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12/1/2014 2:43:00 PM | Browse: 1284 | Download: 1558
Publication Name World Journal of Cardiology
Manuscript ID 11653
Country United States
Received
2014-05-29 08:44
Peer-Review Started
2014-05-29 20:36
First Decision by Editorial Office Director
Return for Revision
2014-07-11 15:34
Revised
2014-07-29 09:46
Publication Fee Transferred
Second Decision by Editor
2014-09-10 09:05
Second Decision by Editor-in-Chief
Final Decision by Editorial Office Director
2014-09-10 09:30
Articles in Press
2014-09-10 09:30
Edit the Manuscript by Language Editor
Typeset the Manuscript
2014-11-20 15:38
Publish the Manuscript Online
2014-12-01 14:43
ISSN 1949-8462 (online)
Open Access
Copyright
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Cardiac & Cardiovascular Systems
Manuscript Type Topic Highlights
Article Title Importance of genetic evaluation and testing in pediatric cardiomyopathy
Manuscript Source Invited Manuscript
All Author List Muhammad Tariq and Stephanie M Ware
Funding Agency and Grant Number
Funding Agency Grant Number
Children’s Cardiomyopathy Foundation
Cincinnati Children’s Hospital’s Clinical and Translational Science Award NIH-ULlRR026314 (to Ware SM)
AHA Postdoctoral Fellowship Award 12POST10370002 (to Tariq M)
Corresponding Author Stephanie M Ware, MD, PhD, Department of Pediatrics and Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, 1044 W. Walnut Street Indianapolis, IN 46202, United States. stware@iu.edu
Key Words Pediatric; Mutation; Exome sequencing; Sarcomere
Core Tip Pediatric cardiomyopathy is a clinically and genetically heterogeneous heart muscle disease with five major phenotypes: hypertrophic cardiomyopathy, dilated cardiomyopathy, restrictive cardiomyopathy, left ventricular noncompaction cardiomyopathy, and arrhythmogenic right ventricular cardiomyopathy. The genetic basis of these cardiomyopathies has been identified using traditional linkage analysis and sequencing. Novel gene discovery has been increased using modern next generation sequencing technologies, however the exact mechanisms of disease development are not fully known. In this review we focus on the current genetic knowledge of cardiomyopathies and their importance in diagnostic settings.
Publish Date 2014-12-01 14:43
Citation Tariq M, Ware SM. Importance of genetic evaluation and testing in pediatric cardiomyopathy. World J Cardiol 2014; 6(11): 1156-1165
URL http://www.wjgnet.com/1949-8462/full/v6/i11/1156.htm
DOI http://dx.doi.org/10.4330/wjc.v6.i11.1156
Full Article (PDF) WJC-6-1156.pdf
Full Article (Word) WJC-6-1156.doc
Manuscript File 11653-Review.docx
Answering Reviewers 11653-Answering reviewers.pdf
Copyright License Agreement 11653-Copyright assignment.pdf
Peer-review Report 11653-Peer review(s).pdf
Scientific Misconduct Check 11653-CrossCheck.jpg
Scientific Editor Work List 11653-Scientific editor work list.pdf