HuGE Literature Finder
Records 1-30
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An NGS-based genotyping in LQTS; minor genes are no longer minor.
Journal of human genetics 2020 Jul . Ohno Seiko, Ozawa Junichi, Fukuyama Megumi, Makiyama Takeru, Horie Mino |
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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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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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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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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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- Page last updated:Mar 02, 2021
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