Professor Louise Gallagher

Professor Louise Gallagher

Professor Child & Adolescent Psychiatry, Psychiatry

Professor Child & Adolescent Psychiatry, Trinity Inst. of Neurosciences (TCIN)

3531896 2464http://people.tcd.ie/lgallagh

Publications and Further Research Outputs

  • 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, 2015Journal Article, 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, 1366-72Journal Article, 2015, DOI , TARA - Full Text
  • 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, p34Journal 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, p209-15Journal Article, 2014, DOI , TARA - Full Text
  • 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, p4871Journal Article, 2014, DOI
  • 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, p199-209Journal Article, 2015
  • 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
  • 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, p1-7Journal Article, 2014, DOI , TARA - Full Text
  • 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, p136-152Journal Article, 2015, 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 - 667Journal Article, 2014, DOI , URL , TARA - Full Text
  • 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 - 251Journal Article, 2015, DOI , URL
  • 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
  • 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, 2016Journal Article, 2016, DOI
  • Gallagher L, Begley C, Clarke M, Determinants of breastfeeding initiation in Ireland., Irish journal of medical science, 185, (3), 2015, p663 - 668Journal Article, 2015, DOI , URL , TARA - Full Text
  • 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- 010551Journal Article, 2016, DOI , URL
  • 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), 2016Journal Article, 2016, URL , TARA - Full Text
  • 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 - 593Journal Article, 2004, DOI , URL
  • Kindregan D. Gallagher, L. Gormley J., Gait Deviations in Children with Autism Spectrum Disorders: A Review, Autism Research and Treatment, 2015, 2015, p1--8Journal Article, 2015
  • 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, p234-239Journal 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, p170010Journal Article, 2017, DOI , URL , TARA - Full Text
  • Fitzgerald J, Gallagher L, McGrath J, Widespread Disrupted White Matter Microstructure in Autism Spectrum Disorders, 2016, 1 - 11Miscellaneous, 2016, DOI , URL
  • Salomone E, Beranová Å , 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 - 249Journal Article, 2016, DOI , URL
  • 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, p652-661Journal Article, 2018, DOI
  • 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, p359-369Journal Article, 2018, 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, p1030-1036Journal Article, 2017, DOI
  • Reilly J, Gallagher L, Chen JL, Leader G, Shen S., Bio-collections in autism research., Molecular autism, 8, 2017, p34Journal Article, 2017, DOI , TARA - Full Text
  • 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, p21Journal Article, 2017, DOI , TARA - Full Text
  • 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, p978-985Journal 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, DOI , URL , TARA - Full Text
  • 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, p602-611Journal Article, 2017, DOI , URL
  • 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, p45-51Journal Article, 2017, DOI , URL
  • 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, p235-246Journal Article, 2017, DOI , URL
  • 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, p204-209Journal Article, 2019, DOI , URL , 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, p357Journal Article, 2019, DOI , TARA - Full Text
  • 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
  • Gallagher, L., Skuse, D., Molecular and genetic influences on the neural substrate of social cognition in humans, Social Behaviour: Genes, Ecology and Evolution, 2010, p446-469Journal Article, 2010
  • 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, p1147-1151Journal Article, 2009
  • 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, p64-67Journal Article, 2004
  • 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), 2001Journal Article, 2001
  • 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, 948-956Journal Article, 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, p1-12Journal Article, 2019, DOI , TARA - Full Text
  • 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), 2019Journal Article, 2019, DOI , URL
  • 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, pp259-262Conference Paper, 2019, DOI , URL
  • 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 - 169Journal Article, 2020, DOI
  • 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 - 67Journal Article, 2004, DOI , URL
  • 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 - 108Journal Article, 2003, DOI , URL
  • , Altered structural brain asymmetry in autism spectrum disorder: large-scale analysis via the ENIGMA Consortium, 2019Journal 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, 2019Journal Article, 2019
  • 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), 2019Journal Article, 2019
  • 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, 2019Journal Article, 2019
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  • 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 O†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), 2021Journal Article, 2021, DOI , URL
  • Schwartz, L. and Caixàs, 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), 2021Journal Article, 2021, DOI , URL
  • 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), 2021Journal Article, 2021, DOI , URL
  • 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), 2021Journal Article, 2021, DOI , URL
  • Fitzgerald, J. and Wilson, C. and Kelly, C. and Gallagher, L., â€~More than a box of puzzles†: Understanding the parental experience of having a child with a rare genetic condition†, European Journal of Medical Genetics, 64, (4), 2021Journal Article, 2021, DOI , URL
  • Molloy, C.J. and Gallagher, L., Can stratification biomarkers address the heterogeneity of autism spectrum disorder?, Irish Journal of Psychological Medicine, 2021Journal Article, 2021, DOI , URL
  • Fitzgerald, J. and Gallagher, L., Parental stress and adjustment in the context of rare genetic syndromes: A scoping review, Journal of Intellectual Disabilities, 2021Journal Article, 2021, DOI , URL
  • 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, 2021Journal Article, 2021, DOI , URL
  • 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, p77-86Journal Article, 2021, DOI , URL
  • 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, pe0267465Journal Article, 2022, DOI
  • 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, p806990Journal Article, 2022, DOI
  • Gallagher, L. and McGrath, J., Autism spectrum disorders: current issues and future directions, Irish Journal of Psychological Medicine, 39, (3), 2022, p237-239Journal Article, 2022, DOI , URL
  • 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-Rodríguez, 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 Díaz-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, p299-313Journal Article, 2022, DOI , URL
  • 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), 2022Journal Article, 2022, DOI , URL
  • 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), 2023Journal Article, 2023, DOI , URL
  • 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, 2023Journal Article, 2023, DOI , URL
  • 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.e18Journal Article, 2022, DOI , URL
  • 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), 2023Journal Article, 2023, DOI , URL
  • 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, p3747-3752Journal Article, 2023, DOI , URL
  • 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), 2023Journal Article, 2023, DOI , URL
  • Dinneen, T.J. and Ní 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), 2024Journal Article, 2024, DOI , URL
  • 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), 2024Journal Article, 2024, DOI , URL
  • 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), 2024Journal Article, 2024, DOI , URL
  • 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), 2024Journal Article, 2024, DOI , URL
  • Ní 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, p157-158Journal Article, 2024, DOI , URL
  • 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 - 965Journal Article, 2005, DOI , URL , TARA - Full Text
  • 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
  • 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 - 41Journal 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 - 2245Journal Article, 2007, DOI , URL , TARA - Full Text
  • Johnson K, Robertson I, Kelly S, Silk T, Barry E, Daibhis A, Watchorn A, Keavey M, Fitzgerald M, Gallagher L, Gill M, Bellgrove M, Dissociation in performance of children with ADHD and high-functioning autism on a task of sustained attention. , Neuropsychologia, 45, (10), 2007, p2234 - 2245Journal Article, 2007, 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 - 16Journal 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, p1685-1699Journal Article, 2008, DOI , TARA - Full Text
  • 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, p535-544Journal Article, 2009, 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 - 808Journal Article, 2009, DOI , URL , TARA - Full Text
  • 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, p2777-2781Journal 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, p163-167Journal 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, p841-848Journal 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, p4072-4082Journal Article, 2010, DOI , URL , 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 - 344Journal Article, 2010, DOI
  • Heron Elizabeth A, O'Dushlane C, Segurado R, Gallagher L, Gill M., Exploration of empirical Bayes hierarchical modeling for the analysis of genome-wide association study data., Oxford Journal Mathematics & Physical Sciences Biostatistics, 12, (3), 2011, p445-461Journal Article, 2011, DOI , URL , 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, p368-372Journal Article, 2010, 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), 2011Journal Article, 2011, DOI , URL , TARA - Full Text
  • Casey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bolton PF, Bourgeron T, Brennan S, Cali P, Correia C, Corsello C, Coutanche M, Dawson G, de Jonge M, Delorme R, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Foley S, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Green J, Guter SJ, Hakonarson H, Holt R, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Lamb JA, Leboyer M, Le Couteur A, Leventhal BL, Lord C, Lund SC, Maestrini E, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Merikangas A, Miller J, Minopoli F, Mirza GK, Munson J, Nelson SF, Nygren G, Oliveira G, Pagnamenta AT, Papanikolaou K, Parr JR, Parrini B, Pickles A, Pinto D, Piven J, Posey DJ, Poustka A, Poustka F, Ragoussis J, Roge B, Rutter ML, Sequeira AF, Soorya L, Sousa I, Sykes N, Stoppioni V, Tancredi R, Tauber M, Thompson AP, Thomson S, Tsiantis J, Van Engeland H, Vincent JB, Volkmar F, Vorstman JA, Wallace S, Wang K, Wassink TH, White K, Wing K, Wittemeyer K, Yaspan BL, Zwaigenbaum L, Betancur C, Buxbaum JD, Cantor RM, Cook EH, Coon H, Cuccaro ML, Geschwind DH, Haines JL, Hallmayer J, Monaco AP, Nurnberger JI Jr, Pericak-Vance MA, Schellenberg GD, Scherer SW, Sutcliffe JS, Szatmari P, Vieland VJ, Wijsman EM, Green A, Gill M, Gallagher L, Vicente A, Ennis S, A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. , Human Genetics, 131, (4), 2011, p565-579Journal Article, 2011, DOI , TARA - Full Text
  • Anney RJ, Kenny EM, O'Dushlaine C, Yaspan BL, Parkhomenka E, Buxbaum JD, Sutcliffe J, Gill M, Gallagher L; Autism Genome Project, Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders., Eur J Human Genetics, 19, (10), 2011, p1082 - 1089Journal Article, 2011, DOI , TARA - Full Text
  • 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 - 169Journal Article, 2012, TARA - Full Text
  • Vorstman JA, Anney RJ, Derks EM, Gallagher L, Gill M, de Jonge MV, van Engeland H, Kahn RS, Ophoff RA, 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, p55-60Journal Article, 2013, 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, p4781-92Journal Article, 2012, DOI , TARA - Full Text
  • 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, p1141-7Journal 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, p565-79Journal Article, 2012, DOI , TARA - Full Text
  • Merikangas AK, Corvin AP, Gallagher L, Copy-number variants in neurodevelopmental disorders: promises and challenges., Trends in genetics : TIG, 25, (12), 2009, p536-44Journal Article, 2009, 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, p314-30Journal Article, 2012, DOI
  • Corvin A, Donohoe G, Hargreaves A, Gallagher L, Gill M., The Cognitive Genetics of Neuropsychiatric Disorders. , Current Topics in Behavioral Neurosciences, 12, 2012, p579-613Journal Article, 2012, 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, p430Journal Article, 2013, DOI , TARA - Full Text
  • 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, p872-879Journal Article, 2014, DOI , TARA - Full Text
  • Bolton, S, McDonald, D, Curtis, E, Kelly, S, Gallagher, L, Autism in a recently arrived immigrant population, EUROPEAN JOURNAL OF PEDIATRICS, 173, (3), 2014, p337-343Journal Article, 2014, 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, 2013Journal 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, p307-319Journal Article, 2013, DOI
  • 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, p77-694Journal Article, 2014, DOI , TARA - Full Text
  • 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, 2013Journal Article, 2013, DOI , TARA - Full Text
  • 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, 2012Journal 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, p194-203Journal 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, p335-9Journal 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, p400-8Journal Article, 2012, DOI
  • Skokauskas N, Gallagher L, Mental health aspects of autistic spectrum disorders in children., Journal of intellectual disability research : JIDR, 56, (3), 2012, p248-57Journal Article, 2012, DOI
  • Skuse, DH, Gallagher, L, Genetic Influences on Social Cognition, PEDIATRIC RESEARCH, 69, (5), 2011, p85R-91RJournal Article, 2011
  • 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, p49ra68Journal 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, p2777-2781Journal Article, 2010, DOI
  • 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, p1147-1151Journal Article, 2009, DOI
  • Skokauskas N, Gallagher L, Psychosis, affective disorders and anxiety in autistic spectrum disorder: prevalence and nosological considerations., Psychopathology, 43, (1), 2010, p8-16Journal Article, 2010, 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, p1223-7Journal Article, 2009, DOI
  • Skuse DH, Gallagher L, Dopaminergic-neuropeptide interactions in the social brain., Trends in cognitive sciences, 13, (1), 2009, p27-35Journal 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, p987-989Journal Article, 2008, DOI
  • 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-U5Journal Article, 2005
  • 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, 543Journal Article, 2000, URL
  • 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, p8Journal Article, 2014, DOI , URL