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Showing results (771-780 of 1,201) with videos related to

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Cell Reports. Medicine|December 13, 2022
Correlations between complex human phenotypes vary by genetic background, gender, and environmentMichael Elgart, Matthew O Goodman, Carmen Isasi, et al.
Nature|November 7, 2018
Publisher Correction: Functional aspects of meningeal lymphatics in ageing and Alzheimer's diseaseSandro Da Mesquita, Antoine Louveau, Andrea Vaccari, et al.
Communications Biology|August 22, 2022
Non-linear machine learning models incorporating SNPs and PRS improve polygenic prediction in diverse human populationsMichael Elgart, Genevieve Lyons, Santiago Romero-Brufau, et al.
American Journal of Human Genetics|January 5, 2024
Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effectsSilva Kasela, François Aguet, Sarah Kim-Hellmuth, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2023
Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effectsSilva Kasela, François Aguet, Sarah Kim-Hellmuth, et al.
Communications Biology|August 16, 2023
Genome-wide association studies and fine-mapping identify genomic loci for n-3 and n-6 polyunsaturated fatty acids in Hispanic American and African American cohortsChaojie Yang, Jenna Veenstra, Traci M Bartz, et al.
Arthritis Research|September 11, 2001
Genetic linkage and transmission disequilibrium of marker haplotypes at chromosome 1q41 in human systemic lupus erythematosusR R Graham, C D Langefeld, P M Gaffney, et al.
Diabetes Care|November 21, 2018
Variations in Risk of End-Stage Renal Disease and Risk of Mortality in an International Study of Patients With Type 1 Diabetes and Advanced NephropathyJan Skupien, Adam M Smiles, Erkka Valo, et al.
Human Molecular Genetics|November 5, 1999
Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)T Sahoo, E W Johnson, J W Thomas, et al.
Mayo Clinic Proceedings|August 23, 2025
Association of Pathogenic/Likely Pathogenic Inherited Cardiomyopathy Variants With Heart Failure: A TOPMed Multiancestry AnalysisNaman S Shetty, Mokshad Gaonkar, Akhil Pampana, et al.
Pageof 121

Showing results (771-780 of 1,201) with videos related to

Sort By:
Pageof 121
Cell Reports. Medicine|December 13, 2022
Correlations between complex human phenotypes vary by genetic background, gender, and environmentMichael Elgart, Matthew O Goodman, Carmen Isasi, et al.
Nature|November 7, 2018
Publisher Correction: Functional aspects of meningeal lymphatics in ageing and Alzheimer's diseaseSandro Da Mesquita, Antoine Louveau, Andrea Vaccari, et al.
Communications Biology|August 22, 2022
Non-linear machine learning models incorporating SNPs and PRS improve polygenic prediction in diverse human populationsMichael Elgart, Genevieve Lyons, Santiago Romero-Brufau, et al.
American Journal of Human Genetics|January 5, 2024
Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effectsSilva Kasela, François Aguet, Sarah Kim-Hellmuth, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2023
Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effectsSilva Kasela, François Aguet, Sarah Kim-Hellmuth, et al.
Communications Biology|August 16, 2023
Genome-wide association studies and fine-mapping identify genomic loci for n-3 and n-6 polyunsaturated fatty acids in Hispanic American and African American cohortsChaojie Yang, Jenna Veenstra, Traci M Bartz, et al.
Arthritis Research|September 11, 2001
Genetic linkage and transmission disequilibrium of marker haplotypes at chromosome 1q41 in human systemic lupus erythematosusR R Graham, C D Langefeld, P M Gaffney, et al.
Diabetes Care|November 21, 2018
Variations in Risk of End-Stage Renal Disease and Risk of Mortality in an International Study of Patients With Type 1 Diabetes and Advanced NephropathyJan Skupien, Adam M Smiles, Erkka Valo, et al.
Human Molecular Genetics|November 5, 1999
Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)T Sahoo, E W Johnson, J W Thomas, et al.
Mayo Clinic Proceedings|August 23, 2025
Association of Pathogenic/Likely Pathogenic Inherited Cardiomyopathy Variants With Heart Failure: A TOPMed Multiancestry AnalysisNaman S Shetty, Mokshad Gaonkar, Akhil Pampana, et al.
Pageof 121