Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 36 Records) |
| Query Trace: Disease and KCNE1[original query] |
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| D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndrome. Journal of the American College of Cardiology 2009 Aug 54 (9): 812-9. Nishio Yukiko, Makiyama Takeru, Itoh Hideki, Sakaguchi Tomoko, Ohno Seiko, Gong Yin-Zhi, Yamamoto Satoshi, Ozawa Tomoya, Ding Wei-Guang, Toyoda Futoshi, Kawamura Mihoko, Akao Masaharu, Matsuura Hiroshi, Kimura Takeshi, Kita Toru, Horie Mino |
| Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population. American journal of medical genetics. Part A 2010 Jan 152A (1): 1. Campbell CA, Della Santina CC, Meyer NC, Smith NB, Myrie OA, Stone EM, Fukushima K, Califano J, Carey JP, Hansen MR, Gantz BJ, Minor LB, Smith RJ |
| Confirmed rare copy number variants implicate novel genes in schizophrenia. Biochemical Society transactions 2010 Apr 38 (2): 445-51. Tam Gloria W C, van de Lagemaat Louie N, Redon Richard, Strathdee Karen E, Croning Mike D R, Malloy Mary P, Muir Walter J, Pickard Ben S, Deary Ian J, Blackwood Douglas H R, Carter Nigel P, Grant Seth G |
| 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, |
| 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 |
| 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 |
| The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study. Journal of negative results in biomedicine 2011 10 (1): 12. Hedley Paula L, Haundrup Ole, Andersen Paal S, Aidt Frederik H, Jensen Morten, Moolman-Smook Johanna C, Bundgaard Henning, Christiansen Micha |
| 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 |
| A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies. International journal of audiology 2012 Aug . Hietikko E, Kotimäki J, Okuloff A, Sorri M, Männikkö M |
| 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 |
| 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 |
| Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation. Biomarkers in medicine 2014 8 (4): 557-70. Nielsen Jonas Bille, Bentzen Bo Hjorth, Olesen Morten Salling, David Jens-Peter, Olesen Søren-Peter, Haunsø Stig, Svendsen Jesper Hastrup, Schmitt Nico |
| An Examination of KCNE1 Mutations and Common Variants in Chronic Tinnitus. Genes 2014 4 1 (1): 23-37. Sand Philipp G, Luettich Alexander, Kleinjung Tobias, Hajak Goeran, Langguth Bertho |
| 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 |
| Sports Participation in Genotype Positive Children With Long QT Syndrome. JACC. Clinical electrophysiology 0 1 (1-2): 62-70. Aziz Peter F, Sweeten Tammy, Vogel Ramon L, Bonney William J, Henderson Jacqueline, Patel Akash R, Shah Maully |
| Ménière's Disease: Molecular Analysis of Aquaporins 2, 3 and Potassium Channel KCNE1 Genes in Brazilian Patients. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2016 09 37 (8): 1117-21. Lopes Karen de Carvalho, Sartorato Edi Lúcia, da Silva-Costa Sueli M, de Macedo Adamov Nadya Soares, Ganança Fernando Freit |
| Epilepsy-related sudden unexpected death: targeted molecular analysis of inherited heart disease genes using next-generation DNA sequencing. Brain pathology (Zurich, Switzerland) 2016 May . Hata Yukiko, Yoshida Koji, Kinoshita Koshi, Nishida Nao |
| Variants in the KCNE1 or KCNE3 gene and risk of Ménière's disease: A meta-analysis. Journal of vestibular research : equilibrium & orientation 2016 Jan 25 (5-6): 211-8. Li Yuan-Jun, Jin Zhan-Guo, Xu Xian-Ro |
| Retrospective Genetic Analysis of 200 Cases of Sudden Infant Death Syndrome and Its Relationship with Long QT Syndrome in Korea. Journal of Korean medical science 2018 8 33 (32): e200. Son Min-Jeong, Kim Min-Kyoung, Yang Kyung-Moo, Choi Byung-Ha, Lee Bong Woo, Yoo Seong |
| Effect of GRM7 polymorphisms on the development of noise-induced hearing loss in Chinese Han workers: a nested case-control study. BMC medical genetics 2018 Jan 19 (1): 4. Yu Peipei, Jiao Jie, Chen Guoshun, Zhou Wenhui, Zhang Huanling, Wu Hui, Li Yanhong, Gu Guizhen, Zheng Yuxin, Yu Yue, Yu Shan |
| Cardiac Arrest Associated with Both an Anomalous Left Coronary Artery and KCNE1 Polymorphism. International heart journal 2019 7 60 (4): 1003-1005. Kawai Hideki, Watanabe Eiichi, Ohno Seiko, Horie Minoru, Ozaki Yuk |
| The Polymorphic Analysis of the Human Potassium Channel KCNE Gene Family in Meniere's Disease-A Preliminary Study. The journal of international advanced otology 2019 Apr 15 (1): 130-134. Dai Qingqing, Wang Dan, Zheng Ho |
| Mutation Screening of KCNQ1 and KCNE1 Genes in Iranian Patients With Jervell and Lange-Nielsen Syndrome. Fetal and pediatric pathology 2019 Apr 1-9. Vojdani Samaneh, Amirsalari Susan, Milanizadeh Saman, Molaei Fatemeh, Ajalloueyane Mohammad, Khosravi Arezoo, Hamzehzadeh Leila, Ghasemi Mohammad Mehdi, Talee Mohammad Reza, Abbaszadegan Mohammad Re |
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
Circulation 2020 Jul 142 (4): 324-338. Lahrouchi Najim, Tadros Rafik, Crotti Lia, Mizusawa Yuka, Postema Pieter G, Beekman Leander, Walsh Roddy, Hasegawa Kanae, Barc Julien, Ernsting Marko, Turkowski Kari L, Mazzanti Andrea, Beckmann Britt M, Shimamoto Keiko, Diamant Ulla-Britt, Wijeyeratne Yanushi D, Kucho Yu, Robyns Tomas, Ishikawa Taisuke, Arbelo Elena, Christiansen Michael, Winbo Annika, Jabbari Reza, Lubitz Steven A, Steinfurt Johannes, Rudic Boris, Loeys Bart, Shoemaker M Ben, Weeke Peter E, Pfeiffer Ryan, Davies Brianna, Andorin Antoine, Hofman Nynke, Dagradi Federica, Pedrazzini Matteo, Tester David J, Bos J Martijn, Sarquella-Brugada Georgia, Campuzano Óscar, Platonov Pyotr G, Stallmeyer Birgit, Zumhagen Sven, Nannenberg Eline A, Veldink Jan H, van den Berg Leonard H, Al-Chalabi Ammar, Shaw Christopher E, Shaw Pamela J, Morrison Karen E, Andersen Peter M, Müller-Nurasyid Martina, Cusi Daniele, Barlassina Cristina, Galan Pilar, Lathrop Mark, Munter Markus, Werge Thomas, Ribasés Marta, Aung Tin, Khor Chiea C, Ozaki Mineo, Lichtner Peter, Meitinger Thomas, van Tintelen J Peter, Hoedemaekers Yvonne, Denjoy Isabelle, Leenhardt Antoine, Napolitano Carlo, Shimizu Wataru, Schott Jean-Jacques, Gourraud Jean-Baptiste, Makiyama Takeru, Ohno Seiko, Itoh Hideki, Krahn Andrew D, Antzelevitch Charles, Roden Dan M, Saenen Johan, Borggrefe Martin, Odening Katja E, Ellinor Patrick T, Tfelt-Hansen Jacob, Skinner Jonathan R, van den Berg Maarten P, Olesen Morten Salling, Brugada Josep, Brugada Ramón, Makita Naomasa, Breckpot Jeroen, Yoshinaga Masao, Behr Elijah R, Rydberg Annika, Aiba Takeshi, Kääb Stefan, Priori Silvia G, Guicheney Pascale, Tan Hanno L, Newton-Cheh Christopher, Ackerman Michael J, Schwartz Peter J, Schulze-Bahr Eric, Probst Vincent, Horie Minoru, Wilde Arthur A, Tanck Michael W T, Bezzina Connie |
| The rs2236609 Polymorphism Is Related to Increased Risk Susceptibility of Atrial Fibrillation. Public health genomics 2020 Apr 1-5. Alzoughool Foad, Atoum Manar, Abu-Awad Aymen, Ghanma Issa, Halalsheh Ra |
| Genetic Susceptibility Study of Chinese Sudden Sensorineural Hearing Loss Patients with Vertigo. Current medical science 2021 Aug 41 (4): 673-679. Gao Yun, Wang Hong-Yang, Guan Jing, Lan Lan, Zhao Cui, Xie Lin-Yi, Wang Da-Yong, Wang Qiu- |
| Genetic predictors of sick sinus syndrome. Molecular biology reports 2021 7 48 (6): 5355-5362. Timasheva Yanina, Badykov Marat, Akhmadishina Leysan, Nasibullin Timur, Badykova Elena, Pushkareva Alfiya, Plechev Vladimir, Sagitov Ildus, Zagidullin Nauf |
| Role of genetic testing in young patients with idiopathic atrioventricular conduction disease. 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 2022 11 25 (2): 643-650. Auricchio Angelo, Demarchi Andrea, Özkartal Tardu, Campanale Daniela, Caputo Maria Luce, di Valentino Marcello, Menafoglio Andrea, Regoli Francois, Facchini Marco, Del Bufalo Alessandro, Foglia Pietro, Ferrari Nicola, Bomio Fulvio, Medeiros-Domingo Argelia, Moccetti Tiziano, Pedrazzini Giovanni B, Klersy Catherine, Conte Giul |
| Genetic variants in Colombian patients with inherited cardiac conditions. Molecular genetics & genomic medicine 2022 10 10 (11): e2046. Rucinski Cynthia, Yunis Luz Karime, Rosas Fernando, Santacruz David, Camargo Juan Manuel, Yunis Juan Jo |
| Escitalopram-induced QTc prolongation and its relationship with KCNQ1, KCNE1, and KCNH2 gene polymorphisms. Journal of affective disorders 2023 11 . Zimu Chen, Zhi Xu, Chenjie Gao, Lei Chen, Tingting Tan, Wenhao Jiang, Bingwei Chen, Yonggui Yuan, Zhijun Zha |
- Page last reviewed:Feb 1, 2024
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