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Showing results (131-140 of 161) with videos related to

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Biorxiv : the Preprint Server for Biology|November 14, 2023
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Diabetes|February 15, 2023
Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic TraitsKenneth E Westerman, Maura E Walker, Sheila M Gaynor, et al.
American Journal of Epidemiology|April 16, 2021
A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) ProgramAdrienne M Stilp, Leslie S Emery, Jai G Broome, et al.
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|June 10, 2021
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomesJulia K Goodrich, Moriel Singer-Berk, Rachel Son, et al.
Nature Genetics|October 18, 2011
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasmaJohn C Chambers, Weihua Zhang, Joban Sehmi, et al.
Nature|May 24, 2019
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controlsJason Flannick, Josep M Mercader, Christian Fuchsberger, et al.
Nature|September 18, 2012
FTO genotype is associated with phenotypic variability of body mass indexJian Yang, Ruth J F Loos, Joseph E Powell, et al.
American Journal of Human Genetics|December 21, 2021
Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomesGeorge Hindy, Peter Dornbos, Mark D Chaffin, et al.
Nature|February 11, 2021
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed ProgramDaniel Taliun, Daniel N Harris, Michael D Kessler, et al.
Pageof 17

Showing results (131-140 of 161) with videos related to

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Pageof 17
Biorxiv : the Preprint Server for Biology|November 14, 2023
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.
Diabetes|February 15, 2023
Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic TraitsKenneth E Westerman, Maura E Walker, Sheila M Gaynor, et al.
American Journal of Epidemiology|April 16, 2021
A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) ProgramAdrienne M Stilp, Leslie S Emery, Jai G Broome, et al.
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|June 10, 2021
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomesJulia K Goodrich, Moriel Singer-Berk, Rachel Son, et al.
Nature Genetics|October 18, 2011
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasmaJohn C Chambers, Weihua Zhang, Joban Sehmi, et al.
Nature|May 24, 2019
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controlsJason Flannick, Josep M Mercader, Christian Fuchsberger, et al.
Nature|September 18, 2012
FTO genotype is associated with phenotypic variability of body mass indexJian Yang, Ruth J F Loos, Joseph E Powell, et al.
American Journal of Human Genetics|December 21, 2021
Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomesGeorge Hindy, Peter Dornbos, Mark D Chaffin, et al.
Nature|February 11, 2021
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed ProgramDaniel Taliun, Daniel N Harris, Michael D Kessler, et al.
Pageof 17