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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.Nature|October 4, 2015
An integrated map of structural variation in 2,504 human genomesPeter H Sudmant, Tobias Rausch, Eugene J Gardner, et al.The New England Journal of Medicine|August 8, 2022
Germline Mutations in CIDEB and Protection against Liver DiseaseNiek Verweij, Mary E Haas, Jonas B Nielsen, et al.Nature Communications|March 10, 2015
Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levelsElisabeth M van Leeuwen, Lennart C Karssen, Joris Deelen, 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.Nature Genetics|August 5, 2024
Genetic risk factors for COVID-19 and influenza are largely distinctJack A Kosmicki, Anthony Marcketta, Deepika Sharma, et al.Pageof 11