Professor Louise Gallagher
Professor Child & Adolescent Psychiatry, Psychiatry
Professor Child & Adolescent Psychiatry, Trinity Inst. of Neurosciences (TCIN)
Publications and Further Research Outputs
Peer-Reviewed Publications
Dinneen, T.J. and Nà Ghrálaigh, F. and Ormond, C. and Heron, E.A. and Kirov, G. and Lopez, L.M. and Gallagher, L., Polygenic scores stratify neurodevelopmental copy number variant carrier cognitive outcomes in the UK Biobank, npj Genomic Medicine, 9, (1), 2024
Summers, J. and Baribeau, D. and Perlman, P. and Hoang, N. and Cui, S. and Krakowski, A. and Ambrozewicz, P. and Ho, A. and Selvanayagam, T. and Sándor-Bajusz, K.A. and Palad, K. and Patel, N. and McGaughey, S. and Gallagher, L. and Scherer, S.W. and Szatmari, P. and Vorstman, J., An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructure, Journal of Neurodevelopmental Disorders, 16, (1), 2024
Bloomfield, M. and Lautarescu, A. and Heraty, S. and Douglas, S. and Violland, P. and Plas, R. and Ghosh, A. and Van Den Bosch, K. and Eaton, E. and Absoud, M. and Battini, R. and Blázquez Hinojosa, A. and Bolshakova, N. and Bölte, S. and Bonanni, P. and Borg, J. and Calderoni, S. and Calvo Escalona, R. and Castelo-Branco, M. and Castro-Fornieles, J. and Caro, P. and Cliquet, F. and Danieli, A. and Delorme, R. and Elia, M. and Hempel, M. and Leblond, C.S. and Madeira, N. and McAlonan, G. and Milone, R. and Molloy, C.J. and Mouga, S. and Montiel, V. and Pina Rodrigues, A. and Schaaf, C.P. and Serrano, M. and Tammimies, K. and Tye, C. and Vigevano, F. and Oliveira, G. and Mazzone, B. and O'Neill, C. and Pender, J. and Romero, V. and Tillmann, J. and Oakley, B. and Murphy, D.G.M. and Gallagher, L. and Bourgeron, T. and Chatham, C. and Charman, T., European Autism GEnomics Registry (EAGER): Protocol for a multicentre cohort study and registry, BMJ Open, 14, (6), 2024
Nà Ghrálaigh, F. and Brennan, A. and Bolshakova, N. and Foley, M. and Gallagher, L. and Lopez, L.M., Establishing an Irish autism research network, Irish Journal of Psychological Medicine, 41, (1), 2024, p157-158
Kurth, F. and Schijven, D. and van den Heuvel, O.A. and Hoogman, M. and van Rooij, D. and Stein, D.J. and Buitelaar, J.K. and Bölte, S. and Auzias, G. and Kushki, A. and Venkatasubramanian, G. and Rubia, K. and Bollmann, S. and Isaksson, J. and Jaspers-Fayer, F. and Marsh, R. and Batistuzzo, M.C. and Arnold, P.D. and Bressan, R.A. and Stewart, S.E. and Gruner, P. and Sorensen, L. and Pan, P.M. and Silk, T.J. and Gur, R.C. and Cubillo, A.I. and Haavik, J. and O'Gorman Tuura, R.L. and Hartman, C.A. and Calvo, R. and McGrath, J. and Calderoni, S. and Jackowski, A. and Chantiluke, K.C. and Satterthwaite, T.D. and Busatto, G.F. and Nigg, J.T. and Gur, R.E. and Retico, A. and Tosetti, M. and Gallagher, L. and Szeszko, P.R. and Neufeld, J. and Ortiz, A.E. and Ghisleni, C. and Lazaro, L. and Hoekstra, P.J. and Anagnostou, E. and Hoekstra, L. and Simpson, B. and Plessen, J.K. and Deruelle, C. and Soreni, N. and James, A. and Narayanaswamy, J. and Reddy, J.Y. and Fitzgerald, J. and Bellgrove, M.A. and Salum, G.A. and Janssen, J. and Muratori, F. and Vila, M. and Giral, M.G. and Ameis, S.H. and Bosco, P. and Remnélius, K.L. and Huyser, C. and Pariente, J.C. and Jalbrzikowski, M. and Rosa, P.G. and O'Hearn, K.M. and Ehrlich, S. and Mollon, J. and Zugman, A. and Christakou, A. and Arango, C. and Fisher, S.E. and Kong, X. and Franke, B. and Medland, S.E. and Thomopoulos, S.I. and Jahanshad, N. and Glahn, D.C. and Thompson, P.M. and Francks, C. and Luders, E., Large-scale analysis of structural brain asymmetries during neurodevelopment: Associations with age and sex in 4265 children and adolescents, Human Brain Mapping, 45, (11), 2024
Molloy, C.J. and Cooke, J. and Gatford, N.J.F. and Rivera-Olvera, A. and Avazzadeh, S. and Homberg, J.R. and Grandjean, J. and Fernandes, C. and Shen, S. and Loth, E. and Srivastava, D.P. and Gallagher, L., Bridging the translational gap: what can synaptopathies tell us about autism?, Frontiers in Molecular Neuroscience, 16, (1191323), 2023
Heraty, S. and Lautarescu, A. and Belton, D. and Boyle, A. and Cirrincione, P. and Doherty, M. and Douglas, S. and Plas, J.R.D. and Van Den Bosch, K. and Violland, P. and Tercon, J. and Ruigrok, A. and Murphy, D.G.M. and Bourgeron, T. and Chatham, C. and Loth, E. and Oakley, B. and McAlonan, G.M. and Charman, T. and Puts, N. and Gallagher, L. and Jones, E.J.H., Bridge-building between communities: Imagining the future of biomedical autism research, Cell, 186, (18), 2023, p3747-3752
Bölte, S. and Neufeld, J. and Marschik, P.B. and Williams, Z.J. and Gallagher, L. and Lai, M.-C., Sex and gender in neurodevelopmental conditions, Nature Reviews Neurology, 2023
Molloy, C.J. and Quigley, C. and McNicholas, Ã . and Lisanti, L. and Gallagher, L., A review of the cognitive impact of neurodevelopmental and neuropsychiatric associated copy number variants, Translational Psychiatry, 13, (1), 2023
Vibert, B. and Segura, P. and Gallagher, L. and Georgiades, S. and Pervanidou, P. and Thurm, A. and Alexander, L. and Anagnostou, E. and Aoki, Y. and Birken, C.S. and Bishop, S.L. and Boi, J. and Bravaccio, C. and Brentani, H. and Canevini, P. and Carta, A. and Charach, A. and Costantino, A. and Cost, K.T. and Cravo, E.A. and Crosbie, J. and Davico, C. and Donno, F. and Fujino, J. and Gabellone, A. and Geyer, C.T. and Hirota, T. and Kanne, S. and Kawashima, M. and Kelley, E. and Kim, H. and Kim, Y.S. and Kim, S.H. and Korczak, D.J. and Lai, M.-C. and Margari, L. and Marzulli, L. and Masi, G. and Mazzone, L. and McGrath, J. and Monga, S. and Morosini, P. and Nakajima, S. and Narzisi, A. and Nicolson, R. and Nikolaidis, A. and Noda, Y. and Nowell, K. and Polizzi, M. and Portolese, J. and Riccio, M.P. and Saito, M. and Schwartz, I. and Simhal, A.K. and Siracusano, M. and Sotgiu, S. and Stroud, J. and Sumiya, F. and Tachibana, Y. and Takahashi, N. and Takahashi, R. and Tamon, H. and Tancredi, R. and Vitiello, B. and Zuddas, A. and Leventhal, B. and Merikangas, K. and Milham, M.P. and Di Martino, A., CRISIS AFAR: an international collaborative study of the impact of the COVID-19 pandemic on mental health and service access in youth with autism and neurodevelopmental conditions, Molecular Autism, 14, (1), 2023
Gallagher L, Smith V, Carroll M, Hannon K, Lawler D, Begley C., What would reduce caesarean section rates?-Views from pregnant women and clinicians in Ireland., PloS one, 17, (4), 2022, pe0267465
Patel, Y. and Shin, J. and Abé, C. and Agartz, I. and Alloza, C. and AlnÊs, D. and Ambrogi, S. and Antonucci, L.A. and Arango, C. and Arolt, V. and Auzias, G. and Ayesa-Arriola, R. and Banaj, N. and Banaschewski, T. and Bandeira, C. and BaÅ göze, Z. and Cupertino, R.B. and Bau, C.H.D. and Bauer, J. and Baumeister, S. and Bernardoni, F. and Bertolino, A. and Bonnin, C.D.M. and Brandeis, D. and Brem, S. and Bruggemann, J. and BÃŒlow, R. and Bustillo, J.R. and Calderoni, S. and Calvo, R. and Canales-RodrÃguez, E.J. and Cannon, D.M. and Carmona, S. and Carr, V.J. and Catts, S.V. and Chenji, S. and Chew, Q.H. and Coghill, D. and Connolly, C.G. and Conzelmann, A. and Craven, A.R. and Crespo-Facorro, B. and Cullen, K. and Dahl, A. and Dannlowski, U. and Davey, C.G. and Deruelle, C. and DÃaz-Caneja, C.M. and Dohm, K. and Ehrlich, S. and Epstein, J. and Erwin-Grabner, T. and Eyler, L.T. and Fedor, J. and Fitzgerald, J. and Foran, W. and Ford, J.M. and Fortea, L. and Fuentes-Claramonte, P. and Fullerton, J. and Furlong, L. and Gallagher, L. and Gao, B. and Gao, S. and Goikolea, J.M. and Gotlib, I. and Goya-Maldonado, R. and Grabe, H.J. and Green, M. and Grevet, E.H. and Groenewold, N.A. and Grotegerd, D. and Gruber, O. and Haavik, J. and Hahn, T. and Harrison, B.J. and Heindel, W. and Henskens, F. and Heslenfeld, D.J. and Hilland, E. and Hoekstra, P.J. and Hohmann, S. and Holz, N. and Howells, F.M. and Ipser, J.C. and Jahanshad, N. and Jakobi, B. and Jansen, A. and Janssen, J. and Jonassen, R. and Kaiser, A. and Kaleda, V. and Karantonis, J. and King, J.A. and Kircher, T. and Kochunov, P. and Koopowitz, S.-M. and Landén, M. and LandrÞ, N.I. and Lawrie, S. and Lebedeva, I. and Luna, B. and Lundervold, A.J. and MacMaster, F.P. and Maglanoc, L.A. and Mathalon, D.H. and McDonald, C. and McIntosh, A. and Meinert, S. and Michie, P.T. and Mitchell, P. and Moreno-Alcázar, A. and Mowry, B. and Muratori, F. and Nabulsi, L. and NenadiÄ , I. and O'Gorman Tuura, R. and Oosterlaan, J. and Overs, B. and Pantelis, C. and Parellada, M. and Pariente, J.C. and Pauli, P. and Pergola, G. and Piarulli, F.M. and Picon, F. and Piras, F. and Pomarol-Clotet, E. and Pretus, C. and Quidé, Y. and Radua, J. and Ramos-Quiroga, J.A. and Rasser, P.E. and Reif, A. and Retico, A. and Roberts, G. and Rossell, S. and Rovaris, D.L. and Rubia, K. and Sacchet, M. and Salavert, J. and Salvador, R. and Sarró, S. and Sawa, A. and Schall, U. and Scott, R. and Selvaggi, P. and Silk, T. and Sim, K. and Skoch, A. and Spalletta, G. and Spaniel, F. and Stein, D.J. and SteinstrÀter, O. and Stolicyn, A. and Takayanagi, Y. and Tamm, L. and Tavares, M. and Teumer, A. and Thiel, K. and Thomopoulos, S.I. and Tomecek, D. and Tomyshev, A.S. and Tordesillas-Gutiérrez, D. and Tosetti, M. and Uhlmann, A. and Van Rheenen, T. and Vazquez-Bourgón, J. and Vernooij, M.W. and Vieta, E. and Vilarroya, O. and Weickert, C. and Weickert, T. and Westlye, L.T. and Whalley, H. and Willinger, D. and Winter, A. and Wittfeld, K. and Yang, T.T. and Yoncheva, Y. and Zijlmans, J.L. and Hoogman, M. and Franke, B. and van Rooij, D. and Buitelaar, J. and Ching, C.R.K. and Andreassen, O.A. and Pozzi, E. and Veltman, D. and Schmaal, L. and van Erp, T.G.M. and Turner, J. and Castellanos, F.X. and Pausova, Z. and Thompson, P. and Paus, T., Virtual Ontogeny of Cortical Growth Preceding Mental Illness, Biological Psychiatry, 92, (4), 2022, p299-313
Cooke J, Molloy CJ, Cáceres ASJ, Dinneen T, Bourgeron T, Murphy D, Gallagher L, Loth E., The Synaptic Gene Study: Design and Methodology to Identify Neurocognitive Markers in Phelan-McDermid Syndrome and NRXN1 Deletions., Frontiers in neuroscience, 16, 2022, p806990
Gallagher, L. and McGrath, J., Autism spectrum disorders: current issues and future directions, Irish Journal of Psychological Medicine, 39, (3), 2022, p237-239
Dinneen, T.J. and Ghrálaigh, F.N. and Walsh, R. and Lopez, L.M. and Gallagher, L., How does genetic variation modify ND-CNV phenotypes?, Trends in Genetics, 38, (2), 2022, p140-151
Trost, B. and Thiruvahindrapuram, B. and Chan, A.J.S. and Engchuan, W. and Higginbotham, E.J. and Howe, J.L. and Loureiro, L.O. and Reuter, M.S. and Roshandel, D. and Whitney, J. and Zarrei, M. and Bookman, M. and Somerville, C. and Shaath, R. and Abdi, M. and Aliyev, E. and Patel, R.V. and Nalpathamkalam, T. and Pellecchia, G. and Hamdan, O. and Kaur, G. and Wang, Z. and MacDonald, J.R. and Wei, J. and Sung, W.W.L. and Lamoureux, S. and Hoang, N. and Selvanayagam, T. and Deflaux, N. and Geng, M. and Ghaffari, S. and Bates, J. and Young, E.J. and Ding, Q. and Shum, C. and D'Abate, L. and Bradley, C.A. and Rutherford, A. and Aguda, V. and Apresto, B. and Chen, N. and Desai, S. and Du, X. and Fong, M.L.Y. and Pullenayegum, S. and Samler, K. and Wang, T. and Ho, K. and Paton, T. and Pereira, S.L. and Herbrick, J.-A. and Wintle, R.F. and Fuerth, J. and Noppornpitak, J. and Ward, H. and Magee, P. and Al Baz, A. and Kajendirarajah, U. and Kapadia, S. and Vlasblom, J. and Valluri, M. and Green, J. and Seifer, V. and Quirbach, M. and Rennie, O. and Kelley, E. and Masjedi, N. and Lord, C. and Szego, M.J. and Zawati, M.H. and Lang, M. and Strug, L.J. and Marshall, C.R. and Costain, G. and Calli, K. and Iaboni, A. and Yusuf, A. and Ambrozewicz, P. and Gallagher, L. and Amaral, D.G. and Brian, J. and Elsabbagh, M. and Georgiades, S. and Messinger, D.S. and Ozonoff, S. and Sebat, J. and Sjaarda, C. and Smith, I.M. and Szatmari, P. and Zwaigenbaum, L. and Kushki, A. and Frazier, T.W. and Vorstman, J.A.S. and Fakhro, K.A. and Fernandez, B.A. and Lewis, M.E.S. and Weksberg, R. and Fiume, M. and Yuen, R.K.C. and Anagnostou, E. and Sondheimer, N. and Glazer, D. and Hartley, D.M. and Scherer, S.W., Genomic architecture of autism from comprehensive whole-genome sequence annotation, Cell, 185, (23), 2022, p4409-4427.e18
Sha, Z. and van Rooij, D. and Anagnostou, E. and Arango, C. and Auzias, G. and Behrmann, M. and Bernhardt, B. and Bolte, S. and Busatto, G.F. and Calderoni, S. and Calvo, R. and Daly, E. and Deruelle, C. and Duan, M. and Duran, F.L.S. and Durston, S. and Ecker, C. and Ehrlich, S. and Fair, D. and Fedor, J. and Fitzgerald, J. and Floris, D.L. and Franke, B. and Freitag, C.M. and Gallagher, L. and Glahn, D.C. and Haar, S. and Hoekstra, L. and Jahanshad, N. and Jalbrzikowski, M. and Janssen, J. and King, J.A. and Lazaro, L. and Luna, B. and McGrath, J. and Medland, S.E. and Muratori, F. and Murphy, D.G.M. and Neufeld, J. and Oâ Hearn, K. and Oranje, B. and Parellada, M. and Pariente, J.C. and Postema, M.C. and Remnelius, K.L. and Retico, A. and Rosa, P.G.P. and Rubia, K. and Shook, D. and Tammimies, K. and Taylor, M.J. and Tosetti, M. and Wallace, G.L. and Zhou, F. and Thompson, P.M. and Fisher, S.E. and Buitelaar, J.K. and Francks, C., Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium, Molecular Psychiatry, 2022
Nà Ghrálaigh, F. and McCarthy, E. and Murphy, D.N. and Gallagher, L. and Lopez, L.M., Brief Report: Evaluating the Diagnostic Yield of Commercial Gene Panels in Autism, Journal of Autism and Developmental Disorders, 2022
Carter, M. and Casey, S. and O'Keeffe, G.W. and Gibson, L. and Gallagher, L. and Murray, D.M., Maternal Immune Activation and Interleukin 17A in the Pathogenesis of Autistic Spectrum Disorder and Why It Matters in the COVID-19 Era, Frontiers in Psychiatry, 13, (823096), 2022
Conlan, K. and McGrath, J. and Teeling, M. and Macavin, M.J. and Bennett, K. and Gallagher, L., Antipsychotic prescribing in GMS paediatric and young adult population in Ireland 2005-2015: Repeated cross-sectional study, Irish Journal of Psychological Medicine, 2021
Chawner, S.J.R.A. and Doherty, J.L. and Anney, R.J.L. and Antshel, K.M. and Bearden, C.E. and Bernier, R. and Chung, W.K. and Clements, C.C. and Curran, S.R. and Cuturilo, G. and Fiksinski, A.M. and Gallagher, L. and Goin-Kochel, R.P. and Gur, R.E. and Hanson, E. and Jacquemont, S. and Kates, W.R. and Kushan, L. and Maillard, A.M. and McDonald-McGinn, D.M. and Mihaljevic, M. and Miller, J.S. and Moss, H. and Pejovic-Milovancevic, M. and Schultz, R.T. and Green-Snyder, L. and Vorstman, J.A. and Wenger, T.L. and Hall, J. and Owen, M.J. and van den Bree, M.B.M., A genetics-first approach to dissecting the heterogeneity of autism: Phenotypic comparison of autism risk copy number variants, American Journal of Psychiatry, 178, (1), 2021, p77-86
Schwartz, L. and Caixà s, A. and Dimitropoulos, A. and Dykens, E. and Duis, J. and Einfeld, S. and Gallagher, L. and Holland, A. and Rice, L. and Roof, E. and Salehi, P. and Strong, T. and Taylor, B. and Woodcock, K., Behavioral features in Prader-Willi syndrome (PWS): consensus paper from the International PWS Clinical Trial Consortium, Journal of Neurodevelopmental Disorders, 13, (1), 2021
Ding, Y. and O'Brien, A. and de la Cruz, B.M. and Yang, M. and Fitzgerald, J. and Yang, G. and Li, W. and McInerney, V. and Krawczyk, J. and Lynch, S.A. and Howard, L. and Allen, N.M. and O'Brien, T. and Gallagher, L. and Shen, S., Derivation of iPSC lines from two patients with autism spectrum disorder carrying NRXN1α deletion (NUIGi041-A, NUIG041-B; NUIGi045-A) and one sibling control (NUIGi042-A, NUIGi042-B), Stem Cell Research, 52, (102222), 2021
Postema, M.C. and van Rooij, D. and Anagnostou, E. and Arango, C. and Auzias, G. and Behrmann, M. and Filho, G.B. and Calderoni, S. and Calvo, R. and Daly, E. and Deruelle, C. and Di Martino, A. and Dinstein, I. and Duran, F.L.S. and Durston, S. and Ecker, C. and Ehrlich, S. and Fair, D. and Fedor, J. and Feng, X. and Fitzgerald, J. and Floris, D.L. and Freitag, C.M. and Gallagher, L. and Glahn, D.C. and Gori, I. and Haar, S. and Hoekstra, L. and Jahanshad, N. and Jalbrzikowski, M. and Janssen, J. and King, J.A. and Kong, X.Z. and Lazaro, L. and Lerch, J.P. and Luna, B. and Martinho, M.M. and McGrath, J. and Medland, S.E. and Muratori, F. and Murphy, C.M. and Murphy, D.G.M. and Oâ Hearn, K. and Oranje, B. and Parellada, M. and Puig, O. and Retico, A. and Rosa, P. and Rubia, K. and Shook, D. and Taylor, M.J. and Tosetti, M. and Wallace, G.L. and Zhou, F. and Thompson, P.M. and Fisher, S.E. and Buitelaar, J.K. and Francks, C., Author Correction: Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets (Nature Communications, (2019), 10, 1, (4958), 10.1038/s41467-019-13005-8), Nature Communications, 12, (1), 2021
Avazzadeh, S. and Quinlan, L.R. and Reilly, J. and McDonagh, K. and Jalali, A. and Wang, Y. and McInerney, V. and Krawczyk, J. and Ding, Y. and Fitzgerald, J. and Oâ Sullivan, M. and Forman, E.B. and Lynch, S.A. and Ennis, S. and Feerick, N. and Reilly, R. and Li, W. and Shen, X. and Yang, G. and Lu, Y. and Peeters, H. and Dockery, P. and Oâ Brien, T. and Shen, S. and Gallagher, L., NRXN1α+/- is associated with increased excitability in ASD iPSC-derived neurons, BMC Neuroscience, 22, (1), 2021
Oakley, B. and Tillmann, J. and Ruigrok, A. and Baranger, A. and Takow, C. and Charman, T. and Jones, E. and Cusack, J. and Doherty, M. and Violland, P. and WroczyÅ"ska, A. and Simonoff, E. and Buitelaar, J.K. and Gallagher, L. and Murphy, D.G.M., COVID-19 health and social care access for autistic people: European policy review, BMJ Open, 11, (6), 2021
Mezinska, S. and Gallagher, L. and Verbrugge, M. and Bunnik, E.M., Ethical issues in genomics research on neurodevelopmental disorders: a critical interpretive review, Human Genomics, 15, (1), 2021
Fitzgerald, J. and Wilson, C. and Kelly, C. and Gallagher, L., â~More than a box of puzzlesâ : Understanding the parental experience of having a child with a rare genetic conditionâ , European Journal of Medical Genetics, 64, (4), 2021
Fitzgerald, J. and Gallagher, L., Parental stress and adjustment in the context of rare genetic syndromes: A scoping review, Journal of Intellectual Disabilities, 2021
Ding, Y. and O'Brien, A. and Marcó de la Cruz, B. and Yang, M. and Lu, Y. and Qian, X. and Yang, G. and McInerney, V. and Krawczyk, J. and Lynch, S.A. and Howard, L. and Allen, N.M. and O'Brien, T. and Gallagher, L. and Shen, S., Derivation of four iPSC lines from a male ASD patient carrying a deletion in the middle coding region of NRXN1α gene (NUIGi039-A and NUIGi039-B) and a male sibling control (NUIGi040-A and NUIGi040-B), Stem Cell Research, 53, (102254), 2021
Molloy, C.J. and Gallagher, L., Can stratification biomarkers address the heterogeneity of autism spectrum disorder?, Irish Journal of Psychological Medicine, 2021
Foley C, Heron EA, Harold D, Walters J, Owen M, O'Donovan M, Sebat J, Kelleher E, Mooney C, Durand A, Pinto C, Cormican P, Morris D, Donohoe G, Gill M, Gallagher L, Corvin A., Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study., The British journal of psychiatry : the journal of mental science, 216, (5), 2020, p275-279
Hoogman, M. and van Rooij, D. and Klein, M. and Boedhoe, P. and Ilioska, I. and Li, T. and Patel, Y. and Postema, M.C. and Zhang-James, Y. and Anagnostou, E. and Arango, C. and Auzias, G. and Banaschewski, T. and Bau, C.H.D. and Behrmann, M. and Bellgrove, M.A. and Brandeis, D. and Brem, S. and Busatto, G.F. and Calderoni, S. and Calvo, R. and Castellanos, F.X. and Coghill, D. and Conzelmann, A. and Daly, E. and Deruelle, C. and Dinstein, I. and Durston, S. and Ecker, C. and Ehrlich, S. and Epstein, J.N. and Fair, D.A. and Fitzgerald, J. and Freitag, C.M. and Frodl, T. and Gallagher, L. and Grevet, E.H. and Haavik, J. and Hoekstra, P.J. and Janssen, J. and Karkashadze, G. and King, J.A. and Konrad, K. and Kuntsi, J. and Lazaro, L. and Lerch, J.P. and Lesch, K.-P. and Louza, M.R. and Luna, B. and Mattos, P. and McGrath, J. and Muratori, F. and Murphy, C. and Nigg, J.T. and Oberwelland-Weiss, E. and O'Gorman Tuura, R.L. and O'Hearn, K. and Oosterlaan, J. and Parellada, M. and Pauli, P. and Plessen, K.J. and Ramos-Quiroga, J.A. and Reif, A. and Reneman, L. and Retico, A. and Rosa, P.G.P. and Rubia, K. and Shaw, P. and Silk, T.J. and Tamm, L. and Vilarroya, O. and Walitza, S. and Jahanshad, N. and Faraone, S.V. and Francks, C. and van den Heuvel, O.A. and Paus, T. and Thompson, P.M. and Buitelaar, J.K. and Franke, B., Consortium neuroscience of attention deficit/hyperactivity disorder and autism spectrum disorder: The ENIGMA adventure, Human Brain Mapping, 2020
Feighan SM, Hughes M, Maunder K, Roche E, Gallagher L. , A profile of mental health and behaviour in Prader Willi Syndrome, J Intellect Disabil Res. , 64, (2), 2020, p158 - 169
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Lin BD, Colas F, Nijman IJ, Medic J, Brands W, Parr JR, van Eijk KR, Klauck SM, Chiocchetti AG, Freitag CM, Maestrini E, Bacchelli E, Coon H, Vicente A, Oliveira G, Pagnamenta AT, Gallagher L, Ennis S, Anney R, Bourgeron T, Luykx JJ, Vorstman J., The role of rare compound heterozygous events in autism spectrum disorder., Translational psychiatry, 10, (1), 2020, p204
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Oliva-Teles, N. and de Stefano, M.C. and Gallagher, L. and Rakic, S. and Jorge, P. and Cuturilo, G. and Markovska-Simoska, S. and Borg, I. and Wolstencroft, J. and TÃŒmer, Z. and Harwood, A.J. and Kodra, Y. and Skuse, D., Rare pathogenic copy number variation in the 16p11.2 (bp4â"bp5) region associated with neurodevelopmental and neuropsychiatric disorders: A review of the literature, International Journal of Environmental Research and Public Health, 17, (24), 2020, p1-16
Reilly, J. and Gallagher, L. and Leader, G. and Shen, S., Coupling of autism genes to tissue-wide expression and dysfunction of synapse, calcium signalling and transcriptional regulation, PLoS ONE, 15, (12 December), 2020
Haworth S, Shapland CY, Hayward C, Prins BP, Felix JF, Medina-Gomez C, Rivadeneira F, Wang C, Ahluwalia TS, Vrijheid M, Guxens M, Sunyer J, Tachmazidou I, Walter K, Iotchkova V, Jackson A, Cleal L, Huffmann J, Min JL, Sass L, Timmers PRHJ, UK10K consortium, Davey Smith G, Fisher SE, Wilson JF, Cole TJ, Fernandez-Orth D, Bønnelykke K, Bisgaard H, Pennell CE, Jaddoe VWV, Dedoussis G, Timpson N, Zeggini E, Vitart V, St Pourcain B., Low-frequency variation in TP53 has large effects on head circumference and intracranial volume., Nature communications, 10, (1), 2019, p357
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Orkeeffe, C. and Taboada, L.P. and Feerick, N. and Gallagher, L. and Lynch, T. and Reilly, R.B., Employing an entropy-based measure of sway to probe postural stability in Fragile X Premutation carriers, 2019-March, (8717071), 2019, pp259-262
Gorman KM, Meyer E, Grozeva D, Spinelli E, McTague A, Sanchis-Juan A, Carss KJ, Bryant E, Reich A, Schneider AL, Pressler RM, Simpson MA, Debelle GD, Wassmer E, Morton J, Sieciechowicz D, Jan-Kamsteeg E, Paciorkowski AR, King MD, Cross JH, Poduri A, Mefford HC, Scheffer IE, Haack TB, McCullagh G, Deciphering Developmental Disorders Study, UK10K Consortium, NIHR BioResource, Millichap JJ, Carvill GL, Clayton-Smith J, Maher ER, Raymond FL, Kurian MA., Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia., American journal of human genetics, 104, (5), 2019, 948-956
Chouinard B., Gallagher L., Kelly C., He said, she said_ Autism spectrum diagnosis and gender differentially affect relationships between executive functions and social communication, Autism, 2019, p1-12
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O'Keeffe, C. and Taboada, L.P. and Feerick, N. and Gallagher, L. and Lynch, T. and Reilly, R.B., Complexity based measures of postural stability provide novel evidence of functional decline in fragile X premutation carriers, Journal of NeuroEngineering and Rehabilitation, 16, (1), 2019
Al Shehhi, M. and Forman, E.B. and Fitzgerald, J.E. and McInerney, V. and Krawczyk, J. and Shen, S. and Betts, D.R. and Ardle, L.M. and Gorman, K.M. and King, M.D. and Green, A. and Gallagher, L. and Lynch, S.A., NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families, European Journal of Medical Genetics, 62, (3), 2019, p204-209
Ding, Y., Marcó de la Cruz, B., Xia, Y., Liu, M., Lu, Y., McInerney, V., Krawczyk, J., Lynch, S.A., Howard, L., O'Brien, T., Gallagher, L., Shen, S., Derivation of familial iPSC lines from three ASD patients carrying NRXN1"+/" and two controls (NUIGi022-A, NUIGi022-B; NUIGi023-A, NUIGi023-B; NUIGi025-A, NUIGi025-B; NUIGi024-A, NUIGi024-B; NUIGi026-A, NUIGi026-B), Stem Cell Research, 41, 2019
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, Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk, 2018
Fitzgerald J, Leemans A, Kehoe E, O'Hanlon E, Gallagher L, McGrath J., Abnormal fronto-parietal white matter organisation in the superior longitudinal fasciculus branches in autism spectrum disorders., The European journal of neuroscience, 47, (6), 2018, p652-661
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
Reilly J, Gallagher L, Chen JL, Leader G, Shen S., Bio-collections in autism research., Molecular autism, 8, 2017, p34
Connolly, S., Anney, R., Gallagher, L., Heron, E.A., A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3, European Journal of Human Genetics, 25, (2), 2017, p234-239
Balsters, J.H. and Apps, M.A. and Bolis, D. and Lehner, R. and Gallagher, L. and Wenderoth, N., Disrupted prediction errors index social deficits in autism spectrum disorder, Brain : a journal of neurology, 140, (1), 2017, p235-246
Kerley CP, Power C, Gallagher L, Coghlan D., Lack of effect of vitamin D3 supplementation in autism: a 20-week, placebo-controlled RCT., Archives of disease in childhood, 102, (11), 2017, p1030-1036
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Di Martino A, O'Connor D, Chen B, Alaerts K, Anderson J.S, Assaf M, Balsters J.H, Baxter L, Beggiato A, Bernaerts S, Blanken L.M.E, Bookheimer S.Y, Braden B.B, Byrge L, Castellanos F.X, Dapretto M, Delorme R, Fair D.A, Fishman I, Fitzgerald J, Gallagher L, Keehn R.J.J, Kennedy D.P, Lainhart J.E, Luna B, Mostofsky S.H, MÃ"ller R.-A, Nebel M.B, Nigg J.T, O'Hearn K, Solomon M, Toro R, Vaidya C.J, Wenderoth N, White T, Craddock R.C, Lord C, Leventhal B, Milham M.P, Enhancing studies of the connectome in autism using the autism brain imaging data exchange II, Scientific Data, 4, 2017, p170010
Uduehi, E. and Gallagher, L. and Alugo, T., Monitoring of prolactin levels in children and adolescents prescribed antipsychotic medication: A complete audit cycle, Irish Journal of Psychological Medicine, 34, (1), 2017, p45-51
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
Salomone E, Beranová Š, Bonnet-Brilhault F, Briciet Lauritsen M, Budisteanu M, Buitelaar J, Canal-Bedia R, Felhosi G, Fletcher-Watson S, Freitag C, Fuentes J, Gallagher L, Garcia Primo P, Gliga F, Gomot M, Green J, Heimann M, Jónsdóttir S.L, Kaale A, Kawa R, Kylliainen A, Lemcke S, Markovska-Simoska S, Marschik P.B, McConachie H, Moilanen I, Muratori F, Narzisi A, Noterdaeme M, Oliveira G, Oosterling I, Pijl M, Pop-Jordanova N, Poustka L, Roeyers H, Rogé B, Sinzig J, Vicente A, Warreyn P, Charman T, Use of early intervention for young children with autism spectrum disorder across Europe, Autism, 20, (2), 2016, p233 - 249
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
Fitzgerald J, Gallagher L, McGrath J, Widespread Disrupted White Matter Microstructure in Autism Spectrum Disorders, 2016, 1 - 11
Yvonne L. Hauck, Ingrid Blixt, Ingegerd Hildingsson, Louise Gallagher, Christine Rubertsson, Brooke Thomson and Lucy Lewis, Australian, Irish and Swedish women's perceptions of what assisted them to breastfeed for six months: exploratory design using critical incident technique, BMC Public Health, 16, (1067), 2016
Clare Quigley, Cristina Taut, Tamara Zigman, Louise Gallagher, Harry Campbell, Lina Zgaga, Association between Home Birth and Breast Feeding Outcomes: a Cross-Sectional Study in 28,125 Mother-Infant Pairs from Ireland and UK, British Medical Journal Open, 6, (e010551), 2016, p10.1136/bmjopen-2015- 010551
Maier R, Moser G, Chen GB, Ripke S, Coryell W, Potash JB, Scheftner WA, Shi J, Weissman MM, Hultman CM, Landén M, Levinson DF, Kendler KS, Smoller JW, Wray NR, Lee SH, Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder., American journal of human genetics, 2015
Gallagher L, Begley C, Clarke M, Determinants of breastfeeding initiation in Ireland., Irish journal of medical science, 185, (3), 2015, p663 - 668
Ding Y, Howard L, Gallagher L, Shen S, Regulation and postsynaptic binding of neurexins - drug targets for neurodevelopmental and neuropsychiatric disorders, Frontiers in Biology, 10, (3), 2015, p239 - 251
Kindregan D. Gallagher, L. Gormley J., Gait Deviations in Children with Autism Spectrum Disorders: A Review, Autism Research and Treatment, 2015, 2015, p1--8
Molecular pathways in autistic spectrum disorders in, editor(s)Leboyer M. (Créteil) Chaste P. (Paris) , Autism Spectrum Disorders. Phenotypes, Mechanisms and Treatments. Key Issues , Karger, 2015, 97-112 , [Gallagher L, Shen S, Anney R]
Network and Pathway Analysis Subgroup of the Psychiatric Genomics Consortium; International Inflammatory Bowel Disease Genetics Consortium (IIBDGC); International Inflammatory Bowel Disease Genetics Consortium IIBDGC., Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways., Nature neuroscience, 18, (2), 2015, p199-209
Huang, J., Howie, B., McCarthy, S., Memari, Y., Walter, K., Min, J.L., Danecek, P., Malerba, G., Trabetti, E., Zheng, H.-F., Gambaro, G., Richards, J.B., Durbin, R., Timpson, N.J., Marchini, J., Soranzo, N., Al Turki, S., Amuzu, A., Anderson, C.A., Anney, R., Antony, D., Artigas, M.S., Ayub, M., Bala, S., Barrett, J.C., Barroso, I., Beales, P., Benn, M., Bentham, J., Bhattacharya, S., Birney, E., Blackwood, D., Bobrow, M., Bochukova, E., Bolton, P.F., Bounds, R., Boustred, C., Breen, G., Calissano, M., Carss, K., Casas, J.P., Chambers, J.C., Charlton, R., Chatterjee, K., Chen, L., Ciampi, A., Cirak, S., Clapham, P., Clement, G., Coates, G., Cocca, M., Collier, D.A., Cosgrove, C., Cox, T., Craddock, N., Crooks, L., Curran, S., Curtis, D., Daly, A., Day, I.N.M., Day-Williams, A., Dedoussis, G., Down, T., Du, Y., Van Duijn, C.M., Dunham, I., Edkins, S., Ekong, R., Ellis, P., Evans, D.M., Farooqi, I.S., Fitzpatrick, D.R., Flicek, P., Floyd, J., Foley, A.R., Franklin, C.S., Futema, M., Gallagher, L., Gasparini, P., Gaunt, T.R., Geihs, M., Geschwind, D., Greenwood, C., Griffin, H., Grozeva, D., Guo, X., Guo, X., Gurling, H., Hart, D., Hendricks, A.E., Holmans, P., Huang, L., Hubbard, T., Humphries, S.E., Hurles, M.E., Hysi, P., Iotchkova, V., Isaacs, A., Jackson, D.K., Jamshidi, Y., Johnson, J., Joyce, C., Karczewski, K.J., Kaye, J., Keane, T., Kemp, J.P., Kennedy, K., Kent, A., Keogh, J., Khawaja, F., Kleber, M.E., Van Kogelenberg, M., Kolb-Kokocinski, A., Kooner, J.S., Lachance, G., Langenberg, C., Langford, C., Lawson, D., Lee, I., Van Leeuwen, E.M., Lek, M., Li, R., Li, Y., Liang, J., Lin, H., Liu, R., Lönnqvist, J., Lopes, L.R., Lopes, M., Luan, J., MacArthur, D.G., Mangino, M., Marenne, G., März, W., Maslen, J., Matchan, A., Mathieson, I., McGuffin, P., McIntosh, A.M., McKechanie, A.G., McQuillin, A., Metrustry, S., Migone, N., Mitchison, H.M., Moayyeri, A., Morris, J., Morris, R., Muddyman, D., Muntoni, F., Nordestgaard, B.G., Northstone, K., O'Donovan, M.C., O'Rahilly, S., Onoufriadis, A., Oualkacha, K., Owen, M.J., Palotie, A., Panoutsopoulou, K., Parker, V., Parr, J.R., Paternoster, L., Paunio, T., Payne, F., Payne, S.J., Perry, J.R.B., Pietilainen, O., Plagnol, V., Pollitt, R.C., Povey, S., Quail, M.A., Quaye, L., Raymond, L., Rehnström, K., Ridout, C.K., Ring, S., Ritchie, G.R.S., Roberts, N., Robinson, R.L., Savage, D.B., Scambler, P., Schiffels, S., Schmidts, M., Schoenmakers, N., Scott, R.H., Scott, R.A., Semple, R.K., Serra, E., Sharp, S.I., Shaw, A., Shihab, H.A., Shin, S.-Y., Skuse, D., Small, K.S., Smee, C., Smith, G.D., Southam, L., Spasic-Boskovic, O., Spector, T.D., St. Clair, D., St. Pourcain, B., Stalker, J., Stevens, E., Sun, J., Surdulescu, G., Suvisaari, J., Syrris, P., Tachmazidou, I., Taylor, R., Tian, J., Tobin, M.D., Toniolo, D., Traglia, M., Tybjaerg-Hansen, A., Valdes, A.M., Vandersteen, A.M., Varbo, A., Vijayarangakannan, P., Visscher, P.M., Wain, L.V., Walters, J.T.R., Wang, G., Wang, J., Wang, Y., Ward, K., Wheeler, E., Whincup, P., Whyte, T., Williams, H.J., Williamson, K.A., Wilson, C., Wilson, S.G., Wong, K., Xu, C., Yang, J., Zaza, G., Zeggini, E., Zhang, F., Zhang, P., Zhang, W., Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel, Nature Communications, 2015
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
Fitzgerald J, Johnson K, Kehoe E, Bokde AL, Garavan H, Gallagher L, McGrath J, Disrupted Functional Connectivity in Dorsal and Ventral Attention Networks During Attention Orienting in Autism Spectrum Disorders., Autism research : official journal of the International Society for Autism Research, 8, (2), 2015, p136-152
Bolton, S, McDonald, D, Curtis, E, Kelly, S, Gallagher, L, Autism in a recently arrived immigrant population, EUROPEAN JOURNAL OF PEDIATRICS, 173, (3), 2014, p337-343
Buxbaum JD, Bolshakova N, Brownfeld JM, Anney RJ, Bender P, Bernier R, Cook EH, Coon H, Cuccaro M, Freitag CM, Hallmayer J, Geschwind D, Klauck SM, Nurnberger JI, Oliveira G, Pinto D, Poustka F, Scherer SW, Shih A, Sutcliffe JS, Szatmari P, Vicente AM, Vieland V, Gallagher L, The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses., Molecular autism, 5, 2014, p34
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
Cleary l., Brady N., Fitzgerald M., Gallagher L., Holistic processing of faces as measured by the Thatcher illusion is intact in autism spectrum disorders., Autism : the international journal of research and practice, 1, 2014, p8
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
Timpson NJ, Walter K, Min JL, Tachmazidou I, Malerba G, Shin SY, Chen L, Futema M, Southam L, Iotchkova V, Cocca M, Huang J, Memari Y, McCarthy S, Danecek P, Muddyman D, Mangino M, Menni C, Perry JR, Ring SM, Gaye A, Dedoussis G, Farmaki AE, Burton P, Talmud PJ, Gambaro G, Spector TD, Smith GD, Durbin R, Richards JB, Humphries SE, Zeggini E, Soranzo N, A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans., Nature communications, 5, 2014, p4871
Di Martino, A. Yan, C.-G. Li, Q. Denio, E. Castellanos, F.X. Alaerts, K. Anderson, J.S. Assaf, M. Bookheimer, S.Y. Dapretto, M. Deen, B. Delmonte, S. Dinstein, I. Ertl-Wagner, B. Fair, D.A. Gallagher, L. Kennedy, D.P. Keown, C.L. Keysers, C. Lainhart, J.E. Lord, C. Luna, B. Menon, V. Minshew, N.J. Monk, C.S. Mueller, S. Müller, R.-A. Nebel, M.B. Nigg, J.T. O'Hearn, K. Pelphrey, K.A. Peltier, S.J. Rudie, J.D. Sunaert, S. Thioux, M. Tyszka, J.M. Uddin, L.Q. Verhoeven, J.S. Wenderoth, N. Wiggins, J.L. Mostofsky, S.H. Milham, M.P., The autism brain imaging data exchange: Towards a large-scale evaluation of the intrinsic brain architecture in autism, Nature, 19, (6), 2014, p659 - 667
Molecular Pathways in Autistic Spectrum Disorders in, editor(s)Leboyer M, Chaste P (eds) , Autism Spectrum Disorders. Phenotypes, Mechanisms and Treatments. Key Issues Ment Health. Basel, Karger, 2014, vol 179, pp 1-15, Basel, Karger, 2014, pp0.1159/000363593 , [Gallagher, Shen, Anney]
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-
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
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, p77-694
McGrath, J, Johnson, K, O'Hanlon, E, Garavan, H, Gallagher, L, Leemans, A, White Matter and Visuospatial Processing in Autism: A Constrained Spherical Deconvolution Tractography Study, AUTISM RESEARCH, 6, (5), 2013, p307-319
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
Delmonte S, Gallagher L, O'Hanlon E, McGrath J, Balsters JH, Functional and structural connectivity of frontostriatal circuitry in Autism Spectrum Disorder., Frontiers in human neuroscience, 7, 2013, p430
McGrath, J., Johnson, K., O'Hanlon, E., (...), Leemans, A., Gallagher, L., Abnormal functional connectivity in autism spectrum disorder is associated with disrupted white matter microstructural organisation, Frontiers in Human Neuroscience, July, 2013
McGrath, J, Johnson, K, O'Hanlon, E, Garavan, H, Leemans, A, Gallagher, L, Abnormal functional connectivity during visuospatial processing is associated with disrupted organisation of white matter in autism, FRONTIERS IN HUMAN NEUROSCIENCE, 7, 2013
Thevenon J, Lopez E, Keren B, Heron D, Mignot C, Altuzarra C, Béri-Dexheimer M, Bonnet C, Magnin E, Burglen L, Minot D, Vigneron J, Morle S, Anheim M, Charles P, Brice A, Gallagher L, Amiel J, Haffen E, Mach C, Depienne C, Doummar D, Bonnet M, Duplomb L, Carmignac V, Callier P, Marle N, Mosca-Boidron AL, Roze V, Aral B, Razavi F, Jonveaux P, Faivre L, Thauvin-Robinet C, Intragenic CAMTA1 rearrangements cause non-progressive congenital ataxia with or without intellectual disability., Journal of medical genetics, 49, (6), 2012, p400-8
Delmonte, S, Balsters, JH, McGrath, J, Fitzgerald, J, Brennan, S, Fagan, AJ, Gallagher, L, Social and monetary reward processing in autism spectrum disorders, MOLECULAR AUTISM, 3, 2012
Skokauskas N, Sweeny E, Meehan J, Gallagher L, Mental health problems in children with prader-willi syndrome., Journal of the Canadian Academy of Child and Adolescent Psychiatry = Journal de l'Académie canadienne de psychiatrie de l'enfant et de l'adolescent, 21, (3), 2012, p194-203
Skokauskas N, Gallagher L, Mental health aspects of autistic spectrum disorders in children., Journal of intellectual disability research : JIDR, 56, (3), 2012, p248-57
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, 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), 2012, p565-79
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
Holt R, Sykes NH, Conceição IC, Cazier JB, Anney RJ, Oliveira G, Gallagher L, Vicente A, Monaco AP, Pagnamenta AT, CNVs leading to fusion transcripts in individuals with autism spectrum disorder., European journal of human genetics : EJHG, 20, (11), 2012, p1141-7
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
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
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
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
Skuse, DH, Gallagher, L, Genetic Influences on Social Cognition, PEDIATRIC RESEARCH, 69, (5), 2011, p85R-91R
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
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
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
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
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
Noor A, Whibley A, Marshall CR, Gianakopoulos PJ, Piton A, Carson AR, Orlic-Milacic M, Lionel AC, Sato D, Pinto D, Drmic I, Noakes C, Senman L, Zhang X, Mo R, Gauthier J, Crosbie J, Pagnamenta AT, Munson J, Estes AM, Fiebig A, Franke A, Schreiber S, Stewart AF, Roberts R, McPherson R, Guter SJ, Cook EH, Dawson G, Schellenberg GD, Battaglia A, Maestrini E, Jeng L, Hutchison T, Rajcan-Separovic E, Chudley AE, Lewis SM, Liu X, Holden JJ, Fernandez B, Zwaigenbaum L, Bryson SE, Roberts W, Szatmari P, Gallagher L, Stratton MR, Gecz J, Brady AF, Schwartz CE, Schachar RJ, Monaco AP, Rouleau GA, Hui CC, Lucy Raymond F, Scherer SW, Vincent JB, Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability., Science translational medicine, 2, (49), 2010, p49ra68
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
Skokauskas N, Gallagher L, Psychosis, affective disorders and anxiety in autistic spectrum disorder: prevalence and nosological considerations., Psychopathology, 43, (1), 2010, p8-16
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
Gallagher, L., Skuse, D., Molecular and genetic influences on the neural substrate of social cognition in humans, Social Behaviour: Genes, Ecology and Evolution, 2010, p446-469
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
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
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
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
Skuse DH, Gallagher L, Dopaminergic-neuropeptide interactions in the social brain., Trends in cognitive sciences, 13, (1), 2009, p27-35
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
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
Correia, C., Coutinho, A.M., Almeida, J., Lontro, R., Lobo, C., Miguel, T.S., Martins, M., Gallagher, L., Conroy, J., Gill, M., Oliveira, G., Vicente, A.M., Association of the "4 integrin subunit gene (ITGA4) with autism, American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 150, (8), 2009, p1147-1151
McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S, Perkins DO, Dickel DE, Kusenda M, Krastoshevsky O, Krause V, Kumar RA, Grozeva D, Malhotra D, Walsh T, Zackai EH, Kaplan P, Ganesh J, Krantz ID, Spinner NB, Roccanova P, Bhandari A, Pavon K, Lakshmi B, Leotta A, Kendall J, Lee YH, Vacic V, Gary S, Iakoucheva LM, Crow TJ, Christian SL, Lieberman JA, Stroup TS, Lehtimäki T, Puura K, Haldeman-Englert C, Pearl J, Goodell M, Willour VL, Derosse P, Steele J, Kassem L, Wolff J, Chitkara N, McMahon FJ, Malhotra AK, Potash JB, Schulze TG, Nöthen MM, Cichon S, Rietschel M, Leibenluft E, Kustanovich V, Lajonchere CM, Sutcliffe JS, Skuse D, Gill M, Gallagher L, Mendell NR, Craddock N, Owen MJ, O'Donovan MC, Shaikh TH, Susser E, Delisi LE, Sullivan PF, Deutsch CK, Rapoport J, Levy DL, King MC, Sebat J, Microduplications of 16p11.2 are associated with schizophrenia., Nature genetics, 41, (11), 2009, p1223-7
Merikangas AK, Corvin AP, Gallagher L, Copy-number variants in neurodevelopmental disorders: promises and challenges., Trends in genetics : TIG, 25, (12), 2009, p536-44
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
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
Kent, L, Gallagher, L, Elliott, HR, Mowbray, C, Chinnery, PF, An investigation of mitochondrial haplogroups in autism, AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 147B, (6), 2008, p987-989
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
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
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
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
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
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
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
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
Gallagher, L., Hawi, Z., Kearney, G., Fitzgerald, M., Gill, M., No Association between Allelic Variants of HOXA1/HOXB1 and Autism, American Journal of Medical Genetics - Neuropsychiatric Genetics, 124 B, (1), 2004, p64-67
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
Gallagher, L., Hawi, Z., Kearney, G., Fitzgerald, M., Gill, M., No association of allelic variant of HOXA1 and autism, American Journal of Medical Genetics - Neuropsychiatric Genetics, 105, (7), 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
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