A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta-Reference-Cited by-同舟云学术

A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta

Published:2018-03-24 Issue:34 Volume:39 Page:3243-3249
ISSN:0195-668X
Container-title:European Heart Journal
language:en
Short-container-title:

Author:

Bjornsson Thorsteinn¹,Thorolfsdottir Rosa B¹,Sveinbjornsson Gardar¹,Sulem Patrick¹,Norddahl Gudmundur L¹,Helgadottir Anna¹,Gretarsdottir Solveig¹,Magnusdottir Audur¹,Danielsen Ragnar²,Sigurdsson Emil L³⁴,Adalsteinsdottir Berglind⁵⁶,Gunnarsson Sverrir I⁷,Jonsdottir Ingileif¹⁶⁸,Arnar David O¹²⁶,Helgason Hrodmar⁹,Gudbjartsson Tomas⁶¹⁰,Gudbjartsson Daniel F¹¹¹,Thorsteinsdottir Unnur¹⁶,Holm Hilma¹,Stefansson Kari¹⁶

Affiliation:

1. deCODE genetics/Amgen, Inc., Sturlugata 8, Reykjavik, Iceland

2. Department of Medicine, Landspitali—The National University Hospital of Iceland, Hringbraut, Reykjavik, Iceland

3. Department of Family Medicine, University of Iceland, Vatnsmyrarvegur 16, Reykjavik, Iceland

4. Department of Development, Primary Health Care of the Capital Area, Alfabakki 16, Reykjavik, Iceland

5. Department of Cardiology, Haukeland University Hospital, Jonas Lies vei 83, Bergen, Norway

6. Faculty of Medicine, University of Iceland, Vatnsmyrarvegur 16, Reykjavik, Iceland

7. Division of Cardiovascular Medicine, Department of Medicine, University of Wisconsin, 600 Highland Ave, Madison, WI, USA

8. Department of Immunology, Landspitali—The National University Hospital of Iceland, Hringbraut, Reykjavik, Iceland

9. Children's Hospital, Landspitali—The National University Hospital of Iceland, Hringbraut, Reykjavik, Iceland

10. Department of Cardiothoracic Surgery, Landspitali—The National University Hospital of Iceland, Hringbraut, Reykjavik, Iceland

11. School of Engineering and Natural Sciences, University of Iceland, Hjardarhagi 4, Reykjavik, Iceland

Funder

deCODE genetics/Amgen, Inc

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

Link

http://academic.oup.com/eurheartj/article-pdf/39/34/3243/25694668/ehy142.pdf

Reference41 articles.

1. The incidence of congenital heart disease;Hoffman;J Am Coll Cardiol,2002

2. Left ventricular outflow obstruction: subaortic stenosis, bicuspid aortic valve, supravalvar aortic stenosis, and coarctation of the aorta;Aboulhosn;Circulation,2006

3. Prevalence of congenital cardiovascular malformations among relatives of infants with hypoplastic left heart, coarctation of the aorta, and d-transposition of the great arteries;Loffredo;Am J Med Genet A,2004

Cited by 61 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. From genes to therapy: A comprehensive exploration of congenital heart disease through the lens of genetics and emerging technologies;Current Problems in Cardiology;2024-09

2. Whole-exome sequencing uncovers the genetic complexity of bicuspid aortic valve in families with early-onset complications;The American Journal of Human Genetics;2024-09

3. Conotruncal Heart Defects: A Narrative Review of Molecular Genetics, Genomics Research and Innovation;OMICS: A Journal of Integrative Biology;2024-07-01

4. Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects;BMC Genomics;2024-03-07

5. 2024 Heart Disease and Stroke Statistics: A Report of US and Global Data From the American Heart Association;Circulation;2024-02-20