ISL1 loss-of-function variation causes familial atrial fibrillation-Reference-Cited by-同舟云学术

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ISL1 loss-of-function variation causes familial atrial fibrillation

Published:2020-11 Issue:11 Volume:63 Page:104029
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Wu Shao-Hui,Wang Xin-Hua,Xu Ying-Jia,Gu Jia-Ning,Yang Chen-Xi,Qiao Qi,Guo Xiao-Juan,Guo Yu-Han,Qiu Xing-Biao,Jiang Wei-Feng,Yang Yi-Qing

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference63 articles.

1. Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation;Ahlberg;Nat. Commun.,2018

2. Underdiagnoses resulting from variant misinterpretation: time for systematic reanalysis of whole exome data?;Al-Murshedi;Eur. J. Med. Genet.,2019

3. Identification of a genetic locus for familial atrial fibrillation;Brugada;N. Engl. J. Med.,1997

4. Human ISL1 heart progenitors generate diverse multipotent cardiovascular cell lineages;Bu;Nature,2009

5. Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation and contributes a majority of cells to the heart;Cai;Dev. Cell,2003

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Single-cell Transcriptomic Atlas of Human Atrial Fibrillation;2024-09-11

2. Genetic Variants of ISL1 Gene Promoter Identified from Congenital Tetralogy of Fallot Patients Alter Cellular Function Forming Disease Basis;Biomolecules;2023-02-13

3. Genetics of atrial fibrillation;Current Opinion in Cardiology;2023-02-10

4. Identification and functional analysis of genetic variants of ISL1 gene promoter in human atrial septal defects;The Journal of Gene Medicine;2022-10-27

5. Regulation of cardiac ion channels by transcription factors: Looking for new opportunities of druggable targets for the treatment of arrhythmias;Biochemical Pharmacology;2022-10

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