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Professor Louise Gallagher

Professor Child & Adolescent Psychiatry (Psychiatry)
TRINITY CENTRE, S J H

 lgallagh@tcd.ie

 3531896 2464

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
Dinneen, T.J. and Ghrálaigh, F.N. and Walsh, R. and Lopez, L.M. and Gallagher, L., How does genetic variation modify ND-CNV phenotypes?, Trends in Genetics, 38, (2), 2022, p140-151 , Notes: [cited By 0], Journal Article, PUBLISHED  DOI
Sha, Z. and van Rooij, D. and Anagnostou, E. and Arango, C. and Auzias, G. and Behrmann, M. and Bernhardt, B. and Bolte, S. and Busatto, G.F. and Calderoni, S. and Calvo, R. and Daly, E. and Deruelle, C. and Duan, M. and Duran, F.L.S. and Durston, S. and Ecker, C. and Ehrlich, S. and Fair, D. and Fedor, J. and Fitzgerald, J. and Floris, D.L. and Franke, B. and Freitag, C.M. and Gallagher, L. and Glahn, D.C. and Haar, S. and Hoekstra, L. and Jahanshad, N. and Jalbrzikowski, M. and Janssen, J. and King, J.A. and Lazaro, L. and Luna, B. and McGrath, J. and Medland, S.E. and Muratori, F. and Murphy, D.G.M. and Neufeld, J. and O†Hearn, K. and Oranje, B. and Parellada, M. and Pariente, J.C. and Postema, M.C. and Remnelius, K.L. and Retico, A. and Rosa, P.G.P. and Rubia, K. and Shook, D. and Tammimies, K. and Taylor, M.J. and Tosetti, M. and Wallace, G.L. and Zhou, F. and Thompson, P.M. and Fisher, S.E. and Buitelaar, J.K. and Francks, C., Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium, Molecular Psychiatry, 2022, Notes: [cited By 0], Journal Article, PUBLISHED  DOI
Ní Ghrálaigh, F. and McCarthy, E. and Murphy, D.N. and Gallagher, L. and Lopez, L.M., Brief Report: Evaluating the Diagnostic Yield of Commercial Gene Panels in Autism, Journal of Autism and Developmental Disorders, 2022, Notes: [cited By 0], Journal Article, PUBLISHED  DOI
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
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), 2021, Notes: [cited By 0], Journal Article, PUBLISHED  DOI
Avazzadeh, S. and Quinlan, L.R. and Reilly, J. and McDonagh, K. and Jalali, A. and Wang, Y. and McInerney, V. and Krawczyk, J. and Ding, Y. and Fitzgerald, J. and O†Sullivan, M. and Forman, E.B. and Lynch, S.A. and Ennis, S. and Feerick, N. and Reilly, R. and Li, W. and Shen, X. and Yang, G. and Lu, Y. and Peeters, H. and Dockery, P. and O†Brien, T. and Shen, S. and Gallagher, L., NRXN1α+/- is associated with increased excitability in ASD iPSC-derived neurons, BMC Neuroscience, 22, (1), 2021, Notes: [cited By 0], Journal Article, PUBLISHED  DOI
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), 2021, Notes: [cited By 2], Journal Article, PUBLISHED  DOI
Mezinska, S. and Gallagher, L. and Verbrugge, M. and Bunnik, E.M., Ethical issues in genomics research on neurodevelopmental disorders: a critical interpretive review, Human Genomics, 15, (1), 2021, Notes: [cited By 0], Journal Article, PUBLISHED  DOI
Oakley, B. and Tillmann, J. and Ruigrok, A. and Baranger, A. and Takow, C. and Charman, T. and Jones, E. and Cusack, J. and Doherty, M. and Violland, P. and WroczyÅ"ska, A. and Simonoff, E. and Buitelaar, J.K. and Gallagher, L. and Murphy, D.G.M., COVID-19 health and social care access for autistic people: European policy review, BMJ Open, 11, (6), 2021, Notes: [cited By 8], Journal Article, PUBLISHED  DOI
  

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