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Maureen E Smith

Showing results (21-30 of 46) with videos related to

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Journal of Personalized Medicine|December 24, 2021
Defining the Critical Components of Informed Consent for Genetic TestingKelly E Ormond, Maia J Borensztein, Miranda L G Hallquist, et al.
Healthcare (Basel, Switzerland)|July 18, 2018
Harmonizing Outcomes for Genomic Medicine: Comparison of eMERGE Outcomes to ClinGen Outcome/Intervention PairsJanet L Williams, Wendy K Chung, Alex Fedotov, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 14, 2013
Stakeholder engagement: a key component of integrating genomic information into electronic health recordsAndrea Hartzler, Catherine A McCarty, Luke V Rasmussen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2020
Participant choices for return of genomic results in the eMERGE NetworkChristin Hoell, Julia Wynn, Luke V Rasmussen, et al.
Journal of the American Medical Informatics Association : JAMIA|December 28, 2018
Enrichment sampling for a multi-site patient survey using electronic health records and census dataNathaniel D Mercaldo, Kyle B Brothers, David S Carrell, et al.
The Journal of Molecular Diagnostics : JMD|May 16, 2017
Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx StudyLaura J Rasmussen-Torvik, Berta Almoguera, Kimberly F Doheny, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 25, 2012
Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) NetworkStephanie M Fullerton, Wendy A Wolf, Kyle B Brothers, et al.
BMC Research Notes|March 3, 2024
Genetic sex validation for sample tracking in next-generation sequencing clinical testingJianhong Hu, Viktoriya Korchina, Hana Zouk, et al.
Research Square|October 4, 2023
Genetic Sex Validation for Sample Tracking in Clinical TestingJianhong Hu, Viktoriya Korchina, Hana Zouk, et al.
Plos One|May 17, 2023
Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithmYoonjung Yoonie Joo, Jennifer A Pacheco, William K Thompson, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
Journal of Personalized Medicine|December 24, 2021
Defining the Critical Components of Informed Consent for Genetic TestingKelly E Ormond, Maia J Borensztein, Miranda L G Hallquist, et al.
Healthcare (Basel, Switzerland)|July 18, 2018
Harmonizing Outcomes for Genomic Medicine: Comparison of eMERGE Outcomes to ClinGen Outcome/Intervention PairsJanet L Williams, Wendy K Chung, Alex Fedotov, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 14, 2013
Stakeholder engagement: a key component of integrating genomic information into electronic health recordsAndrea Hartzler, Catherine A McCarty, Luke V Rasmussen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2020
Participant choices for return of genomic results in the eMERGE NetworkChristin Hoell, Julia Wynn, Luke V Rasmussen, et al.
Journal of the American Medical Informatics Association : JAMIA|December 28, 2018
Enrichment sampling for a multi-site patient survey using electronic health records and census dataNathaniel D Mercaldo, Kyle B Brothers, David S Carrell, et al.
The Journal of Molecular Diagnostics : JMD|May 16, 2017
Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx StudyLaura J Rasmussen-Torvik, Berta Almoguera, Kimberly F Doheny, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 25, 2012
Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) NetworkStephanie M Fullerton, Wendy A Wolf, Kyle B Brothers, et al.
BMC Research Notes|March 3, 2024
Genetic sex validation for sample tracking in next-generation sequencing clinical testingJianhong Hu, Viktoriya Korchina, Hana Zouk, et al.
Research Square|October 4, 2023
Genetic Sex Validation for Sample Tracking in Clinical TestingJianhong Hu, Viktoriya Korchina, Hana Zouk, et al.
Plos One|May 17, 2023
Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithmYoonjung Yoonie Joo, Jennifer A Pacheco, William K Thompson, et al.
Pageof 5