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Anna C F Lewis

Showing results (21-30 of 33) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|June 22, 2026
Long-term Penetrance of Disease Variants in Genes Prioritized for Genomic Newborn Screening: Evidence from Adult BiobanksNina B Gold, Hana Zouk, Julie Yeo, et al.
European Journal of Human Genetics : EJHG|May 8, 2026
Genomic newborn screening: a scoping review of the field's evolution and associated ethical, legal, and social implicationsGemma L Brown, Loren Walker, Mutiat A Afolabi, et al.
Journal of the American College of Cardiology|April 29, 2026
Development and Validation of a Clinical Polygenic Risk Report in U.S.-Based Health Systems for 8 Cardiovascular ConditionsAnika Misra, Amanda Jowell, Sara Haidermota, et al.
Genome Medicine|October 7, 2022
Patient and provider perspectives on polygenic risk scores: implications for clinical reporting and utilizationAnna C F Lewis, Emma F Perez, Anya E R Prince, et al.
Nature Genetics|September 9, 2024
Defining and pursuing diversity in human genetic studiesMaili C Raven-Adams, Tina Hernandez-Boussard, Yann Joly, et al.
Science (New York, N.Y.)|April 14, 2022
Getting genetic ancestry right for science and societyAnna C F Lewis, Santiago J Molina, Paul S Appelbaum, et al.
American Journal of Human Genetics|November 3, 2023
The GenoVA study: Equitable implementation of a pragmatic randomized trial of polygenic-risk scoring in primary careJason L Vassy, Charles A Brunette, Matthew S Lebo, et al.
Perspectives in Biology and Medicine|September 27, 2023
An Ethical Framework for Research Using Genetic AncestryAnna C F Lewis, Santiago J Molina, Paul S Appelbaum, et al.
Nature Medicine|April 19, 2022
Development of a clinical polygenic risk score assay and reporting workflowLimin Hao, Peter Kraft, Gabriel F Berriz, et al.
American Journal of Human Genetics|April 30, 2026
Navigating data sharing in researchAnna C F Lewis, Ellen W Clayton, Hana Bangash, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Medrxiv : the Preprint Server for Health Sciences|June 22, 2026
Long-term Penetrance of Disease Variants in Genes Prioritized for Genomic Newborn Screening: Evidence from Adult BiobanksNina B Gold, Hana Zouk, Julie Yeo, et al.
European Journal of Human Genetics : EJHG|May 8, 2026
Genomic newborn screening: a scoping review of the field's evolution and associated ethical, legal, and social implicationsGemma L Brown, Loren Walker, Mutiat A Afolabi, et al.
Journal of the American College of Cardiology|April 29, 2026
Development and Validation of a Clinical Polygenic Risk Report in U.S.-Based Health Systems for 8 Cardiovascular ConditionsAnika Misra, Amanda Jowell, Sara Haidermota, et al.
Genome Medicine|October 7, 2022
Patient and provider perspectives on polygenic risk scores: implications for clinical reporting and utilizationAnna C F Lewis, Emma F Perez, Anya E R Prince, et al.
Nature Genetics|September 9, 2024
Defining and pursuing diversity in human genetic studiesMaili C Raven-Adams, Tina Hernandez-Boussard, Yann Joly, et al.
Science (New York, N.Y.)|April 14, 2022
Getting genetic ancestry right for science and societyAnna C F Lewis, Santiago J Molina, Paul S Appelbaum, et al.
American Journal of Human Genetics|November 3, 2023
The GenoVA study: Equitable implementation of a pragmatic randomized trial of polygenic-risk scoring in primary careJason L Vassy, Charles A Brunette, Matthew S Lebo, et al.
Perspectives in Biology and Medicine|September 27, 2023
An Ethical Framework for Research Using Genetic AncestryAnna C F Lewis, Santiago J Molina, Paul S Appelbaum, et al.
Nature Medicine|April 19, 2022
Development of a clinical polygenic risk score assay and reporting workflowLimin Hao, Peter Kraft, Gabriel F Berriz, et al.
American Journal of Human Genetics|April 30, 2026
Navigating data sharing in researchAnna C F Lewis, Ellen W Clayton, Hana Bangash, et al.
Pageof 4