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Shannon Rego

Showing results (21-30 of 32) with videos related to

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Journal of Genetic Counseling|December 5, 2020
A review and definition of 'usual care' in genetic counseling trials to standardize use in researchBarbara B Biesecker, Sarah E Lillie, Laura M Amendola, et al.
Journal of Personalized Medicine|April 3, 2021
Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER ConsortiumSabrina A Suckiel, Julianne M O'Daniel, Katherine E Donohue, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 1, 2022
Integration of stakeholder engagement from development to dissemination in genomic medicine research: Approaches and outcomes from the CSER ConsortiumJulianne M O'Daniel, Sara Ackerman, Lauren R Desrosiers, et al.
Human Mutation|October 13, 2018
Evidence-based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working GroupElizabeth M Webber, Jessica Ezzell Hunter, Leslie G Biesecker, et al.
Human Mutation|May 4, 2021
New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency DisorderJustin O Szot, Anne Slavotinek, Karen Chong, et al.
Nature Medicine|May 10, 2019
A longitudinal big data approach for precision healthSophia Miryam Schüssler-Fiorenza Rose, Kévin Contrepois, Kegan J Moneghetti, et al.
Cell Systems|January 24, 2018
Integrative Personal Omics Profiles during Periods of Weight Gain and LossBrian D Piening, Wenyu Zhou, Kévin Contrepois, et al.
NPJ Genomic Medicine|May 26, 2023
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse populationAnne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
Nature|May 31, 2019
Longitudinal multi-omics of host-microbe dynamics in prediabetesWenyu Zhou, M Reza Sailani, Kévin Contrepois, et al.
American Journal of Human Genetics|February 24, 2022
Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndromeFederico Tessadori, Karen Duran, Karen Knapp, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Journal of Genetic Counseling|December 5, 2020
A review and definition of 'usual care' in genetic counseling trials to standardize use in researchBarbara B Biesecker, Sarah E Lillie, Laura M Amendola, et al.
Journal of Personalized Medicine|April 3, 2021
Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER ConsortiumSabrina A Suckiel, Julianne M O'Daniel, Katherine E Donohue, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 1, 2022
Integration of stakeholder engagement from development to dissemination in genomic medicine research: Approaches and outcomes from the CSER ConsortiumJulianne M O'Daniel, Sara Ackerman, Lauren R Desrosiers, et al.
Human Mutation|October 13, 2018
Evidence-based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working GroupElizabeth M Webber, Jessica Ezzell Hunter, Leslie G Biesecker, et al.
Human Mutation|May 4, 2021
New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency DisorderJustin O Szot, Anne Slavotinek, Karen Chong, et al.
Nature Medicine|May 10, 2019
A longitudinal big data approach for precision healthSophia Miryam Schüssler-Fiorenza Rose, Kévin Contrepois, Kegan J Moneghetti, et al.
Cell Systems|January 24, 2018
Integrative Personal Omics Profiles during Periods of Weight Gain and LossBrian D Piening, Wenyu Zhou, Kévin Contrepois, et al.
NPJ Genomic Medicine|May 26, 2023
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse populationAnne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
Nature|May 31, 2019
Longitudinal multi-omics of host-microbe dynamics in prediabetesWenyu Zhou, M Reza Sailani, Kévin Contrepois, et al.
American Journal of Human Genetics|February 24, 2022
Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndromeFederico Tessadori, Karen Duran, Karen Knapp, et al.
Pageof 4