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Flavia Chen

Showing results (1-10 of 13) with videos related to

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The Hastings Center Report|August 23, 2018
Sequencing Newborns: A Call for Nuanced Use of Genomic TechnologiesJosephine Johnston, John D Lantos, Aaron Goldenberg, et al.
Pediatrics|January 6, 2016
Parental Views on Expanded Newborn Screening Using Whole-Genome SequencingGalen Joseph, Flavia Chen, Julie Harris-Wai, et al.
Human Mutation|October 26, 2017
Whole exome and whole genome sequencing with dried blood spot DNA without whole genome amplificationLaia Bassaganyas, George Freedman, Dedeepya Vaka, et al.
Health Affairs (Project Hope)|March 6, 2023
Community-Based Outbreak Investigation And Response: Enhancing Preparedness, Public Health Capacity, And EquityShefali Oza, Flavia Chen, Victoria Selser, et al.
Prenatal Diagnosis|May 31, 2021
Preference for secondary findings in prenatal and pediatric exome sequencingKate Swanson, Teresa N Sparks, Billie R Lianoglou, et al.
NPJ Genomic Medicine|December 17, 2019
FDA oversight of NSIGHT genomic research: the need for an integrated systems approach to regulationLaura V Milko, Flavia Chen, Kee Chan, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2022
Cost-effectiveness frameworks for comparing genome and exome sequencing versus conventional diagnostic pathways: A scoping review and recommended methodsBart S Ferket, Zach Baldwin, Priyanka Murali, et al.
HGG Advances|June 16, 2022
Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experienceKathleen D Muenzen, Laura M Amendola, Tia L Kauffman, et al.
Nature Medicine|August 12, 2020
The role of exome sequencing in newborn screening for inborn errors of metabolismAashish N Adhikari, Renata C Gallagher, Yaqiong Wang, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
The Hastings Center Report|August 23, 2018
Sequencing Newborns: A Call for Nuanced Use of Genomic TechnologiesJosephine Johnston, John D Lantos, Aaron Goldenberg, et al.
Pediatrics|January 6, 2016
Parental Views on Expanded Newborn Screening Using Whole-Genome SequencingGalen Joseph, Flavia Chen, Julie Harris-Wai, et al.
Human Mutation|October 26, 2017
Whole exome and whole genome sequencing with dried blood spot DNA without whole genome amplificationLaia Bassaganyas, George Freedman, Dedeepya Vaka, et al.
Health Affairs (Project Hope)|March 6, 2023
Community-Based Outbreak Investigation And Response: Enhancing Preparedness, Public Health Capacity, And EquityShefali Oza, Flavia Chen, Victoria Selser, et al.
Prenatal Diagnosis|May 31, 2021
Preference for secondary findings in prenatal and pediatric exome sequencingKate Swanson, Teresa N Sparks, Billie R Lianoglou, et al.
NPJ Genomic Medicine|December 17, 2019
FDA oversight of NSIGHT genomic research: the need for an integrated systems approach to regulationLaura V Milko, Flavia Chen, Kee Chan, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2022
Cost-effectiveness frameworks for comparing genome and exome sequencing versus conventional diagnostic pathways: A scoping review and recommended methodsBart S Ferket, Zach Baldwin, Priyanka Murali, et al.
HGG Advances|June 16, 2022
Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experienceKathleen D Muenzen, Laura M Amendola, Tia L Kauffman, et al.
Nature Medicine|August 12, 2020
The role of exome sequencing in newborn screening for inborn errors of metabolismAashish N Adhikari, Renata C Gallagher, Yaqiong Wang, et al.
Pageof 2