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Professor Louise Gallagher

Professor Child & Adolescent Psychiatry (Psychiatry)


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

  Attention Deficit Hyperactivity Disorder (ADHD)   Autism   Child Mental Health   Genetics of Neurodevelopmental Disorders   Neurodevelopmental Disorders
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 , Notes: [cited By 0; Article in Press], Journal Article, PUBLISHED  TARA - Full Text  DOI
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, PUBLISHED  TARA - Full Text  DOI
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, PUBLISHED  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, PUBLISHED  TARA - Full Text  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, p359-369 , Journal Article, PUBLISHED  DOI
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, PUBLISHED  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, PUBLISHED  TARA - Full Text  DOI  URL
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, PUBLISHED  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, PUBLISHED  DOI
Reilly J, Gallagher L, Chen JL, Leader G, Shen S., Bio-collections in autism research., Molecular autism, 8, 2017, p34 , Journal Article, PUBLISHED  TARA - Full Text  DOI

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