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Alyna T Khan

Showing results (1-10 of 17) with videos related to

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Forensic Science International. Synergy|June 16, 2023
Perceptions of forensic scientists on statistical models, sequence data, and ethical implications for DNA evidence evaluations: A qualitative assessmentSanne E Aalbers, Alyna T Khan, Bruce S Weir
Cell Genomics|September 19, 2022
Recommendations on the use and reporting of race, ethnicity, and ancestry in genetic research: Experiences from the NHLBI TOPMed programAlyna T Khan, Stephanie M Gogarten, Caitlin P McHugh, et al.
American Journal of Human Genetics|June 13, 2025
A data model for population descriptors in genomic researchAlyna T Khan, Clement Adebamowo, Stephanie M Fullerton, et al.
Nature Genetics|November 25, 2025
Recommendations for responsible use of population descriptors in polygenic risk score developmentJohanna L Smith, Clement A Adebamowo, Sally N Adebamowo, et al.
Biorxiv : the Preprint Server for Biology|February 17, 2023
Full-length isoform sequencing for resolving the molecular basis of Charcot-Marie-Tooth 2AAndrew B Stergachis, Elizabeth E Blue, Madelyn A Gillentine, et al.
Neurology. Genetics|August 10, 2023
Full-length Isoform Sequencing for Resolving the Molecular Basis of Charcot-Marie-Tooth 2AAndrew B Stergachis, Elizabeth E Blue, Madelyn A Gillentine, et al.
Nature Communications|June 2, 2023
Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groupsNuzulul Kurniansyah, Matthew O Goodman, Alyna T Khan, et al.
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Journal of the American Heart Association|February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural VariantsKruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.
Medrxiv : the Preprint Server for Health Sciences|August 30, 2023
Rare damaging <i>CCR2</i> variants are associated with lower lifetime cardiovascular riskMarios K Georgakis, Rainer Malik, Omar El Bounkari, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Forensic Science International. Synergy|June 16, 2023
Perceptions of forensic scientists on statistical models, sequence data, and ethical implications for DNA evidence evaluations: A qualitative assessmentSanne E Aalbers, Alyna T Khan, Bruce S Weir
Cell Genomics|September 19, 2022
Recommendations on the use and reporting of race, ethnicity, and ancestry in genetic research: Experiences from the NHLBI TOPMed programAlyna T Khan, Stephanie M Gogarten, Caitlin P McHugh, et al.
American Journal of Human Genetics|June 13, 2025
A data model for population descriptors in genomic researchAlyna T Khan, Clement Adebamowo, Stephanie M Fullerton, et al.
Nature Genetics|November 25, 2025
Recommendations for responsible use of population descriptors in polygenic risk score developmentJohanna L Smith, Clement A Adebamowo, Sally N Adebamowo, et al.
Biorxiv : the Preprint Server for Biology|February 17, 2023
Full-length isoform sequencing for resolving the molecular basis of Charcot-Marie-Tooth 2AAndrew B Stergachis, Elizabeth E Blue, Madelyn A Gillentine, et al.
Neurology. Genetics|August 10, 2023
Full-length Isoform Sequencing for Resolving the Molecular Basis of Charcot-Marie-Tooth 2AAndrew B Stergachis, Elizabeth E Blue, Madelyn A Gillentine, et al.
Nature Communications|June 2, 2023
Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groupsNuzulul Kurniansyah, Matthew O Goodman, Alyna T Khan, et al.
Nature Communications|October 9, 2024
Rare variant contribution to the heritability of coronary artery diseaseGhislain Rocheleau, Shoa L Clarke, Gaëlle Auguste, et al.
Journal of the American Heart Association|February 14, 2025
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural VariantsKruthika R Iyer, Shoa L Clarke, Rodrigo Guarischi-Sousa, et al.
Medrxiv : the Preprint Server for Health Sciences|August 30, 2023
Rare damaging <i>CCR2</i> variants are associated with lower lifetime cardiovascular riskMarios K Georgakis, Rainer Malik, Omar El Bounkari, et al.
Pageof 2