Showing results (121-130 of 191) with videos related to
Sort By:
Pageof 20
American Journal of Human Genetics|April 7, 2026
Neurodevelopmental copy-number variants increase risk of internalizing and cardiometabolic multimorbidity: Findings from the UK BiobankIoanna K Katzourou, , Inês Barroso, et al.Biological Psychiatry|January 21, 2004
Support for RGS4 as a susceptibility gene for schizophreniaNigel M Williams, Anna Preece, Gillian Spurlock, et al.Journal of Affective Disorders|March 31, 2009
Case-control association study of 65 candidate genes revealed a possible association of a SNP of HTR5A to be a factor susceptible to bipolar disease in Bulgarian populationAdelina Yosifova, Taisei Mushiroda, Drozdstoi Stoianov, et al.Plos Genetics|May 7, 2016
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental DisordersAnthony R Isles, Andrés Ingason, Chelsea Lowther, et al.Archives of General Psychiatry|October 6, 2005
Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13Marian L Hamshere, Phil Bennett, Nigel Williams, et al.Human Molecular Genetics|November 16, 2007
Strong evidence that GNB1L is associated with schizophreniaNigel M Williams, Beate Glaser, Nadine Norton, et al.Schizophrenia Bulletin|January 1, 2019
Convergent Evidence That ZNF804A Is a Regulator of Pre-messenger RNA Processing and Gene ExpressionRia M Chapman, Caroline L Tinsley, Matthew J Hill, et al.Archives of General Psychiatry|April 6, 2006
Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorderNigel M Williams, Elaine K Green, Stuart Macgregor, et al.Investigative Ophthalmology & Visual Science|March 28, 2009
An international collaborative family-based whole-genome linkage scan for high-grade myopiaYi-Ju Li, Jeremy A Guggenheim, Anuradha Bulusu, et al.Archives of General Psychiatry|April 7, 2010
Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophreniaDetelina Grozeva, George Kirov, Dobril Ivanov, et al.Pageof 20