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Stacey Gabriel

Showing results (51-60 of 195) with videos related to

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International Journal of Obesity (2005)|December 3, 2022
Gene expression associations with body mass index in the Multi-Ethnic Study of AtherosclerosisLuciana B Vargas, Leslie A Lange, Kendra Ferrier, et al.
Science (New York, N.Y.)|December 16, 2021
Pangenomics enables genotyping of known structural variants in 5202 diverse genomesJouni Sirén, Jean Monlong, Xian Chang, et al.
Nature|December 2, 2016
Genomic evolution and chemoresistance in germ-cell tumoursAmaro Taylor-Weiner, Travis Zack, Elizabeth O'Donnell, et al.
Circulation. Cardiovascular Genetics|July 17, 2016
Association of Exome Sequences With Cardiovascular Traits Among Blacks in the Jackson Heart StudyGina M Peloso, Leslie A Lange, Tibor V Varga, et al.
The New England Journal of Medicine|June 22, 2017
Clonal Hematopoiesis and Risk of Atherosclerotic Cardiovascular DiseaseSiddhartha Jaiswal, Pradeep Natarajan, Alexander J Silver, et al.
American Journal of Human Genetics|July 26, 2016
Biallelic Mutations in Citron Kinase Link Mitotic Cytokinesis to Human Primary MicrocephalyHongda Li, Stephanie L Bielas, Maha S Zaki, et al.
Nature Genetics|May 25, 2023
Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architectureLinda Kachuri, Angel C Y Mak, Donglei Hu, et al.
Genome Medicine|March 29, 2022
Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research ProgramEric Venner, Donna Muzny, Joshua D Smith, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Integration of dilated cardiomyopathy genomics with transcriptomics from the human heart implicates regulatory molecular mechanismsConnor S Murray, Chaojie Yang, Suet Nee Chen, et al.
American Journal of Human Genetics|March 5, 2013
Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasiaNaiara Akizu, Nuri M Shembesh, Tawfeg Ben-Omran, et al.
Pageof 20

Showing results (51-60 of 195) with videos related to

Sort By:
Pageof 20
International Journal of Obesity (2005)|December 3, 2022
Gene expression associations with body mass index in the Multi-Ethnic Study of AtherosclerosisLuciana B Vargas, Leslie A Lange, Kendra Ferrier, et al.
Science (New York, N.Y.)|December 16, 2021
Pangenomics enables genotyping of known structural variants in 5202 diverse genomesJouni Sirén, Jean Monlong, Xian Chang, et al.
Nature|December 2, 2016
Genomic evolution and chemoresistance in germ-cell tumoursAmaro Taylor-Weiner, Travis Zack, Elizabeth O'Donnell, et al.
Circulation. Cardiovascular Genetics|July 17, 2016
Association of Exome Sequences With Cardiovascular Traits Among Blacks in the Jackson Heart StudyGina M Peloso, Leslie A Lange, Tibor V Varga, et al.
The New England Journal of Medicine|June 22, 2017
Clonal Hematopoiesis and Risk of Atherosclerotic Cardiovascular DiseaseSiddhartha Jaiswal, Pradeep Natarajan, Alexander J Silver, et al.
American Journal of Human Genetics|July 26, 2016
Biallelic Mutations in Citron Kinase Link Mitotic Cytokinesis to Human Primary MicrocephalyHongda Li, Stephanie L Bielas, Maha S Zaki, et al.
Nature Genetics|May 25, 2023
Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architectureLinda Kachuri, Angel C Y Mak, Donglei Hu, et al.
Genome Medicine|March 29, 2022
Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research ProgramEric Venner, Donna Muzny, Joshua D Smith, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Integration of dilated cardiomyopathy genomics with transcriptomics from the human heart implicates regulatory molecular mechanismsConnor S Murray, Chaojie Yang, Suet Nee Chen, et al.
American Journal of Human Genetics|March 5, 2013
Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasiaNaiara Akizu, Nuri M Shembesh, Tawfeg Ben-Omran, et al.
Pageof 20