The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.
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Marc S. Williams | W. Chung | H. Hakonarson | E. Clayton | D. Roden | J. Ralston | J. Denny | S. Pratap | J. Peterson | P. Appelbaum | I. Kullo | G. Jarvik | R. Sharp | J. Wynn | Maureen E. Smith | N. Lindor | I. Holm | M. Myers | S. V. Van Driest | M. Marasà | M. Harr | K. Leppig | K. Christensen | A. Gordon | D. Crosslin | S. Bland | G. Wiesner | C. Prows | A. Buchanan | H. Rasouly | H. Thiese | C. Hoell | S. Aufox | P. Lammers | Alanna Kulchak Rahm | Shannon DeVange | R. C. Green | N. Henrikson | E. B. Larson | E. Perez | Rajbir Singh | G. Shaibi | Amy Sturm | Janet L. Williams | C. L. Blout Zawatsky | Sarah T Bland | E. Larson | A. Kulchak Rahm | Heidi A. Thiese | Christin Hoell
[1] W. Chung,et al. 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) , 2021, Genetics in Medicine.
[2] J. Ralston,et al. Preferences of biobank participants for receiving actionable genomic test results: results of a re-contacting study , 2021, Genetics in Medicine.
[3] John A. Lynch,et al. Returning negative results from large‐scale genomic screening: Experiences from the eMERGE III network , 2020, American journal of medical genetics. Part A.
[4] A. Slonim,et al. Population genetic screening efficiently identifies carriers of autosomal dominant diseases , 2020, Nature Medicine.
[5] John J. Connolly,et al. Participant choices for return of genomic results in the eMERGE Network , 2020, Genetics in Medicine.
[6] K. Marsolo,et al. Adapting Clinical Systems to Enable Adolescents' Genomic Choices , 2020, ACI Open.
[7] Magalie S Leduc,et al. Frequency of genomic incidental findings among 21,915 eMERGE network participants , 2020, Genetics in Medicine.
[8] Marc S. Williams,et al. Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network , 2020, Journal of personalized medicine.
[9] Lisa J. Martin,et al. Adolescents' and Parents' Genomic Testing Decisions: Associations With Age, Race, and Sex. , 2020, The Journal of adolescent health : official publication of the Society for Adolescent Medicine.
[10] Robert C. Green,et al. Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network. , 2019, American journal of human genetics.
[11] A. Philippakis,et al. The "All of Us" Research Program. , 2019, The New England journal of medicine.
[12] Heidi L. Rehm,et al. Harmonizing Clinical Sequencing And Interpretation For The Emerge III Network , 2018, bioRxiv.
[13] N. Risch,et al. The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations. , 2018, American journal of human genetics.
[14] S. Hurvitz,et al. Advances in the use of PARP inhibitor therapy for breast cancer , 2018, Drugs in context.
[15] Stephanie A Cohen,et al. The past, present and future of service delivery in genetic counseling: Keeping up in the era of precision medicine , 2018, American journal of medical genetics. Part C, Seminars in medical genetics.
[16] Matthew S. Lebo,et al. A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort , 2017, bioRxiv.
[17] W. Chung,et al. 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 , 2016, Genetics in Medicine.
[18] Diane Hauser,et al. The IGNITE network: a model for genomic medicine implementation and research , 2015, BMC Medical Genomics.
[19] L. Brooks,et al. ClinGen--the Clinical Genome Resource. , 2015, The New England journal of medicine.
[20] T. Sellers,et al. Modes of delivery of genetic testing services and the uptake of cancer risk management strategies in BRCA1 and BRCA2 carriers , 2014, Clinical genetics.
[21] I. Bates,et al. Institutionalized paternalism? Stakeholders' views on public access to genetic testing , 2006, Journal of health services research & policy.