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
To Make the First Decision	2014-07-10 17:23
Return for Revision	2014-07-11 15:34
Revised	2014-07-29 09:46
Second Decision	2014-09-10 09:05
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2014-09-10 09:30
Articles in Press	2014-09-10 09:30
Publication Fee Transferred
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