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Showing results (441-450 of 590) with videos related to

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Cell|September 5, 2020
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global PopulationsMing-Huei Chen, Laura M Raffield, Abdou Mousas, et al.
American Journal of Human Genetics|June 24, 2014
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP ConsortiaJeannette Simino, Gang Shi, Joshua C Bis, et al.
Nature Genetics|March 6, 2025
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation riskSeung Hoan Choi, Sean J Jurgens, Ling Xiao, et al.
Nature Genetics|February 7, 2017
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targetsLouise V Wain, Nick Shrine, María Soler Artigas, et al.
JAMA|November 6, 2019
Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry, Michael A Hauser, R Rand Allingham, et al.
Nature Communications|April 13, 2021
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indicesPradeep Natarajan, Akhil Pampana, Sarah E Graham, et al.
Nature Communications|May 24, 2024
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genesRebecca Keener, Surya B Chhetri, Carla J Connelly, et al.
Diabetes|September 12, 2020
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early AdiposityHanieh Yaghootkar, Yiying Zhang, Cassandra N Spracklen, et al.
Nature Human Behaviour|September 29, 2020
Genome-wide association study identifies 48 common genetic variants associated with handednessGabriel Cuellar-Partida, Joyce Y Tung, Nicholas Eriksson, et al.
Nature Genetics|October 10, 2018
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome mapsAnubha Mahajan, Daniel Taliun, Matthias Thurner, et al.
Pageof 59

Showing results (441-450 of 590) with videos related to

Sort By:
Pageof 59
Cell|September 5, 2020
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global PopulationsMing-Huei Chen, Laura M Raffield, Abdou Mousas, et al.
American Journal of Human Genetics|June 24, 2014
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP ConsortiaJeannette Simino, Gang Shi, Joshua C Bis, et al.
Nature Genetics|March 6, 2025
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation riskSeung Hoan Choi, Sean J Jurgens, Ling Xiao, et al.
Nature Genetics|February 7, 2017
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targetsLouise V Wain, Nick Shrine, María Soler Artigas, et al.
JAMA|November 6, 2019
Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry, Michael A Hauser, R Rand Allingham, et al.
Nature Communications|April 13, 2021
Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indicesPradeep Natarajan, Akhil Pampana, Sarah E Graham, et al.
Nature Communications|May 24, 2024
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genesRebecca Keener, Surya B Chhetri, Carla J Connelly, et al.
Diabetes|September 12, 2020
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early AdiposityHanieh Yaghootkar, Yiying Zhang, Cassandra N Spracklen, et al.
Nature Human Behaviour|September 29, 2020
Genome-wide association study identifies 48 common genetic variants associated with handednessGabriel Cuellar-Partida, Joyce Y Tung, Nicholas Eriksson, et al.
Nature Genetics|October 10, 2018
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome mapsAnubha Mahajan, Daniel Taliun, Matthias Thurner, et al.
Pageof 59