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Professor Louise Gallagher

Professor Child & Adolescent Psychiatry (Psychiatry)

 lgallagh@tcd.ie

 

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


Research Tags

  Attention Deficit Hyperactivity Disorder (ADHD)   Autism   Child Mental Health   Genetics of Neurodevelopmental Disorders   Neurodevelopmental Disorders
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, Notes: [cited By 0], Journal Article, PUBLISHED  TARA - Full Text  DOI
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, Notes: [cited By 0], Journal Article, PUBLISHED  TARA - Full Text  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, PUBLISHED  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 , Notes: [cited By 0], Journal Article, PUBLISHED  TARA - Full Text  DOI
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, Notes: [cited By 0], Journal Article, PUBLISHED  TARA - Full Text  DOI
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, Notes: [cited By 0], Journal Article, PUBLISHED  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 , Notes: [cited By 7], Journal Article, PUBLISHED  TARA - Full Text  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, PUBLISHED  TARA - Full Text  DOI
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 , Notes: [cited By 2], Journal Article, PUBLISHED  DOI
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, Notes: [cited By 0], Journal Article, PUBLISHED  TARA - Full Text  DOI
  

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