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European Journal of Human Genetics : EJHG|September 22, 2016
Chromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disordersKate Wolfe, André Strydom, Deborah Morrogh, et al.
Nature Communications|September 28, 2023
Genome-wide association studies and cross-population meta-analyses investigating short and long sleep durationIsabelle Austin-Zimmerman, Daniel F Levey, Olga Giannakopoulou, et al.
Biological Psychiatry|October 6, 2005
Failure to confirm allelic association between markers at the CAPON gene locus and schizophrenia in a British sampleVinay Puri, Andrew McQuillin, Srinivasa Thirumalai, et al.
BMC Medical Genetics|January 7, 2014
Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1Wei Xu, Sarah Cohen-Woods, Qian Chen, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 21, 2009
Support of association between BRD1 and both schizophrenia and bipolar affective disorderMette Nyegaard, Jacob E Severinsen, Thomas D Als, et al.
Psychiatric Genetics|February 13, 2025
Unresolved ethical issues of genetic counseling and testing in clinical psychiatryJulia Perry, Eline Bunnik, Marcella Rietschel, 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.
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.
The American Journal of Gastroenterology|March 15, 2018
Genetic variants in PNPLA3 and TM6SF2 predispose to the development of hepatocellular carcinoma in individuals with alcohol-related cirrhosisFelix Stickel, Stephan Buch, Hans Dieter Nischalke, et al.
Alimentary Pharmacology & Therapeutics|February 10, 2021
Variants in PCSK7, PNPLA3 and TM6SF2 are risk factors for the development of cirrhosis in hereditary haemochromatosisStephan Buch, Aneesh Sharma, Eleanor Ryan, et al.
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