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Nature Genetics
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September 26, 2006
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC
Paul I W de Bakker, Gil McVean, Pardis C Sabeti, 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 Biobank
Louise V Wain, Nick Shrine, Suzanne Miller, et al.
Nature Genetics
|
June 12, 2023
Rare coding variants in CHRNB2 reduce the likelihood of smoking
Veera 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 individuals
Kathie Y Sun, Xiaodong Bai, Siying Chen, et al.
Nature
|
October 18, 2021
Exome sequencing and analysis of 454,787 UK Biobank participants
Joshua D Backman, Alexander H Li, Anthony Marcketta, et al.
Nature
|
May 20, 2024
A deep catalogue of protein-coding variation in 983,578 individuals
Kathie Y Sun, Xiaodong Bai, Siying Chen, et al.
Nature
|
February 22, 2023
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes
Michael D Kessler, Amy Damask, Sean O'Keeffe, et al.
Nature
|
January 8, 2025
Author Correction: A deep catalogue of protein-coding variation in 983,578 individuals
Kathie Y Sun, Xiaodong Bai, Siying Chen, et al.
Nature
|
January 8, 2025
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes
Michael D Kessler, Amy Damask, Sean O'Keeffe, et al.
Nature
|
February 8, 2024
Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City
Andrey Ziyatdinov, Jason Torres, Jesús Alegre-Díaz, et al.
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of 11
Search research articles
Search
Showing results (61-70 of 102) with videos related to
Sort By:
Page
of 11
Nature Genetics
|
September 26, 2006
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC
Paul I W de Bakker, Gil McVean, Pardis C Sabeti, 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 Biobank
Louise V Wain, Nick Shrine, Suzanne Miller, et al.
Nature Genetics
|
June 12, 2023
Rare coding variants in CHRNB2 reduce the likelihood of smoking
Veera 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 individuals
Kathie Y Sun, Xiaodong Bai, Siying Chen, et al.
Nature
|
October 18, 2021
Exome sequencing and analysis of 454,787 UK Biobank participants
Joshua D Backman, Alexander H Li, Anthony Marcketta, et al.
Nature
|
May 20, 2024
A deep catalogue of protein-coding variation in 983,578 individuals
Kathie Y Sun, Xiaodong Bai, Siying Chen, et al.
Nature
|
February 22, 2023
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes
Michael D Kessler, Amy Damask, Sean O'Keeffe, et al.
Nature
|
January 8, 2025
Author Correction: A deep catalogue of protein-coding variation in 983,578 individuals
Kathie Y Sun, Xiaodong Bai, Siying Chen, et al.
Nature
|
January 8, 2025
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes
Michael D Kessler, Amy Damask, Sean O'Keeffe, et al.
Nature
|
February 8, 2024
Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City
Andrey Ziyatdinov, Jason Torres, Jesús Alegre-Díaz, et al.
Page
of 11