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European Journal of Human Genetics : EJHG|January 6, 2011
Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sampleAndrew McQuillin, Nicholas Bass, Adebayo Anjorin, et al.
BMC Psychiatry|June 2, 2025
Sleep disturbance as a marker of postpartum psychosis risk: a prospective actigraphy studyChiara Petrosellini, Sofia H Eriksson, Nicholas Meyer, et al.
Clinical Epigenetics|May 14, 2016
Hypomethylation of FAM63B in bipolar disorder patientsAnna Starnawska, Ditte Demontis, Andrew McQuillin, et al.
Genes|January 21, 2022
Adolescent Verbal Memory as a Psychosis Endophenotype: A Genome-Wide Association Study in an Ancestrally Diverse SampleBaihan Wang, Olga Giannakopoulou, Isabelle Austin-Zimmerman, et al.
Annals of Human Genetics|November 18, 2017
Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophreniaMariam M Al Eissa, Alessia Fiorentino, Sally I Sharp, et al.
European Journal of Human Genetics : EJHG|June 25, 2002
Linkage disequilibrium and demographic history of the isolated population of the Faroe IslandsTove H Jorgensen, Birte Degn, August G Wang, et al.
Psychiatric Genetics|March 28, 2017
Genetic variation in GABRβ1 and the risk for developing alcohol dependenceWilliam A McCabe, Michael J Way, Kush Ruparelia, et al.
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