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Human genomics

Showing results (221-230 of 1,251) with videos related to

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Human Genomics|November 20, 2012
Strong interaction between T allele of endothelial nitric oxide synthase with B1 allele of cholesteryl ester transfer protein TaqIB highly elevates the risk of coronary artery disease and type 2 diabetes mellitusZohreh Rahimi, Reza Nourozi-Rad, Ziba Rahimi, et al.
Human Genomics|January 11, 2014
On the stability of the Bayenv method in assessing human SNP-environment associationsLily M Blair, Julie M Granka, Marcus W Feldman
Human Genomics|January 23, 2014
A survey of software for genome-wide discovery of differential splicing in RNA-Seq dataJoan E Hooper
Human Genomics|March 12, 2015
Rapid detection of genetic mutations in individual breast cancer patients by next-generation DNA sequencingSuqin Liu, Hongjiang Wang, Lizhi Zhang, et al.
Human Genomics|June 28, 2020
Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discoveryClaudia De Masi, Paola Spitalieri, Michela Murdocca, et al.
Human Genomics|October 25, 2025
Correction: De novo and inherited variants in coding and regulatory regions in genetic cardiomyopathiesNirmal Vadgama, Mohamed Ameen, Laksshman Sundaram, et al.
Human Genomics|October 6, 2018
Identification of gross deletions in FBN1 gene by MLPAHang Yang, Yanyun Ma, Mingyao Luo, et al.
Human Genomics|September 26, 2021
Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 lociChris M Pappas, Moussa A Zouache, Stacie Matthews, et al.
Human Genomics|May 10, 2023
Genetic basis of STEM occupational choice and regional economic performance: a UK biobank genome-wide association studyChen Zhu, Qiran Zhao, Jianbo He, et al.
Human Genomics|May 15, 2023
Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni familiesMaria Asaad, Mona Mahfood, Abdullah Al Mutery, et al.
Pageof 126

Showing results (221-230 of 1,251) with videos related to

Sort By:
Pageof 126
Human Genomics|November 20, 2012
Strong interaction between T allele of endothelial nitric oxide synthase with B1 allele of cholesteryl ester transfer protein TaqIB highly elevates the risk of coronary artery disease and type 2 diabetes mellitusZohreh Rahimi, Reza Nourozi-Rad, Ziba Rahimi, et al.
Human Genomics|January 11, 2014
On the stability of the Bayenv method in assessing human SNP-environment associationsLily M Blair, Julie M Granka, Marcus W Feldman
Human Genomics|January 23, 2014
A survey of software for genome-wide discovery of differential splicing in RNA-Seq dataJoan E Hooper
Human Genomics|March 12, 2015
Rapid detection of genetic mutations in individual breast cancer patients by next-generation DNA sequencingSuqin Liu, Hongjiang Wang, Lizhi Zhang, et al.
Human Genomics|June 28, 2020
Application of CRISPR/Cas9 to human-induced pluripotent stem cells: from gene editing to drug discoveryClaudia De Masi, Paola Spitalieri, Michela Murdocca, et al.
Human Genomics|October 25, 2025
Correction: De novo and inherited variants in coding and regulatory regions in genetic cardiomyopathiesNirmal Vadgama, Mohamed Ameen, Laksshman Sundaram, et al.
Human Genomics|October 6, 2018
Identification of gross deletions in FBN1 gene by MLPAHang Yang, Yanyun Ma, Mingyao Luo, et al.
Human Genomics|September 26, 2021
Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 lociChris M Pappas, Moussa A Zouache, Stacie Matthews, et al.
Human Genomics|May 10, 2023
Genetic basis of STEM occupational choice and regional economic performance: a UK biobank genome-wide association studyChen Zhu, Qiran Zhao, Jianbo He, et al.
Human Genomics|May 15, 2023
Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni familiesMaria Asaad, Mona Mahfood, Abdullah Al Mutery, et al.
Pageof 126