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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 19, 2017
Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophreniaGanna Leonenko, Alexander L Richards, James T Walters, et al.Archives of General Psychiatry|August 9, 2006
Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophreniaHugh M D Gurling, Hugo Critchley, Susmita R Datta, et al.Nature Genetics|June 27, 2017
The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disabilityTarjinder Singh, James T R Walters, Mandy Johnstone, et al.Molecular Psychiatry|September 8, 2019
A polygenic resilience score moderates the genetic risk for schizophreniaJonathan L Hess, Daniel S Tylee, Manuel Mattheisen, et al.Addiction Biology|April 17, 2014
Genetic variants in or near ADH1B and ADH1C affect susceptibility to alcohol dependence in a British and Irish populationMichael Way, Andrew McQuillin, Jit Saini, et al.Translational Psychiatry|September 19, 2019
NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosisNey Alliey-Rodriguez, Tamar A Grey, Rebecca Shafee, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2026
New genotype-phenotype correlations and management recommendations for individuals with RERE variantsDavid Curtis, Xiaonan Zhao, Nichole M Owen, et al.Nature Genetics|April 12, 2022
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophreniaDuncan S Palmer, Daniel P Howrigan, Sinéad B Chapman, et al.Proceedings of the National Academy of Sciences of the United States of America|June 20, 2020
Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitisEszter Balogh, Jennifer C Chandler, Máté Varga, et al.Nature Neuroscience|March 15, 2016
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disordersTarjinder Singh, Mitja I Kurki, David Curtis, et al.Pageof 17