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Plos One|November 2, 2018
Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic strokeJohn W Cole, Huichun Xu, Kathleen Ryan, et al.Human Molecular Genetics|June 6, 2014
Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degenerationRinki Ratnapriya, Xiaowei Zhan, Robert N Fariss, et al.Science (New York, N.Y.)|October 13, 2022
Real-time dynamic single-molecule protein sequencing on an integrated semiconductor deviceBrian D Reed, Michael J Meyer, Valentin Abramzon, et al.American Journal of Human Genetics|June 11, 2021
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individualsJack A Kosmicki, Julie E Horowitz, Nilanjana Banerjee, et al.Nature Genetics|June 2, 2014
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancerYufei Wang, James D McKay, Thorunn Rafnar, et al.Medrxiv : the Preprint Server for Health Sciences|March 3, 2021
A catalog of associations between rare coding variants and COVID-19 outcomesJ A Kosmicki, J E Horowitz, N Banerjee, et al.Nature Genetics|October 11, 2011
Genome-wide association study identifies three new melanoma susceptibility lociJennifer H Barrett, Mark M Iles, Mark Harland, et al.Nature Genetics|August 4, 2015
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanomaMatthew H Law, D Timothy Bishop, Jeffrey E Lee, et al.Nature Medicine|April 17, 2023
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel diseaseMarie-Gabrielle Duperron, Maria J Knol, Quentin Le Grand, et al.Circulation Research|December 10, 2021
Common Genetic Variants Contribute to Risk of Transposition of the Great ArteriesDoris Škorić-Milosavljević, Rafik Tadros, Fernanda M Bosada, et al.Pageof 139