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Cynthia A Prows

Showing results (71-80 of 87) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2019
Multi-site investigation of strategies for the clinical implementation of CYP2D6 genotyping to guide drug prescribingLarisa H Cavallari, Sara L Van Driest, Cynthia A Prows, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2025
Covering medical care costs for participants in the eMERGE Network: Challenges for equity and implementationLaura J Rasmussen-Torvik, Katherine E Bonini, Margaret H Harr, et al.
Journal of Medical Genetics|December 7, 2014
Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromesRobert B Hufnagel, Gavin Arno, Nichole D Hein, et al.
Journal of Personalized Medicine|January 6, 2018
Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) ExperienceRobyn Fossey, David Kochan, Erin Winkler, et al.
Journal of Genetic Counseling|October 19, 2021
Do research participants share genomic screening results with family members?Julia Wynn, Hila Milo Rasouly, Tania Vasquez-Loarte, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 7, 2026
Sequencing and health data resource of children of African ancestryLeah C Kottyan, Scott Richards, Morgan E Tracy, et al.
American Journal of Medical Genetics. Part A|February 8, 2023
A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall statureAlanna Strong, Soumya Rao, Sandra von Hardenberg, et al.
Journal of Personalized Medicine|May 1, 2020
Returning Results in the Genomic Era: Initial Experiences of the eMERGE NetworkGeorgia L Wiesner, Alanna Kulchak Rahm, Paul Appelbaum, et al.
Journal of Personalized Medicine|May 17, 2020
Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research NetworkJohn A Lynch, Richard R Sharp, Sharon A Aufox, et al.
Nature Genetics|July 14, 2015
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorderAlexander J Abrams, Robert B Hufnagel, Adriana Rebelo, et al.
Pageof 9

Showing results (71-80 of 87) with videos related to

Sort By:
Pageof 9
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2019
Multi-site investigation of strategies for the clinical implementation of CYP2D6 genotyping to guide drug prescribingLarisa H Cavallari, Sara L Van Driest, Cynthia A Prows, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2025
Covering medical care costs for participants in the eMERGE Network: Challenges for equity and implementationLaura J Rasmussen-Torvik, Katherine E Bonini, Margaret H Harr, et al.
Journal of Medical Genetics|December 7, 2014
Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromesRobert B Hufnagel, Gavin Arno, Nichole D Hein, et al.
Journal of Personalized Medicine|January 6, 2018
Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) ExperienceRobyn Fossey, David Kochan, Erin Winkler, et al.
Journal of Genetic Counseling|October 19, 2021
Do research participants share genomic screening results with family members?Julia Wynn, Hila Milo Rasouly, Tania Vasquez-Loarte, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 7, 2026
Sequencing and health data resource of children of African ancestryLeah C Kottyan, Scott Richards, Morgan E Tracy, et al.
American Journal of Medical Genetics. Part A|February 8, 2023
A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall statureAlanna Strong, Soumya Rao, Sandra von Hardenberg, et al.
Journal of Personalized Medicine|May 1, 2020
Returning Results in the Genomic Era: Initial Experiences of the eMERGE NetworkGeorgia L Wiesner, Alanna Kulchak Rahm, Paul Appelbaum, et al.
Journal of Personalized Medicine|May 17, 2020
Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research NetworkJohn A Lynch, Richard R Sharp, Sharon A Aufox, et al.
Nature Genetics|July 14, 2015
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorderAlexander J Abrams, Robert B Hufnagel, Adriana Rebelo, et al.
Pageof 9