M. A. Al Eissa

Genetic association and functional characterization of MCPH1 gene variation in bipolar disorder and schizophrenia

A. McQuillin, N. Bass, D. Curtis, 2019, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia

M. Owen, M. O’Donovan, P. Sullivan, 2017, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genome-wide association study of over 40,000 bipolar disorder cases provides novel biological insights

John P. Rice, Melissa J. Green, Janice M. Fullerton, 2020, medRxiv.

Rare variant analysis in multiply affected families, association studies and functional analysis suggest a role for the ITGΒ4 gene in schizophrenia and bipolar disorder

A. McQuillin, N. Bass, D. Curtis, 2018, Schizophrenia Research.

Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology

Dan J Stein, Melissa J. Green, Janice M. Fullerton, 2021, Nature Genetics.

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

Michael F. Green, Max W. Y. Lam, Catherine A. Sugar, 2022, Nature.

Rare coding variants in ten genes confer substantial risk for schizophrenia

S. Gabriel, M. Daly, H. Kang, 2022, Nature.

Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia

S. Gabriel, N. Craddock, L. DeLisi, 2020, medRxiv.

Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia

A. McQuillin, N. Bass, D. Curtis, 2017, Annals of human genetics.