HuGE Literature Finder
Records 1-30
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Association between (GT)n promoter polymorphism and recovery from concussion: A Pilot Study.
Journal of neurotrauma 2019 Dec . McDevitt Jane, Rubin Leah, De Simone Francesca Isabella, Phillips Jacqueline, Langford Dian |
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Genetic Variants on SCN5A, KCNQ1, and KCNH2 in Patients with Ventricular Arrhythmias during Acute Myocardial Infarction in a Chinese Population.
Cardiology 2019 Nov 1-8. Wang Feng, Liu Yang, Liao Hongtao, Xue Yumei, Zhan Xianzhang, Fang Xianhong, Liang Yuanhong, Wei Wei, Rao Fang, Zhang Qianhuan, Deng Hai, Lin Yubi, Liu Fangzhou, Lin Weidong, Zhang Bin, Wu Shul |
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Variant frequencies of KCNQ1, KCNH2, and SCN5A in a Chinese inherited arrhythmia cohort and other disease cohorts undergoing genetic testing.
Annals of human genetics 2019 Nov . Li Xin, Liu Nian, Bai Ro |
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Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy.
BMC cardiovascular disorders 2019 Jul 19 (1): 174. Raju Hariharan, Ware James S, Skinner Jonathan R, Hedley Paula L, Arno Gavin, Love Donald R, van der Werf Christian, Tfelt-Hansen Jacob, Winkel Bo Gregers, Cohen Marta C, Li Xinzhong, John Shibu, Sharma Sanjay, Jeffery Steve, Wilde Arthur A M, Christiansen Michael, Sheppard Mary N, Behr Elijah |
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Analysis of KCNH2 and CACNA1C schizophrenia risk genes on EEG functional network modulation during an auditory odd-ball task.
European archives of psychiatry and clinical neuroscience 2019 Jan . Lubeiro Alba, Fatjó-Vilas Mar, Guardiola Maria, Almodóvar Carmen, Gomez-Pilar Javier, Cea-Cañas Benjamin, Poza Jesús, Palomino Aitor, Gómez-García Marta, Zugasti Jone, Molina Vicen |
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Corrected QT Interval Prolongation in Psychopharmacological Treatment and Its Modulation by Genetic Variation.
Neuropsychobiology 2019 77 (2): 67-72. Corponi Filippo, Fabbri Chiara, Boriani Giuseppe, Diemberger Igor, Albani Diego, Forloni Gianluigi, Serretti Alessand |
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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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Relationship between KCNQ1 (LQT1) and KCNH2 (LQT2) gene mutations and sudden death during illegal drug use.
Scientific reports 2018 May 8 (1): 8443. Nagasawa Sayaka, Saitoh Hisako, Kasahara Shiori, Chiba Fumiko, Torimitsu Suguru, Abe Hiroko, Yajima Daisuke, Iwase Hirota |
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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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Re-evaluating pathogenicity of variants associated with the long-QT syndrome.
Journal of cardiovascular electrophysiology 2017 Oct . Kaltman Jonathan R, Evans Frank, Fu Yi-Pi |
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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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KCNQ1 p.L353L affects splicing and modifies the phenotype in a founder population with long QT syndrome type 1.
Journal of medical genetics 2017 Mar . Kapplinger Jamie D, Erickson Anders, Asuri Sirisha, Tester David J, McIntosh Sarah, Kerr Charles R, Morrison Julie, Tang Anthony, Sanatani Shubhayan, Arbour Laura, Ackerman Michael |
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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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Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases.
International journal of legal medicine 2016 Feb . Neubauer Jacqueline, Haas Cordula, Bartsch Christine, Domingo-Medeiros Argelia, Berger Wolfga |
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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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eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants.
BMC medical genomics 2016 9 Suppl 1 32. Verma Anurag, Verma Shefali S, Pendergrass Sarah A, Crawford Dana C, Crosslin David R, Kuivaniemi Helena, Bush William S, Bradford Yuki, Kullo Iftikhar, Bielinski Suzette J, Li Rongling, Denny Joshua C, Peissig Peggy, Hebbring Scott, De Andrade Mariza, Ritchie Marylyn D, Tromp Gera |
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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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Differential Response to Risperidone in Schizophrenia Patients by KCNH2 Genotype and Drug Metabolizer Status.
The American journal of psychiatry 2015 Oct appiajp201514050653. Heide Juliane, Zhang Fengyu, Bigos Kristin L, Mann Stefan A, Carr Vaughan J, Shannon Weickert Cynthia, Green Melissa J, Weinberger Daniel R, Vandenberg Jamie |
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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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Genetic variants of potassium voltage-gated channel genes (KCNQ1, KCNH2, and KCNE1) affected the risk of atrial fibrillation in elderly patients.
Genetic testing and molecular biomarkers 2015 Jul 19 (7): 359-65. Li Li, Shen Chao, Yao Zhaohui, Liang Jinjun, Huang Congx |
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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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herg1b expression as a potential specific marker in pediatric acute myeloid leukemia patients with HERG 897K/K genotype.
Pediatric hematology and oncology 2015 Apr 32 (3): 182-92. Erdem Merve, Tekiner Tugce Ayca, Fejzullahu Arta, Akan Gokce, Anak Sema, Saribeyoglu Ebru Tugrul, Ozbek Ugur, Atalar Fatmah |
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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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Association between polymorphisms in NOS3 and KCNH2 and social memory.
Frontiers in neuroscience 2015 9 393. Henningsson Susanne, Zettergren Anna, Hovey Daniel, Jonsson Lina, Svärd Joakim, Cortes Diana S, Melke Jonas, Ebner Natalie C, Laukka Petri, Fischer Håkan, Westberg La |
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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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High incidence of functional ion-channel abnormalities in a consecutive Long QT cohort with novel missense genetic variants of unknown significance.
Scientific reports 2015 5 10009. Steffensen Annette Buur, Refaat Marwan M, David Jens-Peter, Mujezinovic Amer, Calloe Kirstine, Wojciak Julianne, Nussbaum Robert L, Scheinman Melvin M, Schmitt Nico |
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Mutation Analysis of KCNQ1, KCNH2 and SCN5A Genes in Taiwanese Long QT Syndrome Patients.
International heart journal 2015 56 (4): 450-3. Chang Ya-Sian, Yang Yi-Wen, Lin Yen-Nien, Lin Kuo-Hung, Chang Kuan-Cheng, Chang Jan-Gow |
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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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The compounding dilemma of genetic noise: identification of the genetic noise rate in genes associated with cardiac channelopathies.
Heart rhythm : the official journal of the Heart Rhythm Society 2013 Nov 10 (11): 11. Kapplinger J, Tester DJ, Ackerman MJ |
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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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Mutations in genes encoding cardiac ion channels previously associated with sudden infant death syndrome (SIDS) are present with high frequency in new exome data.
The Canadian journal of cardiology 2013 Sep 29 (9): 1104-9. Andreasen Charlotte, Refsgaard Lena, Nielsen Jonas B, Sajadieh Ahmad, Winkel Bo G, Tfelt-Hansen Jacob, Haunsø Stig, Holst Anders G, Svendsen Jesper H, 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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The KCNH2 gene is associated with neurocognition and the risk of schizophrenia.
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2013 Mar 14 (2): 114-20. Hashimoto Ryota, Ohi Kazutaka, Yasuda Yuka, Fukumoto Motoyuki, Yamamori Hidenaga, Kamino Kouzin, Morihara Takashi, Iwase Masao, Kazui Hiroaki, Takeda Masatos |
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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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The KCNH2 genetic polymorphism (1956, C>T) is a novel biomarker that is associated with CCB and ?,?-ADR blocker response in EH patients in China.
PloS one 2013 8 (4): e61317. He Fazhong, Luo Jianquan, Luo Zhiying, Fan Lan, He Yijing, Zhu Dingliang, Gao Jinping, Deng Sheng, Wang Yan, Qian Yuesheng, Zhou Honghao, Chen Xiaoping, Zhang W |
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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 |
Impact of ancestry and common genetic variants on QT interval in African Americans.
Circulation. Cardiovascular genetics 2012 Dec 5 (6): 647-55. Smith J Gustav, Avery Christy L, Evans Daniel S, Nalls Michael A, Meng Yan A, Smith Erin N, Palmer Cameron, Tanaka Toshiko, Mehra Reena, Butler Anne M, Young Taylor, Buxbaum Sarah G, Kerr Kathleen F, Berenson Gerald S, Schnabel Renate B, Li Guo, Ellinor Patrick T, Magnani Jared W, Chen Wei, Bis Joshua C, Curb J David, Hsueh Wen-Chi, Rotter Jerome I, Liu Yongmei, Newman Anne B, Limacher Marian C, North Kari E, Reiner Alexander P, Quibrera P Miguel, Schork Nicholas J, Singleton Andrew B, Psaty Bruce M, Soliman Elsayed Z, Solomon Allen J, Srinivasan Sathanur R, Alonso Alvaro, Wallace Robert, Redline Susan, Zhang Zhu-Ming, Post Wendy S, Zonderman Alan B, Taylor Herman A, Murray Sarah S, Ferrucci Luigi, Arking Dan E, Evans Michele K, Fox Ervin R, Sotoodehnia Nona, Heckbert Susan R, Whitsel Eric A, Newton-Cheh Christopher, |
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Integration of genetics into a systems model of electrocardiographic traits using HumanCVD BeadChip.
Circulation. Cardiovascular genetics 2012 Dec 5 (6): 630-8. Gaunt Tom R, Shah Sonia, Nelson Christopher P, Drenos Fotios, Braund Peter S, Adeniran Ismail, Folkersen Lasse, Lawlor Debbie A, Casas Juan-Pablo, Amuzu Antoinette, Kivimaki Mika, Whittaker John, Eriksson Per, Zhang Henggui, Hancox Jules C, Tomaszewski Maciej, Burton Paul R, Tobin Martin D, Humphries Steve E, Talmud Philippa J, Macfarlane Peter W, Hingorani Aroon D, Samani Nilesh J, Kumari Meena, Day Ian N |
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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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Exome sequencing and digital PCR analyses reveal novel mutated genes related to the metastasis of pancreatic ductal adenocarcinoma.
Cancer biology & therapy 2012 Aug 13 (10): 871-9. Zhou Bin, Irwanto Astrid, Guo Yun-Miao, Bei Jin-Xin, Wu Qiao, Chen Ge, Zhang Tai-Ping, Lei Jin-Jv, Feng Qi-Sheng, Chen Li-Zhen, Liu Jianjun, Zhao Yu-P |
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Genetic variation in KCNH2 associated with expression in the brain of a unique hERG isoform modulates treatment response in patients with schizophrenia.
The American journal of psychiatry 2012 Jul 169 (7): 725-34. Apud José A, Zhang Fengyu, Decot Heather, Bigos Kristin L, Weinberger Daniel |
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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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Domperidone treatment for gastroparesis: demographic and pharmacogenetic characterization of clinical efficacy and side-effects.
Digestive diseases and sciences 2011 Jan 56 (1): 115-24. Parkman Henry P, Jacobs Michael R, Mishra Anurag, Hurdle Jessica A, Sachdeva Priyanka, Gaughan John P, Krynetskiy Evge |
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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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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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Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Diabetes care 2010 Oct 33 (10): 2250-3. Bailey Swneke D, Xie Changchun, Do Ron, Montpetit Alexandre, Diaz Rafael, Mohan Viswanathan, Keavney Bernard, Yusuf Salim, Gerstein Hertzel C, Engert James C, Anand Sonia, |
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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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Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutation.
Heart rhythm : the official journal of the Heart Rhythm Society 2010 Jul 7 (7): 912-9. Tester David J, Valdivia Carmen, Harris-Kerr Carole, Alders Marielle, Salisbury Benjamin A, Wilde Arthur A M, Makielski Jonathan C, 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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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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