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Literature DB >> 23611745

Prevalence and spectrum of PITX2c mutations associated with familial atrial fibrillation.

Yi-Qing Yang¹, Ying-Jia Xu, Ruo-Gu Li, Xin-Kai Qu, Wei-Yi Fang, Xu Liu.

Abstract

Entities: Disease Gene

Keywords: Atrial fibrillation; Genetics; Transcription factor

Mesh：

Substances：

Year: 2013 PMID： 23611745 DOI： 10.1016/j.ijcard.2013.03.141

Source DB: PubMed Journal: Int J Cardiol ISSN： 0167-5273 Impact factor: 4.164

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Cited

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8 in total

1. Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.

Authors: Juan Wang; Yuan-Feng Xin; Wen-Jun Xu; Zhong-Min Liu; Xing-Biao Qiu; Xin-Kai Qu; Lei Xu; Xin Li; Yi-Qing Yang
Journal: DNA Cell Biol Date: 2013-10-01 Impact factor: 3.311

2. Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation.

Authors: Zeynep H Coban-Akdemir; Wu-Lin Charng; Mahshid Azamian; Ingrid S Paine; Jaya Punetha; Christopher M Grochowski; Tomasz Gambin; Santiago O Valdes; Bryan Cannon; Gladys Zapata; Patricia P Hernandez; Shalini Jhangiani; Harsha Doddapaneni; Jianhong Hu; Fatima Boricha; Donna M Muzny; Eric Boerwinkle; Yaping Yang; Richard A Gibbs; Jennifer E Posey; Xander H T Wehrens; John W Belmont; Jeffrey J Kim; Christina Y Miyake; James R Lupski; Seema R Lalani
Journal: Am J Med Genet A Date: 2020-03-31 Impact factor: 2.802

3. PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome.

Authors: Cui-Mei Zhao; Lu-Ying Peng; Li Li; Xing-Yuan Liu; Juan Wang; Xian-Ling Zhang; Fang Yuan; Ruo-Gu Li; Xing-Biao Qiu; Yi-Qing Yang
Journal: PLoS One Date: 2015-04-20 Impact factor: 3.240

4. Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial Fibrillation.

Authors: Zhan-Cheng Wang; Wen-Hui Ji; Chang-Wu Ruan; Xing-Yuan Liu; Xing-Biao Qiu; Fang Yuan; Ruo-Gu Li; Ying-Jia Xu; Xu Liu; Ru-Tai Huang; Song Xue; Yi-Qing Yang
Journal: Int J Med Sci Date: 2016-01-23 Impact factor: 3.738

5. Accurate prediction of functional, structural, and stability changes in PITX2 mutations using in silico bioinformatics algorithms.

Authors: Morteza Seifi; Michael A Walter
Journal: PLoS One Date: 2018-04-17 Impact factor: 3.240

Prevalence and spectrum of PITX2c mutations associated with familial atrial fibrillation.

1. Prevalence and spectrum of PITX2c mutations associated with congenital heart disease.

2. Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation.

3. PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome.

4. Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial Fibrillation.

5. Accurate prediction of functional, structural, and stability changes in PITX2 mutations using in silico bioinformatics algorithms.

6. Proarrhythmia in the p.Met207Val PITX2c-Linked Familial Atrial Fibrillation-Insights From Modeling.

7. PITX2c loss-of-function mutations responsible for congenital atrial septal defects.

8. PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation.