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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

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 Journal Article, 2021 DOI TARA - Full Text

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 Journal Article, 2021 DOI TARA - Full Text

de la Cruz, B.M. and Ding, Y. and McInerney, V. and Krawczyk, J. and Lu, Y. and Yang, G. and Qian, X. and Li, W. and Howard, L. and Allen, N.M. and O'Brien, T. and Gallagher, L. and Shen, S., Derivation of two iPSC lines from a sporadic ASD patient (NUIGi033-A) and a paternal control (NUIGi034-A), Stem Cell Research, 44, (101722), 2020 Journal Article, 2020 DOI TARA - Full Text

Ding, Y. and de la Cruz, B.M. and McInerney, V. and Lu, Y. and Yang, G. and Qian, X. and Li, W. and Krawczyk, J. and Howard, L. and O'Brien, T. and Gallagher, L. and Shen, S., Derivation of iPSC lines from three young healthy donors of Caucasian origin (NUIGi035-A; NUIGi036-A; NUIGi037-A), Stem Cell Research, 49, (102101), 2020 Journal Article, 2020 TARA - Full Text DOI

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 Journal Article, 2020 DOI TARA - Full Text

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 Journal Article, 2020 DOI TARA - Full Text

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 Journal Article, 2020 DOI

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 Journal Article, 2020 DOI TARA - Full Text

Cosemans, N. and Vandenhove, L. and Vogels, A. and Devriendt, K. and Van Esch, H. and Van Buggenhout, G. and Olivié, H. and De Ravel, T. and Ortibus, E. and Legius, E. and Aerssens, P. and Breckpot, J. and Vermeesch, J.R. and Shen, S. and Fitzgerald, J. and Gallagher, L. and Peeters, H., The clinical relevance of intragenic NRXN1 deletions, Journal of Medical Genetics, 57, (5), 2020, p347-355 Journal Article, 2020 DOI

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 Journal Article, 2020 DOI TARA - Full Text

Satterstrom, F.K. and Kosmicki, J.A. and Wang, J. and Breen, M.S. and De Rubeis, S. and An, J.-Y. and Peng, M. and Collins, R. and Grove, J. and Klei, L. and Stevens, C. and Reichert, J. and Mulhern, M.S. and Artomov, M. and Gerges, S. and Sheppard, B. and Xu, X. and Bhaduri, A. and Norman, U. and Brand, H. and Schwartz, G. and Nguyen, R. and Guerrero, E.E. and Dias, C. and Aleksic, B. and Anney, R. and Barbosa, M. and Bishop, S. and Brusco, A. and Bybjerg-Grauholm, J. and Carracedo, A. and Chan, M.C.Y. and Chiocchetti, A.G. and Chung, B.H.Y. and Coon, H. and Cuccaro, M.L. and Curró, A. and Dalla Bernardina, B. and Doan, R. and Domenici, E. and Dong, S. and Fallerini, C. and Fernández-Prieto, M. and Ferrero, G.B. and Freitag, C.M. and Fromer, M. and Gargus, J.J. and Geschwind, D. and Giorgio, E. and González-Peñas, J. and Guter, S. and Halpern, D. and Hansen-Kiss, E. and He, X. and Herman, G.E. and Hertz-Picciotto, I. and Hougaard, D.M. and Hultman, C.M. and Ionita-Laza, I. and Jacob, S. and Jamison, J. and Jugessur, A. and Kaartinen, M. and Knudsen, G.P. and Kolevzon, A. and Kushima, I. and Lee, S.L. and LehtimÀki, T. and Lim, E.T. and Lintas, C. and Lipkin, W.I. and Lopergolo, D. and Lopes, F. and Ludena, Y. and Maciel, P. and Magnus, P. and Mahjani, B. and Maltman, N. and Manoach, D.S. and Meiri, G. and Menashe, I. and Miller, J. and Minshew, N. and Montenegro, E.M.S. and Moreira, D. and Morrow, E.M. and Mors, O. and Mortensen, P.B. and Mosconi, M. and Muglia, P. and Neale, B.M. and Nordentoft, M. and Ozaki, N. and Palotie, A. and Parellada, M. and Passos-Bueno, M.R. and Pericak-Vance, M. and Persico, A.M. and Pessah, I. and Puura, K. and Reichenberg, A. and Renieri, A. and Riberi, E. and Robinson, E.B. and Samocha, K.E. and Sandin, S. and Santangelo, S.L. and Schellenberg, G. and Scherer, S.W. and Schlitt, S. and Schmidt, R. and Schmitt, L. and Silva, I.M.W. and Singh, T. and Siper, P.M. and Smith, M. and Soares, G. and Stoltenberg, C. and Suren, P. and Susser, E. and Sweeney, J. and Szatmari, P. and Tang, L. and Tassone, F. and Teufel, K. and Trabetti, E. and Trelles, M.D.P. and Walsh, C.A. and Weiss, L.A. and Werge, T. and Werling, D.M. and Wigdor, E.M. and Wilkinson, E. and Willsey, A.J. and Yu, T.W. and Yu, M.H.C. and Yuen, R. and Zachi, E. and Agerbo, E. and Als, T.D. and Appadurai, V. and BÊkvad-Hansen, M. and Belliveau, R. and Buil, A. and Carey, C.E. and Cerrato, F. and Chambert, K. and Churchhouse, C. and Dalsgaard, S. and Demontis, D. and Dumont, A. and Goldstein, J. and Hansen, C.S. and Hauberg, M.E. and Hollegaard, M.V. and Howrigan, D.P. and Huang, H. and Maller, J. and Martin, A.R. and Martin, J. and Mattheisen, M. and Moran, J. and Pallesen, J. and Palmer, D.S. and Pedersen, C.B. and Pedersen, M.G. and Poterba, T. and Poulsen, J.B. and Ripke, S. and Schork, A.J. and Thompson, W.K. and Turley, P. and Walters, R.K. and Betancur, C. and Cook, E.H. and Gallagher, L. and Gill, M. and Sutcliffe, J.S. and Thurm, A. and Zwick, M.E. and BÞrglum, A.D. and State, M.W. and Cicek, A.E. and Talkowski, M.E. and Cutler, D.J. and Devlin, B. and Sanders, S.J. and Roeder, K. and Daly, M.J. and Buxbaum, J.D., Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism, Cell, 180, (3), 2020, p568-584.e23 Journal Article, 2020 TARA - Full Text DOI

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 Journal Article, 2020 TARA - Full Text DOI

Schaaf, C.P. and Betancur, C. and Yuen, R.K.C. and Parr, J.R. and Skuse, D.H. and Gallagher, L. and Bernier, R.A. and Buchanan, J.A. and Buxbaum, J.D. and Chen, C.-A. and Dies, K.A. and Elsabbagh, M. and Firth, H.V. and Frazier, T. and Hoang, N. and Howe, J. and Marshall, C.R. and Michaud, J.L. and Rennie, O. and Szatmari, P. and Chung, W.K. and Bolton, P.F. and Cook, E.H. and Scherer, S.W. and Vorstman, J.A.S., A framework for an evidence-based gene list relevant to autism spectrum disorder, Nature Reviews Genetics, 21, (6), 2020, p367-376 Journal Article, 2020 DOI TARA - Full Text

Postema, M.C., van Rooij, D., Anagnostou, E., Arango, C., Auzias, G., Behrmann, M., Filho, G.B., Calderoni, S., Calvo, R., Daly, E., Deruelle, C., Di Martino, A., Dinstein, I., Duran, F.L.S., Durston, S., Ecker, C., Ehrlich, S., Fair, D., Fedor, J., Feng, X., Fitzgerald, J., Floris, D.L., Freitag, C.M., Gallagher, L., Glahn, D.C., Gori, I., Haar, S., Hoekstra, L., Jahanshad, N., Jalbrzikowski, M., Janssen, J., King, J.A., Kong, X.Z., Lazaro, L., Lerch, J.P., Luna, B., Martinho, M.M., McGrath, J., Medland, S.E., Muratori, F., Murphy, C.M., Murphy, D.G.M., O"Hearn, K., Oranje, B., Parellada, M., Puig, O., Retico, A., Rosa, P., Rubia, K., Shook, D., Taylor, M.J., Tosetti, M., Wallace, G.L., Zhou, F., Thompson, P.M., Fisher, S.E., Buitelaar, J.K., Francks, C., Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets, Nature Communications, 10, (1), 2019 Journal Article, 2019

Avazzadeh, S., McDonagh, K., Reilly, J., Wang, Y., Boomkamp, S.D., McInerney, V., Krawczyk, J., Fitzgerald, J., Feerick, N., O'Sullivan, M., Jalali, A., Forman, E.B., Lynch, S.A., Ennis, S., Cosemans, N., Peeters, H., Dockery, P., O'Brien, T., Quinlan, L.R., Gallagher, L., Shen, S., Increased Ca2+ signaling in NRXN1" +/- neurons derived from ASD induced pluripotent stem cells, Molecular Autism, 10, (1), 2019 Journal Article, 2019

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 Journal Article, 2019 DOI

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 Journal Article, 2019 DOI TARA - Full Text

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 Journal Article, 2019

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 Journal Article, 2019 DOI

, Altered structural brain asymmetry in autism spectrum disorder: large-scale analysis via the ENIGMA Consortium, 2019 Journal Article, 2019

, He said, she said: Autism spectrum diagnosis and gender differentially affect relationships between executive functions and social communication, Autism : the international journal of research and practice, 2019 Journal Article, 2019

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 Conference Paper, 2019 DOI

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 Journal Article, 2019 DOI TARA - Full Text

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 Journal Article, 2019 DOI TARA - Full Text

van Rooij D, Anagnostou E, Arango C, Auzias G, Behrmann M, Busatto GF, Calderoni S, Daly E, Deruelle C, Di Martino A, Dinstein I, Duran FLS, Durston S, Ecker C, Fair D, Fedor J, Fitzgerald J, Freitag CM, Gallagher L, Gori I, Haar S, Hoekstra L, Jahanshad N, Jalbrzikowski M, Janssen J, Lerch J, Luna B, Martinho MM, McGrath J, Muratori F, Murphy CM, Murphy DGM, O'Hearn K, Oranje B, Parellada M, Retico A, Rossa P, Rubia K, Shook D, Taylor M, Thompson PM, Tosetti M, Wallace GL, Zhou F, Buitelaar JK., Cortical and Subcortical Brain Morphometry Differences Between Patients With Autism Spectrum Disorder and Healthy Individuals Across the Lifespan: Results From the ENIGMA ASD Working Group., The American journal of psychiatry, 175, (4), 2018, p359-369 Journal Article, 2018 DOI

, Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk, 2018 Journal Article, 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 Journal Article, 2018 DOI

Reilly J, Gallagher L, Chen JL, Leader G, Shen S., Bio-collections in autism research., Molecular autism, 8, 2017, p34 Journal Article, 2017 TARA - Full Text 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

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 Journal Article, 2017 DOI

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

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 Journal Article, 2017 DOI

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 Journal Article, 2017 DOI TARA - Full Text URL

Yuen, R.K.C. and Merico, D. and Bookman, M. and Howe, J.L. and Thiruvahindrapuram, B. and Patel, R.V. and Whitney, J. and Deflaux, N. and Bingham, J. and Wang, Z. and Pellecchia, G. and Buchanan, J.A. and Walker, S. and Marshall, C.R. and Uddin, M. and Zarrei, M. and Deneault, E. and D'Abate, L. and Chan, A.J.S. and Koyanagi, S. and Paton, T. and Pereira, S.L. and Hoang, N. and Engchuan, W. and Higginbotham, E.J. and Ho, K. and Lamoureux, S. and Li, W. and MacDonald, J.R. and Nalpathamkalam, T. and Sung, W.W.L. and Tsoi, F.J. and Wei, J. and Xu, L. and Tasse, A.-M. and Kirby, E. and Van Etten, W. and Twigger, S. and Roberts, W. and Drmic, I. and Jilderda, S. and Modi, B.M. and Kellam, B. and Szego, M. and Cytrynbaum, C. and Weksberg, R. and Zwaigenbaum, L. and Woodbury-Smith, M. and Brian, J. and Senman, L. and Iaboni, A. and Doyle-Thomas, K. and Thompson, A. and Chrysler, C. and Leef, J. and Savion-Lemieux, T. and Smith, I.M. and Liu, X. and Nicolson, R. and Seifer, V. and Fedele, A. and Cook, E.H. and Dager, S. and Estes, A. and Gallagher, L. and Malow, B.A. and Parr, J.R. and Spence, S.J. and Vorstman, J. and Frey, B.J. and Robinson, J.T. and Strug, L.J. and Fernandez, B.A. and Elsabbagh, M. and Carter, M.T. and Hallmayer, J. and Knoppers, B.M. and Anagnostou, E. and Szatmari, P. and Ring, R.H. and Glazer, D. and Pletcher, M.T. and Scherer, S.W., Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder, Nature Neuroscience, 20, (4), 2017, p602-611 Journal Article, 2017 DOI

Hendricks, A.E. and Bochukova, E.G. and Marenne, G. and Keogh, J.M. and Atanassova, N. and Bounds, R. and Wheeler, E. and Mistry, V. and Henning, E. and Körner, A. and Muddyman, D. and McCarthy, S. and Hinney, A. and Hebebrand, J. and Scott, R.A. and Langenberg, C. and Wareham, N.J. and Surendran, P. and Howson, J.M. and Butterworth, A.S. and Danesh, J. and Nordestgaard, BÃ".G. and Nielsen, S.F. and Afzal, S. and Papadia, S. and Ashford, S. and Garg, S. and Millhauser, G.L. and Palomino, R.I. and Kwasniewska, A. and Tachmazidou, I. and O'Rahilly, S. and Zeggini, E. and Barroso, I. and Farooqi, I.S. and Benzeval, M. and Burton, J. and Buck, N. and JÃ"ckle, A. and Kumari, M. and Laurie, H. and Lynn, P. and Pudney, S. and Rabe, B. and Wolke, D. and Overvad, K. and TjÃ"nneland, A. and Clavel-Chapelon, F. and Kaaks, R. and Boeing, H. and Trichopoulou, A. and Ferrari, P. and Palli, D. and Krogha, V. and Panico, S. and Tuminoa, R. and Matullo, G. and Boer, J. and Van Der Schouw, Y. and Weiderpass, E. and Quiros, J.R. and Sánchez, M.-J. and Navarro, C. and Moreno-Iribas, C. and Arriola, L. and Melander, O. and Wennberg, P. and Key, T.J. and Riboli, E. and Turki, S.A. and Anderson, C.A. and Anney, R. and Antony, D. and Soler Artigas, M. and Ayub, M. and Bala, S. and Barrett, J.C. and Beales, P. and Bentham, J. and Bhattacharyaa, S. and Birney, E. and Blackwooda, D. and Bobrow, M. and Bolton, P.F. and Boustred, C. and Breen, G. and Calissanoa, M. and Carss, K. and Charlton, R. and Chatterjee, K. and Chen, L. and Ciampia, A. and Cirak, S. and Clapham, P. and Clement, G. and Coates, G. and Coccaa, M. and Collier, D.A. and Cosgrove, C. and Coxa, T. and Craddock, N. and Crooks, L. and Curran, S. and Curtis, D. and Daly, A. and Danecek, P. and Day, I.N.M. and Day-Williams, A. and Dominiczak, A. and Down, T. and Du, Y. and Dunham, I. and Durbin, R. and Edkins, S. and Ekong, R. and Ellis, P. and Evansa, D.M. and Fitzpatrick, D.R. and Flicek, P. and Floyd, J. and Foley, A.R. and Franklin, C.S. and Futema, M. and Gallagher, L. and Gaunt, T.R. and Geihs, M. and Geschwind, D. and Greenwood, C.M.T. and Griffin, H. and Grozeva, D. and Guo, X. and Guo, X. and Gurling, H. and Hart, D. and Holmans, P. and Howie, B. and Huang, J. and Huang, L. and Hubbard, T. and Humphries, S.E. and Hurles, M.E. and Hysi, P. and Iotchkova, V. and Jackson, D.K. and Jamshidi, Y. and Joyce, C. and Karczewski, K.J. and Kaye, J. and Keane, T. and Kemp, J.P. and Kennedy, K. and Kent, A. and Khawaja, F. and Van Kogelenberg, M. and Kolb-Kokocinski, A. and Lachance, G. and Langford, C. and Lawson, D. and Lee, I. and Lek, M. and Li, R. and Li, Y. and Liang, J. and Lin, H. and Liu, R. and Lönnqvist, J. and Lopes, L.R. and Lopes, M. and MacArthur, D.G. and Mangino, M. and Marchini, J. and Maslen, J. and Mathieson, I. and McGuffin, P. and McIntosh, A.M. and McKechanie, A.G. and McQuillin, A. and Memari, Y. and Metrustry, S. and Migone, N. and Min, J.L. and Mitchison, H.M. and Moayyeri, A. and Morris, A. and Morris, J. and Muntoni, F. and Northstone, K. and O'Donovan, M.C. and Onoufriadis, A. and Oualkacha, K. and Owen, M.J. and Palotie, A. and Panoutsopoulou, K. and Parker, V. and Parr, J.R. and Paternoster, L. and Paunio, T. and Payne, F. and Payne, S.J. and Perry, J.R.B. and Pietilainen, O. and Plagnol, V. and Pollitt, R.C. and Porteous, D.J. and Povey, S. and Quail, M.A. and Quaye, L. and Raymond, F.L. and Rehnström, K. and Richards, J.B. and Ridout, C.K. and Ring, S. and Ritchie, G.R.S. and Roberts, N. and Robinson,, Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity, Scientific Reports, 7, (1), 2017, p4394 - Journal Article, 2017 TARA - Full Text DOI

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 Journal Article, 2017 DOI

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 Journal Article, 2017 DOI

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 Journal Article, 2016 DOI

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, Molecular Psychiatry, 21, 2016, p728-730 Journal Article, 2016 DOI

Fitzgerald J, Gallagher L, McGrath J, Widespread Disrupted White Matter Microstructure in Autism Spectrum Disorders, 2016, 1 - 11 Miscellaneous, 2016 URL DOI

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 Journal Article, 2016 TARA - Full Text URL

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 Journal Article, 2016 DOI URL

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 Journal Article, 2015

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 Journal Article, 2015

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] Book Chapter, 2015 DOI URL

Gallagher L, Begley C, Clarke M, Determinants of breastfeeding initiation in Ireland., Irish journal of medical science, 185, (3), 2015, p663 - 668 Journal Article, 2015 TARA - Full Text 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 TARA - Full Text DOI

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 Journal Article, 2015 DOI

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 Journal Article, 2015 URL DOI

Kindregan D. Gallagher, L. Gormley J., Gait Deviations in Children with Autism Spectrum Disorders: A Review, Autism Research and Treatment, 2015, 2015, p1--8 Journal Article, 2015

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 Journal Article, 2015

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 Journal Article, 2014 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

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 Journal Article, 2014 TARA - Full Text URL DOI

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] Book Chapter, 2014

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 Journal Article, 2014 DOI TARA - Full Text

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

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

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

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 Journal Article, 2014 DOI

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 Journal Article, 2014 URL DOI

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 Journal Article, 2014 DOI

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 Journal Article, 2013 TARA - Full Text DOI

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 Journal Article, 2013 DOI TARA - Full Text

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

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 Journal Article, 2013 DOI

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 Journal Article, 2013 DOI

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 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 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

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 Journal Article, 2012 DOI

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

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 Journal Article, 2012 TARA - Full Text DOI

Skokauskas N, Gallagher L, Mental health aspects of autistic spectrum disorders in children., Journal of intellectual disability research : JIDR, 56, (3), 2012, p248-57 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

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

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 Journal Article, 2012 DOI

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 Journal Article, 2012 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 DOI TARA - Full Text

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 TARA - Full Text DOI URL

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 DOI TARA - Full Text

Skuse, DH, Gallagher, L, Genetic Influences on Social Cognition, PEDIATRIC RESEARCH, 69, (5), 2011, p85R-91R Journal Article, 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 Journal Article, 2011 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

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

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 Journal Article, 2010

Skokauskas N, Gallagher L, Psychosis, affective disorders and anxiety in autistic spectrum disorder: prevalence and nosological considerations., Psychopathology, 43, (1), 2010, p8-16 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 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

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 Journal Article, 2010 DOI

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

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

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

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

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

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

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 Journal Article, 2009 DOI

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 Journal Article, 2009

Skuse DH, Gallagher L, Dopaminergic-neuropeptide interactions in the social brain., Trends in cognitive sciences, 13, (1), 2009, p27-35 Journal Article, 2009 DOI

Merikangas AK, Corvin AP, Gallagher L, Copy-number variants in neurodevelopmental disorders: promises and challenges., Trends in genetics : TIG, 25, (12), 2009, p536-44 Journal Article, 2009 DOI

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 Journal Article, 2008 DOI

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 DOI 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

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

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 DOI TARA - Full Text URL

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 DOI TARA - Full Text

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, 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 DOI URL TARA - Full Text 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 DOI URL

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 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 URL DOI

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 URL DOI URL

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 Journal Article, 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

Child Protection in Ireland in, editor(s)M. Harder and K. Pringle , Protecting Children in Europe: Towards a New Millennium, Aalborg, Aalborg University Press, 1997, pp101 - 126, [Buckley, H] Book Chapter, 1997

Research Expertise

Keywords

Attention Deficit Hyperactivity Disorder (ADHD); Autism; Child Mental Health; Genetics of Neurodevelopmental Disorders; Neurodevelopmental Disorders