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Literature DB >> 15547041

Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation.

P T Ellinor, R K Moore, K K Patton, J N Ruskin, M R Pollak, C A Macrae.

Abstract

Entities: Disease Gene Mutation

Mesh：

Substances：

Year: 2004 PMID： 15547041 PMCID： PMC1768565 DOI： 10.1136/hrt.2003.027227

Source DB: PubMed Journal: Heart ISSN： 1355-6037 Impact factor: 5.994

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5 in total

Review 1. New ideas about atrial fibrillation 50 years on.

Authors: Stanley Nattel
Journal: Nature Date: 2002-01-10 Impact factor: 49.962

Review 2. Epidemiology and natural history of atrial fibrillation: clinical implications.

Authors: S S Chugh; J L Blackshear; W K Shen; S C Hammill; B J Gersh
Journal: J Am Coll Cardiol Date: 2001-02 Impact factor: 24.094

3. Identification of a genetic locus for familial atrial fibrillation.

Authors: R Brugada; T Tapscott; G Z Czernuszewicz; A J Marian; A Iglesias; L Mont; J Brugada; J Girona; A Domingo; L L Bachinski; R Roberts
Journal: N Engl J Med Date: 1997-03-27 Impact factor: 91.245

4. Locus for atrial fibrillation maps to chromosome 6q14-16.

Authors: Patrick T Ellinor; Jordan T Shin; Rachel K Moore; Danita M Yoerger; Calum A MacRae
Journal: Circulation Date: 2003-06-02 Impact factor: 29.690

5. KCNQ1 gain-of-function mutation in familial atrial fibrillation.

Authors: Yi-Han Chen; Shi-Jie Xu; Said Bendahhou; Xiao-Liang Wang; Ying Wang; Wen-Yuan Xu; Hong-Wei Jin; Hao Sun; Xiao-Yan Su; Qi-Nan Zhuang; Yi-Qing Yang; Yue-Bin Li; Yi Liu; Hong-Ju Xu; Xiao-Fei Li; Ning Ma; Chun-Ping Mou; Zhu Chen; Jacques Barhanin; Wei Huang
Journal: Science Date: 2003-01-10 Impact factor: 47.728

5 in total

26 in total

1. Ion channel mutations in AF: signal or noise?

Authors: Patrick T Ellinor; Calum A MacRae
Journal: Heart Rhythm Date: 2008-01-17 Impact factor: 6.343

2. 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 3. Genetics of atrial fibrillation.

Authors: Steven A Lubitz; B Alexander Yi; Patrick T Ellinor
Journal: Heart Fail Clin Date: 2010-04 Impact factor: 3.179

4. Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation.

Authors: Marylyn D Ritchie; Shane Rowan; Gayle Kucera; Tanya Stubblefield; Marcia Blair; Shannon Carter; Dan M Roden; Dawood Darbar
Journal: J Am Coll Cardiol Date: 2012-07-18 Impact factor: 24.094

Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation.

Review 1. New ideas about atrial fibrillation 50 years on.

Review 2. Epidemiology and natural history of atrial fibrillation: clinical implications.

3. Identification of a genetic locus for familial atrial fibrillation.

4. Locus for atrial fibrillation maps to chromosome 6q14-16.

5. KCNQ1 gain-of-function mutation in familial atrial fibrillation.

1. Ion channel mutations in AF: signal or noise?

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

Review 3. Genetics of atrial fibrillation.

4. Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation.

5. Comprehensive mutation scanning of KCNQ1 in 111 Han Chinese patients with lone atrial fibrillation.

Review 6. Monogenic atrial fibrillation as pathophysiological paradigms.

7. Familial aggregation in lone atrial fibrillation.

Review 8. Genetic mechanisms of atrial fibrillation: impact on response to treatment.

Review 9. Next-Generation Sequencing in the Genetics of Human Atrial Fibrillation.

10. Molecular genetics of atrial fibrillation.