Defining purpose: a key step in genetic test evaluation.

Suppr

超能文献

作者信息

Burke Wylie, Zimmern Ronald L, Kroese Mark

机构信息

Department of Medical History and Ethics, University of Washington, Seattle, Washington 98195-7120, USA.

出版信息

Genet Med. 2007 Oct;9(10):675-81. doi: 10.1097/gim.0b013e318156e45b.

DOI:10.1097/gim.0b013e318156e45b

PMID:18073580

Abstract

摘要

相似文献

Defining purpose: a key step in genetic test evaluation.

Genet Med. 2007 Oct;9(10):675-81. doi: 10.1097/gim.0b013e318156e45b.

Genetic testing and medical decision making.

Arch Intern Med. 2001 Nov 12;161(20):2406-8. doi: 10.1001/archinte.161.20.2406.

Prenatal genetic testing.

Pediatr Ann. 2009 Aug;38(8):426-30. doi: 10.3928/00904481-20090723-05.

US panel rejects routine use of BRCA cancer screening in women.

BMJ. 2013 Apr 4;346:f2160. doi: 10.1136/bmj.f2160.

Genomic testing: a struggle for oncologists.

J Natl Cancer Inst. 2014 Jun 6;106(6):dju172. doi: 10.1093/jnci/dju172. Print 2014 Jun.

Drifting Away from Informed Consent in the Era of Personalized Medicine.

Hastings Cent Rep. 2015 Jul-Aug;45(4):16-20. doi: 10.1002/hast.470.

Research directions in genetic counselling: a review of the literature.

Patient Educ Couns. 2001 Aug;44(2):95-105. doi: 10.1016/s0738-3991(00)00181-6.

When to consider a genetic test.

J Am Assoc Nurse Pract. 2018 Jul;30(7):366-367. doi: 10.1097/JXX.0000000000000067.

Predictive testing: more than just another test.

Intern Med J. 2013 Dec;43(12):1261-2. doi: 10.1111/imj.12312.

Incorporating genetic testing ancestry results into medical decisions.

Virtual Mentor. 2014 Jun 1;16(6):428-33. doi: 10.1001/virtualmentor.2014.16.06.ecas2-1406.

引用本文的文献

Beyond severity: utility as a criterion for setting the scope of RGCS.

Eur J Hum Genet. 2025 Mar;33(2):226-230. doi: 10.1038/s41431-024-01640-9. Epub 2024 May 29.

Knowledge of genetic eye diseases and genetic services and attitudes toward genetic testing and gene therapy.

Taiwan J Ophthalmol. 2021 Nov 15;11(4):372-379. doi: 10.4103/tjo.tjo_34_21. eCollection 2021 Oct-Dec.

Understanding polygenic models, their development and the potential application of polygenic scores in healthcare.

J Med Genet. 2020 Nov;57(11):725-732. doi: 10.1136/jmedgenet-2019-106763. Epub 2020 May 6.

Healthcare System Priorities for Successful Integration of Genomics: An Australian Focus.

Front Public Health. 2019 Mar 11;7:41. doi: 10.3389/fpubh.2019.00041. eCollection 2019.

Paediatricians underuse recommended genetic tests in children with global developmental delay.

Paediatr Child Health. 2018 Dec;23(8):e156-e162. doi: 10.1093/pch/pxy033. Epub 2018 Apr 5.

Integrative omics for health and disease.

Nat Rev Genet. 2018 May;19(5):299-310. doi: 10.1038/nrg.2018.4. Epub 2018 Feb 26.

Conceptual issues for screening in the genomic era - time for an update?

Epidemiol Biostat Public Health. 2014 Dec 11;11(4). doi: 10.2427/9944.

Giving and withholding of information following genomic screening: challenges identified in a study of primary care physicians in Estonia.

J Genet Couns. 2012 Aug;21(4):591-604. doi: 10.1007/s10897-011-9424-3. Epub 2011 Dec 8.

A formal risk-benefit framework for genomic tests: facilitating the appropriate translation of genomics into clinical practice.

Genet Med. 2010 Nov;12(11):686-93. doi: 10.1097/GIM.0b013e3181eff533.

Debating clinical utility.

Public Health Genomics. 2010;13(4):215-23. doi: 10.1159/000279623. Epub 2010 Apr 15.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

相似文献

Defining purpose: a key step in genetic test evaluation.

Genet Med. 2007 Oct;9(10):675-81. doi: 10.1097/gim.0b013e318156e45b.

Genetic testing and medical decision making.

Arch Intern Med. 2001 Nov 12;161(20):2406-8. doi: 10.1001/archinte.161.20.2406.

Prenatal genetic testing.

Pediatr Ann. 2009 Aug;38(8):426-30. doi: 10.3928/00904481-20090723-05.

US panel rejects routine use of BRCA cancer screening in women.

BMJ. 2013 Apr 4;346:f2160. doi: 10.1136/bmj.f2160.

Genomic testing: a struggle for oncologists.

J Natl Cancer Inst. 2014 Jun 6;106(6):dju172. doi: 10.1093/jnci/dju172. Print 2014 Jun.

Drifting Away from Informed Consent in the Era of Personalized Medicine.

Hastings Cent Rep. 2015 Jul-Aug;45(4):16-20. doi: 10.1002/hast.470.

Research directions in genetic counselling: a review of the literature.

Patient Educ Couns. 2001 Aug;44(2):95-105. doi: 10.1016/s0738-3991(00)00181-6.

When to consider a genetic test.

J Am Assoc Nurse Pract. 2018 Jul;30(7):366-367. doi: 10.1097/JXX.0000000000000067.

Predictive testing: more than just another test.

Intern Med J. 2013 Dec;43(12):1261-2. doi: 10.1111/imj.12312.

Incorporating genetic testing ancestry results into medical decisions.

Virtual Mentor. 2014 Jun 1;16(6):428-33. doi: 10.1001/virtualmentor.2014.16.06.ecas2-1406.

引用本文的文献

Beyond severity: utility as a criterion for setting the scope of RGCS.

Eur J Hum Genet. 2025 Mar;33(2):226-230. doi: 10.1038/s41431-024-01640-9. Epub 2024 May 29.

Knowledge of genetic eye diseases and genetic services and attitudes toward genetic testing and gene therapy.

Taiwan J Ophthalmol. 2021 Nov 15;11(4):372-379. doi: 10.4103/tjo.tjo_34_21. eCollection 2021 Oct-Dec.

Understanding polygenic models, their development and the potential application of polygenic scores in healthcare.

J Med Genet. 2020 Nov;57(11):725-732. doi: 10.1136/jmedgenet-2019-106763. Epub 2020 May 6.

Healthcare System Priorities for Successful Integration of Genomics: An Australian Focus.

Front Public Health. 2019 Mar 11;7:41. doi: 10.3389/fpubh.2019.00041. eCollection 2019.

Paediatricians underuse recommended genetic tests in children with global developmental delay.

Paediatr Child Health. 2018 Dec;23(8):e156-e162. doi: 10.1093/pch/pxy033. Epub 2018 Apr 5.

Integrative omics for health and disease.

Nat Rev Genet. 2018 May;19(5):299-310. doi: 10.1038/nrg.2018.4. Epub 2018 Feb 26.

Conceptual issues for screening in the genomic era - time for an update?

Epidemiol Biostat Public Health. 2014 Dec 11;11(4). doi: 10.2427/9944.

Giving and withholding of information following genomic screening: challenges identified in a study of primary care physicians in Estonia.

J Genet Couns. 2012 Aug;21(4):591-604. doi: 10.1007/s10897-011-9424-3. Epub 2011 Dec 8.

A formal risk-benefit framework for genomic tests: facilitating the appropriate translation of genomics into clinical practice.

Genet Med. 2010 Nov;12(11):686-93. doi: 10.1097/GIM.0b013e3181eff533.

Debating clinical utility.

Public Health Genomics. 2010;13(4):215-23. doi: 10.1159/000279623. Epub 2010 Apr 15.