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Lisa R Yanek

Showing results (131-140 of 245) with videos related to

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HGG Advances|October 4, 2021
Genetic discovery and risk characterization in type 2 diabetes across diverse populationsLinda M Polfus, Burcu F Darst, Heather Highland, et al.
Diabetes Care|November 18, 2021
Obesity Partially Mediates the Diabetogenic Effect of Lowering LDL CholesterolPeitao Wu, Jee-Young Moon, Iyas Daghlas, 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.
Nature Aging|June 4, 2024
Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rateTaralynn M Mack, Michael A Raddatz, Yash Pershad, 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.
Journal of Thrombosis and Haemostasis : JTH|April 20, 2021
FGL1 as a modulator of plasma D-dimer levels: Exome-wide marker analysis of plasma tPA, PAI-1, and D-dimerFlorian Thibord, Ci Song, Jack Pattee, et al.
Nature Genetics|March 8, 2022
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence dataPierrick Wainschtein, Deepti Jain, Zhili Zheng, et al.
Human Genetics|January 24, 2019
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing dataKaren Y He, Xiaoyin Li, Tanika N Kelly, et al.
Nature Communications|March 27, 2026
An integrated germline and somatic genomic model for coronary artery diseaseXiong Yang, Min Seo Kim, Xinyu Zhu, et al.
Nature Genetics|December 23, 2022
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studiesXihao Li, Corbin Quick, Hufeng Zhou, et al.
Pageof 25

Showing results (131-140 of 245) with videos related to

Sort By:
Pageof 25
HGG Advances|October 4, 2021
Genetic discovery and risk characterization in type 2 diabetes across diverse populationsLinda M Polfus, Burcu F Darst, Heather Highland, et al.
Diabetes Care|November 18, 2021
Obesity Partially Mediates the Diabetogenic Effect of Lowering LDL CholesterolPeitao Wu, Jee-Young Moon, Iyas Daghlas, 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.
Nature Aging|June 4, 2024
Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rateTaralynn M Mack, Michael A Raddatz, Yash Pershad, 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.
Journal of Thrombosis and Haemostasis : JTH|April 20, 2021
FGL1 as a modulator of plasma D-dimer levels: Exome-wide marker analysis of plasma tPA, PAI-1, and D-dimerFlorian Thibord, Ci Song, Jack Pattee, et al.
Nature Genetics|March 8, 2022
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence dataPierrick Wainschtein, Deepti Jain, Zhili Zheng, et al.
Human Genetics|January 24, 2019
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing dataKaren Y He, Xiaoyin Li, Tanika N Kelly, et al.
Nature Communications|March 27, 2026
An integrated germline and somatic genomic model for coronary artery diseaseXiong Yang, Min Seo Kim, Xinyu Zhu, et al.
Nature Genetics|December 23, 2022
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studiesXihao Li, Corbin Quick, Hufeng Zhou, et al.
Pageof 25