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Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Rare protein-coding variation and the genetic architecture of height in >1.4 million individualsJack A Kosmicki, Liron Ganel, Kyoko Watanabe, et al.Proceedings of the National Academy of Sciences of the United States of America|January 23, 2020
De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder populationMichael D Kessler, Douglas P Loesch, James A Perry, et al.Nature Genetics|June 12, 2023
Rare coding variants in CHRNB2 reduce the likelihood of smokingVeera M Rajagopal, Kyoko Watanabe, Joelle Mbatchou, et al.Biorxiv : the Preprint Server for Biology|May 22, 2023
A deep catalog of protein-coding variation in 985,830 individualsKathie Y Sun, Xiaodong Bai, Siying Chen, et al.Nature|October 18, 2021
Exome sequencing and analysis of 454,787 UK Biobank participantsJoshua D Backman, Alexander H Li, Anthony Marcketta, et al.Nature|May 20, 2024
A deep catalogue of protein-coding variation in 983,578 individualsKathie Y Sun, Xiaodong Bai, Siying Chen, et al.Nature|November 30, 2022
Common and rare variant associations with clonal haematopoiesis phenotypesMichael D Kessler, Amy Damask, Sean O'Keeffe, et al.Nature Genetics|August 5, 2024
Genetic risk factors for COVID-19 and influenza are largely distinctJack A Kosmicki, Anthony Marcketta, Deepika Sharma, et al.American Journal of Human Genetics|January 14, 2025
Genomic and phenotypic correlates of mosaic loss of chromosome Y in bloodYasminka A Jakubek, Xiaolong Ma, Adrienne M Stilp, 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.Pageof 19