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Circulation. Cardiovascular Genetics|May 6, 2014
Genome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohortRicha Saxena, Andrew Bjonnes, Jennifer Prescott, et al.Journal of Medical Genetics|January 28, 2015
DCAF4, a novel gene associated with leucocyte telomere lengthMassimo Mangino, Lene Christiansen, Rivka Stone, et al.Human Molecular Genetics|January 12, 2018
Deep molecular phenotypes link complex disorders and physiological insult to CpG methylationShaza B Zaghlool, Dennis O Mook-Kanamori, Sara Kader, et al.Nature|September 3, 2011
Human metabolic individuality in biomedical and pharmaceutical researchKarsten Suhre, So-Youn Shin, Ann-Kristin Petersen, et al.Circulation|March 26, 2008
Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery diseaseHeribert Schunkert, Anika Götz, Peter Braund, et al.The New England Journal of Medicine|July 20, 2007
Genomewide association analysis of coronary artery diseaseNilesh J Samani, Jeanette Erdmann, Alistair S Hall, et al.Human Molecular Genetics|April 17, 2018
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in uteroNicole M Warrington, Enisa Shevroja, Gibran Hemani, et al.Medrxiv : the Preprint Server for Health Sciences|September 19, 2025
Human germline biallelic loss-of-function OSMR variants cause severe allergic diseaseMehul Sharma, Simran Samra, Yihui Liu, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 19, 2007
Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone massJohn Pa Ioannidis, Mandy Y Ng, Pak C Sham, et al.Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|October 4, 2012
A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterolIda Surakka, John B Whitfield, Markus Perola, et al.Pageof 36