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Nathan Pankratz

Showing results (111-120 of 173) with videos related to

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Diabetologia|September 15, 2017
Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortiumStephanie A Bien, James S Pankow, Jeffrey Haessler, et al.
Human Molecular Genetics|June 16, 2024
Multi-ancestry polygenic risk scores for venous thromboembolismYon Ho Jee, Florian Thibord, Alicia Dominguez, et al.
Human Molecular Genetics|May 13, 2022
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factorsNathan Pankratz, Peng Wei, Jennifer A Brody, et al.
Human Molecular Genetics|June 8, 2018
Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) studyJonathan M Kocarnik, Melissa Richard, Misa Graff, et al.
HGG Advances|August 2, 2021
BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportionTamar Sofer, Jiwon Lee, Nuzulul Kurniansyah, et al.
Circulation. Cardiovascular Genetics|March 14, 2014
Multiancestral analysis of inflammation-related genetic variants and C-reactive protein in the population architecture using genomics and epidemiology studyJonathan M Kocarnik, Sarah A Pendergrass, Cara L Carty, et al.
Circulation. Genomic and Precision Medicine|March 24, 2023
Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine ProgramAmanda A Seyerle, Cecelia A Laurie, Brandon J Coombes, et al.
Genetic Epidemiology|January 20, 2019
A large-scale exome array analysis of venous thromboembolismSara Lindström, Jennifer A Brody, Constance Turman, et al.
Cell Genomics|January 17, 2022
Association of mitochondrial DNA copy number with cardiometabolic diseasesXue Liu, Ryan J Longchamps, Kerri L Wiggins, et al.
Scientific Reports|October 25, 2019
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairmentAndries Paul Nagtegaal, Linda Broer, Nuno R Zilhao, et al.
Pageof 18

Showing results (111-120 of 173) with videos related to

Sort By:
Pageof 18
Diabetologia|September 15, 2017
Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortiumStephanie A Bien, James S Pankow, Jeffrey Haessler, et al.
Human Molecular Genetics|June 16, 2024
Multi-ancestry polygenic risk scores for venous thromboembolismYon Ho Jee, Florian Thibord, Alicia Dominguez, et al.
Human Molecular Genetics|May 13, 2022
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factorsNathan Pankratz, Peng Wei, Jennifer A Brody, et al.
Human Molecular Genetics|June 8, 2018
Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) studyJonathan M Kocarnik, Melissa Richard, Misa Graff, et al.
HGG Advances|August 2, 2021
BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportionTamar Sofer, Jiwon Lee, Nuzulul Kurniansyah, et al.
Circulation. Cardiovascular Genetics|March 14, 2014
Multiancestral analysis of inflammation-related genetic variants and C-reactive protein in the population architecture using genomics and epidemiology studyJonathan M Kocarnik, Sarah A Pendergrass, Cara L Carty, et al.
Circulation. Genomic and Precision Medicine|March 24, 2023
Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine ProgramAmanda A Seyerle, Cecelia A Laurie, Brandon J Coombes, et al.
Genetic Epidemiology|January 20, 2019
A large-scale exome array analysis of venous thromboembolismSara Lindström, Jennifer A Brody, Constance Turman, et al.
Cell Genomics|January 17, 2022
Association of mitochondrial DNA copy number with cardiometabolic diseasesXue Liu, Ryan J Longchamps, Kerri L Wiggins, et al.
Scientific Reports|October 25, 2019
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairmentAndries Paul Nagtegaal, Linda Broer, Nuno R Zilhao, et al.
Pageof 18