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Nature Communications|February 24, 2026
Rare coding variants in CHRNB3 associate with reduced daily cigarette smoking across ancestriesVeera M Rajagopal, Andrey Ziyatdinov, Tyler Joseph, et al.Nature|April 8, 2026
Population-scale repeat expansions elucidate disease risk and brain atrophyVijay Kumar Pounraja, Jae Hoon Sul, Joseph Herman, et al.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.Nature Genetics|September 26, 2006
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHCPaul I W de Bakker, Gil McVean, Pardis C Sabeti, et al.European Journal of Human Genetics : EJHG|May 30, 2013
The Genome of the Netherlands: design, and project goalsDorret I Boomsma, Cisca Wijmenga, Eline P Slagboom, 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.The Lancet. Respiratory Medicine|October 2, 2015
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK BiobankLouise V Wain, Nick Shrine, Suzanne Miller, 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.Pageof 11