Literature DB >> 10807545

Twenty single nucleotide polymorphisms (SNPs) and their allelic frequencies in four genes that are responsible for familial long QT syndrome in the Japanese population.

H Iwasa1, T Itoh, R Nagai, Y Nakamura, T Tanaka.   

Abstract

We report here 20 single nucleotide polymorphisms (SNPs), including 10 novel ones, and their allelic frequencies detected in four genes that are known to be responsible for familial long QT syndrome in the Japanese population; 7 polymorphisms are in the KCNQ1 gene, 6 in the KCNH2 gene, 5 in the SCN5A gene, and 2 in the KCNE1 gene. These data will be of use for genetic association studies of acquired cardiac arrhythmias.

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Year:  2000        PMID: 10807545     DOI: 10.1007/s100380050207

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  21 in total

1.  Detection of genetic variation in KCNQ1 gene by high-resolution melting analysis in a prospective-based series of postmortem negative sudden death: comparison of results obtained in fresh frozen and formalin-fixed paraffin-embedded tissues.

Authors:  Audrey Farrugia; Christine Keyser; Bertrand Ludes
Journal:  Int J Legal Med       Date:  2012-03-09       Impact factor: 2.686

2.  Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms.

Authors:  Ling-Ping Lai; Yi-Ning Su; Fu-Tien Chiang; Jyh-Ming Juang; Yen-Bin Liu; Yi-Lwun Ho; Wen-Jone Chen; San-Jou Yeh; Chun-Chieh Wang; Yu-Lin Ko; Tsu-Juey Wu; Kwo-Chang Ueng; Meng-Huan Lei; Hsuan-Ming Tsao; Shih-Ann Chen; Tin-Kwang Lin; Mei-Hwan Wu; Huey-Ming Lo; Shoei K Stephen Huang; Jiunn-Lee Lin
Journal:  J Hum Genet       Date:  2005-09-10       Impact factor: 3.172

3.  Genetic polymorphisms in KCNQ1, HERG, KCNE1 and KCNE2 genes in the Chinese, Malay and Indian populations of Singapore.

Authors:  Seok Hwee Koo; Woon Fei Ho; Edmund Jon Deoon Lee
Journal:  Br J Clin Pharmacol       Date:  2006-03       Impact factor: 4.335

4.  Pharmacological and electrophysiological characterization of nine, single nucleotide polymorphisms of the hERG-encoded potassium channel.

Authors:  Roope Männikkö; G Overend; C Perrey; C L Gavaghan; J-P Valentin; J Morten; M Armstrong; C E Pollard
Journal:  Br J Pharmacol       Date:  2009-08-10       Impact factor: 8.739

5.  The antihistamine fexofenadine does not affect I(Kr) currents in a case report of drug-induced cardiac arrhythmia.

Authors:  Constanze R Scherer; Christian Lerche; Niels Decher; Adrienne T Dennis; Patrick Maier; Eckhard Ficker; Andreas E Busch; Bernd Wollnik; Klaus Steinmeyer
Journal:  Br J Pharmacol       Date:  2002-11       Impact factor: 8.739

6.  Cardiac channelopathy causing sudden death as revealed by molecular autopsy.

Authors:  Silke Kauferstein; Nadine Kiehne; Steve Peigneur; Jan Tytgat; Hansjürgen Bratzke
Journal:  Int J Legal Med       Date:  2012-02-28       Impact factor: 2.686

7.  Genetics can contribute to the prognosis of Brugada syndrome: a pilot model for risk stratification.

Authors:  Elena Sommariva; Carlo Pappone; Filippo Martinelli Boneschi; Chiara Di Resta; Maria Rosaria Carbone; Erika Salvi; Pasquale Vergara; Simone Sala; Daniele Cusi; Maurizio Ferrari; Sara Benedetti
Journal:  Eur J Hum Genet       Date:  2013-01-16       Impact factor: 4.246

8.  Genetic analysis of the cardiac sodium channel gene SCN5A in Koreans with Brugada syndrome.

Authors:  Dong-Jik Shin; Yangsoo Jang; Hyun-Young Park; Jong Eun Lee; Keumjin Yang; Eunmin Kim; Yoonjung Bae; Jongmin Kim; Jeongki Kim; Sung Soon Kim; Moon Hyoung Lee; Mohamed Chahine; Sungjoo Kim Yoon
Journal:  J Hum Genet       Date:  2004-08-26       Impact factor: 3.172

9.  Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval.

Authors:  Honghuang Lin; Jessica van Setten; Albert V Smith; Nathan A Bihlmeyer; Helen R Warren; Jennifer A Brody; Farid Radmanesh; Leanne Hall; Niels Grarup; Martina Müller-Nurasyid; Thibaud Boutin; Niek Verweij; Henry J Lin; Ruifang Li-Gao; Marten E van den Berg; Jonathan Marten; Stefan Weiss; Bram P Prins; Jeffrey Haessler; Leo-Pekka Lyytikäinen; Hao Mei; Tamara B Harris; Lenore J Launer; Man Li; Alvaro Alonso; Elsayed Z Soliman; John M Connell; Paul L Huang; Lu-Chen Weng; Heather S Jameson; William Hucker; Alan Hanley; Nathan R Tucker; Yii-Der Ida Chen; Joshua C Bis; Kenneth M Rice; Colleen M Sitlani; Jan A Kors; Zhijun Xie; Chengping Wen; Jared W Magnani; Christopher P Nelson; Jørgen K Kanters; Moritz F Sinner; Konstantin Strauch; Annette Peters; Melanie Waldenberger; Thomas Meitinger; Jette Bork-Jensen; Oluf Pedersen; Allan Linneberg; Igor Rudan; Rudolf A de Boer; Peter van der Meer; Jie Yao; Xiuqing Guo; Kent D Taylor; Nona Sotoodehnia; Jerome I Rotter; Dennis O Mook-Kanamori; Stella Trompet; Fernando Rivadeneira; André Uitterlinden; Mark Eijgelsheim; Sandosh Padmanabhan; Blair H Smith; Henry Völzke; Stephan B Felix; Georg Homuth; Uwe Völker; Massimo Mangino; Timothy D Spector; Michiel L Bots; Marco Perez; Mika Kähönen; Olli T Raitakari; Vilmundur Gudnason; Dan E Arking; Patricia B Munroe; Bruce M Psaty; Cornelia M van Duijn; Emelia J Benjamin; Jonathan Rosand; Nilesh J Samani; Torben Hansen; Stefan Kääb; Ozren Polasek; Pim van der Harst; Susan R Heckbert; J Wouter Jukema; Bruno H Stricker; Caroline Hayward; Marcus Dörr; Yalda Jamshidi; Folkert W Asselbergs; Charles Kooperberg; Terho Lehtimäki; James G Wilson; Patrick T Ellinor; Steven A Lubitz; Aaron Isaacs
Journal:  Circ Genom Precis Med       Date:  2018-05

10.  Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention.

Authors:  Alica M Goldman; Elijah R Behr; Christopher Semsarian; Richard D Bagnall; Sanjay Sisodiya; Paul N Cooper
Journal:  Epilepsia       Date:  2016-01       Impact factor: 5.864

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