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Plos One|May 11, 2019
Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart diseaseCavin K Ward-Caviness, Paul S de Vries, Kerri L Wiggins, et al.Diabetes|July 16, 2016
Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity LociGeoffrey A Walford, Stefan Gustafsson, Denis Rybin, et al.International Journal of Epidemiology|May 17, 2015
Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysisEveline Nüesch, Caroline Dale, Tom M Palmer, et al.Journal of the American Society of Nephrology : JASN|April 1, 2017
NFAT5 and SLC4A10 Loci Associate with Plasma OsmolalityCarsten A Böger, Mathias Gorski, Gearoid M McMahon, et al.The Lancet. Diabetes & Endocrinology|June 2, 2017
Relations between lipoprotein(a) concentrations, LPA genetic variants, and the risk of mortality in patients with established coronary heart disease: a molecular and genetic association studyStephen Zewinger, Marcus E Kleber, Vinicius Tragante, et al.European Journal of Epidemiology|May 9, 2020
Mendelian randomization analysis does not support causal associations of birth weight with hypertension risk and blood pressure in adulthoodYan Zheng, Tao Huang, Tiange Wang, et al.JAMA Network Open|September 21, 2019
Association of Birth Weight With Type 2 Diabetes and Glycemic Traits: A Mendelian Randomization Study, Tao Huang, Tiange Wang, et al.Nature Communications|January 17, 2024
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elementsMarkus Scholz, Katrin Horn, Janne Pott, et al.Nature Genetics|April 19, 2017
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillationIngrid E Christophersen, Michiel Rienstra, Carolina Roselli, et al.Circulation. Genomic and Precision Medicine|March 22, 2019
Association of Chromosome 9p21 With Subsequent Coronary Heart Disease EventsRiyaz S Patel, Amand F Schmidt, Vinicius Tragante, et al.Pageof 7