The impact of unsolicited findings in clinical exome sequencing, a qualitative interview study
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/s41431-021-00834-9.pdf
Reference39 articles.
1. Srivastava S, Love-Nichols JA, Dies KA, Ledbetter DH, Martin CL, Chung WK, et al. Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders. Genet Med. 2019;21:2413–21.
2. Berg JS, Khoury MJ, Evans JP. Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time. Genet Med. 2011;13:499–504.
3. Christenhusz GM, Devriendt K, Dierickx K. Secondary variants-in defense of a more fitting term in the incidental findings debate. Eur J Hum Genet. 2013;21:1331–4.
4. Tan N, Amendola LM, O’Daniel JM, Burt A, Horike-Pyne MJ, Boshe L, et al. Is “incidental finding” the best term?: a study of patients’ preferences. Genet Med. 2017;19:176–81.
5. van El CG, Cornel MC, Borry P, Hastings RJ, Fellmann F, Hodgson SV, et al. Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics. Eur J Hum Genet. 2013;21:S1–5.
Cited by 10 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Expectations, needs and mid-term outcomes in people accessing to secondary findings from ES: 1st French mixed study (FIND Study);European Journal of Human Genetics;2024-05-27
2. Exploring uncertainties regarding unsolicited findings in genetic testing;Patient Education and Counseling;2024-02
3. Systematic review of the uptake and outcomes from returning secondary findings to adult participants in research genomic testing;Journal of Genetic Counseling;2024-01-10
4. Machine learning in onco-pharmacogenomics: a path to precision medicine with many challenges;Frontiers in Pharmacology;2024-01-09
5. Copy number variations (CNVs) and karyotyping analysis in males with azoospermia and oligospermia;BMC Medical Genomics;2023-09-08
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3