相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Returning negative results from large-scale genomic screening: Experiences from the eMERGE III network
Kelsey Stuttgen Finn et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2021)
Preferences of biobank participants for receiving actionable genomic test results: results of a recontacting study
Nora B. Henrikson et al.
GENETICS IN MEDICINE (2021)
ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)
David T. Miller et al.
GENETICS IN MEDICINE (2021)
Adolescents' and Parents' Genomic Testing Decisions: Associations With Age, Race, and Sex
Melanie F. Myers et al.
JOURNAL OF ADOLESCENT HEALTH (2020)
Frequency of genomic secondary findings among 21,915 eMERGE network participants
Adam S. Gordon et al.
GENETICS IN MEDICINE (2020)
Participant choices for return of genomic results in the eMERGE Network
Christin Hoell et al.
GENETICS IN MEDICINE (2020)
Population genetic screening efficiently identifies carriers of autosomal dominant diseases
J. J. Grzymski et al.
NATURE MEDICINE (2020)
Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network
Hana Zouk et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2019)
The All of Us Research Program
NEW ENGLAND JOURNAL OF MEDICINE (2019)
The past, present and future of service delivery in genetic counseling: Keeping up in the era of precision medicine
Katie Stoll et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2018)
A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort
Marci L. B. Schwartz et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2018)
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations
Laura M. Amendola et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2018)
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics
Sarah S. Kalia et al.
GENETICS IN MEDICINE (2017)
The IGNITE network: a model for genomic medicine implementation and research
Kristin Wiisanen Weitzel et al.
BMC MEDICAL GENOMICS (2016)
ClinGen - The Clinical Genome Resource
Heidi L. Rehm et al.
NEW ENGLAND JOURNAL OF MEDICINE (2015)
Modes of delivery of genetic testing services and the uptake of cancer risk management strategies in BRCA1 and BRCA2 carriers
T. Pal et al.
CLINICAL GENETICS (2014)