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Human Molecular Genetics|August 7, 2014
Trans-ethnic meta-analysis of white blood cell phenotypesMargaux F Keller, Alexander P Reiner, Yukinori Okada, et al.BMC Medical Genetics|July 23, 2013
Genetics of coronary artery calcification among African Americans, a meta-analysisMary K Wojczynski, Mingyao Li, Lawrence F Bielak, et al.Journal of Thrombosis and Haemostasis : JTH|April 20, 2021
FGL1 as a modulator of plasma D-dimer levels: Exome-wide marker analysis of plasma tPA, PAI-1, and D-dimerFlorian Thibord, Ci Song, Jack Pattee, et al.Human Genetics|January 24, 2019
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing dataKaren Y He, Xiaoyin Li, Tanika N Kelly, et al.American Journal of Human Genetics|August 4, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.Nature Communications|March 27, 2026
An integrated germline and somatic genomic model for coronary artery diseaseXiong Yang, Min Seo Kim, Xinyu Zhu, et al.Nature|September 17, 2020
A giant planet candidate transiting a white dwarfAndrew Vanderburg, Saul A Rappaport, Siyi Xu, et al.Nature Communications|December 9, 2022
Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed programMarsha M Wheeler, Adrienne M Stilp, Shuquan Rao, et al.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.Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.Pageof 251