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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.Nature|April 12, 2023
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesisJoshua S Weinstock, Jayakrishnan Gopakumar, Bala Bharathi Burugula, 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.Medrxiv : the Preprint Server for Health Sciences|September 4, 2023
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELEXinruo Zhang, Jennifer A Brody, Mariaelisa Graff, 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.Science Advances|April 6, 2022
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potentialTetsushi Nakao, Alexander G Bick, Margaret A Taub, et al.Nature|October 15, 2020
Inherited causes of clonal haematopoiesis in 97,691 whole genomesAlexander G Bick, Joshua S Weinstock, Satish K Nandakumar, et al.Nature Genetics|April 19, 2017
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillationIngrid E Christophersen, Michiel Rienstra, Carolina Roselli, et al.Cell Genomics|May 9, 2022
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMedMargaret A Taub, Matthew P Conomos, Rebecca Keener, et al.Nature Genetics|March 6, 2025
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 casesCarolina Roselli, Ida Surakka, Morten S Olesen, et al.Pageof 72