D. Morris

M. Gill, J. Waddington, P. Scully, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC

S Purcell, D. Grozeva, M. Gill, 2013, Molecular Psychiatry.

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

D. Rujescu, S. Cichon, A. Ingason, 2011, Molecular Psychiatry.

Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders

M. Gill, L. Gallagher, R. Anney, 2014, Molecular Psychiatry.

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2

M C O'Donovan, M J Owen, T G Schulze, 2009, Molecular Psychiatry.

Common variant at 16p11.2 conferring risk of psychosis

M. Pirinen, H. Stefánsson, D. Rujescu, 2014, Molecular Psychiatry.

Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha

D. Rujescu, G. Kirov, D. Grozeva, 2010, Molecular Psychiatry.

Clinical symptomatology and the psychosis risk gene ZNF804A

C. Mcdonald, T. Dinan, F. O’Neill, 2010, Schizophrenia Research.

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC

S Purcell, D. Grozeva, M. Gill, 2013, Molecular Psychiatry.

Evidence that duplications of 22q11.2 protect against schizophrenia

G. Kirov, M. Gill, N. Craddock, 2013, Molecular Psychiatry.

Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137

J. Waddington, A. Corvin, D. Morris, 2013, Neuroscience Letters.

Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study

Daniel P. Newman, N. Wray, M. Gill, 2017, Molecular Psychiatry.

Confirmation and refinement of an ‘at-risk’ haplotype for schizophrenia suggests the EST cluster, Hs.97362, as a potential susceptibility gene at the Neuregulin-1 locus

D. Clair, P. Scully, A. Corvin, 2004, Molecular Psychiatry.

Association analysis of two candidate phospholipase genes that map to the chromosome 15q15.1‐15.3 region associated with reading disability

L. Robinson, D. Morris, D. Ivanov, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

National scientific medical meeting 1997 abstracts

G. S. Nesbitt, R. Segurado, D. Sibley, 1998, Irish journal of medical science.

Mendelian randomisation analysis using GWAS and eQTL data to investigate the relationship between chronotype and neuropsychiatric disorders and their molecular basis

G. Donohoe, D. Morris, C. Wyse, 2023, medRxiv.

The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis

M. Gill, R. Anney, D. Morris, 2013, Psychological Medicine.

BDNF Val66Met polymorphism is associated with aggressive behavior in schizophrenia

C Caltagirone, I A Rubino, M. Gill, 2010, European Psychiatry.

Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility

M. Fornage, S. Cichon, B. Franke, 2014, Molecular Psychiatry.

Edinburgh Research Explorer GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function

D. Rujescu, I. Giegling, S. Djurovic, 2017 .