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Showing results (1131-1140 of 1,201) with videos related to

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Communications Biology|July 28, 2022
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed programDaniel DiCorpo, Sheila M Gaynor, Emily M Russell, et al.
Blood|February 6, 2024
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levelsPaul S de Vries, Paula Reventun, Michael R Brown, et al.
American Journal of Human Genetics|June 28, 2016
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated DiseasesSalman M Tajuddin, Ursula M Schick, John D Eicher, et al.
Nature Human Behaviour|August 4, 2022
Rare genetic variants explain missing heritability in smokingSeon-Kyeong Jang, Luke Evans, Allison Fialkowski, 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.
Cell|September 5, 2020
The Polygenic and Monogenic Basis of Blood Traits and DiseasesDragana Vuckovic, Erik L Bao, Parsa Akbari, et al.
Wellcome Open Research|September 4, 2018
Meta-analysis of exome array data identifies six novel genetic loci for lung functionVictoria E Jackson, Jeanne C Latourelle, Louise V Wain, et al.
Nature Communications|August 1, 2018
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary functionAnnah B Wyss, Tamar Sofer, Mi Kyeong Lee, et al.
Nature Communications|January 19, 2018
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levelsXia Jiang, Paul F O'Reilly, Hugues Aschard, 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.
Pageof 121

Showing results (1131-1140 of 1,201) with videos related to

Sort By:
Pageof 121
Communications Biology|July 28, 2022
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed programDaniel DiCorpo, Sheila M Gaynor, Emily M Russell, et al.
Blood|February 6, 2024
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levelsPaul S de Vries, Paula Reventun, Michael R Brown, et al.
American Journal of Human Genetics|June 28, 2016
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated DiseasesSalman M Tajuddin, Ursula M Schick, John D Eicher, et al.
Nature Human Behaviour|August 4, 2022
Rare genetic variants explain missing heritability in smokingSeon-Kyeong Jang, Luke Evans, Allison Fialkowski, 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.
Cell|September 5, 2020
The Polygenic and Monogenic Basis of Blood Traits and DiseasesDragana Vuckovic, Erik L Bao, Parsa Akbari, et al.
Wellcome Open Research|September 4, 2018
Meta-analysis of exome array data identifies six novel genetic loci for lung functionVictoria E Jackson, Jeanne C Latourelle, Louise V Wain, et al.
Nature Communications|August 1, 2018
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary functionAnnah B Wyss, Tamar Sofer, Mi Kyeong Lee, et al.
Nature Communications|January 19, 2018
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levelsXia Jiang, Paul F O'Reilly, Hugues Aschard, 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.
Pageof 121