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Joshua D Smith

Showing results (121-130 of 194) with videos related to

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Head & Neck|December 15, 2018
Mutational profiles of persistent/recurrent laryngeal squamous cell carcinomaJoshua D Smith, Andrew C Birkeland, Andrew J Rosko, et al.
Circulation. Cardiovascular Genetics|October 6, 2009
Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replicationDaniel I Chasman, Guillaume Paré, Robert Y L Zee, et al.
Circulation. Cardiovascular Genetics|July 17, 2016
Association of Exome Sequences With Cardiovascular Traits Among Blacks in the Jackson Heart StudyGina M Peloso, Leslie A Lange, Tibor V Varga, et al.
Frontiers in Genetics|March 8, 2021
Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify <i>MYRIP</i>, <i>TRAPPC11</i>, and <i>SLC27A6</i> of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry PopulationMarguerite R Irvin, Praful Aggarwal, Steven A Claas, et al.
Communications Biology|January 31, 2023
An integrated multi-omics analysis of sleep-disordered breathing traits implicates P2XR4 purinergic signalingNuzulul Kurniansyah, Danielle A Wallace, Ying Zhang, et al.
American Journal of Human Genetics|January 1, 2013
Whole-genome analysis reveals that mutations in inositol polyphosphate phosphatase-like 1 cause opsismodysplasiaJennifer E Below, Dawn L Earl, Kathryn M Shively, et al.
Biorxiv : the Preprint Server for Biology|April 27, 2026
Long-read MitoScope reveals tissue-resolved somatic mitochondrial variation and landscape of nuclear-embedded mitochondrial sequencesChristina Zakarian, Joshua D Smith, Chee Hong Wong, et al.
American Journal of Human Genetics|April 29, 2008
Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive proteinAlexander P Reiner, Mathew J Barber, Yongtao Guan, et al.
Genome Medicine|March 29, 2022
Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research ProgramEric Venner, Donna Muzny, Joshua D Smith, et al.
Human Genetics|February 27, 2019
Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein-Taybi syndrome: the interconnections of epigenetic machinery disordersGloria Negri, Pamela Magini, Donatella Milani, et al.
Pageof 20

Showing results (121-130 of 194) with videos related to

Sort By:
Pageof 20
Head & Neck|December 15, 2018
Mutational profiles of persistent/recurrent laryngeal squamous cell carcinomaJoshua D Smith, Andrew C Birkeland, Andrew J Rosko, et al.
Circulation. Cardiovascular Genetics|October 6, 2009
Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replicationDaniel I Chasman, Guillaume Paré, Robert Y L Zee, et al.
Circulation. Cardiovascular Genetics|July 17, 2016
Association of Exome Sequences With Cardiovascular Traits Among Blacks in the Jackson Heart StudyGina M Peloso, Leslie A Lange, Tibor V Varga, et al.
Frontiers in Genetics|March 8, 2021
Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify <i>MYRIP</i>, <i>TRAPPC11</i>, and <i>SLC27A6</i> of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry PopulationMarguerite R Irvin, Praful Aggarwal, Steven A Claas, et al.
Communications Biology|January 31, 2023
An integrated multi-omics analysis of sleep-disordered breathing traits implicates P2XR4 purinergic signalingNuzulul Kurniansyah, Danielle A Wallace, Ying Zhang, et al.
American Journal of Human Genetics|January 1, 2013
Whole-genome analysis reveals that mutations in inositol polyphosphate phosphatase-like 1 cause opsismodysplasiaJennifer E Below, Dawn L Earl, Kathryn M Shively, et al.
Biorxiv : the Preprint Server for Biology|April 27, 2026
Long-read MitoScope reveals tissue-resolved somatic mitochondrial variation and landscape of nuclear-embedded mitochondrial sequencesChristina Zakarian, Joshua D Smith, Chee Hong Wong, et al.
American Journal of Human Genetics|April 29, 2008
Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive proteinAlexander P Reiner, Mathew J Barber, Yongtao Guan, et al.
Genome Medicine|March 29, 2022
Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research ProgramEric Venner, Donna Muzny, Joshua D Smith, et al.
Human Genetics|February 27, 2019
Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein-Taybi syndrome: the interconnections of epigenetic machinery disordersGloria Negri, Pamela Magini, Donatella Milani, et al.
Pageof 20