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Professor Michael Gill

Professor Consultant/ Head of Department (Psychiatry)

Professor Consultant/ Head of Department (Molecular Medicine Ireland)

  Nonlinear Dynamics and Systems
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Member, DMMC Gene Bank Management Group, A trans-institutional committee with responsibility for providing strategic and scientific direction in the management of DMMC's combined bioresource collections.
Member, Cycle 2 PI's & Researchers, All Cycle 2 Researchers & PI's
Ferentinos P, Koukounari A, Power R, Rivera M, Uher R, Craddock N, Owen MJ, Korszun A, Jones L, Jones I, Gill M, Rice JP, Ising M, Maier W, Mors O, Rietschel M, Preisig M, Binder EB, Aitchison KJ, Mendlewicz J, Souery D, Hauser J, Henigsberg N, Breen G, Craig IW, Farmer AE, Müller-Myhsok B, McGuffin P, Lewis CM, Familiality and SNP heritability of age at onset and episodicity in major depressive disorder., Psychological medicine, 2015, p1-11 , Journal Article, PUBLISHED  TARA - Full Text  DOI
Gentil G P, Gill M, Murray R, Vallada H, Caracteristicas Clinicas da Esquizofrenia Familiar: estudo em uma populacao brasileira., 2014, Journal Article, SUBMITTED
Webb B, Oord E, Knight J, Breen G, Brewster S, Tozzi F, Craddock N, Gill M, Korzun A, Maier W, Middleton L, Mors O, Owen M, Perry J, Preisig M, Rice J, Rietschel M, Jones L, Farmer A, Muglia P, McGuffin P., Genome-wide linkage analysis of waves 1 and 2 of the Depression Network Study , 2014, Journal Article, SUBMITTED
Mothersill O, Morris DW, Kelly S, Rose EJ, Fahey C, O'Brien C, Lyne R, Reilly R, Gill M, Corvin AP, Donohoe G, Effects of MIR137 on fronto-amygdala functional connectivity., NeuroImage, 90, 2014, p189-95 , Journal Article, PUBLISHED  TARA - Full Text  DOI
Fahey C, Byrne S, McLaughlin R, Kenna K, Shatunov A, Donohoe G, Gill M, Al-Chalabi A, Bradley DG, Hardiman O, Corvin AP, Morris DW, Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample., Neurobiology of aging, 35, (6), 2014, p1510.e1-1510.e5 , Journal Article, PUBLISHED  TARA - Full Text  DOI
Heron, E.A., Cormican, P., Donohoe, G., O'Neill, F.A., Kendler, K.S., Riley, B.P., Gill, M., Corvin, A.P., Morris, D.W., No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset, Schizophrenia Research, 154, (1-3), 2014, p79-82 , Journal Article, PUBLISHED  TARA - Full Text  DOI
Rees E, Walters JT, Chambert KD, O'Dushlaine C, Szatkiewicz J, Richards AL, Georgieva L, Mahoney-Davies G, Legge SE, Moran JL, Genovese G, Levinson D, Morris DW, Cormican P, Kendler KS, O'Neill FA, Riley B, Gill M, Corvin A, Sklar P, Hultman C, Pato C, Pato M, Sullivan PF, Gejman PV, McCarroll SA, O'Donovan MC, Owen MJ, Kirov G, CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1., Human molecular genetics, 23, (6), 2014, 1669-1676 , Journal Article, PUBLISHED  TARA - Full Text  DOI
O'Donoghue T, Morris DW, Fahey C, Da Costa A, Moore S, Cummings E, Leicht G, Karch S, Hoerold D, Tropea D, Foxe JJ, Gill M, Corvin A, Donohoe G, Effects of ZNF804A on auditory P300 response in schizophrenia., Translational psychiatry, 4, 2014, pe345 , Journal Article, PUBLISHED  TARA - Full Text  DOI
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, p872-879 , Journal Article, PUBLISHED  DOI
McCarthy, S.E., Gillis, J., Kramer, M., (...), McCombie, W.R., Corvin, A. , De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability, Molecular Psychiatry, 19, 2014, p652-658 , Journal Article, PUBLISHED  DOI

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215. Dagger D, Rogers C, Wade V, Gaffney C, Armstrong K, Fitxmaurice B, Gill M, Walsh E.(ed.), Proceedings of 2nd International Workshop on Personalisation for E-Health at the 11th International Conference on User Modelling,, corfu, Greece, 25-29 June 2007, 2007, Proceedings of a Conference, ACCEPTED
Corvin AP, McGhee K, Murphy K, Walsh C, Kenny N, Nangle J, Schwaiger S, Baldwin P, Scully P, Quinn J, Crumlish N, O'Callaghan E, Waddington J, Morris D, Gill M, Evidence for association and interaction between G72 and DAAO markers in an Irish case-control schizophrenia sample, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, SEP 5, 138B, (1), 2005, pp25 - 25, Meeting Abstract, PUBLISHED
Hawi Z, Sheehan K, Conroy J, Lowe N, Kirley A, Seguardo R, Gallagher L, Shields D, Fitzgerald M, Gill M, Preferential transmission of paternal alleles at risk genes in ADHD, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, SEP 5, 138B, (1), 2005, pp56 - 57, Meeting Abstract, PUBLISHED
Johnson KA, Bellgrove MA, Barry E, Cox M, Hawi Z, Kirley A, Robertson IH, Gill M, Movement variability in children with ADHD, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, SEP 5, 138B, (1), 2005, pp57 - 57, Meeting Abstract, PUBLISHED
Lowe N, Hawi Z, Brophy K, Kirley A, Mullins C, Sheehen K, Fitzgerald M, Gill M, Phenotype : genotype analysis of DRD4, DRD5 and SNAP-25 in an Irish ADHD sample, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, SEP 5, 138B, (1), 2005, pp59 - 59, Meeting Abstract, PUBLISHED
Corvin A, Gill M, Wright P in, editor(s)Padraig Wright, Julian Stern, Michael Phelan , Core Psychiatry, UK, Elsevier Saunders, 2004, pp35 - 53, [M. Gill], Notes: [ (], Book Chapter, PUBLISHED
Morris DW, Nangle JM, Kiely B, Corvin A, Gill M. , The molecular basis of schizophrenia: a complex genetic disorder. , Irish Psychiatrist, 5, 2004, p134 - 137, Journal Article, PUBLISHED