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Nature Communications|June 13, 2018
A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk lociHélène Choquet, Seyyedhassan Paylakhi, Stephen C Kneeland, et al.International Journal of Molecular Sciences|November 21, 2019
Y-chromosome and Surname Analyses for Reconstructing Past Population Structures: The Sardinian Population as a Test CaseViola Grugni, Alessandro Raveane, Giulia Colombo, et al.Proceedings of the National Academy of Sciences of the United States of America|April 30, 2003
Natural variation in human membrane transporter genes reveals evolutionary and functional constraintsMaya K Leabman, Conrad C Huang, Joseph DeYoung, et al.Human Genetics|March 29, 2008
Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery diseaseThemistocles L Assimes, Joshua W Knowles, James R Priest, et al.Plos One|September 18, 2012
An overview of the genetic structure within the Italian population from genome-wide dataCornelia Di Gaetano, Floriana Voglino, Simonetta Guarrera, et al.American Journal of Human Genetics|October 29, 2002
A highly significant association between a COMT haplotype and schizophreniaSagiv Shifman, Michal Bronstein, Meira Sternfeld, et al.Nature|January 10, 2020
A brief history of human disease geneticsMelina Claussnitzer, Judy H Cho, Rory Collins, et al.Medrxiv : the Preprint Server for Health Sciences|May 4, 2026
Determinants of DNA-sequence-based Diagnostic Yield in the CSER ConsortiumYusuph Mavura, David Crosslin, Kathleen Ferar, et al.Atherosclerosis|October 26, 2007
A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery diseaseThemistocles L Assimes, Joshua W Knowles, James R Priest, et al.Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Clinical validation of a statin-benefit polygenic score using real-world cohorts of primary prevention participantsTanushree Haldar, Kyung Min Lee, Craig C Teerlink, et al.Pageof 18