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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 Communications|September 13, 2024
NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with strokeJuan Lorenzo Rodriguez-Flores, Shareef Khalid, Neelroop Parikshak, 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|October 11, 2023
Genotyping, sequencing and analysis of 140,000 adults from Mexico CityAndrey Ziyatdinov, Jason Torres, Jesús Alegre-Díaz, et al.The New England Journal of Medicine|August 8, 2022
Germline Mutations in <i>CIDEB</i> and Protection against Liver DiseaseNiek Verweij, Mary E Haas, Jonas B Nielsen, et al.Nature|October 22, 2020
Exome sequencing and characterization of 49,960 individuals in the UK BiobankCristopher V Van Hout, Ioanna Tachmazidou, Joshua D Backman, et al.Plos Genetics|June 10, 2011
Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancerIan P M Tomlinson, Luis G Carvajal-Carmona, Sara E Dobbins, et al.American Journal of Respiratory and Critical Care Medicine|October 4, 2011
Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung functionMaría Soler Artigas, Louise V Wain, Emmanouela Repapi, et al.Pageof 10