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Richard M Sherva

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

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Neoplasia (New York, N.Y.)|February 23, 2018
Single Nucleotide Polymorphism Facilitated Down-Regulation of the Cohesin Stromal Antigen-1: Implications for Colorectal Cancer Racial DisparitiesSomenath Datta, Richard M Sherva, Mart De La Cruz, et al.
Exploration of Medicine|February 8, 2021
Identifying factors associated with opioid cessation in a biracial sample using machine learningJiayi W Cox, Richard M Sherva, Kathryn L Lunetta, et al.
Journal of Clinical Medicine|January 16, 2020
Genome-Wide Association Study of Opioid CessationJiayi W Cox, Richard M Sherva, Kathryn L Lunetta, et al.
JAMA Psychiatry|June 4, 2020
Association of OPRM1 Functional Coding Variant With Opioid Use Disorder: A Genome-Wide Association StudyHang Zhou, Christopher T Rentsch, Zhongshan Cheng, et al.
International Journal of Molecular Sciences|March 29, 2023
Heritable Risk and Protective Genetic Components of Glaucoma Medication Non-AdherenceJulie L Barr, Michael Feehan, Casey Tak, et al.
Cells|December 9, 2023
Patterns of Gene Expression, Splicing, and Allele-Specific Expression Vary among Macular Tissues and Clinical Stages of Age-Related Macular DegenerationTreefa Shwani, Charles Zhang, Leah A Owen, et al.
Blood|March 10, 2011
A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expressionJohn J Farrell, Richard M Sherva, Zhi-Yi Chen, et al.
Cell Reports. Medicine|April 16, 2025
A structural haplotype in the 17q21.31 MAPT region is associated with increased risk for chronic traumatic encephalopathy endophenotypesXudong Han, Yichi Zhang, Jillian N Petrosky, et al.
Medrxiv : the Preprint Server for Health Sciences|July 18, 2023
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies <i>LRRC4C, LHX5-AS1</i> and nominates ancestry-specific loci <i>PTPRK</i> , <i>GRB14</i> , and <i>KIAA0825</i> as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics ConsortiumFarid Rajabli, Penelope Benchek, Giuseppe Tosto, et al.
Genome Biology|July 17, 2025
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's diseaseFarid Rajabli, Penelope Benchek, Giuseppe Tosto, et al.
Pageof 1

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

Sort By:
Pageof 1
Neoplasia (New York, N.Y.)|February 23, 2018
Single Nucleotide Polymorphism Facilitated Down-Regulation of the Cohesin Stromal Antigen-1: Implications for Colorectal Cancer Racial DisparitiesSomenath Datta, Richard M Sherva, Mart De La Cruz, et al.
Exploration of Medicine|February 8, 2021
Identifying factors associated with opioid cessation in a biracial sample using machine learningJiayi W Cox, Richard M Sherva, Kathryn L Lunetta, et al.
Journal of Clinical Medicine|January 16, 2020
Genome-Wide Association Study of Opioid CessationJiayi W Cox, Richard M Sherva, Kathryn L Lunetta, et al.
JAMA Psychiatry|June 4, 2020
Association of OPRM1 Functional Coding Variant With Opioid Use Disorder: A Genome-Wide Association StudyHang Zhou, Christopher T Rentsch, Zhongshan Cheng, et al.
International Journal of Molecular Sciences|March 29, 2023
Heritable Risk and Protective Genetic Components of Glaucoma Medication Non-AdherenceJulie L Barr, Michael Feehan, Casey Tak, et al.
Cells|December 9, 2023
Patterns of Gene Expression, Splicing, and Allele-Specific Expression Vary among Macular Tissues and Clinical Stages of Age-Related Macular DegenerationTreefa Shwani, Charles Zhang, Leah A Owen, et al.
Blood|March 10, 2011
A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expressionJohn J Farrell, Richard M Sherva, Zhi-Yi Chen, et al.
Cell Reports. Medicine|April 16, 2025
A structural haplotype in the 17q21.31 MAPT region is associated with increased risk for chronic traumatic encephalopathy endophenotypesXudong Han, Yichi Zhang, Jillian N Petrosky, et al.
Medrxiv : the Preprint Server for Health Sciences|July 18, 2023
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies <i>LRRC4C, LHX5-AS1</i> and nominates ancestry-specific loci <i>PTPRK</i> , <i>GRB14</i> , and <i>KIAA0825</i> as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics ConsortiumFarid Rajabli, Penelope Benchek, Giuseppe Tosto, et al.
Genome Biology|July 17, 2025
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies known and novel cross-population and ancestry-specific associations as novel risk loci for Alzheimer's diseaseFarid Rajabli, Penelope Benchek, Giuseppe Tosto, et al.
Pageof 1