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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 Communications|May 24, 2024
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genesRebecca Keener, Surya B Chhetri, Carla J Connelly, 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.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.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|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.Nature Communications|September 1, 2022
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathwaysWilliam J Young, Najim Lahrouchi, Aaron Isaacs, et al.Nature|February 11, 2021
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed ProgramDaniel Taliun, Daniel N Harris, Michael D Kessler, et al.Nature Genetics|June 13, 2018
Multi-ethnic genome-wide association study for atrial fibrillationCarolina Roselli, Mark D Chaffin, Lu-Chen Weng, et al.Pageof 18