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Genetic Epidemiology|February 5, 2023
A fast linkage method for population GWAS cohorts with related individualsGregory J M Zajac, Sarah A Gagliano Taliun, Carlo Sidore, et al.Plos One|February 8, 2021
Exposure and risk factors for COVID-19 and the impact of staying home on Michigan residentsKuan-Han H Wu, Whitney E Hornsby, Bethany Klunder, et al.Diabetes|August 29, 2006
Association of transcription factor 7-like 2 (TCF7L2) variants with type 2 diabetes in a Finnish sampleLaura J Scott, Lori L Bonnycastle, Cristen J Willer, et al.Genetic Epidemiology|December 24, 2005
Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap databaseCristen J Willer, Laura J Scott, Lori L Bonnycastle, et al.Human Molecular Genetics|April 15, 2014
No large-effect low-frequency coding variation found for myocardial infarctionOddgeir L Holmen, He Zhang, Wei Zhou, et al.Scientific Reports|September 2, 2017
A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitorsIngrid Brænne, Christina Willenborg, Vinicius Tragante, et al.Nature Genetics|December 17, 2013
Meta-analysis of gene-level tests for rare variant associationDajiang J Liu, Gina M Peloso, Xiaowei Zhan, et al.American Journal of Human Genetics|August 30, 2016
Genetic Variants in LRP1 and ULK4 Are Associated with Acute Aortic DissectionsDong-Chuan Guo, Megan L Grove, Siddharth K Prakash, et al.Nature Genetics|August 15, 2018
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studiesWei Zhou, Jonas B Nielsen, Lars G Fritsche, et al.Cephalalgia : an International Journal of Headache|February 15, 2020
Mitochondrial genome-wide association study of migraine - the HUNT StudySigrid Børte, John-Anker Zwart, Anne Heidi Skogholt, et al.Pageof 20