The molecular genetic basis of atrial fibrillation-Reference-Cited by-同舟云学术

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The molecular genetic basis of atrial fibrillation

Published:2020-07-02 Issue:12 Volume:139 Page:1485-1498
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Huang Xin,Li Yuhui,Zhang Junguo,Wang Xiaojie,Li Ziyi,Li Guowei

Funder

the research grant from the Science Foundation of Guangdong Second Provincial General Hospital

Medical Scientific Research Foundation of Guangdong Province of China

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-020-02203-w.pdf

Reference121 articles.

1. Ackerman MJ et al (2011) HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA). Europace 13:1077–1109. https://doi.org/10.1093/europace/eur245

2. Alkan C, Coe BP, Eichler EE (2011) Genome structural variation discovery and genotyping. Nat Rev Genet 12:363–376. https://doi.org/10.1038/nrg2958

3. Andersson R, Sandelin A (2020) Determinants of enhancer and promoter activities of regulatory elements. Nat Rev Genet 21:71–87. https://doi.org/10.1038/s41576-019-0173-8

4. Arnar DO, Thorvaldsson S, Manolio TA, Thorgeirsson G, Kristjansson K, Hakonarson H, Stefansson K (2006) Familial aggregation of atrial fibrillation in Iceland. Eur Heart J 27:708–712. https://doi.org/10.1093/eurheartj/ehi727

5. Ball J, Carrington MJ, McMurray JJ, Stewart S (2013) Atrial fibrillation: profile and burden of an evolving epidemic in the 21st century. Int J Cardiol 167:1807–1824. https://doi.org/10.1016/j.ijcard.2012.12.093

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1. A novel PRRX1 loss-of-function variation contributing to familial atrial fibrillation and congenital patent ductus arteriosus;Genetics and Molecular Biology;2022

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3. Targeting of Potassium Channels in Cardiac Arrhythmias;Trends in Pharmacological Sciences;2021-06

4. Multiomics Analysis of Genetics and Epigenetics Reveals Pathogenesis and Therapeutic Targets for Atrial Fibrillation;BioMed Research International;2021-03-25

5. KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy;Genes;2021-03-12

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