High-resolution analysis of copy number variants in adults with simple-to-moderate congenital heart disease-Reference-Cited by-同舟云学术

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High-resolution analysis of copy number variants in adults with simple-to-moderate congenital heart disease

Published:2013-09-24 Issue:12 Volume:161 Page:3087-3094
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Zhao Wei¹,Niu Guannan²,Shen Botao¹,Zheng Yang¹,Gong Fangchao¹,Wang Xianfu³,Lee Jiyun³⁴,Mulvihill John J.³,Chen Xiaohui⁵,Li Shibo³

Affiliation:

1. The Cardiovascular Center; The First Hospital of Jilin University; Changchun China

2. Fuwai Cardiovascular Hospital; Beijing China

3. Department of Pediatrics; University of Oklahoma Health Sciences Center; Oklahoma City Oklahoma

4. Department of Pathology; College of Medicine of Korea University; Seoul South Korea

5. Department of Internal Medicine; Kezuozhongqi People's Hospital; Tongliao China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36177/fullpdf

Reference34 articles.

1. Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients;Carlson;Am J Hum Genet,1997

2. VEGF and RANKL regulation of NFATc1 in heart valve development;Combs;Circ Res,2009

3. An inherited atypical 1 Mb 22q11.2 deletion within the DGS/VCFS 3 Mb region in a child with obesity and aggressive behavior;D'Angelo;Am J Med Genet Part A,2007

4. Embryological Development of the Ventricular Inlets. Septation and Atrioventricular Valve Apparatus

5. A common molecular basis for rearrangement disorders on chromosome 22q11;Edelmann;Hum Mol Genet,1999

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2. Association of Myocardial Changes and Gene Expression of the NFATC1 and NFATC4—Calcineurin Signaling Pathway in Children with Bicuspid Aortic Valve;Children;2023-08-23

3. Copy number variation-associated lncRNAs may contribute to the etiologies of congenital heart disease;Communications Biology;2023-02-17

4. Congenital heart disease risk loci identified by genome-wide association study in European patients;Journal of Clinical Investigation;2021-01-19

5. Genome-wide association study in European patients with congenital heart disease identifies risk loci for transposition of the great arteries and anomalies of the thoracic arteries and veins and expression of discovered candidate genes in the developing heart;2020-06-20

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