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Nature Genetics|March 6, 2025
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation riskSeung Hoan Choi, Sean J Jurgens, Ling Xiao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2023
Returning integrated genomic risk and clinical recommendations: The eMERGE studyJodell E Linder, Aimee Allworth, Harris T Bland, et al.
Nature|April 12, 2023
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesisJoshua S Weinstock, Jayakrishnan Gopakumar, Bala Bharathi Burugula, et al.
The Lancet. Respiratory Medicine|December 12, 2018
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysisChristopher J Rhodes, Ken Batai, Marta Bleda, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controlsRoddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.
Nature Communications|July 27, 2018
PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activityJessica van Setten, Jennifer A Brody, Yalda Jamshidi, et al.
The Lancet. Diabetes & Endocrinology|December 3, 2016
PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation studyAmand F Schmidt, Daniel I Swerdlow, Michael V Holmes, et al.
Nature Communications|April 11, 2025
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk alleleXinruo Zhang, Jennifer A Brody, Mariaelisa Graff, et al.
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