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Charles Kooperberg

Showing results (221-230 of 530) with videos related to

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American Journal of Human Genetics|April 18, 2024
MagicalRsq-X: A cross-cohort transferable genotype imputation quality metricQuan Sun, Yingxi Yang, Jonathan D Rosen, et al.
Genetic Epidemiology|January 15, 2025
General Kernel Machine Methods for Multi-Omics Integration and Genome-Wide Association Testing With Related IndividualsAmarise Little, Ni Zhao, Anna Mikhaylova, et al.
JAMA Neurology|May 12, 2015
Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence ProjectPaul L Auer, Mike Nalls, James F Meschia, et al.
Genetics|June 22, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Plos One|July 2, 2021
Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) ProgramChloé Sarnowski, Han Chen, Mary L Biggs, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Plos Genetics|January 24, 2013
A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) studyUlrike Peters, Kari E North, Praveen Sethupathy, et al.
Carcinogenesis|May 17, 2014
Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortiaVeronica Wendy Setiawan, Fredrick Schumacher, Jennifer Prescott, et al.
Medrxiv : the Preprint Server for Health Sciences|March 27, 2026
Local ancestry modulates gene expression: shifting our understanding of genetic regulation and disease association within and across populationsHung-Hsin Chen, Yanwei Cai, MariaElisa Graff, et al.
Human Molecular Genetics|August 20, 2021
Epigenome-wide association study of mitochondrial genome copy numberPenglong Wang, Christina A Castellani, Jie Yao, et al.
Pageof 53

Showing results (221-230 of 530) with videos related to

Sort By:
Pageof 53
American Journal of Human Genetics|April 18, 2024
MagicalRsq-X: A cross-cohort transferable genotype imputation quality metricQuan Sun, Yingxi Yang, Jonathan D Rosen, et al.
Genetic Epidemiology|January 15, 2025
General Kernel Machine Methods for Multi-Omics Integration and Genome-Wide Association Testing With Related IndividualsAmarise Little, Ni Zhao, Anna Mikhaylova, et al.
JAMA Neurology|May 12, 2015
Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence ProjectPaul L Auer, Mike Nalls, James F Meschia, et al.
Genetics|June 22, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Plos One|July 2, 2021
Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) ProgramChloé Sarnowski, Han Chen, Mary L Biggs, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Plos Genetics|January 24, 2013
A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) studyUlrike Peters, Kari E North, Praveen Sethupathy, et al.
Carcinogenesis|May 17, 2014
Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortiaVeronica Wendy Setiawan, Fredrick Schumacher, Jennifer Prescott, et al.
Medrxiv : the Preprint Server for Health Sciences|March 27, 2026
Local ancestry modulates gene expression: shifting our understanding of genetic regulation and disease association within and across populationsHung-Hsin Chen, Yanwei Cai, MariaElisa Graff, et al.
Human Molecular Genetics|August 20, 2021
Epigenome-wide association study of mitochondrial genome copy numberPenglong Wang, Christina A Castellani, Jie Yao, et al.
Pageof 53