Literature DB >> 22483626

Mutational spectrum of the GATA5 gene associated with familial atrial fibrillation.

Yi-Qing Yang, Juan Wang, Xin-Hua Wang, Qian Wang, Hong-Wei Tan, Min Zhang, Fang-Fang Shen, Jin-Qi Jiang, Wei-Yi Fang, Xu Liu.   

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Year:  2012        PMID： 22483626     DOI： 10.1016/j.ijcard.2012.03.132

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


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  15 in total

Review 1.  Emerging directions in the genetics of atrial fibrillation.

Authors:  Nathan R Tucker; Patrick T Ellinor
Journal:  Circ Res       Date:  2014-04-25       Impact factor: 17.367

2.  Compound heterozygous GATA5 mutations in a girl with hydrops fetalis, congenital heart defects and genital anomalies.

Authors:  Maja Hempel; Teresa Casar Tena; Thilo Diehl; Martina S Burczyk; Tim M Strom; Christian Kubisch; Melanie Philipp; Davor Lessel
Journal:  Hum Genet       Date:  2017-02-08       Impact factor: 4.132

Review 3.  Genetics of atrial fibrillation: from families to genomes.

Authors:  Ingrid E Christophersen; Patrick T Ellinor
Journal:  J Hum Genet       Date:  2015-05-21       Impact factor: 3.172

4.  Novel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallot.

Authors:  Juan Wang; Xue-Jiao Luo; Yuan-Feng Xin; Yi Liu; Zhong-Min Liu; Qian Wang; Ruo-Gu Li; Wei-Yi Fang; Xiao-Zhou Wang; Yi-Qing Yang
Journal:  DNA Cell Biol       Date:  2012-09-28       Impact factor: 3.311

5.  Novel and functional DNA sequence variants within the GATA5 gene promoter in ventricular septal defects.

Authors:  Ji-Ping Shan; Xiao-Li Wang; Yuan-Gang Qiao; Hong-Xin Wan Yan; Wen-Hui Huang; Shu-Chao Pang; Bo Yan
Journal:  World J Pediatr       Date:  2014-12-17       Impact factor: 2.764

6.  GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect.

Authors:  Dong Wei; Han Bao; Ning Zhou; Gui-Fen Zheng; Xing-Yuan Liu; Yi-Qing Yang
Journal:  Pediatr Cardiol       Date:  2012-09-09       Impact factor: 1.655

7.  Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation.

Authors:  Jian-Yun Gu; Jia-Hong Xu; Hong Yu; Yi-Qing Yang
Journal:  Clinics (Sao Paulo)       Date:  2012-12       Impact factor: 2.365

8.  GATA5 loss-of-function mutations underlie tetralogy of fallot.

Authors:  Dong Wei; Han Bao; Xing-Yuan Liu; Ning Zhou; Qian Wang; Ruo-Gu Li; Ying-Jia Xu; Yi-Qing Yang
Journal:  Int J Med Sci       Date:  2012-12-10       Impact factor: 3.738

9.  Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation.

Authors:  Wen-Hui Xie; Cheng Chang; Ying-Jia Xu; Ruo-Gu Li; Xin-Kai Qu; Wei-Yi Fang; Xu Liu; Yi-Qing Yang
Journal:  Clinics (Sao Paulo)       Date:  2013-06       Impact factor: 2.365

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

Authors:  Xing-Biao Qiu; Ying-Jia Xu; Ruo-Gu Li; Lei Xu; Xu Liu; Wei-Yi Fang; Yi-Qing Yang; Xin-Kai Qu
Journal:  Clinics (Sao Paulo)       Date:  2014-01       Impact factor: 2.365
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