Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: SNX19[original query] |
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Five common gene variants identify elevated genetic risk for coronary heart disease. Genetics in medicine : official journal of the American College of Medical Genetics 2007 Oct 9 (10): 682-9. Bare Lance A, Morrison Alanna C, Rowland Charles M, Shiffman Dov, Luke May M, Iakoubova Olga A, Kane John P, Malloy Mary J, Ellis Stephen G, Pankow James S, Willerson James T, Devlin James J, Boerwinkle Er |
Genome-wide associations between genetic and epigenetic variation influence mRNA expression and insulin secretion in human pancreatic islets. PLoS genetics 2014 Nov 10 (11): e1004735. Olsson Anders H, Volkov Petr, Bacos Karl, Dayeh Tasnim, Hall Elin, Nilsson Emma A, Ladenvall Claes, Rönn Tina, Ling Charlot |
Epigenetic Markers Are Associated With Differences in Isocyanate Biomarker Levels in Exposed Spray-Painters. Frontiers in genetics 2021 8 12 700636. Taylor Laura W, French John E, Robbins Zachary G, Nylander-French Leena |
Single molecule in situ hybridization reveals distinct localizations of schizophrenia risk-related transcripts SNX19 and AS3MT in human brain. Molecular psychiatry 2021 3 26 (7): 3536-3547. Takahashi Yoichiro, Maynard Kristen R, Tippani Madhavi, Jaffe Andrew E, Martinowich Keri, Kleinman Joel E, Weinberger Daniel R, Hyde Thomas |
Whole-genome sequencing analysis of suicide deaths integrating brain-regulatory eQTLs data to identify risk loci and genes. Molecular psychiatry 2023 10 . Seonggyun Han, Emily DiBlasi, Eric T Monson, Andrey Shabalin, Elliott Ferris, Danli Chen, Alison Fraser, Zhe Yu, Michael Staley, W Brandon Callor, Erik D Christensen, David K Crockett, Qingqin S Li, Virginia Willour, Amanda V Bakian, Brooks Keeshin, Anna R Docherty, Karen Eilbeck, Hilary Co |
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