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Braxton D Mitchell

Showing results (331-340 of 457) with videos related to

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American Journal of Human Genetics|January 15, 2019
Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing StudiesHan Chen, Jennifer E Huffman, Jennifer A Brody, et al.
Journal of Thrombosis and Haemostasis : JTH|May 14, 2025
Genetic study of von Willebrand factor antigen levels ≤ 50 IU/dL identifies variants associated with increased risk of von Willebrand disease and bleedingRachel K Friedman, Adam S Heath, Jennifer E Huffman, et al.
Journal of the American Society of Nephrology : JASN|December 9, 2016
Genetic Variants Associated with Circulating Parathyroid HormoneCassianne Robinson-Cohen, Pamela L Lutsey, Marcus E Kleber, et al.
European Heart Journal. Cardiovascular Pharmacotherapy|September 11, 2019
Pharmacogenomic polygenic response score predicts ischaemic events and cardiovascular mortality in clopidogrel-treated patientsJoshua P Lewis, Joshua D Backman, Jean-Luc Reny, et al.
Nature Communications|August 30, 2022
Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genesJennifer L Halford, Valerie N Morrill, Seung Hoan Choi, et al.
American Journal of Human Genetics|December 30, 2019
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry CohortsLaura M Raffield, Apoorva K Iyengar, Biqi Wang, et al.
Circulation. Genomic and Precision Medicine|July 28, 2021
Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry AnalysisSeung Hoan Choi, Sean J Jurgens, Christopher M Haggerty, et al.
Nature Genetics|October 31, 2023
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencingYasminka A Jakubek, Ying Zhou, Adrienne Stilp, et al.
The Journal of Clinical Investigation|June 4, 2008
Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levelsWei-Min Chen, Michael R Erdos, Anne U Jackson, et al.
Human Molecular Genetics|November 29, 2022
Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney diseaseYang Pan, Xiao Sun, Xuenan Mi, et al.
Pageof 46

Showing results (331-340 of 457) with videos related to

Sort By:
Pageof 46
American Journal of Human Genetics|January 15, 2019
Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing StudiesHan Chen, Jennifer E Huffman, Jennifer A Brody, et al.
Journal of Thrombosis and Haemostasis : JTH|May 14, 2025
Genetic study of von Willebrand factor antigen levels ≤ 50 IU/dL identifies variants associated with increased risk of von Willebrand disease and bleedingRachel K Friedman, Adam S Heath, Jennifer E Huffman, et al.
Journal of the American Society of Nephrology : JASN|December 9, 2016
Genetic Variants Associated with Circulating Parathyroid HormoneCassianne Robinson-Cohen, Pamela L Lutsey, Marcus E Kleber, et al.
European Heart Journal. Cardiovascular Pharmacotherapy|September 11, 2019
Pharmacogenomic polygenic response score predicts ischaemic events and cardiovascular mortality in clopidogrel-treated patientsJoshua P Lewis, Joshua D Backman, Jean-Luc Reny, et al.
Nature Communications|August 30, 2022
Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genesJennifer L Halford, Valerie N Morrill, Seung Hoan Choi, et al.
American Journal of Human Genetics|December 30, 2019
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry CohortsLaura M Raffield, Apoorva K Iyengar, Biqi Wang, et al.
Circulation. Genomic and Precision Medicine|July 28, 2021
Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry AnalysisSeung Hoan Choi, Sean J Jurgens, Christopher M Haggerty, et al.
Nature Genetics|October 31, 2023
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencingYasminka A Jakubek, Ying Zhou, Adrienne Stilp, et al.
The Journal of Clinical Investigation|June 4, 2008
Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levelsWei-Min Chen, Michael R Erdos, Anne U Jackson, et al.
Human Molecular Genetics|November 29, 2022
Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney diseaseYang Pan, Xiao Sun, Xuenan Mi, et al.
Pageof 46