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Medrxiv : the Preprint Server for Health Sciences|September 4, 2024
The Genetic Determinants and Genomic Consequences of Non-Leukemogenic Somatic Point MutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.Nature Communications|October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.HGG Advances|December 26, 2022
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variantsKristin L Young, Virginia Fisher, Xuan Deng, et al.Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.Journal of the American Heart Association|February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural VariantsKruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.Nature Genetics|August 26, 2020
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scaleXihao Li, Zilin Li, Hufeng Zhou, et al.American Journal of Epidemiology|April 16, 2021
A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) ProgramAdrienne M Stilp, Leslie S Emery, Jai G Broome, et al.Science Advances|May 1, 2023
The genetic determinants of recurrent somatic mutations in 43,693 blood genomesJoshua S Weinstock, Cecelia A Laurie, Jai G Broome, et al.Nature Communications|April 13, 2021
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indicesPradeep Natarajan, Akhil Pampana, Sarah E Graham, 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.Pageof 21