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1
Can targeted genetic testing offer useful health information to adoptees?靶向基因检测能为被收养者提供有用的健康信息吗？
Genet Med. 2015 Jul;17(7):533-5. doi: 10.1038/gim.2015.58. Epub 2015 Apr 23.
2
Adult adoptees and their use of direct-to-consumer genetic testing: Searching for family, searching for health.成人被收养者及其对直接面向消费者的基因检测的使用：寻找家庭，寻找健康。
J Genet Couns. 2021 Feb;30(1):144-157. doi: 10.1002/jgc4.1304. Epub 2020 Jun 29.
3
Adoptees' Pursuit of Genomic Testing to Fill Gaps in Family Health History and Reduce Healthcare Disparity.被收养者寻求基因检测以填补家族健康史空白并减少医疗保健差异。
Narrat Inq Bioeth. 2018;8(2):131-135. doi: 10.1353/nib.2018.0050.
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Family Health History: Invaluable for Adoptees' Medical Care and Self Identity.家族健康史：对领养者的医疗护理和自我认知至关重要。
Narrat Inq Bioeth. 2018;8(2):143-149. doi: 10.1353/nib.2018.0052.
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Adopted individuals' interest in elective genomic testing.被收养者对选择性基因组检测的兴趣。
J Med Genet. 2022 Feb;59(2):197-203. doi: 10.1136/jmedgenet-2020-107503. Epub 2020 Dec 21.
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Addressing perceived economic obstacles to genetic testing as a way to mitigate disparities in family health history for adoptees.解决领养人群在遗传检测方面所感知到的经济障碍，以此来减轻他们在家族健康史方面的差异。
Health Econ Policy Law. 2020 Apr;15(2):277-287. doi: 10.1017/S1744133118000488. Epub 2018 Dec 20.
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Adopting genetics: motivations and outcomes of personal genomic testing in adult adoptees.采用遗传学：成年领养者进行个人基因组检测的动机与结果
Genet Med. 2016 Sep;18(9):924-32. doi: 10.1038/gim.2015.192. Epub 2016 Jan 28.
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Adoptees' experiences of using direct-to-consumer genetic testing and determinants of this use: A mixed study in Quebec.领养者使用直接面向消费者的基因检测的经历及其使用的决定因素：魁北克的一项混合研究。
J Genet Couns. 2025 Apr;34(2):e1963. doi: 10.1002/jgc4.1963. Epub 2024 Aug 22.
9
[Genetic screening of adopted individuals].
Ugeskr Laeger. 2021 Mar 29;183(13).
10
Unpacking Reasons for Genetic Testing of Adoptees.
Am J Bioeth. 2016 Dec;16(12):39-40. doi: 10.1080/15265161.2016.1239793.

引用本文的文献

1
Does genetic testing offer utility as a supplement to traditional family health history intake for inherited disease risk?基因检测作为传统家族病史采集的补充，对遗传性疾病风险评估是否有用？
Fam Pract. 2023 Dec 22;40(5-6):760-767. doi: 10.1093/fampra/cmad017.
2
Adoptees' views and experiences of direct-to-consumer (DTC) genomic testing: an exploratory interview study from the UK.领养者对直接面向消费者（DTC）基因检测的看法与体验：一项来自英国的探索性访谈研究
J Community Genet. 2023 Apr;14(2):149-162. doi: 10.1007/s12687-022-00622-y. Epub 2022 Nov 29.
3
Ethics in genetic counselling.遗传咨询中的伦理问题。
J Community Genet. 2019 Jan;10(1):3-33. doi: 10.1007/s12687-018-0371-7. Epub 2018 Jun 14.
4
Autonomy, Well-Being, and the Value of Genetic Testing for Adopted Persons.自主性、幸福与收养者基因检测的价值
HEC Forum. 2018 Sep;30(3):283-295. doi: 10.1007/s10730-017-9345-0.
5
Gallbladder Adenocarcinoma as the First Manifestation of Germline BRCA1 Mutation.
J Gastrointest Cancer. 2019 Mar;50(1):147-150. doi: 10.1007/s12029-017-9995-9.
6
An old problem in a new age: Revisiting the clinical dilemma of misattributed paternity.新时代的老问题：重新审视父子关系误认的临床困境。
Appl Transl Genom. 2016 Feb 1;8:36-9. doi: 10.1016/j.atg.2016.01.004. eCollection 2016 Mar.
7
Adopting genetics: motivations and outcomes of personal genomic testing in adult adoptees.采用遗传学：成年领养者进行个人基因组检测的动机与结果
Genet Med. 2016 Sep;18(9):924-32. doi: 10.1038/gim.2015.192. Epub 2016 Jan 28.

本文引用的文献

1
Genomic screening of the general adult population: key concepts for assessing net benefit with systematic evidence reviews.普通成年人群的基因组筛查：通过系统证据综述评估净效益的关键概念
Genet Med. 2015 Jun;17(6):441-3. doi: 10.1038/gim.2014.129. Epub 2014 Sep 18.
2
Familial transmission of prostate, breast and colorectal cancer in adoptees is related to cancer in biological but not in adoptive parents: a nationwide family study.领养者中前列腺癌、乳腺癌和结直肠癌的家族传播与生物学父母而非养父母的癌症有关：一项全国性家庭研究。
Eur J Cancer. 2014 Sep;50(13):2319-27. doi: 10.1016/j.ejca.2014.05.018. Epub 2014 Jun 18.
3
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.ACMG 临床外显子组和基因组测序中偶然发现报告的推荐标准。
Genet Med. 2013 Jul;15(7):565-74. doi: 10.1038/gim.2013.73. Epub 2013 Jun 20.
4
Characterization of SNPs associated with prostate cancer in men of Ashkenazic descent from the set of GWAS identified SNPs: impact of cancer family history and cumulative SNP risk prediction.鉴定全基因组关联研究 SNPs 中与阿什肯纳兹裔男性前列腺癌相关的单核苷酸多态性的特征：家族癌症史的影响和累积 SNP 风险预测。
PLoS One. 2013;8(4):e60083. doi: 10.1371/journal.pone.0060083. Epub 2013 Apr 3.
5
We screen newborns, don't we?: realizing the promise of public health genomics.我们对新生儿进行筛查，不是吗？：实现公共卫生基因组学的前景。
Genet Med. 2013 May;15(5):332-4. doi: 10.1038/gim.2013.11. Epub 2013 Mar 7.
6
Prospective comparison of family medical history with personal genome screening for risk assessment of common cancers.前瞻性比较家族病史与个人基因组筛查在常见癌症风险评估中的应用。
Eur J Hum Genet. 2012 May;20(5):547-51. doi: 10.1038/ejhg.2011.224. Epub 2012 Jan 4.
7
Comprehensive health evaluation of the newly adopted child.新收养儿童的全面健康评估。
Pediatrics. 2012 Jan;129(1):e214-23. doi: 10.1542/peds.2011-2381. Epub 2011 Dec 26.
8
Using family history information to promote healthy lifestyles and prevent diseases; a discussion of the evidence.利用家族病史信息促进健康生活方式和预防疾病；对证据的讨论。
BMC Public Health. 2010 May 13;10:248. doi: 10.1186/1471-2458-10-248.
9
National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health.美国国立卫生研究院科学会议声明：家族史与增进健康
Ann Intern Med. 2009 Dec 15;151(12):872-7. doi: 10.7326/0003-4819-151-12-200912150-00165.
10
The family history--more important than ever.家族病史——比以往任何时候都更重要。
N Engl J Med. 2004 Nov 25;351(22):2333-6. doi: 10.1056/NEJMsb042979.

Can targeted genetic testing offer useful health information to adoptees?

作者信息

May Thomas, Strong Kimberly A, Khoury Muin J, Evans James P

机构信息

1] Center for Bioethics and Medical Humanities, Medical College of Wisconsin, Milwaukee, Wisconsin, USA [2] Institute for Health and Aging, University of California San Francisco, San Francisco, CA, USA.

Center for Bioethics and Medical Humanities, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

出版信息

Genet Med. 2015 Jul;17(7):533-5. doi: 10.1038/gim.2015.58. Epub 2015 Apr 23.

DOI:10.1038/gim.2015.58
PMID:25905442
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4701205/
Abstract
摘要