M
Min Xia
Researcher at Tongji University
Publications - 3
Citations - 816
Min Xia is an academic researcher from Tongji University. The author has contributed to research in topics: Familial atrial fibrillation & Mutation (genetic algorithm). The author has an hindex of 3, co-authored 3 publications receiving 789 citations.
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Journal ArticleDOI
Identification of a KCNE2 Gain-of-Function Mutation in Patients with Familial Atrial Fibrillation
Yiqing Yang,Min Xia,Qingfeng Jin,Saïd Bendahhou,Jingyi Shi,Yiping Chen,Bo Liang,Jie Lin,Yi Liu,Ban Liu,Qinshu Zhou,Dongwei Zhang,Rong Wang,Ning Ma,Xiaoyan Su,Kaiya Niu,Yan Pei,Wenyuan Xu,Zhaopeng Chen,Haiying Wan,Jianmin Cui,Jacques Barhanin,Yi-Han Chen +22 more
TL;DR: The evaluation of 28 unrelated Chinese kindreds with AF found an arginine-to-cysteine mutation at position 27 (R27C) of KCNE2, the beta subunit of the KCNQ1-KCNE2 channel responsible for a background potassium current, is a gain-of-function mutation associated with the initiation and/or maintenance of AF.
Journal ArticleDOI
A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation.
Min Xia,Qingfeng Jin,Saïd Bendahhou,Yusong He,Marie-Madeleine Larroque,Yiping Chen,Qinshu Zhou,Yiqing Yang,Yi Liu,Ban Liu,Qian Zhu,Yanting Zhou,Jie Lin,Bo Liang,Li Li,Xiongjian Dong,Zhiwen Pan,Rongrong Wang,Haiying Wan,Weiqin Qiu,Wenyuan Xu,Petra M.H. Eurlings,Jacques Barhanin,Yi-Han Chen +23 more
TL;DR: The inward rectifier K(+) channel Kir2.1 mediates the potassium I(K1) current in the heart and a valine-to-isoleucine mutation at position 93 (V93I) of Kir1.1 was found in all affected members in one kindred.
Journal ArticleDOI
Mapping a novel locus for familial atrial fibrillation on chromosome 10p11-q21
Paul G.A. Volders,Qian Zhu,Carl Timmermans,Petra M.H. Eurlings,Xiaoyan Su,Yvonne Arens,Li Li,Roselie J. Jongbloed,Min Xia,Luz-Maria Rodriguez,Yi-Han Chen +10 more
TL;DR: A novel locus for AF is identified on chromosome 10p11-q21, which provides further evidence of genetic heterogeneity in this arrhythmia.