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Sarah C Nelson

Showing results (31-40 of 50) with videos related to

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Human Genetics|February 8, 2011
Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery diseaseMollie A Minear, David R Crosslin, Beth S Sutton, et al.
Cancer Genetics|March 12, 2014
Acquired chromosomal anomalies in chronic lymphocytic leukemia patients compared with more than 50,000 quasi-normal participantsCathy C Laurie, Cecelia A Laurie, Stephanie A Smoley, et al.
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.
Nature Genetics|September 9, 2024
Defining and pursuing diversity in human genetic studiesMaili C Raven-Adams, Tina Hernandez-Boussard, Yann Joly, et al.
American Journal of Human Genetics|November 19, 2024
The PRIMED Consortium: Reducing disparities in polygenic risk assessmentIftikhar J Kullo, Matthew P Conomos, Sarah C Nelson, et al.
BMC Oral Health|December 25, 2012
Genome-wide association scan of dental caries in the permanent dentitionXiaojing Wang, John R Shaffer, Zhen Zeng, 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.
Human Genetics|November 1, 2011
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE NetworkDavid R Crosslin, Andrew McDavid, Noah Weston, 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.
American Journal of Human Genetics|January 26, 2016
Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino AmericansUrsula M Schick, Deepti Jain, Chani J Hodonsky, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Human Genetics|February 8, 2011
Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery diseaseMollie A Minear, David R Crosslin, Beth S Sutton, et al.
Cancer Genetics|March 12, 2014
Acquired chromosomal anomalies in chronic lymphocytic leukemia patients compared with more than 50,000 quasi-normal participantsCathy C Laurie, Cecelia A Laurie, Stephanie A Smoley, et al.
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.
Nature Genetics|September 9, 2024
Defining and pursuing diversity in human genetic studiesMaili C Raven-Adams, Tina Hernandez-Boussard, Yann Joly, et al.
American Journal of Human Genetics|November 19, 2024
The PRIMED Consortium: Reducing disparities in polygenic risk assessmentIftikhar J Kullo, Matthew P Conomos, Sarah C Nelson, et al.
BMC Oral Health|December 25, 2012
Genome-wide association scan of dental caries in the permanent dentitionXiaojing Wang, John R Shaffer, Zhen Zeng, 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.
Human Genetics|November 1, 2011
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE NetworkDavid R Crosslin, Andrew McDavid, Noah Weston, 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.
American Journal of Human Genetics|January 26, 2016
Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino AmericansUrsula M Schick, Deepti Jain, Chani J Hodonsky, et al.
Pageof 5