Tumor profiling and the incidentalome: patient decisions and risks.
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[1] J. Berg,et al. A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing , 2015, Genetics in Medicine.
[2] Bartha Maria Knoppers,et al. Return of genetic testing results in the era of whole-genome sequencing , 2015, Nature Reviews Genetics.
[3] Lacey Smith,et al. Reporting Incidental Findings in Clinical Whole Exome Sequencing: Incorporation of the 2013 ACMG Recommendations into Current Practices of Genetic Counseling , 2015, Journal of Genetic Counseling.
[4] G. Mills,et al. Prevalence of incidental actionable germline mutations in 1,000 advanced cancer patients on a prospective somatic genomic profiling program. , 2015 .
[5] Donavan T. Cheng,et al. Tumor relevant germline findings in targeted tumor sequencing using matched normal DNA of 1,570 unselected cases. , 2015 .
[6] Avni Santani,et al. Actionable exomic incidental findings in 6503 participants: challenges of variant classification , 2015, Genome research.
[7] Christine Weiner,et al. Anticipate and communicate: Ethical management of incidental and secondary findings in the clinical, research, and direct-to-consumer contexts (December 2013 report of the Presidential Commission for the Study of Bioethical Issues). , 2014, American journal of epidemiology.
[8] Seema M Jamal,et al. Attitudes of genetics professionals toward the return of incidental results from exome and whole-genome sequencing. , 2014, American journal of human genetics.
[9] S. Hull,et al. The unintended implications of blurring the line between research and clinical care in a genomic age. , 2014, Personalized medicine.
[10] L. Garraway,et al. Cancer patients' preferences for return of somatic and germline whole-exome sequencing results: Data from the CANSEQ study. , 2014 .
[11] A. McGuire,et al. Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group , 2014, Genetics in Medicine.
[12] N. Holtzman. ACMG recommendations on incidental findings are flawed scientifically and ethically , 2013, Genetics in Medicine.
[13] Y. Bombard,et al. Revealing the incidentalome when targeting the tumor genome. , 2013, JAMA.
[14] E. Hofstatter,et al. The promise and pitfalls of genomics-driven cancer medicine. , 2013, The virtual mentor : VM.
[15] Fiona A Miller,et al. Testing personalized medicine: patient and physician expectations of next-generation genomic sequencing in late-stage cancer care , 2013, European Journal of Human Genetics.
[16] M. Driessnack,et al. ‘Information is information’: a public perspective on incidental findings in clinical and research genome‐based testing , 2013, Clinical genetics.
[17] Marc S. Williams,et al. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing , 2013, Genetics in Medicine.
[18] Robert C. Green,et al. Ethics and Genomic Incidental Findings , 2013, Science.
[19] Levi A Garraway,et al. Genomics-driven oncology: framework for an emerging paradigm. , 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[20] C. Hudis,et al. ASCO's approach to a learning health care system in oncology. , 2013, Journal of oncology practice.
[21] E. V. Van Allen,et al. Clinical analysis and interpretation of cancer genome data. , 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[22] E. Cuppen,et al. Ethical, legal, and counseling challenges surrounding the return of genetic results in oncology. , 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[23] M. Minden,et al. Cancer patient perceptions on the ethical and legal issues related to biobanking , 2013, BMC Medical Genomics.
[24] Ellen Wright Clayton,et al. Managing incidental genomic findings: legal obligations of clinicians , 2013, Genetics in Medicine.
[25] R. Weinshilboum,et al. Incidental genetic findings in randomized clinical trials: recommendations from the Genomics and Randomized Trials Network (GARNET) , 2013, Genome Medicine.
[26] Tina Hambuch,et al. Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology. , 2012, The Journal of molecular diagnostics : JMD.
[27] L. Garraway,et al. Attitudes of patients with cancer about personalized medicine and somatic genetic testing. , 2012, Journal of oncology practice.
[28] Kris Dierickx,et al. To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts , 2012, European Journal of Human Genetics.
[29] Martha Driessnack,et al. Researcher and institutional review board chair perspectives on incidental findings in genomic research. , 2012, Genetic testing and molecular biomarkers.
[30] R. Steiner,et al. “I'm fine; I'm just waiting for my disease” , 2011, Neurology.
[31] Boris Pasche,et al. Whole-genome sequencing: a step closer to personalized medicine. , 2011, JAMA.
[32] Mildred K. Cho,et al. Understanding Incidental Findings in the Context of Genetics and Genomics , 2008, The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics.
[33] Harry Ostrer,et al. Translating genomic research into clinical practice: promise and pitfalls. , 2013, American Society of Clinical Oncology educational book. American Society of Clinical Oncology. Annual Meeting.