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Jennifer A Smith

Showing results (271-280 of 414) with videos related to

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Nature Communications|March 27, 2026
An integrated germline and somatic genomic model for coronary artery diseaseXiong Yang, Min Seo Kim, Xinyu Zhu, et al.
The Lancet. Global Health|July 17, 2020
Potential impact of the COVID-19 pandemic on HIV, tuberculosis, and malaria in low-income and middle-income countries: a modelling studyAlexandra B Hogan, Britta L Jewell, Ellie Sherrard-Smith, et al.
Nature Communications|October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Nature Methods|December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regionsEric Van Buren, Yi Zhang, Xihao Li, et al.
Nature Communications|June 29, 2021
A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipidsMin-A Jhun, Michael Mendelson, Rory Wilson, et al.
Epigenomics|September 20, 2019
Comparison of smoking-related DNA methylation between newborns from prenatal exposure and adults from personal smokingSinjini Sikdar, Roby Joehanes, Bonnie R Joubert, et al.
American Journal of Human Genetics|December 5, 2017
DNA Methylation Analysis Identifies Loci for Blood Pressure RegulationMelissa A Richard, Tianxiao Huan, Symen Ligthart, et al.
Journal of Thrombosis and Haemostasis : JTH|January 30, 2023
DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in bloodJulie Hahn, Jan Bressler, Arce Domingo-Relloso, et al.
Alzheimer'S Research & Therapy|January 20, 2024
Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performanceHao Mei, Jeannette Simino, Lianna Li, 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 42

Showing results (271-280 of 414) with videos related to

Sort By:
Pageof 42
Nature Communications|March 27, 2026
An integrated germline and somatic genomic model for coronary artery diseaseXiong Yang, Min Seo Kim, Xinyu Zhu, et al.
The Lancet. Global Health|July 17, 2020
Potential impact of the COVID-19 pandemic on HIV, tuberculosis, and malaria in low-income and middle-income countries: a modelling studyAlexandra B Hogan, Britta L Jewell, Ellie Sherrard-Smith, et al.
Nature Communications|October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Nature Methods|December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regionsEric Van Buren, Yi Zhang, Xihao Li, et al.
Nature Communications|June 29, 2021
A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipidsMin-A Jhun, Michael Mendelson, Rory Wilson, et al.
Epigenomics|September 20, 2019
Comparison of smoking-related DNA methylation between newborns from prenatal exposure and adults from personal smokingSinjini Sikdar, Roby Joehanes, Bonnie R Joubert, et al.
American Journal of Human Genetics|December 5, 2017
DNA Methylation Analysis Identifies Loci for Blood Pressure RegulationMelissa A Richard, Tianxiao Huan, Symen Ligthart, et al.
Journal of Thrombosis and Haemostasis : JTH|January 30, 2023
DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in bloodJulie Hahn, Jan Bressler, Arce Domingo-Relloso, et al.
Alzheimer'S Research & Therapy|January 20, 2024
Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performanceHao Mei, Jeannette Simino, Lianna Li, 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 42