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JAMA|December 12, 2018
Association Between Titin Loss-of-Function Variants and Early-Onset Atrial FibrillationSeung Hoan Choi, Lu-Chen Weng, Carolina Roselli, et al.Nature Aging|June 4, 2024
Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rateTaralynn M Mack, Michael A Raddatz, Yash Pershad, et al.Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophreniaRunjia Li, Sarah A Gagliano Taliun, Kevin Liao, et al.Circulation. Cardiovascular Genetics|November 21, 2012
Impact of ancestry and common genetic variants on QT interval in African AmericansJ Gustav Smith, Christy L Avery, Daniel S Evans, et al.Circulation. Cardiovascular Genetics|November 10, 2012
Novel loci associated with PR interval in a genome-wide association study of 10 African American cohortsAnne M Butler, Xiaoyan Yin, Daniel S Evans, et al.Nature Genetics|March 8, 2022
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence dataPierrick Wainschtein, Deepti Jain, Zhili Zheng, et al.Plos One|May 8, 2020
Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucosePeitao Wu, Denis Rybin, Lawrence F Bielak, et al.Genome Biology|January 15, 2026
Whole genome sequence analysis of pulmonary function and COPD in 44,287 multi-ancestry participantsWonji Kim, Xiaowei Hu, Kangjin Kim, 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.Atherosclerosis|February 25, 2012
Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortiumChristina L Wassel, Claudia Lamina, Vijay Nambi, et al.Pageof 125