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Daniel Taliun

Showing results (21-30 of 44) with videos related to

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Communications Biology|April 2, 2026
Author Correction: HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseasesGuillaume Butler-Laporte, Joseph Farjoun, Tomoko Nakanishi, et al.
Communications Biology|November 4, 2023
HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseasesGuillaume Butler-Laporte, Joseph Farjoun, Tomoko Nakanishi, et al.
Genetic Epidemiology|January 3, 2013
SNP prioritization using a Bayesian probability of associationJohn R Thompson, Martin Gögele, Christian X Weichenberger, et al.
Genetic Epidemiology|January 12, 2013
Importance of different types of prior knowledge in selecting genome-wide findings for follow-upCosetta Minelli, Alessandro De Grandi, Christian X Weichenberger, et al.
Human Molecular Genetics|August 1, 2014
Meta-analysis of genome-wide association studies identifies two loci associated with circulating osteoprotegerin levelsJohnny S H Kwan, Yi-Hsiang Hsu, Ching-Lung Cheung, 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 Communications|February 3, 2026
A multi-ancestry genetic reference for the Quebec populationPeyton McClelland, Georgette Femerling, Rose Laflamme, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2025
A multi-ancestry genetic reference for the Quebec populationPeyton McClelland, Georgette Femerling, Rose Laflamme, et al.
Cell Metabolism|March 24, 2023
The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traitsMaria C Costanzo, Marcin von Grotthuss, Jeffrey Massung, et al.
Nature Communications|December 19, 2020
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular diseaseJonas B Nielsen, Oren Rom, Ida Surakka, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Communications Biology|April 2, 2026
Author Correction: HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseasesGuillaume Butler-Laporte, Joseph Farjoun, Tomoko Nakanishi, et al.
Communications Biology|November 4, 2023
HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseasesGuillaume Butler-Laporte, Joseph Farjoun, Tomoko Nakanishi, et al.
Genetic Epidemiology|January 3, 2013
SNP prioritization using a Bayesian probability of associationJohn R Thompson, Martin Gögele, Christian X Weichenberger, et al.
Genetic Epidemiology|January 12, 2013
Importance of different types of prior knowledge in selecting genome-wide findings for follow-upCosetta Minelli, Alessandro De Grandi, Christian X Weichenberger, et al.
Human Molecular Genetics|August 1, 2014
Meta-analysis of genome-wide association studies identifies two loci associated with circulating osteoprotegerin levelsJohnny S H Kwan, Yi-Hsiang Hsu, Ching-Lung Cheung, 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 Communications|February 3, 2026
A multi-ancestry genetic reference for the Quebec populationPeyton McClelland, Georgette Femerling, Rose Laflamme, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2025
A multi-ancestry genetic reference for the Quebec populationPeyton McClelland, Georgette Femerling, Rose Laflamme, et al.
Cell Metabolism|March 24, 2023
The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traitsMaria C Costanzo, Marcin von Grotthuss, Jeffrey Massung, et al.
Nature Communications|December 19, 2020
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular diseaseJonas B Nielsen, Oren Rom, Ida Surakka, et al.
Pageof 5