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Literature DB >> 17698744

Genes and atrial fibrillation: a new look at an old problem.

Diane Fatkin¹, Robyn Otway, Jamie I Vandenberg.

Abstract

Entities: Disease

Mesh：

Substances：
Potassium Channels

Year: 2007 PMID： 17698744 DOI： 10.1161/CIRCULATIONAHA.106.688889

Source DB: PubMed Journal: Circulation ISSN： 0009-7322 Impact factor: 29.690

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Cited

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28 in total

1. Pro-arrhythmogenic effects of the S140G KCNQ1 mutation in human atrial fibrillation - insights from modelling.

Authors: Sanjay Kharche; Ismail Adeniran; Jonathan Stott; Phillip Law; Mark R Boyett; Jules C Hancox; Henggui Zhang
Journal: J Physiol Date: 2012-04-16 Impact factor: 5.182

2. Identification of a Kir3.4 mutation in congenital long QT syndrome.

Authors: Yanzong Yang; Yiqing Yang; Bo Liang; Jinqiu Liu; Jun Li; Morten Grunnet; Søren-Peter Olesen; Hanne B Rasmussen; Patrick T Ellinor; Lianjun Gao; Xiaoping Lin; Li Li; Lei Wang; Junjie Xiao; Yi Liu; Ying Liu; Shulong Zhang; Dandan Liang; Luying Peng; Thomas Jespersen; Yi-Han Chen
Journal: Am J Hum Genet Date: 2010-06-11 Impact factor: 11.025

3. Common and rare variants in SCN10A modulate the risk of atrial fibrillation.

Authors: Javad Jabbari; Morten S Olesen; Lei Yuan; Jonas B Nielsen; Bo Liang; Vincenzo Macri; Ingrid E Christophersen; Nikolaj Nielsen; Ahmad Sajadieh; Patrick T Ellinor; Morten Grunnet; Stig Haunsø; Anders G Holst; Jesper H Svendsen; Thomas Jespersen
Journal: Circ Cardiovasc Genet Date: 2015-02

4. R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation.

Authors: Daniel C Bartos; Sabine Duchatelet; Don E Burgess; Didier Klug; Isabelle Denjoy; Rachel Peat; Jean-Marc Lupoglazoff; Véronique Fressart; Myriam Berthet; Michael J Ackerman; Craig T January; Pascale Guicheney; Brian P Delisle
Journal: Heart Rhythm Date: 2010-09-17 Impact factor: 6.343

5. Advances in cardiac ATP-sensitive K+ channelopathies from molecules to populations.

Authors: Andre Terzic; Alexey E Alekseev; Satsuki Yamada; Santiago Reyes; Timothy M Olson
Journal: Circ Arrhythm Electrophysiol Date: 2011-08

6. Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation.

Authors: Denice M Hodgson-Zingman; Margaret L Karst; Leonid V Zingman; Denise M Heublein; Dawood Darbar; Kathleen J Herron; Jeffrey D Ballew; Mariza de Andrade; John C Burnett; Timothy M Olson
Journal: N Engl J Med Date: 2008-07-10 Impact factor: 91.245

7. A novel mutation in LAMIN A/C is associated with isolated early-onset atrial fibrillation and progressive atrioventricular block followed by cardiomyopathy and sudden cardiac death.

Authors: Hubert Pan; Ashleigh A Richards; Xiaohui Zhu; Jose A Joglar; Helen L Yin; Vidu Garg
Journal: Heart Rhythm Date: 2009-02-04 Impact factor: 6.343