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Showing results (251-260 of 538) with videos related to

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Journal of Perinatal Medicine|August 19, 2020
COVID-19 in pregnancy: creating an outpatient surveillance model in a public hospital systemMegan E Trostle, Jenna S Silverstein, Elizabeth Tubridy, et al.
JAMA Internal Medicine|June 16, 2025
Diseases Common in Persons With Cystic Fibrosis Among CFTR HeterozygotesChenjie Zeng, Sangwoo T Han, Thomas A Cassini, et al.
Health Equity|November 14, 2019
Translational Health Disparities Research in a Data-Rich WorldNancy Breen, David Berrigan, James S Jackson, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|November 27, 2020
CYP2C19 Loss-of-Function is Associated with Increased Risk of Ischemic Stroke after Transient Ischemic Attack in Intracranial Atherosclerotic DiseasePious D Patel, Praveen Vimalathas, Xinnan Niu, et al.
Clinical Pharmacology and Therapeutics|January 30, 2018
Benefit of Preemptive Pharmacogenetic Information on Clinical OutcomeDan M Roden, Sara L Van Driest, Jonathan D Mosley, et al.
AMIA ... Annual Symposium Proceedings. AMIA Symposium|January 11, 2013
An evaluation of the NQF Quality Data Model for representing Electronic Health Record driven phenotyping algorithmsWilliam K Thompson, Luke V Rasmussen, Jennifer A Pacheco, et al.
Journal of Human Genetics|June 30, 2017
A common deletion in the haptoglobin gene associated with blood cholesterol levels among Chinese womenNeil S Zheng, Lisa A Bastarache, Julie A Bastarache, et al.
JNCI Cancer Spectrum|June 30, 2020
Evaluating the Utility of Polygenic Risk Scores in Identifying High-Risk Individuals for Eight Common CancersGuochong Jia, Yingchang Lu, Wanqing Wen, et al.
Journal of the American Medical Informatics Association : JAMIA|February 26, 2016
Harnessing next-generation informatics for personalizing medicine: a report from AMIA's 2014 Health Policy Invitational MeetingLaura K Wiley, Peter Tarczy-Hornoch, Joshua C Denny, et al.
Physiological Genomics|July 9, 2003
The sld mutation is specific for sublingual salivary mucous cells and disrupts apomucin gene expressionM A Fallon, L R Latchney, A R Hand, et al.
Pageof 54

Showing results (251-260 of 538) with videos related to

Sort By:
Pageof 54
Journal of Perinatal Medicine|August 19, 2020
COVID-19 in pregnancy: creating an outpatient surveillance model in a public hospital systemMegan E Trostle, Jenna S Silverstein, Elizabeth Tubridy, et al.
JAMA Internal Medicine|June 16, 2025
Diseases Common in Persons With Cystic Fibrosis Among CFTR HeterozygotesChenjie Zeng, Sangwoo T Han, Thomas A Cassini, et al.
Health Equity|November 14, 2019
Translational Health Disparities Research in a Data-Rich WorldNancy Breen, David Berrigan, James S Jackson, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|November 27, 2020
CYP2C19 Loss-of-Function is Associated with Increased Risk of Ischemic Stroke after Transient Ischemic Attack in Intracranial Atherosclerotic DiseasePious D Patel, Praveen Vimalathas, Xinnan Niu, et al.
Clinical Pharmacology and Therapeutics|January 30, 2018
Benefit of Preemptive Pharmacogenetic Information on Clinical OutcomeDan M Roden, Sara L Van Driest, Jonathan D Mosley, et al.
AMIA ... Annual Symposium Proceedings. AMIA Symposium|January 11, 2013
An evaluation of the NQF Quality Data Model for representing Electronic Health Record driven phenotyping algorithmsWilliam K Thompson, Luke V Rasmussen, Jennifer A Pacheco, et al.
Journal of Human Genetics|June 30, 2017
A common deletion in the haptoglobin gene associated with blood cholesterol levels among Chinese womenNeil S Zheng, Lisa A Bastarache, Julie A Bastarache, et al.
JNCI Cancer Spectrum|June 30, 2020
Evaluating the Utility of Polygenic Risk Scores in Identifying High-Risk Individuals for Eight Common CancersGuochong Jia, Yingchang Lu, Wanqing Wen, et al.
Journal of the American Medical Informatics Association : JAMIA|February 26, 2016
Harnessing next-generation informatics for personalizing medicine: a report from AMIA's 2014 Health Policy Invitational MeetingLaura K Wiley, Peter Tarczy-Hornoch, Joshua C Denny, et al.
Physiological Genomics|July 9, 2003
The sld mutation is specific for sublingual salivary mucous cells and disrupts apomucin gene expressionM A Fallon, L R Latchney, A R Hand, et al.
Pageof 54