HuGE Literature Finder
Records 1-75
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Mutation Screening of KCNQ1 and KCNE1 Genes in Iranian Patients With Jervell and Lange-Nielsen Syndrome.
Fetal and pediatric pathology 2019 Apr 1-9. Vojdani Samaneh, Milanizadeh Saman, Molaei Fatemeh, Ajalloueyane Mohammad, Khosravi Arezoo, Hamzefzadeh Leila, Ghasemi Mohammad Mehdi, Talee Mohammad Reza, Abbaszadegan Mohammad Re |
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QT length during methadone maintenance treatment: Gene x dose interaction.
Fundamental & clinical pharmacology 2018 Aug . Zerdazi El-Hadi, Vorspan Florence, Marees Andries T, Naccache François, Lepine Jean-Pierre, Laplanche Jean-Louis, Prince Nathalie, Marie-Claire Cynthia, Bellivier Frank, Mouly Stéphane, Bloch Vanes |
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[Association of KCNE1 and KCNE4 gene polymorphisms with atrial fibrillation among Uygur and Han Chinese populations in Xinjiang].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2017 Oct 34 (5): 743-748. Miao Haijun, Zhou Xiaohui, Kabinur Keyimu, Zou Ting, Palida Abulizi, Tang Baope |
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Ethnic Differences in Genetic Ion Channelopathies Associated with Sudden Cardiac Death: A Systematic Review and Meta-Analysis.
Annals of clinical and laboratory science 2017 Aug 47 (4): 481-490. Kong Tim, Feulefack Joseph, Ruether Kim, Shen Fan, Zheng Wang, Chen Xing-Zhen, Sergi Consola |
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Association between KCNE1 G38S gene polymorphism and risk of atrial fibrillation: A PRISMA-compliant meta-analysis.
Medicine 2017 Jun 96 (25): e7253. Jiang Yu-Feng, Chen Min, Zhang Nan-Nan, Yang Hua-Jia, Xu Lang-Biao, Rui Qing, Sun Si-Jia, Yao Jia-Lu, Zhou Ya-Fe |
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The role of known variants of KCNQ1, KCNH2, KCNE1, SCN5A, and NOS1AP in water-related deaths.
International journal of legal medicine 2016 Jul . Tzimas Iliana, Zingraf Jana-Christin, Bajanowski Thomas, Poetsch Micae |
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Latent pathogenicity of the G38S polymorphism of KCNE1 K(+) channel modulator.
Heart and vessels 2016 Jun . Yamaguchi Yoshiaki, Mizumaki Koichi, Hata Yukiko, Sakamoto Tamotsu, Nakatani Yosuke, Kataoka Naoya, Ichida Fukiko, Inoue Hiroshi, Nishida Nao |
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Abnormal repolarization dynamics in a patient with KCNE1(G38S) who presented with torsades de pointes.
Journal of electrocardiology 2015 Oct . Yamaguchi Yoshiaki, Mizumaki Koichi, Hata Yukiko, Inoue Hiros |
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Multiplex ligation-dependent probe amplification copy number variant analysis in patients with acquired long QT syndrome.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2015 Apr 17 (4): 635-41. Williams Victoria S, Cresswell Carl J, Ruspi Gerhard, Yang Tao, Atak Thomas C, McLoughlin Matthew, Ingram Christiana D, Ramirez Andrea H, Roden Dan, Armstrong Mart |
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Genetic analysis, in silico prediction, and family segregation in long QT syndrome.
European journal of human genetics : EJHG 2015 Jan 23 (1): 79-85. Riuró Helena, Campuzano Oscar, Berne Paola, Arbelo Elena, Iglesias Anna, Pérez-Serra Alexandra, Coll-Vidal Mònica, Partemi Sara, Mademont-Soler Irene, Picó Ferran, Allegue Catarina, Oliva Antonio, Gerstenfeld Edward, Sarquella-Brugada Georgia, Castro-Urda Víctor, Fernández-Lozano Ignacio, Mont Lluís, Brugada Josep, Scornik Fabiana S, Brugada Ram |
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Correlation analysis between the delayed rectifier potassium channel KCNE1 (G38S) polymorphism and atrial fibrillation among the senior Uygur population in Xinjiang.
Genetics and molecular research : GMR 2015 14 (4): 15906-12. Wugeti N, Yu-Jun G, Juan S, Mahemuti |
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Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.
PloS one 2015 10 (7): e0133037. Allegue Catarina, Coll Mònica, Mates Jesus, Campuzano Oscar, Iglesias Anna, Sobrino Beatriz, Brion Maria, Amigo Jorge, Carracedo Angel, Brugada Pedro, Brugada Josep, Brugada Ram |
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Evaluation of a new high-throughput next-generation sequencing method based on a custom AmpliSeq™ library and ion torrent PGM™ sequencing for the rapid detection of genetic variations in long QT syndrome.
Molecular diagnosis & therapy 2014 Oct 18 (5): 533-9. Millat Gilles, Chanavat Valérie, Rousson Robe |
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KCNH2 polymorphism and methadone dosage interact to enhance QT duration.
Drug and alcohol dependence 2014 Aug 141 34-8. Hajj Aline, Ksouda Kamilia, Peoc'h Katell, Curis Emmanuel, Messali Anne, Deveaux Laurence Labat, Bloch Vanessa, Prince Nathalie, Mouly Stéphane, Scherrmann Jean-Michel, Lépine Jean-Pierre, Laplanche Jean-Louis, Drici Milou-Daniel, Vorspan Floren |
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Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndrome.
Journal of the American College of Cardiology 2014 Apr 63 (14): 1430-7. Weeke Peter, Mosley Jonathan D, Hanna David, Delaney Jessica T, Shaffer Christian, Wells Quinn S, Van Driest Sara, Karnes Jason H, Ingram Christie, Guo Yan, Shyr Yu, Norris Kris, Kannankeril Prince J, Ramirez Andrea H, Smith Joshua D, Mardis Elaine R, Nickerson Deborah, George Alfred L, Roden Dan |
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Genetic diversity of the KCNE1 gene and susceptibility to postoperative atrial fibrillation.
American heart journal 2014 Feb 167 (2): 274-280.e1. Voudris Konstantinos V, Apostolakis Stavros, Karyofillis Panagiotis, Doukas Konstantinos, Zaravinos Apostolos, Androutsopoulos Vasilis P, Michalis Alkis, Voudris Vassilis, Spandidos Demetrios |
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Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation.
Heart rhythm : the official journal of the Heart Rhythm Society 2014 Feb 11 (2): 246-51. Olesen Morten S, Andreasen Laura, Jabbari Javad, Refsgaard Lena, Haunsø Stig, Olesen Søren-Peter, Nielsen Jonas B, Schmitt Nicole, Svendsen Jesper |
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KCNE1 112G>a polymorphism and atrial fibrillation risk: a meta-analysis.
Genetics and molecular research : GMR 2014 13 (4): 8367-77. Han H G, Wang H S, Yin Z, Jiang H, Fang M, Han |
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Mink S38G gene polymorphism and atrial fibrillation in the Chinese population: a meta-analysis of 1871 participants.
TheScientificWorldJournal 2014 2014 768681. Li Yan-yan, Wang Lian-sheng, Lu Xin-zhe |
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IKs Blockade Contributes Importantly to Drug-Induced Long QT Syndrome.
Circulation. Arrhythmia and electrophysiology 2013 Aug . Veerman CC, Verkerk AO, Blom MT, Klemens CA, Langendijk PN, van Ginneken AC, Wilders R, Tan HL |
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Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory.
Genetic testing and molecular biomarkers 2013 Jul 17 (7): 553-61. Lieve Krystien V, Williams Leah, Daly Amy, Richard Gabriele, Bale Sherri, Macaya Daniela, Chung Wendy |
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Do LQTS gene single nucleotide polymorphisms alter QTc intervals at rest and during exercise stress testing?
Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2013 May 18 (3): 288-93. Aziz Peter F, Wieand Tammy S, Ganley Jamie, Henderson Jacqueline, McBride Michael, Shah Maully |
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Return to play? Athletes with congenital long QT syndrome.
British journal of sports medicine 2013 Jan 47 (1): 28-33. Johnson Jonathan N, Ackerman Michael |
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KCNE1 rs1805127 polymorphism increases the risk of atrial fibrillation: a meta-analysis of 10 studies.
PloS one 2013 8 (7): e68690. Liang Chang, Li Xiankai, Xu Yawei, Chen Qingyong, Wu Yadong, Wang Wan, Li Weiming, Qiu Manta |
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Association between KCNE1 (G38S) genetic polymorphism and non-valvular atrial fibrillation in an Uygur population.
Wiener klinische Wochenschrift 2012 Nov . Haijun M, Xiaohui Z, Ting M, Renner W, Abulizi P, Baopeng T |
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Association of KCNE1 genetic polymorphisms with atrial fibrillation in a Chinese Han population.
Genetic testing and molecular biomarkers 2012 Nov 16 (11): 1343-6. Yao Juan, Ma Yi-Tong, Xie Xiang, Liu Fen, Chen Bang-Da |
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Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing.
Mayo Clinic proceedings 2012 Jun 87 (6): 524-39. Tester David J, Medeiros-Domingo Argelia, Will Melissa L, Haglund Carla M, Ackerman Michael |
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A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes.
Circulation. Cardiovascular genetics 2012 Feb 5 (1): 91-9. Kääb Stefan, Crawford Dana C, Sinner Moritz F, Behr Elijah R, Kannankeril Prince J, Wilde Arthur A M, Bezzina Connie R, Schulze-Bahr Eric, Guicheney Pascale, Bishopric Nanette H, Myerburg Robert J, Schott Jean-Jacques, Pfeufer Arne, Beckmann Britt-Maria, Martens Eimo, Zhang Taifang, Stallmeyer Birgit, Zumhagen Sven, Denjoy Isabelle, Bardai Abdennasser, Van Gelder Isabelle C, Jamshidi Yalda, Dalageorgou Chrysoula, Marshall Vanessa, Jeffery Steve, Shakir Saad, Camm A John, Steinbeck Gerhard, Perz Siegfried, Lichtner Peter, Meitinger Thomas, Peters Annette, Wichmann H-Erich, Ingram Christiana, Bradford Yuki, Carter Shannon, Norris Kris, Ritchie Marylyn D, George Alfred L, Roden Dan |
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Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing.
BMC cardiovascular disorders 2012 12 (1): 95. Stattin Eva-Lena, Boström Ida Maria, Winbo Annika, Cederquist Kristina, Jonasson Jenni, Jonsson Björn-Anders, Diamant Ulla-Britt, Jensen Steen M, Rydberg Annika, Norberg An |
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[Association of rs1805127 polymorphism of KCNE1 gene with atrial fibrillation in Uigur population of Xinjiang].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2011 Aug 28 (4): 436-40. Yao Juan, Ma Yi-tong, Xie Xiang, Liu Fen, Chen Bang-dang, An Yo |
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Mutation analysis ion channel genes ventricular fibrillation survivors with coronary artery disease.
Pacing and clinical electrophysiology : PACE 2011 Jun 34 (6): 742-9. Novotny Tomas, Kadlecova Jitka, Raudenska Martina, Bittnerova Alexandra, Andrsova Irena, Florianova Alena, Vasku Anna, Neugebauer Petr, Kozak Milan, Sepsi Milan, Krivan Lubomir, Gaillyova Renata, Spinar Jindri |
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Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals.
Hypertension 2011 May 57 (5): 903-10. Johnson Andrew D, Newton-Cheh Christopher, Chasman Daniel I, Ehret Georg B, Johnson Toby, Rose Lynda, Rice Kenneth, Verwoert Germaine C, Launer Lenore J, Gudnason Vilmundur, Larson Martin G, Chakravarti Aravinda, Psaty Bruce M, Caulfield Mark, van Duijn Cornelia M, Ridker Paul M, Munroe Patricia B, Levy Daniel, , , |
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Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds.
Heart rhythm : the official journal of the Heart Rhythm Society 2011 Mar 8 (3): 412-9. Skinner Jonathan R, Crawford Jackie, Smith Warren, Aitken Andrew, Heaven David, Evans Cary-Anne, Hayes Ian, Neas Katherine R, Stables Simon, Koelmeyer Timothy, Denmark Lloyd, Vuletic Jane, Maxwell Fraser, White Kate, Yang Tao, Roden Dan M, Leren Trond P, Shelling Andrew, Love Donald R, |
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KCNE1 D85N polymorphism--a sex-specific modifier in type 1 long QT syndrome?
BMC medical genetics 2011 12 (1): 11. Lahtinen Annukka M, Marjamaa Annukka, Swan Heikki, Kontula Kim |
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Large-scale candidate gene analysis of HDL particle features.
PloS one 2011 6 (1): e14529. Kaess Bernhard M, Tomaszewski Maciej, Braund Peter S, Stark Klaus, Rafelt Suzanne, Fischer Marcus, Hardwick Robert, Nelson Christopher P, Debiec Radoslaw, Huber Fritz, Kremer Werner, Kalbitzer Hans Robert, Rose Lynda M, Chasman Daniel I, Hopewell Jemma, Clarke Robert, Burton Paul R, Tobin Martin D, Hengstenberg Christian, Samani Nilesh |
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The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.
Journal of negative results in biomedicine 2011 10 (1): 12. Hedley Paula L, Haundrup Ole, Andersen Paal S, Aidt Frederik H, Jensen Morten, Moolman-Smook Johanna C, Bundgaard Henning, Christiansen Micha |
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Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing.
The American journal of cardiology 2010 Oct 106 (8): 1124-8. Tester David J, Benton Amber J, Train Laura, Deal Barbara, Baudhuin Linnea M, Ackerman Michael |
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Relationship of common candidate gene variants to electrocardiographic T-wave peak to T-wave end interval and T-wave morphology parameters.
Heart rhythm : the official journal of the Heart Rhythm Society 2010 Jul 7 (7): 898-903. Porthan Kimmo, Marjamaa Annukka, Viitasalo Matti, Väänänen Heikki, Jula Antti, Toivonen Lauri, Nieminen Markku S, Newton-Cheh Christopher, Salomaa Veikko, Kontula Kimmo, Oikarinen Las |
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Common variants in cardiac ion channel genes are associated with sudden cardiac death.
Circulation. Arrhythmia and electrophysiology 2010 Jun 3 (3): 222-9. Albert Christine M, MacRae Calum A, Chasman Daniel I, VanDenburgh Martin, Buring Julie E, Manson JoAnn E, Cook Nancy R, Newton-Cheh Christoph |
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Torsades de pointes during complete atrioventricular block: Genetic factors and electrocardiogram correlates.
The Canadian journal of cardiology 2010 Apr 26 (4): 208-12. Subbiah Rajesh N, Gollob Michael H, Gula Lorne J, Davies Robert W, Leong-Sit Peter, Skanes Allan C, Yee Raymond, Klein George J, Krahn Andrew |
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S38G single-nucleotide polymorphism at the KCNE1 locus is associated with heart failure.
Heart rhythm : the official journal of the Heart Rhythm Society 2010 Mar 7 (3): 363-7. Fatini Cinzia, Sticchi Elena, Marcucci Rossella, Verdiani Valerio, Nozzoli Carlo, Vassallo Cristina, Emdin Michele, Abbate Rosanna, Gensini Gian Fran |
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Cardiac ion channel gene mutations in Greek long QT syndrome patients.
Journal of applied genetics 2010 51 (4): 515-8. Kotta C-M, Anastasakis A, Gatzoulis K, Papagiannis J, Geleris P, Stefanadis |
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Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
American journal of human genetics 2009 Nov 85 (5): 628-42. Talmud Philippa J, Drenos Fotios, Shah Sonia, Shah Tina, Palmen Jutta, Verzilli Claudio, Gaunt Tom R, Pallas Jacky, Lovering Ruth, Li Kawah, Casas Juan Pablo, Sofat Reecha, Kumari Meena, Rodriguez Santiago, Johnson Toby, Newhouse Stephen J, Dominiczak Anna, Samani Nilesh J, Caulfield Mark, Sever Peter, Stanton Alice, Shields Denis C, Padmanabhan Sandosh, Melander Olle, Hastie Claire, Delles Christian, Ebrahim Shah, Marmot Michael G, Smith George Davey, Lawlor Debbie A, Munroe Patricia B, Day Ian N, Kivimaki Mika, Whittaker John, Humphries Steve E, Hingorani Aroon D, , , |
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Interactions of MinK and e-NOS gene polymorphisms appear to be inconsistent predictors of atrial fibrillation propensity, but long alleles of ESR1 promoter TA repeat may be a promising marker.
Collegium antropologicum 2009 Sep 33 (3): 933-7. Smalcelj Anton, Serti? Jadranka, Golubi? Karlo, Jurci? Ljiljana, Banfi? Ljiljana, Brida Margari |
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Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
Heart rhythm : the official journal of the Heart Rhythm Society 2009 Sep 6 (9): 1297-303. Kapplinger Jamie D, Tester David J, Salisbury Benjamin A, Carr Janet L, Harris-Kerr Carole, Pollevick Guido D, Wilde Arthur A M, Ackerman Michael |
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D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndrome.
Journal of the American College of Cardiology 2009 Aug 54 (9): 812-9. Nishio Yukiko, Makiyama Takeru, Itoh Hideki, Sakaguchi Tomoko, Ohno Seiko, Gong Yin-Zhi, Yamamoto Satoshi, Ozawa Tomoya, Ding Wei-Guang, Toyoda Futoshi, Kawamura Mihoko, Akao Masaharu, Matsuura Hiroshi, Kimura Takeshi, Kita Toru, Horie Mino |
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Common candidate gene variants are associated with QT interval duration in the general population.
Journal of internal medicine 2009 Apr 265 (4): 448-58. Marjamaa A, Newton-Cheh C, Porthan K, Reunanen A, Lahermo P, Väänänen H, Jula A, Karanko H, Swan H, Toivonen L, Nieminen M S, Viitasalo M, Peltonen L, Oikarinen L, Palotie A, Kontula K, Salomaa |
Common variants at ten loci influence QT interval duration in the QTGEN Study.
Nature genetics 2009 Apr 41 (4): 4. Newton-Cheh C, Eijgelsheim M, Rice KM, de Bakker PI, Yin X, Estrada K, Bis JC, Marciante K, Rivadeneira F, Noseworthy PA, Sotoodehnia N, Smith NL, Rotter JI, Kors JA, Witteman JC, Hofman A, Heckbert SR, O'Donnell CJ, Uitterlinden AG, Psaty BM, Lumley T, Larson MG, Stricker BH |
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Contribution of Long-QT Syndrome Genetic Variants in Sudden Infant Death Syndrome.
Pediatric cardiology 2009 Mar . Millat G, Kugener B, Chevalier P, Chahine M, Huang H, Malicier D, Rodriguez-Lafrasse C, Rousson R |
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A Genotype Dependent Intermediate ECG Phenotype in Patients with Persistent Lone Atrial Fibrillation.
Circulation. Arrhythmia and electrophysiology 2009 Feb 2 (1): 1. Husser D, Stridh M, Sörnmo L, Roden DM, Darbar D, Bollmann A |
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Relationship between genetic variants in myocardial sodium and potassium channel genes and QT interval duration in diabetics: the Diabetes Heart Study.
Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2009 Jan 14 (1): 72-9. Lehtinen Allison B, Daniel Kurt R, Shah Sidharth A, Nelson Matthew R, Ziegler Julie T, Freedman Barry I, Carr J Jeffrey, Herrington David M, Langefeld Carl D, Bowden Donald |
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Effect of common KCNE1 and SCN5A ion channel gene variants on T-wave alternans, a marker of cardiac repolarization, during clinical exercise stress test: the Finnish Cardiovascular Study.
Translational research : the journal of laboratory and clinical medicine 2008 Aug 152 (2): 49-58. Koskela Jenni, Kähönen Mika, Fan Meng, Nieminen Tuomo, Lehtinen Rami, Viik Jari, Nikus Kjell, Niemelä Kari, Kööbi Tiit, Turjanmaa Väinö, Pörsti Ilkka, Lehtimäki Ter |
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The association between SCN5A, KCNQ1 and KCNE1 gene polymorphisms and complex ventricular arrhythmias in survivors of myocardial infarction.
Kardiologia polska 2008 Aug 66 (8): 845-53; discussion 854-5. Olszak-Wa?kiewicz Marlena, Kubik Leszek, Dziuk Miros?aw, Sid?o Ewa, Kucharczyk Krzysztof, Kaczanowski Rados? |
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[Study on the correlation between CETP TaqIB, KCNE1 S38G and eNOS T-786C gene polymorphisms for predisposition and non-valvular atrial fibrillation].
Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi 2008 May 29 (5): 486-92. Xu Li-Xin, Yang Wei-Yu, Zhang Huai-Qin, Tao Zhi-Hua, Duan Cheng-Che |
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Single nucleotide polymorphisms and haplotype of four genes encoding cardiac ion channels in Chinese and their association with arrhythmia.
Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2008 Apr 13 (2): 180-90. Zhang Yu, Chang Bingxi, Hu Songnian, Wang Duenmei, Fang Quan, Huang Xianyong, Zeng Qiang, Qi Mi |
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Long QT and Brugada syndrome gene mutations in New Zealand.
Heart rhythm : the official journal of the Heart Rhythm Society 2007 Oct 4 (10): 1306-14. Chung Seo-Kyung, MacCormick Judith M, McCulley Caroline H, Crawford Jackie, Eddy Carey-Anne, Mitchell Edwin A, Shelling Andrew N, French John K, Skinner Jonathan R, Rees Mark |
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Torsades de pointes complicating atrioventricular block: evidence for a genetic predisposition.
Heart rhythm : the official journal of the Heart Rhythm Society 2007 Feb 4 (2): 170-4. Chevalier Philippe, Bellocq Chloé, Millat Gilles, Piqueras Eric, Potet Franck, Schott Jean-Jacques, Baró Isabelle, Lemarec Hervé, Barhanin Jacques, Rousson Robert, Rodriguez-Lafrasse Clai |
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Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.
Circulation 2007 Jan 115 (3): 361-7. Arnestad Marianne, Crotti Lia, Rognum Torleiv O, Insolia Roberto, Pedrazzini Matteo, Ferrandi Chiara, Vege Ashild, Wang Dao W, Rhodes Troy E, George Alfred L, Schwartz Peter |
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The single nucleotide polymorphisms of I(Ks) potassium channel genes and their association with atrial fibrillation in a Chinese population.
Cardiology 2007 108 (2): 97-103. Zeng Zhiyu, Tan Chen, Teng Siyong, Chen Jianhong, Su Shaoyong, Zhou Xiaoyang, Wang Fangzheng, Zhang Shu, Gu Dongfeng, Makielski Jonathan C, Pu Jiel |
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Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative results.
Heart rhythm : the official journal of the Heart Rhythm Society 2006 Jul 3 (7): 815-21. Tester David J, Cronk Lisa B, Carr Janet L, Schulz Vincent, Salisbury Benjamin A, Judson Richard S, Ackerman Michael |
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Genetic polymorphisms in KCNQ1, HERG, KCNE1 and KCNE2 genes in the Chinese, Malay and Indian populations of Singapore.
British journal of clinical pharmacology 2006 Mar 61 (3): 301-8. Koo Seok Hwee, Ho Woon Fei, Lee Edmund Jon Deo |
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Effect of clinical phenotype on yield of long QT syndrome genetic testing.
Journal of the American College of Cardiology 2006 Feb 47 (4): 764-8. Tester David J, Will Melissa L, Haglund Carla M, Ackerman Michael |
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Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.
JAMA 2005 Dec 294 (23): 2975-80. Napolitano Carlo, Priori Silvia G, Schwartz Peter J, Bloise Raffaella, Ronchetti Elena, Nastoli Janni, Bottelli Georgia, Cerrone Marina, Leonardi Serg |
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[The association of single nucleotide polymorphism of slow delayed rectifier K+ channel genes with atrial fibrillation in Han nationality Chinese].
Zhonghua xin xue guan bing za zhi 2005 Nov 33 (11): 987-91. Zeng Zhi-yu, Pu Jie-lin, Tan Chen, Teng Si-yong, Chen Jian-hong, Su Shao-yong, Zhou Xiao-yang, Zhang Shu, Li Yi-shi, Wang Fang-zheng, Gu Dong-fe |
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Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population.
European journal of human genetics : EJHG 2005 Nov 13 (11): 1213-22. Gouas L, Nicaud V, Berthet M, Forhan A, Tiret L, Balkau B, Guicheney P |
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Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
Heart rhythm : the official journal of the Heart Rhythm Society 2005 May 2 (5): 507-17. Tester David J, Will Melissa L, Haglund Carla M, Ackerman Michael |
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Common variants in myocardial ion channel genes modify the QT interval in the general population: results from the KORA study.
Circulation research 2005 Apr 96 (6): 693-701. Pfeufer Arne, Jalilzadeh Shapour, Perz Siegfried, Mueller Jakob C, Hinterseer Martin, Illig Thomas, Akyol Mahmut, Huth Cornelia, Schöpfer-Wendels Andreas, Kuch Bernhard, Steinbeck Gerhard, Holle Rolf, Näbauer Michael, Wichmann H-Erich, Meitinger Thomas, Kääb Stef |
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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.
Journal of human genetics 2005 50 (9): 490-6. Lai Ling-Ping, Su Yi-Ning, Hsieh Fon-Jou, Chiang Fu-Tien, Juang Jyh-Ming, Liu Yen-Bin, Ho Yi-Lwun, Chen Wen-Jone, Yeh San-Jou, Wang Chun-Chieh, Ko Yu-Lin, Wu Tsu-Juey, Ueng Kwo-Chang, Lei Meng-Huan, Tsao Hsuan-Ming, Chen Shih-Ann, Lin Tin-Kwang, Wu Mei-Hwan, Lo Huey-Ming, Huang Shoei K Stephen, Lin Jiunn-L |
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Compound mutations: a common cause of severe long-QT syndrome.
Circulation 2004 Apr 109 (15): 1834-41. Westenskow Peter, Splawski Igor, Timothy Katherine W, Keating Mark T, Sanguinetti Michael |
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Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients.
Journal of molecular medicine (Berlin, Germany) 2004 Mar 82 (3): 182-8. Paulussen Aimée D C, Gilissen Ronaldus A H J, Armstrong Martin, Doevendans Pieter A, Verhasselt Peter, Smeets Hubert J M, Schulze-Bahr Eric, Haverkamp Wilhelm, Breithardt Günter, Cohen Nadine, Aerssens Jero |
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Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland.
Annals of medicine 2004 36 Suppl 1 (): 53-63. Fodstad Heidi, Swan Heikki, Laitinen Päivi, Piippo Kirsi, Paavonen Kristian, Viitasalo Matti, Toivonen Lauri, Kontula Kim |
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Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome.
Mayo Clinic proceedings 2003 Dec 78 (12): 1479-87. Ackerman Michael J, Tester David J, Jones Gregg S, Will Melissa L, Burrow Christopher R, Curran Mark |
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Association of the human minK gene 38G allele with atrial fibrillation: evidence of possible genetic control on the pathogenesis of atrial fibrillation.
American heart journal 2002 Sep 144 (3): 485-90. Lai Ling-Ping, Su Ming-Jai, Yeh Huei-Ming, Lin Jiunn-Lee, Chiang Fu-Tien, Hwang Juey-Jen, Hsu Kwan-Li, Tseng Chuen-Den, Lien Wen-Pin, Tseng Yung-Zu, Huang Shoei K Steph |
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Correlation of genetic etiology with response to beta-adrenergic blockade among symptomatic patients with familial long-QT syndrome.
Journal of human genetics 2001 46 (1): 38-40. Itoh T, Kikuchi K, Odagawa Y, Takata S, Yano K, Okada S, Haneda N, Ogawa S, Nakano O, Kawahara Y, Kasai H, Nakayama T, Fukutomi T, Sakurada H, Shimizu A, Yazaki Y, Nagai R, Nakamura Y, Tanaka T |
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The electrocardiographic abnormalities in highly trained athletes compared to the genetic study related to causes of unexpected sudden cardiac death.
Journal of medicine and life 0 2 (4): 361-72. Macarie C, Stoian Ioana, Dermengiu D, Barbarii Ligia, Piser Ileana Tepes, Chioncel O, Carp A, Stoian |
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- Page last updated:Feb 20, 2020
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