• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions: a viewpoint paper of the European Society of Cardiology working group on myocardial and pericardial diseases and members of the European Society of Human Genetics.

作者信息

Mogensen Jens, van Tintelen J Peter, Fokstuen Siv, Elliott Perry, van Langen Irene M, Meder Benjamin, Richard Pascale, Syrris Petros, Caforio Alida L P, Adler Yehuda, Anastasakis Aris, Gimeno Juan R, Klingel Karin, Linhart Ales, Imazio Massimo, Pinto Yigal, Newbery Ruth, Schmidtke Joerg, Charron Philippe

机构信息

Department of Cardiology, Odense University Hospital, Odense, Denmark

Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands Department of Genetics, University Medical Centre Groningen, University of Groningen, the Netherlands.

出版信息

Eur Heart J. 2015 Jun 7;36(22):1367-70. doi: 10.1093/eurheartj/ehv122. Epub 2015 Apr 5.

DOI:10.1093/eurheartj/ehv122
PMID:25845928
Abstract
摘要

相似文献

1
The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions: a viewpoint paper of the European Society of Cardiology working group on myocardial and pericardial diseases and members of the European Society of Human Genetics.下一代DNA测序在遗传性心血管疾病患者常规护理中的当前作用:欧洲心脏病学会心肌和心包疾病工作组及欧洲人类遗传学学会成员的观点文件
Eur Heart J. 2015 Jun 7;36(22):1367-70. doi: 10.1093/eurheartj/ehv122. Epub 2015 Apr 5.
2
[Medical genetics and the genome].[医学遗传学与基因组]
Ugeskr Laeger. 2014 Nov 10;176(46).
3
Managing the ethical challenges of next-generation sequencing in genomic medicine.应对基因组医学中下一代测序的伦理挑战。
Br Med Bull. 2014 Sep;111(1):17-30. doi: 10.1093/bmb/ldu017. Epub 2014 Aug 13.
4
Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases.遗传性心脏病咨询和检测:欧洲心脏病学会心肌和心包疾病工作组立场声明。
Eur Heart J. 2010 Nov;31(22):2715-26. doi: 10.1093/eurheartj/ehq271. Epub 2010 Sep 7.
5
Ethical challenges of the use of whole exome sequencing in the clinic.临床应用全外显子组测序的伦理挑战。
World J Pediatr Congenit Heart Surg. 2013 Jan;4(1):58-61. doi: 10.1177/2150135112462590.
6
[Practical guidelines for genetic testing in cardiovascular diseases].[心血管疾病基因检测实用指南]
Herz. 2017 Aug;42(5):485-491. doi: 10.1007/s00059-017-4571-4.
7
NGS-Based genetic testing for heritable cardiovascular diseases. Specific requirements for obtaining informed consent.基于下一代测序的遗传性心血管疾病基因检测。获取知情同意的特定要求。
Mol Cell Probes. 2019 Jun;45:70-78. doi: 10.1016/j.mcp.2019.04.005. Epub 2019 May 3.
8
Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy.欧洲医学辅助生殖与遗传学的当前问题:研究、临床实践、伦理、法律问题及政策
Hum Reprod. 2014 Aug;29(8):1603-9. doi: 10.1093/humrep/deu130. Epub 2014 Jul 8.
9
Whole-genome sequencing and the physician.全基因组测序与医生。
Clin Genet. 2012 Jun;81(6):511-3. doi: 10.1111/j.1399-0004.2012.01868.x. Epub 2012 Apr 9.
10
Whole-exome/genome sequencing and genomics.全外显子组/基因组测序和基因组学。
Pediatrics. 2013 Dec;132(Suppl 3):S211-5. doi: 10.1542/peds.2013-1032E.

引用本文的文献

1
Hemodynamics in Left-Sided Cardiomyopathies.左心心肌病的血流动力学
Rev Cardiovasc Med. 2024 Dec 24;25(12):455. doi: 10.31083/j.rcm2512455. eCollection 2024 Dec.
2
International policies guiding the selection, analysis, and clinical management of secondary findings from genomic sequencing: A systematic review.国际政策指导基因组测序中次生发现的选择、分析和临床管理:系统评价。
Am J Hum Genet. 2024 Oct 3;111(10):2079-2093. doi: 10.1016/j.ajhg.2024.08.012. Epub 2024 Sep 18.
3
Fabry Disease in Women: Genetic Basis, Available Biomarkers, and Clinical Manifestations.
女性法布里病:遗传基础、可用生物标志物和临床表现。
Genes (Basel). 2023 Dec 26;15(1):37. doi: 10.3390/genes15010037.
4
Sex Differences in Anderson-Fabry Cardiomyopathy: Clinical, Genetic, and Imaging Analysis in Women.安德森-法布里心肌病的性别差异:女性的临床、遗传和影像学分析。
Genes (Basel). 2023 Sep 15;14(9):1804. doi: 10.3390/genes14091804.
5
Whole-Exome Sequencing Revealed New Candidate Genes for Human Dilated Cardiomyopathy.全外显子组测序揭示了人类扩张型心肌病的新候选基因。
Diagnostics (Basel). 2022 Oct 5;12(10):2411. doi: 10.3390/diagnostics12102411.
6
An Overview of Molecular Mechanisms in Fabry Disease.《法布瑞氏病的分子机制概述》
Biomolecules. 2022 Oct 12;12(10):1460. doi: 10.3390/biom12101460.
7
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases.欧洲心律协会(EHRA)/心律学会(HRS)/亚太心律学会(APHRS)/拉丁美洲心律学会(LAHRS)关于心脏病基因检测现状的专家共识声明。
J Arrhythm. 2022 May 31;38(4):491-553. doi: 10.1002/joa3.12717. eCollection 2022 Aug.
8
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases.欧洲心律协会(EHRA)/心律协会(HRS)/亚太心律协会(APHRS)/拉丁美洲心律协会(LAHRS)关于心脏病基因检测现状的专家共识声明。
Europace. 2022 Sep 1;24(8):1307-1367. doi: 10.1093/europace/euac030.
9
Non-pharmaceutical Interventions for Hypertrophic Cardiomyopathy: A Mini Review.肥厚型心肌病的非药物干预:一篇综述短文
Front Cardiovasc Med. 2021 Oct 15;8:695247. doi: 10.3389/fcvm.2021.695247. eCollection 2021.
10
A comparative study of single nucleotide variant detection performance using three massively parallel sequencing methods.三种高通量测序方法检测单核苷酸变异性能的比较研究。
PLoS One. 2020 Sep 28;15(9):e0239850. doi: 10.1371/journal.pone.0239850. eCollection 2020.