with differing chromosomal abnormalities, American Journal of Medical Genetics - Neuropsychiatric Genetics, 96, (4), 2000, 543 Journal Article, 2000 URL URL

C. Burgess, A. O'Donohoe and M. Gill, Agony and ecstasy: a review of MDMA effects and toxicity, European Psychiatry, 15, (5), 2000, p287-294 Journal Article, 2000 DOI URL

Cosgrave M, Tyrrell J, McCarron M, Gill M, Lawlor M. , A Five-Year Follow-up Study of Dementia in Persons with Down's Syndrome: Early Symptoms and Patterns of Deterioration. , Ir. Journal of Psych Med, 17, (1), 2000, p5 - 11 Journal Article, 2000

Z. Hawi, N. Millar, G. Daly, M. Fitzgerald and M. Gill, No association between catechol-O-methyltransferase (COMT) gene polymorphism and attention deficit hyperactivity disorder (ADHD) in an Irish sample, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 96, (3), 2000, p282 - 284 Journal Article, 2000 DOI URL URL

Messas GP, Gentil V, Gill M, Murray R, Vallada HP. , Lack of gender effect on familial schizophrenia. A Brazilian study. , Arq. Neurossiquiatr. Jun, 58, (2B), 2000, p494 - 498 Journal Article, 2000 TARA - Full Text DOI

Corvin A, Gill M. , Psychosis: One process or many disorders?, Irish Journal Psychological Medicine, 2000 Journal Article, 2000

Cosgrove, M., Tyrrell, J., McCarron, M., Gill, M., Lawlor, B., A Five Year Follow up Study of Dementia in Persons with Down's Syndrome: Early Symptoms and Patterns of Deterioration., Irish Journal of Psychological Medicine 17(1) 5-11., 17, (1), 2000, p5 - 11 Journal Article, 2000

Swift G, Larsen B, Hawi Z, Gill M., Novelty Seeking Traits and D4 dopamine Receptors. , American Journal of Medical Genetics, 96, 2000, p222 - 223 Journal Article, 2000 DOI

Z. Hawi, M. McCarron, A. Kirley, G. Daly, M. Fitzgerald and M. Gill, No association of the dopamine DRD4 receptor (DRD4) gene polymorphism with attention deficit hyperactivity disorder (ADHD) in the Irish population, American Journal of Medical Genetics Part A, 96, (3), 2000, p268 - 272 Journal Article, 2000 URL URL DOI

Cosgrove, M., Tyrrell, J., McCarron, M. , Gill, M., Lawlor, B, Age at onset of dementia and age of menopause in women with Down's syndrome., . Journal of Intellectual Disability Research, 43, (6), 1999, p461 - 465 Journal Article, 1999 DOI

G. Daly, Z. Hawi, M. Fitzgerald and M. Gill, Mapping susceptibility loci in attention deficit hyperactivity disorder: preferential transmission of parental alleles at DAT1, DBH and DRD5 to affected children, Molecular Psychiatry, 4, (2), 1999, p192 - 196 Journal Article, 1999 URL URL URL

Rees M, Fenton I, Williams M, Holmans P, Norton N, Cardno A, Asherson P Spurlock G, Roberts E, Parfitt E, Mant R, Vallada H, Li M. Collier D, Powell J, Nanko S, Gill M, McGuffin P, Owen M., Autosome search for schizophrenia susceptibility genes in multiply affected families, Molecular Psychiatry, 4, 1999, p353 - 359 Journal Article, 1999 URL

Khan A, Kelly R, Gill M., Survey of symptoms associated with antidepressant discontinuation., Psychological Medicine, 16, (3), 1999, p89 - 92 Journal Article, 1999 URL

Z. Hawi, L. Mynett-Johnson, V. Murphy, R. E. Straub, K. S. Kendler, D. Walsh, P. McKeon and M. Gill, No evidence to support the association of the potassium channel gene hSKCa3 CAG repeat with schizophrenia or bipolar disorder in the Irish population, Molecular Psychiatry, 4, (5), 1999, p488-491 Journal Article, 1999 URL

Z. Hawi, S. Gibson, R. E. Straub, D. Walsh, K. S. Kendler and M. Gill, Schizophrenia and HLA: No association with PCR-SSOP typed classical loci in a large Irish familial sample, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 88, (4), 1999, p422-429 Journal Article, 1999 DOI URL

J. Tyrrell, M. Cosgrave, J. McPherson, Z. Hawi, V. Trulock, J. Calvert, B. Lawlor and M. Gill, Presenilin 1 and alpha-1-antichymotrypsin polymorphisms in Down syndrome: no effect on the presence of dementia, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 88, (6), 1999, p616-620 Journal Article, 1999 URL DOI

M. P. Cosgrave, J. Tyrrell, M. McCarron, M. Gill and B. A. Lawlor, Determinants of aggression, and adaptive and maladaptive behaviour in older people with Down's syndrome with and without dementia, Journal of intellectual disability research, 43 ( Pt 5), 1999, p393-9 Journal Article, 1999 URL

Cosgrave M, Tyrrell J, McCarron M, Gill M, Lawlor, BA, Determinants of aggression, and adaptive and maladaptive behaviour in older people with Down's syndrome with and without dementia., Journal of Intellectual Disability Research, 43, (5), 1999, p393 - 399 Journal Article, 1999 DOI

S. Gibson, Z. Hawi, R. E. Straub, D. Walsh, K. S. Kendler and M. Gill, HLA and schizophrenia: refutation of reported associations with A9 (A23/A24), DR4, and DQbeta1*0602, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 88, (4), 1999, p416-421 Journal Article, 1999 DOI URL

M. P. Cosgrave, J. Tyrrell, M. McCarron, M. Gill and B. A. Lawlor, Age at onset of dementia and age of menopause in women with Down's syndrome, Journal of Intellectual Disability Research, 43, (6), 1999, p461-465 Journal Article, 1999 DOI

Z. Hawi, L. Mynett-Johnson, M. Gill, V. Murphy, R. E. Straubl, K. S. Kendler, D. Walsh, F. Machen, H. Connell, P. McKeon and D. Shields, Pseudoautosomal gene: possible association with bipolar males but not with schizophrenia, Psychiatric Genetics, 9, (3), 1999, p129-34 Journal Article, 1999 URL

O'Donoghue A, Gill M. , Pharmacogenetics of the hepatic cytochrome P450 enzyme system: Its relevance for prescribing in psychiatry, Irish journal of psychological medicine, 15, (3), 1998, p96-99 Journal Article, 1998 DOI

Spurlock G, Williams J, McGuffin P, Achauer HN, Lenzinger E, Fuchs K, Sieghart WC, Meszaros K, Fathi N, Laurent C, Mallet J, Macciardi F, Pedrini S, Gill M, Hawi Z, Gibson S, Jazin EE, Yang Hai-Tao, Adolfsson R, Pato CN, Dourado AM, Owen MJ. , European Multi-Centre Association Study of Schizophrenia: A Study of the DRD2 Ser311Cys and DRD3 Ser9 Gly Polymorphisms. , American Journal of Medical Genetics, Feb 7 ;81, (1), 1998, p24 - 28 Journal Article, 1998 URL

Vallada HP, Vasques L, Curtis D, Zatz M, Kirov G, Lauriano V, Gentil V, Murray RM, McGuffin P, Owen M, Gill M, Craddock N, Collier DA , Linkage analysis between bipolar affective disorder and markers on chromosome X., Psychiatric Genetics, 8, (3), 1998, p183 - 186 Journal Article, 1998 URL

J. Tyrrell, M. Cosgrave, Z. Hawi, J. McPherson, C. O'Brien, J. McCalvert, M. McLaughlin, B. Lawlor and M. Gill, A protective effect of apolipoprotein E e2 allele on dementia in Down's syndrome, Biological psychiatry, 43, (6), 1998, p397-400 Journal Article, 1998 URL DOI

Wright P., Dawson E., Donaldson P., Underhill J., Sham P., Zhao, J., Gill M., Nanko S., Owen M., McGuffin P., Murray R., A Transmission/disequilibrium Study of the DRB1*04 Gene Locus on Chromosome 6p21.3 with Schizophrenia , Schizophrenia Research, 27, (32(2)), 1998, p75 - 80 Journal Article, 1998 URL

Hawi Z, Gill M, Report on the Fifth International Congress of Psychiatric Genetics, Santa Fe, New Mexico 19-23 October l997, Molecular Psychiatry, 3, 1998, p109 - 111 Journal Article, 1998 URL

Hawi Z, McCabe U, Straub RE, O'Neill A, Kendler KS, Walsh D Gill M , Examination of new and reported data of the DRD3Mscl polymorphism: no support for the proposed association with schizophrenia, Molecular Psychiatry, 3, 1998, p150 - 155 Journal Article, 1998 URL

Cosgrave MP, McCarron M, Anderson M, Tyrrell J, Gill M, Lawlor BA, Cognitive decline in Down syndrome: a validity/reliability study of the test for severe impairment., American journal of mental retardation : AJMR, 103, (2), 1998, p193-7 Journal Article, 1998 DOI

Cosgrave MP, McCarron M, Anderson M, Tyrrell J, Gill M, Lawlor BA. , Cognitive decline in Down syndrome: a validity/reliability study of the test for severe impairment., Am. J. Mental Retard, 103, (2), 1998, p193 - 197 Journal Article, 1998 URL

O'Donoghue A, O'Flynn K, Shields K, Hawi Z, Gill M. , MDMA Toxicity; no evidence for a major influence of metabolic genotype, Addiction Biology, 3, 1998, p309 - 314 Journal Article, 1998

Bowen T, Kirov G, Gill M, Spurlock G, Vallada H, Powell J, Murray R, McGuffin R, Collier D, Owen MJ, Craddock N. , Linkage Studies of Bipolar disorder with chromosome 18 Markers. , American Journal of Medical Genetics, 88, (5), 1998, p503 - 509 Journal Article, 1998 URL

Burgess C, Gill M, Marks I. , Postal Self Exposure Treatment of Recurrent Nightmares: A randomised controlled trial, British Journal of Psychiatry, 172, 1998, p257 - 262 Journal Article, 1998

Z. Hawi, R. E. Straub, A. O'Neill, K. S. Kendler, D. Walsh and M. Gill, No linkage or linkage disequilibrium between brain-derived neurotrophic factor (BDNF) dinucleotide repeat polymorphism and schizophrenia in Irish families, Psychiatry research, 81, (2), 1998, p111-6 Journal Article, 1998 URL

M. Gill, G. Daly, S. Heron, Z. Hawi and M. Fitzgerald, Confirmation of association between attention deficit hyperactivity disorder and a dopamine transporter polymorphism, Molecular psychiatry, 2, (4), 1997, p311 - 313 Journal Article, 1997 DOI URL URL URL

Williams J, McGuffin P, Nothen M, Owen M, EMASS Collaborative Group, Meta-analysis of association between the 5-HT 2a receptor T102C polymorphism and schizophrenia. , Lancet, 349, (9060), 1997, p1221- Journal Article, 1997 URL

Z. Hawi, M. V. Myakishev, R. E. Straub, A. O'Neill, K. S. Kendler, D. Walsh and M. Gill, No association or linkage between the 5-HT2a/T102C polymorphism and schizophrenia in Irish families, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 74, (4), 1997, p370-373 Journal Article, 1997 DOI URL

M. Gill, Z. Hawi, F. A. O'Neill, D. Walsh, R. E. Straub and K. S. Kendler, Neurotrophin-3 gene polymorphisms and schizophrenia: no evidence for linkage or association, Psychiatric genetics, 6, (4), 1996, p183-6 Journal Article, 1996 URL

Parfitt E, Asherson P, Roberts E, Mant R, Nanko S, Gill M, McGuffin P, Owen M. , No Evidence for Linkage between Schizophrenia and Eight Microsatellite markers on Chromosome 19., Human Heredity, 46, 1996, p191 - 196 Journal Article, 1996 DOI

Ashworth A, Abusaad I, Walsh C, Nanko S, Murray RM, Asherson P, McGuffin P, Gill M, Owen MJ, Collier DA , Linkage analysis of the fragile X gene FMR-1 and, Psychiatric Genetics, 6, (2), 1996, p81 - 86 Journal Article, 1996 URL

M. Cosgrave, J. Tyrrell, H. Dreja, Z. Hawi, B. A. Lawlor and M. Gill, Lower frequency of apolipoprotein E4 allele in an "elderly" Down's syndrome population, Biological psychiatry, 40, (8), 1996, p811-3 Journal Article, 1996 DOI

Schizophrenia Linkage Collaborative Group, Additional support for schizophrenia linkage on chromosomes 6 &7. A Multicentre Study, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 67, (6), 1996, p580 - 594 Journal Article, 1996 DOI URL

Kunugi H, Curtis D, Vallada HP, Nanko S, Powell JF, Murray RM, McGuffin P, Owen MJ, Gill M, Collier, A linkage study of schizophrenia with DNA markers from chromosome 8p21-p22 in 25 multiplex families , Schizophrenia Research, 22, (1), 1996, p61 - 68 Journal Article, 1996 URL DOI

Gill M, Genetics and molecular biology of manic-depression. , Molecular and cell biology of human diseases series, 4, 1994, p173 - 193 Journal Article, 1994