HuGE Literature Finder
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Records 1-100
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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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Targeted Next-Generation Sequencing of 406 Genes Identified Genetic Defects Underlying Congenital Heart Disease in Down Syndrome Patients.
Pediatric cardiology 2018 Aug . Alharbi Khalid M, Al-Mazroea Abdelhadi H, Abdallah Atiyeh M, Almohammadi Yousef, Carlus S Justin, Basit Sulm |
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Risk Stratification of Type 2 Long-QT Syndrome Mutation Carriers With Normal QTc Interval: The Value of Sex, T-Wave Morphology, and Mutation Type.
Circulation. Arrhythmia and electrophysiology 2018 Jul 11 (7): e005918. Platonov Pyotr G, McNitt Scott, Polonsky Bronislava, Rosero Spencer Z, Kutyifa Valentina, Huang Allison, Moss Arthur J, Zareba Wojcie |
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Postmortem Analysis of 4 Mutation Hotspots of KCNQ1, KCNH2, and SCN5A Genes in Sudden Unexplained Death in Southwest of China.
The American journal of forensic medicine and pathology 2018 May . Jia Peng-Lin, Wang Yue-Bing, Fu Hua, Huang Wen-Li, Zhong Shu-Rong, Ma Lin, Li Yu-Hua, Dong Yi, Sun Zhong-Chun, Yang Lin, Qu Peng-Fei, Zhao Su, Qu Yong-Qiang, Xi Yan-Mei, Wang Shang-Wen, Tang Xue, Lei Pu-Pi |
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Cardiac Genetic Predisposition in Sudden Infant Death Syndrome.
Journal of the American College of Cardiology 2018 Mar 71 (11): 1217-1227. Tester David J, Wong Leonie C H, Chanana Pritha, Jaye Amie, Evans Jared M, FitzPatrick David R, Evans Margaret J, Fleming Peter, Jeffrey Iona, Cohen Marta C, Tfelt-Hansen Jacob, Simpson Michael A, Behr Elijah R, Ackerman Michael |
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Common variants in the hERG (KCNH2) voltage-gated potassium channel are associated with altered fasting and glucose-stimulated plasma incretin and glucagon responses.
BMC genetics 2018 Mar 19 (1): 15. Engelbrechtsen Line, Mahendran Yuvaraj, Jonsson Anna, Gjesing Anette Prior, Weeke Peter E, Jørgensen Marit E, Færch Kristine, Witte Daniel R, Holst Jens J, Jørgensen Torben, Grarup Niels, Pedersen Oluf, Vestergaard Henrik, Torekov Signe, Kanters Jørgen K, Hansen Torb |
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QTc prolongation in short-term treatment of schizophrenia patients: effects of different antipsychotics and genetic factors.
European archives of psychiatry and clinical neuroscience 2018 Feb . Spellmann Ilja, Reinhard Matthias A, Veverka Diana, Zill Peter, Obermeier Michael, Dehning Sandra, Schennach Rebecca, Müller Norbert, Möller Hans-Jürgen, Riedel Michael, Musil Richa |
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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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Does Sudden Unexplained Nocturnal Death Syndrome Remain the Autopsy-Negative Disorder: A Gross, Microscopic, and Molecular Autopsy Investigation in Southern China.
Mayo Clinic proceedings 2016 Oct . Zhang Liyong, Tester David J, Lang Di, Chen Yili, Zheng Jinxiang, Gao Rui, Corliss Robert F, Tang Shuangbo, Kyle John W, Liu Chao, Ackerman Michael J, Makielski Jonathan C, Cheng Jiandi |
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Genetic biomarkers for the risk of seizures in long QT syndrome.
Neurology 2016 Oct 87 (16): 1660-1668. Auerbach David S, McNitt Scott, Gross Robert A, Zareba Wojciech, Dirksen Robert T, Moss Arthur |
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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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The Influence of Pregnancy in Patients with Congenital Long QT Syndrome.
Cardiology in review 2016 Mar . Garg Lohit, Garg Jalaj, Krishnamoorthy Parasuram, Ahnert Amy, Shah Neeraj, Dusaj Raman S, Bozorgnia Bab |
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Association of the hERG mutation with long?QT syndrome type 2, syncope and epilepsy.
Molecular medicine reports 2016 Feb . Li Guoliang, Shi Rui, Wu Jine, Han Wenqi, Zhang Aifeng, Cheng Gong, Xue Xiaolin, Sun Chaofe |
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Pediatric Cohort With Long QT Syndrome?- KCNH2 Mutation Carriers Present Late Onset But Severe Symptoms.
Circulation journal : official journal of the Japanese Circulation Society 2016 Jan . Ozawa Junichi, Ohno Seiko, Hisamatsu Takashi, Itoh Hideki, Makiyama Takeru, Suzuki Hiroshi, Saitoh Akihiko, Horie Mino |
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Common Genotypes of Long QT Syndrome in China and the Role of ECG Prediction.
Cardiology 2016 133 (2): 73-8. Gao Yuanfeng, Liu Wenling, Li Cuilan, Qiu Xiaoliang, Qin Xuguang, Guo Baojing, Liu Xueqin, Li Jianfeng, Yuan Yue, Li Xiaomei, Liang Lu, Li Lei, Hong Kui, Pu Jielin, Liu Jinqiu, Wang Qing, Zhang Li, Hu Da- |
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[High incidence of sudden cardiac death in one family with type-3 long QT syndrome: molecular genetics and electrophysiology mechanism analysis].
Zhonghua xin xue guan bing za zhi 2015 Dec 43 (12): 1046-50. Zhou Hui, Li Zhang, Ali Raza Ghani, Zhu Wengen, Zhou Qiongqiong, Shen Yang, Xie Jinyan, Cao Qing, Wan Rong, Hu Jinzhu, Hong K |
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Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction.
European journal of human genetics : EJHG 2015 Dec . Itoh Hideki, Berthet Myriam, Fressart Véronique, Denjoy Isabelle, Maugenre Svetlana, Klug Didier, Mizusawa Yuka, Makiyama Takeru, Hofman Nynke, Stallmeyer Birgit, Zumhagen Sven, Shimizu Wataru, Wilde Arthur A M, Schulze-Bahr Eric, Horie Minoru, Tezenas du Montcel Sophie, Guicheney Pasca |
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Exome-based analysis of cardiac arrhythmia, respiratory control and epilepsy genes in sudden unexpected death in epilepsy.
Annals of neurology 2015 Dec . Bagnall Richard D, Crompton Douglas E, Petrovski Slavé, Lam Lien, Cutmore Carina, Garry Sarah I, Sadleir Lynette G, Dibbens Leanne M, Cairns Anita, Kivity Sara, Afawi Zaid, Regan Brigid M, Duflou Johan, Berkovic Samuel F, Scheffer Ingrid E, Semsarian Christoph |
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The genetics underlying acquired long QT syndrome: impact for genetic screening.
European heart journal 2015 Dec . Itoh Hideki, Crotti Lia, Aiba Takeshi, Spazzolini Carla, Denjoy Isabelle, Fressart Véronique, Hayashi Kenshi, Nakajima Tadashi, Ohno Seiko, Makiyama Takeru, Wu Jie, Hasegawa Kanae, Mastantuono Elisa, Dagradi Federica, Pedrazzini Matteo, Yamagishi Masakazu, Berthet Myriam, Murakami Yoshitaka, Shimizu Wataru, Guicheney Pascale, Schwartz Peter J, Horie Mino |
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Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases.
European journal of human genetics : EJHG 2015 Sep . Hertz Christin Loeth, Christiansen Sofie Lindgren, Larsen Maiken Kudahl, Dahl Morten, Ferrero-Miliani Laura, Weeke Peter Ejvind, Pedersen Oluf, Hansen Torben, Grarup Niels, Ottesen Gyda Lolk, Frank-Hansen Rune, Banner Jytte, Morling Nie |
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Time, frequency and information domain analysis of heart period and QT variability in asymptomatic long QT syndrome type 2 patients.
Conference proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference 2015 Aug 2015 294-7. Bari Vlasta, Girardengo Giulia, Marchi Andrea, De Maria Beatrice, Brink Paul A, Crotti Lia, Schwartz Peter J, Porta Alber |
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Coexistence of Andersen-Tawil Syndrome with Polymorphisms in hERG1 Gene (K897T) and SCN5A Gene (H558R) in One Family.
Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2015 Jun . Jagodzi?ska Michalina, Szperl Ma?gorzata, Poni?ska Joanna, Kosiec Agnieszka, Gajda Robert, Kukla Piotr, Biernacka El?bieta Katarzy |
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Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation.
Circulation. Arrhythmia and electrophysiology 2015 Jun . Hayashi Kenshi, Konno Tetsuo, Tada Hayato, Tani Satoyuki, Liu Li, Fujino Noboru, Nohara Atsushi, Hodatsu Akihiko, Tsuda Toyonobu, Tanaka Yoshihiro, Kawashiri Masa-Aki, Ino Hidekazu, Makita Naomasa, Yamagishi Masaka |
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Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population.
Journal of the American Heart Association 2015 May 4 (5): . Chen Shanshan, Wang Chuchu, Wang Xiaojing, Xu Chengqi, Wu Manman, Wang Pengxia, Tu Xin, Wang Qing |
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hERG potassium channel blockade by the HCN channel inhibitor bradycardic agent ivabradine.
Journal of the American Heart Association 2015 Apr 4 (4): . Melgari Dario, Brack Kieran E, Zhang Chuan, Zhang Yihong, El Harchi Aziza, Mitcheson John S, Dempsey Christopher E, Ng G André, Hancox Jules |
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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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Role of mutation and pharmacologic block of human KCNH2 in vasculogenesis and fetal mortality: partial rescue by transforming growth factor-?.
Circulation. Arrhythmia and electrophysiology 2015 Apr 8 (2): 420-8. Teng Guoqi, Zhao Xiang, Lees-Miller James P, Belke Darrell, Shi Chunhua, Chen Yongxiang, O'Brien Edward R, Fedak Paul W, Bracey Nathan, Cross James C, Duff Henry |
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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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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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Molecular analysis of potassium ion channel genes in sudden death cases among patients administered psychotropic drug therapy: are polymorphisms in LQT genes a potential risk factor?
Journal of human genetics 2014 Feb 59 (2): 95-9. Kamei Sayako, Sato Noriko, Harayama Yuta, Nunotani Miyako, Takatsu Kanae, Shiozaki Tetsuya, Hayashi Tokutaro, Asamura Hide |
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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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Single nucleotide polymorphisms in proximity to K-channel genes are associated with decreased longitudinal QTc variance.
Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2014 Jan 19 (1): 63-9. Mints Yuliya, Zipunnikov Vadim, Khurram Irfan, Calkins Hugh, Nazarian Sam |
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Electrophysiological phenotype in the LQTS mutations Y111C and R518X in the KCNQ1 gene.
Journal of applied physiology (Bethesda, Md. : 1985) 2013 Nov 115 (10): 1423-32. Diamant Ulla-Britt, Vahedi Farzad, Winbo Annika, Rydberg Annika, Stattin Eva-Lena, Jensen Steen M, Bergfeldt Lenna |
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Genetic modifier of the QTc interval associated with early-onset atrial fibrillation.
The Canadian journal of cardiology 2013 Oct 29 (10): 1234-40. Andreasen Laura, Nielsen Jonas B, Christophersen Ingrid E, Holst Anders Gaarsdal, Sajadieh Ahmad, Tveit Arnljot, Haunsø Stig, Svendsen Jesper H, Schmitt Nicole, Olesen Morten |
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Arrhythmia Phenotype during Fetal Life Suggests LQTS Genotype: Risk Stratification of Perinatal Long QT Syndrome.
Circulation. Arrhythmia and electrophysiology 2013 Aug . Cuneo BF, Etheridge SP, Horigome H, Sallee D, Moon-Grady A, Weng HY, Ackerman MJ, Benson DW |
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Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome.
Circulation. Cardiovascular genetics 2013 Aug 6 (4): 354-61. Duchatelet Sabine, Crotti Lia, Peat Rachel A, Denjoy Isabelle, Itoh Hideki, Berthet Myriam, Ohno Seiko, Fressart Véronique, Monti Maria Cristina, Crocamo Cristina, Pedrazzini Matteo, Dagradi Federica, Vicentini Alessandro, Klug Didier, Brink Paul A, Goosen Althea, Swan Heikki, Toivonen Lauri, Lahtinen Annukka M, Kontula Kimmo, Shimizu Wataru, Horie Minoru, George Alfred L, Trégouët David-Alexandre, Guicheney Pascale, Schwartz Peter |
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Genetic mutation in Korean patients of sudden cardiac arrest as a surrogating marker of idiopathic ventricular arrhythmia.
Journal of Korean medical science 2013 Jul 28 (7): 1021-6. Son Myoung Kyun, Ki Chang-Seok, Park Seung-Jung, Huh June, Kim June Soo, On Young Ke |
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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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Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population.
Annals of medicine 2013 Jun 45 (4): 328-35. Lahtinen Annukka M, Havulinna Aki S, Noseworthy Peter A, Jula Antti, Karhunen Pekka J, Perola Markus, Newton-Cheh Christopher, Salomaa Veikko, Kontula Kim |
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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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Long QT syndrome-associated mutations in intrauterine fetal death.
JAMA 2013 Apr 309 (14): 1473-82. Crotti Lia, Tester David J, White Wendy M, Bartos Daniel C, Insolia Roberto, Besana Alessandra, Kunic Jennifer D, Will Melissa L, Velasco Ellyn J, Bair Jennifer J, Ghidoni Alice, Cetin Irene, Van Dyke Daniel L, Wick Myra J, Brost Brian, Delisle Brian P, Facchinetti Fabio, George Alfred L, Schwartz Peter J, Ackerman Michael |
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Prognostic Implications of Mutation Specific QTc Standard Deviation in Congenital Long QT Syndrome.
Heart rhythm : the official journal of the Heart Rhythm Society 2013 Jan . Mathias A, Moss AJ, Lopes CM, Barsheshet A, McNitt S, Zareba W, Robinson JL, Locati EH, Ackerman MJ, Benhorin J, Kaufman ES, Platonov PG, Qi M, Shimizu W, Towbin JA, Michael Vincent G, Wilde AA, Zhang L, Goldenberg I |
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Long QT interval in Turner syndrome--a high prevalence of LQTS gene mutations.
PloS one 2013 8 (7): e69614. Trolle Christian, Mortensen Kristian H, Pedersen Lisbeth N, Berglund Agnethe, Jensen Henrik K, Andersen Niels H, Gravholt Claus |
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Genetic polymorphisms for estimating risk of atrial fibrillation: a literature-based meta-analysis.
Journal of internal medicine 2012 Dec 272 (6): 573-82. Smith J G, Almgren P, Engström G, Hedblad B, Platonov P G, Newton-Cheh C, Melander |
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Repeat long QT syndrome genetic testing of phenotype-positive cases: prevalence and etiology of detection misses.
Heart rhythm : the official journal of the Heart Rhythm Society 2012 Dec 9 (12): 1977-82. Medlock Morgan M, Tester David J, Will Melissa L, Bos J Martijn, Ackerman Michael |
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Risk of Life Threatening Cardiac Events among Patients with Long QT Syndrome and Multiple Mutations.
Heart rhythm : the official journal of the Heart Rhythm Society 2012 Nov . Mullally J, Goldenberg I, Moss AJ, Lopes CM, Ackerman MJ, Zareba W, McNitt S, Robinson JL, Benhorin J, Kaufman ES, Towbin JA, Barsheshet A |
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The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.
Journal of cardiovascular electrophysiology 2012 Oct 23 (10): 1092-8. Winkel Bo Gregers, Larsen Maiken Kudahl, Berge Knut Erik, Leren Trond Paul, Nissen Peter Henrik, Olesen Morten Salling, Hollegaard Mads Vilhelm, Jespersen Thomas, Yuan Lei, Nielsen Nikolaj, Haunsø Stig, Svendsen Jesper Hastrup, Wang Yinman, Kristensen Ingrid Bayer, Jensen Henrik Kjaerulf, Tfelt-Hansen Jacob, Banner Jyt |
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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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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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Genotype- and mutation site-specific QT adaptation during exercise, recovery, and postural changes in children with long-QT syndrome.
Circulation. Arrhythmia and electrophysiology 2011 Dec 4 (6): 867-73. Aziz Peter F, Wieand Tammy S, Ganley Jamie, Henderson Jacqueline, Patel Akash R, Iyer V Ramesh, Vogel R Lee, McBride Michael, Vetter Victoria L, Shah Maully |
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Mutation and gender-specific risk in type 2 long QT syndrome: implications for risk stratification for life-threatening cardiac events in patients with long QT syndrome.
Heart rhythm : the official journal of the Heart Rhythm Society 2011 Oct 8 (10): 1537-43. Migdalovich Dimitry, Moss Arthur J, Lopes Coeli M, Costa Jason, Ouellet Gregory, Barsheshet Alon, McNitt Scott, Polonsky Slava, Robinson Jennifer L, Zareba Wojciech, Ackerman Michael J, Benhorin Jesaia, Kaufman Elizabeth S, Platonov Pyotr G, Shimizu Wataru, Towbin Jeffrey A, Vincent G Michael, Wilde Arthur A M, Goldenberg Il |
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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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Prospective evaluation of corrected QT intervals and arrhythmias after exposure to epirubicin, cyclophosphamide, and 5-fluorouracil in women with breast cancer.
Annals of oncology : official journal of the European Society for Medical Oncology / ESMO 2011 Jun . Kitagawa K, Kawada K, Morita S, Inada M, Mitsuma A, Sawaki M, Iino S, Inden Y, Murohara T, Imai T, Ando Y |
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Risk of recurrent cardiac events after onset of menopause in women with congenital long-QT syndrome types 1 and 2.
Circulation 2011 Jun 123 (24): 2784-91. Buber Jonathan, Mathew Jehu, Moss Arthur J, Hall W Jackson, Barsheshet Alon, McNitt Scott, Robinson Jennifer L, Zareba Wojciech, Ackerman Michael J, Kaufman Elizabeth S, Luria David, Eldar Michael, Towbin Jeffrey A, Vincent Michael, Goldenberg Il |
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Post-mortem review and genetic analysis of sudden unexpected death in epilepsy (SUDEP) cases.
Brain pathology (Zurich, Switzerland) 2011 Mar 21 (2): 201-8. Tu Emily, Bagnall Richard D, Duflou Johan, Semsarian Christoph |
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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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Development of a high resolution melting method for the detection of genetic variations in Long QT Syndrome.
Clinica chimica acta; international journal of clinical chemistry 2011 Jan 412 (1-2): 203-7. Millat Gilles, Chanavat Valérie, Créhalet Hervé, Rousson Robe |
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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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Long QT syndrome with compound mutations is associated with a more severe phenotype: a Japanese multicenter study.
Heart rhythm : the official journal of the Heart Rhythm Society 2010 Oct 7 (10): 1411-8. Itoh Hideki, Shimizu Wataru, Hayashi Kenshi, Yamagata Kenichiro, Sakaguchi Tomoko, Ohno Seiko, Makiyama Takeru, Akao Masaharu, Ai Tomohiko, Noda Takashi, Miyazaki Aya, Miyamoto Yoshihiro, Yamagishi Masakazu, Kamakura Shiro, Horie Mino |
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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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Transmural differences in myocardial contraction in long-QT syndrome: mechanical consequences of ion channel dysfunction.
Circulation 2010 Oct 122 (14): 1355-63. Haugaa Kristina Hermann, Amlie Jan P, Berge Knut Erik, Leren Trond P, Smiseth Otto A, Edvardsen Th |
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Gene-specific paradoxical QT responses during rapid eye movement sleep in women with congenital long QT syndrome.
Heart rhythm : the official journal of the Heart Rhythm Society 2010 Aug 7 (8): 1067-74. Lanfranchi Paola A, Ackerman Michael J, Kara Tomas, Shamsuzzaman Abu S M, Wolk Robert, Jurak Pavel, Amin Raouf, Somers Virend |
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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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Utility of the recovery electrocardiogram after exercise: a novel indicator for the diagnosis and genotyping of long QT syndrome?
Heart rhythm : the official journal of the Heart Rhythm Society 2010 Jul 7 (7): 906-11. Chattha Ishvinder S, Sy Raymond W, Yee Raymond, Gula Lorne J, Skanes Allan C, Klein George J, Bennett Matthew T, Krahn Andrew |
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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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The response of the QT interval to the brief tachycardia provoked by standing: a bedside test for diagnosing long QT syndrome.
Journal of the American College of Cardiology 2010 May 55 (18): 1955-61. Viskin Sami, Postema Pieter G, Bhuiyan Zahurul A, Rosso Raphael, Kalman Jonathan M, Vohra Jitendra K, Guevara-Valdivia Milton E, Marquez Manlio F, Kogan Evgeni, Belhassen Bernard, Glikson Michael, Strasberg Boris, Antzelevitch Charles, Wilde Arthur A |
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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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Utility of treadmill testing in identification and genotype prediction in long-QT syndrome.
Circulation. Arrhythmia and electrophysiology 2010 Apr 3 (2): 120-5. Wong Jorge A, Gula Lorne J, Klein George J, Yee Raymond, Skanes Allan C, Krahn Andrew |
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[Genetic predisposition to development of atrial fibrillation in patients with hypertensive disease].
Kardiologiia 2010 50 (5): 19-24. Gorshkova E S, Minushkina L O, Brovkin A N, Brazhnik V A, Nosikov V V, Zate?shchikov D |
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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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Two four-marker haplotypes on 7q36.1 region indicate that the potassium channel gene HERG1 (KCNH2, Kv11.1) is related to schizophrenia: a case control study.
Behavioral and brain functions : BBF 2010 6 (1): 27. Atalar Fatmahan, Acuner Tufan Tevfik, Cine Naci, Oncu Fatih, Yesilbursa Dogan, Ozbek Ugur, Turkcan Solm |
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Genotype-phenotype aspects of type 2 long QT syndrome.
Journal of the American College of Cardiology 2009 Nov 54 (22): 2052-62. Shimizu Wataru, Moss Arthur J, Wilde Arthur A M, Towbin Jeffrey A, Ackerman Michael J, January Craig T, Tester David J, Zareba Wojciech, Robinson Jennifer L, Qi Ming, Vincent G Michael, Kaufman Elizabeth S, Hofman Nynke, Noda Takashi, Kamakura Shiro, Miyamoto Yoshihiro, Shah Samit, Amin Vinit, Goldenberg Ilan, Andrews Mark L, McNitt Sco |
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Genetic polymorphism of KCNH2 confers predisposition of acquired atrial fibrillation in Chinese.
Journal of cardiovascular electrophysiology 2009 Oct 20 (10): 1158-62. Wang Qun-Shan, Wang Xiao-Feng, Chen Xing-Dong, Yu Jie-Fei, Wang Jun, Sun Jian, Lu Shang-Biao, Shen Mu-Yao, Lu Ming, Li Yi-Gang, Jin |
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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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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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Common variants at ten loci modulate the QT interval duration in the QTSCD Study.
Nature genetics 2009 Apr 41 (4): 4. Pfeufer A, Sanna S, Arking DE, Müller M, Gateva V, Fuchsberger C, Ehret GB, Orrú M, Pattaro C, Köttgen A, Perz S, Usala G, Barbalic M, Li M, Pütz B, Scuteri A, Prineas RJ, Sinner MF, Gieger C, Najjar SS, Kao WH, Mühleisen TW, Dei M, Happle C, Möhlenkamp S, Crisponi L, Erbel R, Jöckel KH, Naitza S, Steinbeck G, Marroni F, Hicks AA, Lakatta E, Müller-Myhsok B, Pramstaller PP, Wichmann HE, Schlessinger D, Boerwinkle E, Meitinger T, Uda M, Coresh J, Kääb S, Abecasis GR, Chakravarti A |
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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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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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Common variation in NOS1AP and KCNH2 genes and QT interval duration in young adults. The Cardiovascular Risk in Young Finns Study.
Annals of medicine 2009 41 (2): 144-51. Raitakari Olli T, Blom-Nyholm Jaana, Koskinen Tuomas A, Kähönen Mika, Viikari Jorma S A, Lehtimäki Ter |
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Depressive symptoms in the congenital long QT syndrome.
Annals of medicine 2009 41 (7): 516-21. Hintsa Taina, Keltikangas-Järvinen Liisa, Puttonen Sampsa, Ravaja Niklas, Toivonen Lauri, Kontula Kimmo, Swan Heik |
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High prevalence of four long QT syndrome founder mutations in the Finnish population.
Annals of medicine 2009 41 (3): 234-40. Marjamaa Annukka, Salomaa Veikko, Newton-Cheh Christopher, Porthan Kimmo, Reunanen Antti, Karanko Hannu, Jula Antti, Lahermo Päivi, Väänänen Heikki, Toivonen Lauri, Swan Heikki, Viitasalo Matti, Nieminen Markku S, Peltonen Leena, Oikarinen Lasse, Palotie Aarno, Kontula Kim |
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Mutation site dependent variability of cardiac events in Japanese LQT2 form of congenital long-QT syndrome.
Circulation journal : official journal of the Japanese Circulation Society 2008 May 72 (5): 694-9. Nagaoka Iori, Shimizu Wataru, Itoh Hideki, Yamamoto Satoshi, Sakaguchi Tomoko, Oka Yuko, Tsuji Keiko, Ashihara Takashi, Ito Makoto, Yoshida Hidetada, Ohno Seiko, Makiyama Takeru, Miyamoto Yoshihiro, Noda Takashi, Kamakura Shiro, Akao Masaharu, Horie Mino |
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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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The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG).
European heart journal 2008 Apr 29 (7): 907-14. Sinner Moritz F, Pfeufer Arne, Akyol Mahmut, Beckmann Britt-Maria, Hinterseer Martin, Wacker Annette, Perz Siegfried, Sauter Wiebke, Illig Thomas, Näbauer Michael, Schmitt Claus, Wichmann H-Erich, Schömig Albert, Steinbeck Gerhard, Meitinger Thomas, Kääb Stef |
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Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers.
Scandinavian journal of clinical and laboratory investigation 2008 68 (5): 362-8. Berge K E, Haugaa K H, Früh A, Anfinsen O-G, Gjesdal K, Siem G, Oyen N, Greve G, Carlsson A, Rognum T O, Hallerud M, Kongsgård E, Amlie J P, Leren T |
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Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.
BMC medical genetics 2008 9 (1): 87. Zhang Xianqin, Chen Shenghan, Zhang Li, Liu Mugen, Redfearn Sharon, Bryant Randall M, Oberti Carlos, Vincent G Michael, Wang Qing |
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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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Common genetic variation in KCNH2 is associated with QT interval duration: the Framingham Heart Study.
Circulation 2007 Sep 116 (10): 1128-36. Newton-Cheh Christopher, Guo Chao-Yu, Larson Martin G, Musone Stacy L, Surti Aarti, Camargo Amy L, Drake Jared A, Benjamin Emelia J, Levy Daniel, D'Agostino Ralph B, Hirschhorn Joel N, O'donnell Christopher |
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A mitochondrial DNA polymorphism associated with cardiac arrhythmia investigated in sudden infant death syndrome.
Acta paediatrica (Oslo, Norway : 1992) 2007 Feb 96 (2): 206-10. Arnestad Marianne, Opdal Siri Hauge, Vege Ashild, Rognum Torleiv O |
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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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Long QT syndrome in adults.
Journal of the American College of Cardiology 2007 Jan 49 (3): 329-37. Sauer Andrew J, Moss Arthur J, McNitt Scott, Peterson Derick R, Zareba Wojciech, Robinson Jennifer L, Qi Ming, Goldenberg Ilan, Hobbs Jenny B, Ackerman Michael J, Benhorin Jesaia, Hall W Jackson, Kaufman Elizabeth S, Locati Emanuela H, Napolitano Carlo, Priori Silvia G, Schwartz Peter J, Towbin Jeffrey A, Vincent G Michael, Zhang |
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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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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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Gastrointestinal symptoms in families of patients with an SCN5A-encoded cardiac channelopathy: evidence of an intestinal channelopathy.
The American journal of gastroenterology 2006 Jun 101 (6): 1299-304. Locke G Richard, Ackerman Michael J, Zinsmeister Alan R, Thapa Prabin, Farrugia Gianri |
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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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