Literature DB >> 26487618

Does Atrial Fibrillation Follow Function? Ion Channel Mutations and Lone Atrial Fibrillation.

Sebastian Clauss1, Patrick T Ellinor2.   

Abstract

Entities:  

Keywords:  Editorial; atrial fibrillation; electrophysiology; genetics; human; ion channel; mutation

Mesh：

Year:  2015        PMID： 26487618      PMCID： PMC4751579          DOI： 10.1161/CIRCEP.115.003330

Source DB:  PubMed          Journal:  Circ Arrhythm Electrophysiol        ISSN： 1941-3084


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  13 in total

1.  Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation.

Authors:  Peter Weeke; Babar Parvez; Marcia Blair; Laura Short; Christie Ingram; Gayle Kucera; Tanya Stubblefield; Dan M Roden; Dawood Darbar
Journal:  Heart Rhythm       Date:  2013-10-10       Impact factor: 6.343

Review 2.  The clinical profile and pathophysiology of atrial fibrillation: relationships among clinical features, epidemiology, and mechanisms.

Authors:  Jason Andrade; Paul Khairy; Dobromir Dobrev; Stanley Nattel
Journal:  Circ Res       Date:  2014-04-25       Impact factor: 17.367

3.  Striking In vivo phenotype of a disease-associated human SCN5A mutation producing minimal changes in vitro.

Authors:  Hiroshi Watanabe; Tao Yang; Dina Myers Stroud; John S Lowe; Louise Harris; Thomas C Atack; Dao W Wang; Susan B Hipkens; Brenda Leake; Lynn Hall; Sabina Kupershmidt; Nagesh Chopra; Mark A Magnuson; Naohito Tanabe; Björn C Knollmann; Alfred L George; Dan M Roden
Journal:  Circulation       Date:  2011-08-08       Impact factor: 29.690

Review 4.  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

5.  High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation.

Authors:  Morten S Olesen; Lei Yuan; Bo Liang; Anders G Holst; Nikolaj Nielsen; Jonas B Nielsen; Paula L Hedley; Michael Christiansen; Søren-Peter Olesen; Stig Haunsø; Nicole Schmitt; Thomas Jespersen; Jesper H Svendsen
Journal:  Circ Cardiovasc Genet       Date:  2012-06-08

6.  Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation.

Authors:  Kenshi Hayashi; Tetsuo Konno; Hayato Tada; Satoyuki Tani; Li Liu; Noboru Fujino; Atsushi Nohara; Akihiko Hodatsu; Toyonobu Tsuda; Yoshihiro Tanaka; Masa-aki Kawashiri; Hidekazu Ino; Naomasa Makita; Masakazu Yamagishi
Journal:  Circ Arrhythm Electrophysiol       Date:  2015-06-30

7.  Novel KCNA5 mutation implicates tyrosine kinase signaling in human atrial fibrillation.

Authors:  Tao Yang; Ping Yang; Dan M Roden; Dawood Darbar
Journal:  Heart Rhythm       Date:  2010-06-01       Impact factor: 6.343

8.  Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation.

Authors:  Ingrid E Christophersen; Morten S Olesen; Bo Liang; Martin N Andersen; Anders P Larsen; Jonas B Nielsen; Stig Haunsø; Søren-Peter Olesen; Arnljot Tveit; Jesper H Svendsen; Nicole Schmitt
Journal:  Eur Heart J       Date:  2012-12-21       Impact factor: 29.983

9.  Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation.

Authors:  Morten S Olesen; Laura Andreasen; Javad Jabbari; Lena Refsgaard; Stig Haunsø; Søren-Peter Olesen; Jonas B Nielsen; Nicole Schmitt; Jesper H Svendsen
Journal:  Heart Rhythm       Date:  2013-10-18       Impact factor: 6.343

10.  Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation.

Authors:  Hiroshi Watanabe; Dawood Darbar; Daniel W Kaiser; Kim Jiramongkolchai; Sameer Chopra; Brian S Donahue; Prince J Kannankeril; Dan M Roden
Journal:  Circ Arrhythm Electrophysiol       Date:  2009-03-06
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