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Todd L Edwards

Showing results (151-160 of 203) with videos related to

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Nature Medicine|January 12, 2021
Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associationsJoseph Park, Anastasia M Lucas, Xinyuan Zhang, et al.
American Journal of Hypertension|September 24, 2019
Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working GroupMarguerite R Irvin, Colleen M Sitlani, James S Floyd, et al.
Frontiers in Genetics|January 1, 2024
Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine programNicole D Armstrong, Vinodh Srinivasasainagendra, Farah Ammous, et al.
Nature Genetics|June 17, 2020
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysisMarijana Vujkovic, Jacob M Keaton, Julie A Lynch, et al.
Circulation|September 28, 2020
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran ProgramDerek Klarin, Shefali Setia Verma, Renae Judy, et al.
Hypertension (Dallas, Tex. : 1979)|September 5, 2013
Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure lociTanika N Kelly, Fumihiko Takeuchi, Yasuharu Tabara, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 14, 2020
Mendelian Randomization of Circulating Polyunsaturated Fatty Acids and Colorectal Cancer RiskNikhil K Khankari, Barbara L Banbury, Maria C Borges, et al.
Nature Medicine|April 10, 2021
Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19Liam Gaziano, Claudia Giambartolomei, Alexandre C Pereira, et al.
Human Molecular Genetics|March 19, 2015
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individualsKevin T Nead, Aihua Li, Mackenzie R Wehner, et al.
Science (New York, N.Y.)|February 6, 2025
Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variantsHongbo Liu, Amin Abedini, Eunji Ha, et al.
Pageof 21

Showing results (151-160 of 203) with videos related to

Sort By:
Pageof 21
Nature Medicine|January 12, 2021
Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associationsJoseph Park, Anastasia M Lucas, Xinyuan Zhang, et al.
American Journal of Hypertension|September 24, 2019
Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working GroupMarguerite R Irvin, Colleen M Sitlani, James S Floyd, et al.
Frontiers in Genetics|January 1, 2024
Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine programNicole D Armstrong, Vinodh Srinivasasainagendra, Farah Ammous, et al.
Nature Genetics|June 17, 2020
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysisMarijana Vujkovic, Jacob M Keaton, Julie A Lynch, et al.
Circulation|September 28, 2020
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran ProgramDerek Klarin, Shefali Setia Verma, Renae Judy, et al.
Hypertension (Dallas, Tex. : 1979)|September 5, 2013
Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure lociTanika N Kelly, Fumihiko Takeuchi, Yasuharu Tabara, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 14, 2020
Mendelian Randomization of Circulating Polyunsaturated Fatty Acids and Colorectal Cancer RiskNikhil K Khankari, Barbara L Banbury, Maria C Borges, et al.
Nature Medicine|April 10, 2021
Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19Liam Gaziano, Claudia Giambartolomei, Alexandre C Pereira, et al.
Human Molecular Genetics|March 19, 2015
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individualsKevin T Nead, Aihua Li, Mackenzie R Wehner, et al.
Science (New York, N.Y.)|February 6, 2025
Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variantsHongbo Liu, Amin Abedini, Eunji Ha, et al.
Pageof 21