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Circulation. Genomic and Precision Medicine|March 24, 2023
Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine ProgramAmanda A Seyerle, Cecelia A Laurie, Brandon J Coombes, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 9, 2026
An integrated cardiometabolic genetic testing program in a predominantly Hispanic population within a community settingBo Yuan, Layla A Abushamat, Stacey Pereira, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 19, 2019
Insights into genetics, human biology and disease gleaned from family based genomic studiesJennifer E Posey, Anne H O'Donnell-Luria, Jessica X Chong, et al.Cancer Discovery|August 24, 2022
Proteogenomic Markers of Chemotherapy Resistance and Response in Triple-Negative Breast CancerMeenakshi Anurag, Eric J Jaehnig, Karsten Krug, et al.Cell Reports|March 8, 2016
Multilevel Genomics-Based Taxonomy of Renal Cell CarcinomaFengju Chen, Yiqun Zhang, Yasin Şenbabaoğlu, et al.Cell|April 29, 2014
Human CLP1 mutations alter tRNA biogenesis, affecting both peripheral and central nervous system functionEnder Karaca, Stefan Weitzer, Davut Pehlivan, et al.Science Advances|March 12, 2019
The comparative genomics and complex population history of <i>Papio</i> baboonsJeffrey Rogers, Muthuswamy Raveendran, R Alan Harris, et al.Science Advances|July 3, 2026
A meta-analysis of carbon losses and gains from tropical moist forest degradation and regenerationViola Heinrich, Amelia Holcomb, Simon Besnard, et al.Journal of the National Cancer Institute|December 9, 2014
Germline mutations in shelterin complex genes are associated with familial gliomaMatthew N Bainbridge, Georgina N Armstrong, M Monica Gramatges, et al.American Journal of Human Genetics|December 3, 2014
Mutations in PURA cause profound neonatal hypotonia, seizures, and encephalopathy in 5q31.3 microdeletion syndromeSeema R Lalani, Jing Zhang, Christian P Schaaf, et al.Pageof 117