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Sarah E Topol

Showing results (1-10 of 9) with videos related to

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Science (New York, N.Y.)|December 3, 2003
Mutation of MEF2A in an inherited disorder with features of coronary artery diseaseLejin Wang, Chun Fan, Sarah E Topol, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2017
Mutation of WIF1: a potential novel cause of a Nail-Patella-like disorderMarilyn C Jones, Sarah E Topol, Manuel Rueda, et al.
Frontiers in Cardiovascular Medicine|February 3, 2018
Corrigendum: Molecular Autopsy for Sudden Death in the Young: Is Data Aggregation the Key?Manuel Rueda, Jennifer L Wagner, Tierney C Phillips, et al.
Frontiers in Cardiovascular Medicine|November 29, 2017
Molecular Autopsy for Sudden Death in the Young: Is Data Aggregation the Key?Manuel Rueda, Jennifer L Wagner, Tierney C Phillips, et al.
Genome Medicine|December 19, 2019
Re-analysis of whole-exome sequencing data uncovers novel diagnostic variants and improves molecular diagnostic yields for sudden death and idiopathic diseasesElias L Salfati, Emily G Spencer, Sarah E Topol, et al.
Human Molecular Genetics|November 20, 2018
Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathyDavid Pacheu-Grau, Sylvie Callegari, Sonia Emperador, et al.
Cell|April 27, 2016
Whole-Genome Sequencing of a Healthy Aging CohortGalina A Erikson, Dale L Bodian, Manuel Rueda, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2015
A genome sequencing program for novel undiagnosed diseasesCinnamon S Bloss, Ashley A Scott-Van Zeeland, Sarah E Topol, et al.
Annals of Neurology|April 5, 2014
Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymiaYing-Zhang Chen, Jennifer R Friedman, Dong-Hui Chen, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Science (New York, N.Y.)|December 3, 2003
Mutation of MEF2A in an inherited disorder with features of coronary artery diseaseLejin Wang, Chun Fan, Sarah E Topol, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2017
Mutation of WIF1: a potential novel cause of a Nail-Patella-like disorderMarilyn C Jones, Sarah E Topol, Manuel Rueda, et al.
Frontiers in Cardiovascular Medicine|February 3, 2018
Corrigendum: Molecular Autopsy for Sudden Death in the Young: Is Data Aggregation the Key?Manuel Rueda, Jennifer L Wagner, Tierney C Phillips, et al.
Frontiers in Cardiovascular Medicine|November 29, 2017
Molecular Autopsy for Sudden Death in the Young: Is Data Aggregation the Key?Manuel Rueda, Jennifer L Wagner, Tierney C Phillips, et al.
Genome Medicine|December 19, 2019
Re-analysis of whole-exome sequencing data uncovers novel diagnostic variants and improves molecular diagnostic yields for sudden death and idiopathic diseasesElias L Salfati, Emily G Spencer, Sarah E Topol, et al.
Human Molecular Genetics|November 20, 2018
Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathyDavid Pacheu-Grau, Sylvie Callegari, Sonia Emperador, et al.
Cell|April 27, 2016
Whole-Genome Sequencing of a Healthy Aging CohortGalina A Erikson, Dale L Bodian, Manuel Rueda, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2015
A genome sequencing program for novel undiagnosed diseasesCinnamon S Bloss, Ashley A Scott-Van Zeeland, Sarah E Topol, et al.
Annals of Neurology|April 5, 2014
Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymiaYing-Zhang Chen, Jennifer R Friedman, Dong-Hui Chen, et al.
Pageof 1