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Plos Genetics|October 21, 2016
Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's DiseaseJohanna Jakobsdottir, Sven J van der Lee, Joshua C Bis, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2024
The Genetic Determinants and Genomic Consequences of Non-Leukemogenic Somatic Point MutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Stroke|January 2, 2010
Genome-wide association studies of MRI-defined brain infarcts: meta-analysis from the CHARGE ConsortiumStéphanie Debette, Joshua C Bis, Myriam Fornage, et al.
Translational Psychiatry|December 5, 2021
Association of low-frequency and rare coding variants with information processing speedJan Bressler, Gail Davies, Albert V Smith, et al.
Annals of the Rheumatic Diseases|September 8, 2012
Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 regionMarjolein J Peters, Linda Broer, Hanneke L D M Willemen, et al.
American Journal of Human Genetics|July 1, 2014
Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associationsSanthi K Ganesh, Daniel I Chasman, Martin G Larson, et al.
Nature Genetics|July 15, 2009
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestryEmelia J Benjamin, Kenneth M Rice, Dan E Arking, et al.
The Pharmacogenomics Journal|March 6, 2013
Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT intervalC L Avery, C M Sitlani, D E Arking, et al.
The Lancet. Diabetes & Endocrinology|October 17, 2017
Omega-6 fatty acid biomarkers and incident type 2 diabetes: pooled analysis of individual-level data for 39 740 adults from 20 prospective cohort studiesJason H Y Wu, Matti Marklund, Fumiaki Imamura, et al.
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