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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.Dementia and Geriatric Cognitive Disorders|October 9, 2008
Cortical serotonin 1A receptor levels are associated with depression in patients with dementia with Lewy bodies and Parkinson's disease dementiaSally I Sharp, Clive G Ballard, Iryna Ziabreva, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 13, 2014
Genetic association of the tachykinin receptor 1 TACR1 gene in bipolar disorder, attention deficit hyperactivity disorder, and the alcohol dependence syndromeSally I Sharp, Andrew McQuillin, Michael Marks, et al.Alcohol and Alcoholism (Oxford, Oxfordshire)|August 11, 2022
SLC19A1 Genetic Variation Leads to Altered Thiamine Diphosphate Transport: Implications for the Risk of Developing Wernicke-Korsakoff's SyndromeNiamh L O'Brien, Giorgia Quadri, Iain Lightley, 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.Archives of General Psychiatry|July 7, 2010
Association of plasma clusterin concentration with severity, pathology, and progression in Alzheimer diseaseMadhav Thambisetty, Andrew Simmons, Latha Velayudhan, et al.Nature|April 9, 2022
Rare coding variants in ten genes confer substantial risk for schizophreniaTarjinder Singh, Timothy Poterba, David Curtis, et al.Pageof 2