Louise Gallagher

Carter M, Casey S, O'Keeffe GW, Gibson L, Gallagher L, Murray DM. Maternal Immune Activation and Interleukin 17A in the Pathogenesis of Autistic Spectrum Disorder and Why It Matters in the COVID-19 Era. Front Psychiatry. 2022 Feb 17. doi: 10.3389/fpsyt.2022.823096. PMID: 35250672

Cook J, Molloy C, San José Cáceres A, Dinneen T, Bourgeron T, Murphy DG, Gallagher L, Loth E. The Synaptic Gene Study (SynaG): design and methodology to identify neurocognitive markers in Phelan McDermid Syndrome (PMS) and NRXN1 Deletions. Front Neurosci. 2022 Feb 18; 16:806990. PMID: 35250452.

Patel Y, Shin J, Abé C, Agartz I, Alloza C, Alnæs D, Ambrogi S, Antonucci LA, Arango C, Arolt V, Auzias G, Ayesa-Arriola R, Banaj N, Banaschewski T, Bandeira C, Başgöze Z, Cupertino RB, Bau CHD, Bauer J, Baumeister S, Bernardoni F, Bertolino A, Bonnin CDM, Brandeis D, Brem S, Bruggemann J, Bülow R, Bustillo JR, Calderoni S, Calvo R, Canales-Rodríguez EJ, Cannon DM, Carmona S, Carr VJ, Catts SV, Chenji S, Chew QH, Coghill D, Connolly CG, Conzelmann A, Craven AR, Crespo-Facorro B, Cullen K, Dahl A, Dannlowski U, Davey CG, Deruelle C, Díaz-Caneja CM, Dohm K, Ehrlich S, Epstein J, Erwin-Grabner T, Eyler LT, Fedor J, Fitzgerald J, Foran W, Ford JM, Fortea L, Fuentes-Claramonte P, Fullerton J, Furlong L, Gallagher L, Gao B, Gao S, Goikolea JM, Gotlib I, Goya-Maldonado R, Grabe HJ, Green M, Grevet EH, Groenewold NA, Grotegerd D, Gruber O, Haavik J, Hahn T, Harrison BJ, Heindel W, Henskens F, Heslenfeld DJ, Hilland E, Hoekstra PJ, Hohmann S, Holz N, Howells FM, Ipser JC, Jahanshad N, Jakobi B, Jansen A, Janssen J, Jonassen R, Kaiser A, Kaleda V, Karantonis J, King JA, Kircher T, Kochunov P, Koopowitz SM, Landén M, Landrø NI, Lawrie S, Lebedeva I, Luna B, Lundervold AJ, MacMaster FP, Maglanoc LA, Mathalon DH, McDonald C, McIntosh A, Meinert S, Michie PT, Mitchell P, Moreno-Alcázar A, Mowry B, Muratori F, Nabulsi L, Nenadić I, O'Gorman Tuura R, Oosterlaan J, Overs B, Pantelis C, Parellada M, Pariente JC, Pauli P, Pergola G, Piarulli FM, Picon F, Piras F, Pomarol-Clotet E, Pretus C, Quidé Y, Radua J, Ramos-Quiroga JA, Rasser PE, Reif A, Retico A, Roberts G, Rossell S, Rovaris DL, Rubia K, Sacchet M, Salavert J, Salvador R, Sarró S, Sawa A, Schall U, Scott R, Selvaggi P, Silk T, Sim K, Skoch A, Spalletta G, Spaniel F, Stein DJ, Steinsträter O, Stolicyn A, Takayanagi Y, Tamm L, Tavares M, Teumer A, Thiel K, Thomopoulos SI, Tomecek D, Tomyshev AS, Tordesillas-Gutiérrez D, Tosetti M, Uhlmann A, Van Rheenen T, Vazquez-Bourgón J, Vernooij MW, Vieta E, Vilarroya O, Weickert C, Weickert T, Westlye LT, Whalley H, Willinger D, Winter A, Wittfeld K, Yang TT, Yoncheva Y, Zijlmans JL, Hoogman M, Franke B, van Rooij D, Buitelaar J, Ching CRK, Andreassen OA, Pozzi E, Veltman D, Schmaal L, van Erp TGM, Turner J, Castellanos FX, Pausova Z, Thompson P, Paus T.Biol Psychiatry. 2022 Aug 15;92(4):299-313. doi: 10.1016/j.biopsych.2022.02.959. Epub 2022 Mar 4.PMID: 35489875

Sha Z, van Rooij D, Anagnostou E, Arango C, Auzias G, Behrmann M, Bernhardt B, Bolte B, Busatto Filho G, Calderoni S, Calvo R, Daly E, Deruelle C, Duan M, Duran F, Durston S, Ecker C, Ehrlich S, Fair D, Fedor F, Fitzgerald F, EU-AIMS LEAP group, Franke B, Freitag CM, Gallagher L, Glahn D, Haar S, Hoekstra L, Jahanshad N, Jalbrzikowski M, Janssen J, King JA, Lazaro L, Lerch JP, Luna B, Beatriz Luna, McGrath J, Medland S, Muratori F, Murphy DG, Neufeld J, O'Hearn K, Oranje B, Parellada M,Pariente J, Postema M, Remnélius KL, Retico A, Rosa P, Rubia K, Shook D, Tammimies K,Taylor MJ, Tosetti M, Wallace GL, Zhou F, Thompson PM, Fisher S, Buitelaar JK, Francks C. Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium. Mol Psychiatry. 2022 Apr;27(4):2114-2125. doi: 10.1038/s41380-022-01452-7. PMID: 35136228

Dinneen T, Ní Ghrálaigh F, Walsh R, Lopez LM, Gallagher L. How Does Genetic Variation Modify ND-CNV Phenotypes? Trends in Genetics 2022 Feb;38(2):140-151. PMID: 34364706

Ní Ghrálaigh F, McCarthy E, Murphy DN, Gallagher L, Lopez LM. Brief Report: Evaluating the Diagnostic Yield of Commercial Gene Panels in Autism. J Autism Dev Disord. 2022 Jan 7. PMID: 34994928

Molloy CJ, Gallagher L. Autism Spectrum Conditions: Stratification biomarkers for a heterogeneous condition. Ir J Psychol Med. 2021 Nov 26:1-7. PMID: 34823622

Avazzadeh S, Quinlan LR, Reilly J, McDonagh K, Jalali A, Wang Y, McInerney V, Krawczyk J, Ding Y, Fitzgerald J, O’Sullivan M, Forman EB, Lynch SA, Ennis S, Feerick N, Reilly R， Li W, Shen X, Yang G, Lu Y, Peeters H, Dockery P, O’Brien T, Shen S, Gallagher L. NRXN1α+/- is associated with increased excitability in ASD iPSC-derived neurons. BMC Neurosci. 2021 Sep 15. 22(1):56. PMID: 34525970

Oakley B, Tillmann J, Ruigrok A, Baranger A, Takow C, Charman T, Jones E, Cusack J, Doherty M, Violland P, Wroczyńska A, Simonoff E, Buitelaar JK, Gallagher L, Murphy DGM. COVID-19 health and social care access for autistic people: European policy review. BMJ Open. 2021 May 17;11(6): e045341.

Ding Y, O'Brien A, Marcó de la Cruz B, Yang M, Lu Y, Qian X, Yang G, McInerney V, Krawczyk J, Lynch SA, Howard L, Allen NM, O'Brien T, Gallagher L, 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 Res. 2021 May; 53:102254.

Honours and Awards

International Society for Autism Research (INSAR) Global Leader

Society for the Study of Behavioral Phenotypes – Tom Oppé Distinguished Lecture (2019)

Fellowship Trinity College Dublin  (FTCD) (2011)

Academy of Medicine of Ireland Senior Registrars Prize. (2004)

Wellcome Trust Mental Health Training Fellowship, 1999-2002