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Showing results (331-340 of 364) with videos related to

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Nature Computational Science|February 7, 2025
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Nature Communications|October 11, 2022
Whole genome sequence analysis of blood lipid levels in >66,000 individualsMargaret Sunitha Selvaraj, Xihao Li, Zilin Li, et al.
Research Square|February 13, 2023
Structural variation across 138,134 samples in the TOPMed consortiumGoo Jun, Adam C English, Ginger A Metcalf, et al.
Plos Genetics|August 8, 2014
Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetesMaggie C Y Ng, Daniel Shriner, Brian H Chen, et al.
American Journal of Human Genetics|September 28, 2021
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed programAnna V Mikhaylova, Caitlin P McHugh, Linda M Polfus, et al.
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.
Diabetes|June 11, 2026
Colocalization of eQTLs With Type 2 Diabetes and Glycemic Traits Using Whole-Genome Sequences in Diverse Populations From the NHLBI Trans-Omics in Precision Medicine (TOPMed) ProgramNingyuan Wang, Daniel A DiCorpo, Yixin Zhang, 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 37

Showing results (331-340 of 364) with videos related to

Sort By:
Pageof 37
Nature Computational Science|February 7, 2025
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Nature Communications|October 11, 2022
Whole genome sequence analysis of blood lipid levels in >66,000 individualsMargaret Sunitha Selvaraj, Xihao Li, Zilin Li, et al.
Research Square|February 13, 2023
Structural variation across 138,134 samples in the TOPMed consortiumGoo Jun, Adam C English, Ginger A Metcalf, et al.
Plos Genetics|August 8, 2014
Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetesMaggie C Y Ng, Daniel Shriner, Brian H Chen, et al.
American Journal of Human Genetics|September 28, 2021
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed programAnna V Mikhaylova, Caitlin P McHugh, Linda M Polfus, et al.
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.
Diabetes|June 11, 2026
Colocalization of eQTLs With Type 2 Diabetes and Glycemic Traits Using Whole-Genome Sequences in Diverse Populations From the NHLBI Trans-Omics in Precision Medicine (TOPMed) ProgramNingyuan Wang, Daniel A DiCorpo, Yixin Zhang, 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 37