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Ira M Hall

Showing results (41-50 of 54) with videos related to

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American Journal of Human Genetics|April 2, 2021
Association of structural variation with cardiometabolic traits in FinnsLei Chen, Haley J Abel, Indraniel Das, et al.
Cell|April 17, 2021
Population-scale tissue transcriptomics maps long non-coding RNAs to complex diseaseOlivia M de Goede, Daniel C Nachun, Nicole M Ferraro, et al.
Nature Genetics|March 6, 2012
Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integrationColby Chiang, Jessie C Jacobsen, Carl Ernst, et al.
Cell Genomics|February 24, 2022
Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-spaceMichael C Schatz, Anthony A Philippakis, Enis Afgan, et al.
American Journal of Human Genetics|September 2, 2022
Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease riskXianyong Yin, Debraj Bose, Annie Kwon, et al.
Nature Communications|March 29, 2022
Genome-wide association studies of metabolites in Finnish men identify disease-relevant lociXianyong Yin, Lap Sum Chan, Debraj Bose, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Single cell variant to enhancer to gene map for coronary artery diseaseJunedh M Amrute, Paul C Lee, Ittai Eres, et al.
Nature|April 21, 2022
The Human Pangenome Project: a global resource to map genomic diversityTing Wang, Lucinda Antonacci-Fulton, Kerstin Howe, et al.
Nature|August 2, 2019
Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.
Nature|November 6, 2019
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|April 2, 2021
Association of structural variation with cardiometabolic traits in FinnsLei Chen, Haley J Abel, Indraniel Das, et al.
Cell|April 17, 2021
Population-scale tissue transcriptomics maps long non-coding RNAs to complex diseaseOlivia M de Goede, Daniel C Nachun, Nicole M Ferraro, et al.
Nature Genetics|March 6, 2012
Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integrationColby Chiang, Jessie C Jacobsen, Carl Ernst, et al.
Cell Genomics|February 24, 2022
Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-spaceMichael C Schatz, Anthony A Philippakis, Enis Afgan, et al.
American Journal of Human Genetics|September 2, 2022
Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease riskXianyong Yin, Debraj Bose, Annie Kwon, et al.
Nature Communications|March 29, 2022
Genome-wide association studies of metabolites in Finnish men identify disease-relevant lociXianyong Yin, Lap Sum Chan, Debraj Bose, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Single cell variant to enhancer to gene map for coronary artery diseaseJunedh M Amrute, Paul C Lee, Ittai Eres, et al.
Nature|April 21, 2022
The Human Pangenome Project: a global resource to map genomic diversityTing Wang, Lucinda Antonacci-Fulton, Kerstin Howe, et al.
Nature|August 2, 2019
Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.
Nature|November 6, 2019
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.
Pageof 6