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Charles Kooperberg

Showing results (171-180 of 530) with videos related to

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BMC Genomics|March 16, 2020
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomicsChani J Hodonsky, Antoine R Baldassari, Stephanie A Bien, et al.
Human Genetics|September 1, 2023
Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohortsMohammad Yaser Anwar, Mariaelisa Graff, Heather M Highland, et al.
Cell Genomics|August 21, 2023
Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestriesIda Surakka, Kuan-Han Wu, Whitney Hornsby, et al.
Women'S Health Issues : Official Publication of the Jacobs Institute of Women'S Health|December 7, 2023
Individual and Neighborhood-level Socioeconomic Status and Somatic Mutations Associated With Increased Risk of Cardiovascular Disease and Mortality: A Cross-Sectional Analysis in the Women's Health InitiativeShelly-Ann M Love, Jason M Collins, Kurtis M Anthony, et al.
Human Molecular Genetics|February 10, 2006
Regional and cellular gene expression changes in human Huntington's disease brainAngela Hodges, Andrew D Strand, Aaron K Aragaki, et al.
Frontiers in Genetics|June 11, 2019
Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE StudyBridget M Lin, Girish N Nadkarni, Ran Tao, et al.
Mayo Clinic Proceedings|August 23, 2025
Association of Pathogenic/Likely Pathogenic Inherited Cardiomyopathy Variants With Heart Failure: A TOPMed Multiancestry AnalysisNaman S Shetty, Mokshad Gaonkar, Akhil Pampana, et al.
Genetic Epidemiology|February 1, 2014
A variational Bayes discrete mixture test for rare variant associationBenjamin A Logsdon, James Y Dai, Paul L Auer, et al.
Epidemiology (Cambridge, Mass.)|August 29, 2014
Evidence of heterogeneity by race/ethnicity in genetic determinants of QT intervalAmanda A Seyerle, Alicia M Young, Janina M Jeff, et al.
Clinical Journal of the American Society of Nephrology : CJASN|August 10, 2022
Genome-Wide Epistatic Interaction between <i>DEF1B</i> and <i>APOL1</i> High-Risk Genotypes for Chronic Kidney DiseaseHa My T Vy, Bridget M Lin, Faris F Gulamali, et al.
Pageof 53

Showing results (171-180 of 530) with videos related to

Sort By:
Pageof 53
BMC Genomics|March 16, 2020
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomicsChani J Hodonsky, Antoine R Baldassari, Stephanie A Bien, et al.
Human Genetics|September 1, 2023
Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohortsMohammad Yaser Anwar, Mariaelisa Graff, Heather M Highland, et al.
Cell Genomics|August 21, 2023
Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestriesIda Surakka, Kuan-Han Wu, Whitney Hornsby, et al.
Women'S Health Issues : Official Publication of the Jacobs Institute of Women'S Health|December 7, 2023
Individual and Neighborhood-level Socioeconomic Status and Somatic Mutations Associated With Increased Risk of Cardiovascular Disease and Mortality: A Cross-Sectional Analysis in the Women's Health InitiativeShelly-Ann M Love, Jason M Collins, Kurtis M Anthony, et al.
Human Molecular Genetics|February 10, 2006
Regional and cellular gene expression changes in human Huntington's disease brainAngela Hodges, Andrew D Strand, Aaron K Aragaki, et al.
Frontiers in Genetics|June 11, 2019
Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE StudyBridget M Lin, Girish N Nadkarni, Ran Tao, et al.
Mayo Clinic Proceedings|August 23, 2025
Association of Pathogenic/Likely Pathogenic Inherited Cardiomyopathy Variants With Heart Failure: A TOPMed Multiancestry AnalysisNaman S Shetty, Mokshad Gaonkar, Akhil Pampana, et al.
Genetic Epidemiology|February 1, 2014
A variational Bayes discrete mixture test for rare variant associationBenjamin A Logsdon, James Y Dai, Paul L Auer, et al.
Epidemiology (Cambridge, Mass.)|August 29, 2014
Evidence of heterogeneity by race/ethnicity in genetic determinants of QT intervalAmanda A Seyerle, Alicia M Young, Janina M Jeff, et al.
Clinical Journal of the American Society of Nephrology : CJASN|August 10, 2022
Genome-Wide Epistatic Interaction between <i>DEF1B</i> and <i>APOL1</i> High-Risk Genotypes for Chronic Kidney DiseaseHa My T Vy, Bridget M Lin, Faris F Gulamali, et al.
Pageof 53