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Shannon Rego

Showing results (11-20 of 32) with videos related to

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Prenatal Diagnosis|May 31, 2021
Preference for secondary findings in prenatal and pediatric exome sequencingKate Swanson, Teresa N Sparks, Billie R Lianoglou, et al.
Plos Biology|January 13, 2017
Digital Health: Tracking Physiomes and Activity Using Wearable Biosensors Reveals Useful Health-Related InformationXiao Li, Jessilyn Dunn, Denis Salins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 22, 2023
Information-seeking preferences in diverse patients receiving a genetic testing result in the Clinical Sequencing Evidence-Generating Research (CSER) studyAnne Slavotinek, Hannah Prasad, Simon Outram, et al.
Cell Reports|September 9, 2020
iPSC Modeling of RBM20-Deficient DCM Identifies Upregulation of RBM20 as a Therapeutic StrategyFrancesca Briganti, Han Sun, Wu Wei, et al.
Journal of Genetic Counseling|February 2, 2019
Developing a genomics rotation: Practical training around variant interpretation for genetic counseling studentsMegan E Grove, Shana White, Dianna G Fisk, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 9, 2022
Perspectives and preferences regarding genomic secondary findings in underrepresented prenatal and pediatric populations: A mixed-methods approachShannon Rego, Hannah Hoban, Simon Outram, et al.
American Journal of Medical Genetics. Part A|December 28, 2019
A novel truncating variant in ring finger protein 113A (RNF113A) confirms the association of this gene with X-linked trichothiodystrophyBryce A Mendelsohn, Daniah T Beleford, Aya Abu-El-Haija, et al.
Cold Spring Harbor Molecular Case Studies|November 30, 2018
High-frequency actionable pathogenic exome variants in an average-risk cohortShannon Rego, Orit Dagan-Rosenfeld, Wenyu Zhou, et al.
Plos Genetics|September 21, 2020
Candidate variants in TUB are associated with familial tremorM Reza Sailani, Fereshteh Jahanbani, Charles W Abbott, et al.
Human Genetics|January 6, 2017
Association of AHSG with alopecia and mental retardation (APMR) syndromeM Reza Sailani, Fereshteh Jahanbani, Jafar Nasiri, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Prenatal Diagnosis|May 31, 2021
Preference for secondary findings in prenatal and pediatric exome sequencingKate Swanson, Teresa N Sparks, Billie R Lianoglou, et al.
Plos Biology|January 13, 2017
Digital Health: Tracking Physiomes and Activity Using Wearable Biosensors Reveals Useful Health-Related InformationXiao Li, Jessilyn Dunn, Denis Salins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 22, 2023
Information-seeking preferences in diverse patients receiving a genetic testing result in the Clinical Sequencing Evidence-Generating Research (CSER) studyAnne Slavotinek, Hannah Prasad, Simon Outram, et al.
Cell Reports|September 9, 2020
iPSC Modeling of RBM20-Deficient DCM Identifies Upregulation of RBM20 as a Therapeutic StrategyFrancesca Briganti, Han Sun, Wu Wei, et al.
Journal of Genetic Counseling|February 2, 2019
Developing a genomics rotation: Practical training around variant interpretation for genetic counseling studentsMegan E Grove, Shana White, Dianna G Fisk, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 9, 2022
Perspectives and preferences regarding genomic secondary findings in underrepresented prenatal and pediatric populations: A mixed-methods approachShannon Rego, Hannah Hoban, Simon Outram, et al.
American Journal of Medical Genetics. Part A|December 28, 2019
A novel truncating variant in ring finger protein 113A (RNF113A) confirms the association of this gene with X-linked trichothiodystrophyBryce A Mendelsohn, Daniah T Beleford, Aya Abu-El-Haija, et al.
Cold Spring Harbor Molecular Case Studies|November 30, 2018
High-frequency actionable pathogenic exome variants in an average-risk cohortShannon Rego, Orit Dagan-Rosenfeld, Wenyu Zhou, et al.
Plos Genetics|September 21, 2020
Candidate variants in TUB are associated with familial tremorM Reza Sailani, Fereshteh Jahanbani, Charles W Abbott, et al.
Human Genetics|January 6, 2017
Association of AHSG with alopecia and mental retardation (APMR) syndromeM Reza Sailani, Fereshteh Jahanbani, Jafar Nasiri, et al.
Pageof 4