A framework for reporting secondary and incidental findings in prenatal sequencing: When and for whom?-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

A framework for reporting secondary and incidental findings in prenatal sequencing: When and for whom?

Published:2022-01-19 Issue:6 Volume:42 Page:697-704
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Vears Danya¹²,Amor David J.¹³^ORCID

Affiliation:

1. Murdoch Children's Research Institute Royal Children's Hospital Melbourne Victoria Australia

2. Melbourne Law School University of Melbourne Carlton Victoria Australia

3. Department of Paediatrics University of Melbourne Royal Children's Hospital Melbourne Victoria Australia

Funder

Australian Government

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.6097

Reference41 articles.

1. The use of chromosomal microarray for prenatal diagnosis

2. Whole-genome sequencing in health care

3. Points to consider for laboratories reporting results from diagnostic genomic sequencing

4. 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

5. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

Cited by 17 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. Fetal whole genome sequencing as a clinical diagnostic tool: Advantages, limitations and pitfalls;Best Practice & Research Clinical Obstetrics & Gynaecology;2024-12

2. Guidelines for NGS procedures applied to prenatal diagnosis by the Spanish Society of Gynecology and Obstetrics and the Spanish Association of Prenatal Diagnosis;Journal of Medical Genetics;2024-06-04

3. Screening embryos for polygenic disease risk: a review of epidemiological, clinical, and ethical considerations;Human Reproduction Update;2024-05-28

4. Exome sequencing in every pregnancy? Results of trio exome sequencing in structurally normal fetuses;Prenatal Diagnosis;2024-05-12

5. Az első hazai tapasztalatok összegzése kromoszomális microarray-analízis és teljesexom-szekvenálás módszerekkel a magzati diagnosztikában;Orvosi Hetilap;2024-04-07

同舟云学术

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