Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 118 Records) |
Query Trace: KCNE1[original query] |
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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 |
Association between KCNE1 G38S gene polymorphism and risk of atrial fibrillation: A PRISMA-compliant meta-analysis. Medicine 2017 Jun 96 (25): e7253. Jiang Yu-Feng, Chen Min, Zhang Nan-Nan, Yang Hua-Jia, Xu Lang-Biao, Rui Qing, Sun Si-Jia, Yao Jia-Lu, Zhou Ya-Fe |
GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals.
Scientific reports 2017 Dec 7 (1): 17075. Méndez-Giráldez Raúl, Gogarten Stephanie M, Below Jennifer E, Yao Jie, Seyerle Amanda A, Highland Heather M, Kooperberg Charles, Soliman Elsayed Z, Rotter Jerome I, Kerr Kathleen F, Ryckman Kelli K, Taylor Kent D, Petty Lauren E, Shah Sanjiv J, Conomos Matthew P, Sotoodehnia Nona, Cheng Susan, Heckbert Susan R, Sofer Tamar, Guo Xiuqing, Whitsel Eric A, Lin Henry J, Hanis Craig L, Laurie Cathy C, Avery Christy |
[Association of KCNE1 and KCNE4 gene polymorphisms with atrial fibrillation among Uygur and Han Chinese populations in Xinjiang]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2017 Oct 34 (5): 743-748. Miao Haijun, Zhou Xiaohui, Kabinur Keyimu, Zou Ting, Palida Abulizi, Tang Baope |
QT length during methadone maintenance treatment: gene × 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 |
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 |
Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience. Hong Kong medical journal = Xianggang yi xue za zhi 2018 3 24 (4): 340-349. Mak C M, Chen S Pl, Mok N S, Siu W K, Lee H Hc, Ching C K, Tsui P T, Fong N C, Yuen Y P, Poon W T, Law C Y, Chong Y K, Chan Y W, Yung T C, Fan K Yy, Lam C |
Genetic variants in post myocardial infarction patients presenting with electrical storm of unstable ventricular tachycardia. Indian pacing and electrophysiology journal 2018 2 18 (3): 91-94. Rangaraju Advithi, Krishnan Shuba, Aparna G, Sankaran Satish, Mannan Ashraf U, Rao B Hygr |
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 |
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 |
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 |
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits.
European journal of human genetics : EJHG 2019 Jan . van Setten Jessica, Verweij Niek, Mbarek Hamdi, Niemeijer Maartje N, Trompet Stella, Arking Dan E, Brody Jennifer A, Gandin Ilaria, Grarup Niels, Hall Leanne M, Hemerich Daiane, Lyytikäinen Leo-Pekka, Mei Hao, Müller-Nurasyid Martina, Prins Bram P, Robino Antonietta, Smith Albert V, Warren Helen R, Asselbergs Folkert W, Boomsma Dorret I, Caulfield Mark J, Eijgelsheim Mark, Ford Ian, Hansen Torben, Harris Tamara B, Heckbert Susan R, Hottenga Jouke-Jan, Iorio Annamaria, Kors Jan A, Linneberg Allan, MacFarlane Peter W, Meitinger Thomas, Nelson Christopher P, Raitakari Olli T, Silva Aldana Claudia T, Sinagra Gianfranco, Sinner Moritz, Soliman Elsayed Z, Stoll Monika, Uitterlinden Andre, van Duijn Cornelia M, Waldenberger Melanie, Alonso Alvaro, Gasparini Paolo, Gudnason Vilmundur, Jamshidi Yalda, Kääb Stefan, Kanters Jørgen K, Lehtimäki Terho, Munroe Patricia B, Peters Annette, Samani Nilesh J, Sotoodehnia Nona, Ulivi Sheila, Wilson James G, de Geus Eco J C, Jukema J Wouter, Stricker Bruno, van der Harst Pim, de Bakker Paul I W, Isaacs Aar |
Genetic homozygosity in a diverse population: An experience of long QT syndrome. International journal of cardiology 2020 5 316 117-124. Mahdieh Nejat, Khorgami Mohammadrafi, Soveizi Mahdieh, Seyed Aliakbar Saranaz, Dalili Mohammad, Rabbani Bahar |
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 |
Variations in the potassium voltage-gated channel subfamily E regulatory subunit 1 gene associated with noise-induced hearing loss in the Chinese population. Environmental science and pollution research international 2020 Mar . Ding Enmin, Wang Huan, Han Lei, Zhang Hengdong, Zhu Bao |
Association Analysis of Candidate Gene Polymorphisms and Audiometric Measures of Noise-Induced Hearing Loss in Young Musicians. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2020 3 41 (5): e538-e547. Bhatt Ishan Sunilkumar, Dias Raquel, Washnik Nilesh, Wang Jin, Guthrie O'neil, Skelton Michael, Lane Jeffery, Wilder Jas |
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition. Circulation 2020 1 141 (6): 429-439. Roberts Jason D, Asaki S Yukiko, Mazzanti Andrea, Bos J Martijn, Tuleta Izabela, Muir Alison R, Crotti Lia, Krahn Andrew D, Kutyifa Valentina, Shoemaker M Benjamin, Johnsrude Christopher L, Aiba Takeshi, Marcondes Luciana, Baban Anwar, Udupa Sharmila, Dechert Brynn, Fischbach Peter, Knight Linda M, Vittinghoff Eric, Kukavica Deni, Stallmeyer Birgit, Giudicessi John R, Spazzolini Carla, Shimamoto Keiko, Tadros Rafik, Cadrin-Tourigny Julia, Duff Henry J, Simpson Christopher S, Roston Thomas M, Wijeyeratne Yanushi D, El Hajjaji Imane, Yousif Maisoon D, Gula Lorne J, Leong-Sit Peter, Chavali Nikhil, Landstrom Andrew P, Marcus Gregory M, Dittmann Sven, Wilde Arthur A M, Behr Elijah R, Tfelt-Hansen Jacob, Scheinman Melvin M, Perez Marco V, Kaski Juan Pablo, Gow Robert M, Drago Fabrizio, Aziz Peter F, Abrams Dominic J, Gollob Michael H, Skinner Jonathan R, Shimizu Wataru, Kaufman Elizabeth S, Roden Dan M, Zareba Wojciech, Schwartz Peter J, Schulze-Bahr Eric, Etheridge Susan P, Priori Silvia G, Ackerman Michael |
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- |
Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.
Circulation. Genomic and precision medicine 2021 Jul . Choi Seung Hoan, Jurgens Sean J, Haggerty Christopher M, Hall Amelia W, Halford Jennifer L, Morrill Valerie N, Weng Lu-Chen, Lagerman Braxton, Mirshahi Tooraj, Pettinger Mary, Guo Xiuqing, Lin Henry J, Alonso Alvaro, Soliman Elsayed Z, Kornej Jelena, Lin Honghuang, Moscati Arden, Nadkarni Girish N, Brody Jennifer A, Wiggins Kerri L, Cade Brian E, Lee Jiwon, Austin-Tse Christina, Blackwell Tom, Chaffin Mark D, Lee Christina J-Y, Rehm Heidi L, Roselli Carolina, , Redline Susan, Mitchell Braxton D, Sotoodehnia Nona, Psaty Bruce M, Heckbert Susan R, Loos Ruth J F, Vasan Ramachandran S, Benjamin Emelia J, Correa Adolfo, Boerwinkle Eric, Arking Dan E, Rotter Jerome I, Rich Stephen S, Whitsel Eric A, Perez Marco, Kooperberg Charles, Fornwalt Brandon K, Lunetta Kathryn L, Ellinor Patrick T, Lubitz Steven A, |
Association Analysis of Candidate Gene Polymorphisms and Tinnitus in Young Musicians. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2021 Jul . Bhatt Ishan Sunilkumar, Dias Raquel, Torkamani A |
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 |
Elevation of propofol sensitivity of cardiac I channel by KCNE1 polymorphism D85N. British journal of pharmacology 2021 3 178 (13): 2690-2708. Kojima Akiko, Mi Xinya, Fukushima Yutaka, Ding Wei-Guang, Omatsu-Kanbe Mariko, Matsuura Hiros |
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 |
[Association study between the KCNE family gene polymorphisms of potassium channel gene and the susceptibility of atrial fibrillation]. Zhonghua yi xue za zhi 2022 Oct 102 (38): 3026-3032. Qin M, Tao J R, Liu Z J, Hu W Y, Yan P Y, Wang R, Zhang Y, Xu G |
Impact of rs1805127 and rs55742440 Variants on Atrial Remodeling in Hypertrophic Cardiomyopathy Patients with Atrial Fibrillation: A Romanian Cohort Study. International journal of molecular sciences 2023 12 24 (24): . Nicoleta-Monica Popa-Fotea, Nicoleta Oprescu, Alexandru Scafa-Udriste, Miruna Mihaela Mich |
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 |
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- Page last updated:Apr 22, 2024
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