Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 38 Records) |
Query Trace: Ventricular Fibrillation and SCN5A[original query] |
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Differential effects of cardiac sodium channel mutations on initiation of ventricular arrhythmias in patients with Brugada syndrome. Heart rhythm : the official journal of the Heart Rhythm Society 2009 Apr 6 (4): 4. Morita H, Nagase S, Miura D, Miura A, Hiramatsu S, Tada T, Murakami M, Nishii N, Nakamura K, Morita ST, Oka T, Kusano KF, Ohe T |
The P-selectin gene polymorphism Val168Met: a novel risk marker for the occurrence of primary ventricular fibrillation during acute myocardial infarction. Journal of cardiovascular electrophysiology 2010 Nov 21 (11): 1260-5. Elmas Elif, Bugert Peter, Popp Tatjana, Lang Siegfried, Weiss Christel, Behnes Michael, Borggrefe Martin, Kälsch Thorst |
Atrial electrophysiological and structural remodeling in high-risk patients with Brugada syndrome: assessment with electrophysiology and echocardiography. Heart rhythm : the official journal of the Heart Rhythm Society 2010 7 (2): 218-24. Toh Norihisa, Morita Hiroshi, Nagase Satoshi, Taniguchi Manabu, Miura Daiji, Nishii Nobuhiro, Nakamura Kazufumi, Ohe Tohru, Kusano Kengo F, Ito Hiros |
SCN5A mutation is associated with early and frequent recurrence of ventricular fibrillation in patients with Brugada syndrome. Circulation journal : official journal of the Japanese Circulation Society 2010 Nov 74 (12): 2572-8. Nishii Nobuhiro, Ogawa Masahiro, Morita Hiroshi, Nakamura Kazufumi, Banba Kimikazu, Miura Daiji, Kumagai Naoko, Matsunaga Akira, Kawamura Hiroshi, Urakawa Shigemi, Miyaji Kohei, Nagai Masahiro, Satoh Katsumasa, Nakagawa Koji, Tanaka Masamichi, Hiramatsu Shigeki, Tada Takeshi, Murakami Masato, Nagase Satoshi, Kohno Kunihisa, Kusano Kengo Fukushima, Saku Keijiro, Ohe Tohru, Ito Hiros |
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 |
Genetic testing of patients with long QT syndrome. Revista espanola de cardiologia 2011 1 64 (1): 71-4. Jiménez-Jáimez Juan, Tercedor-Sánchez Luis, Alvarez-López Miguel, Martínez-Espín Esther, Sebastián Galdeano Ricardo, Almansa-Valencia Isabel, Lorente José A, Melgares-Moreno Rafa |
L-type calcium channel mutations in Japanese patients with inherited arrhythmias. Circulation journal : official journal of the Japanese Circulation Society 2013 77 (7): 1799-806. Fukuyama Megumi, Ohno Seiko, Wang Qi, Kimura Hiromi, Makiyama Takeru, Itoh Hideki, Ito Makoto, Horie Mino |
SCN5A mutations and polymorphisms in patients with ventricular fibrillation during acute myocardial infarction. Molecular medicine reports 2014 Oct 10 (4): 2039-44. Boehringer Tim, Bugert Peter, Borggrefe Martin, Elmas El |
Genetics of Brugada syndrome. Journal of human genetics 2015 Jul . Watanabe Hiroshi, Minamino Toh |
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 |
Purkinje-related ventricular fibrillation associated with a homozygous H558R polymorphism in the sodium channel SCN5A gene. 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 Jun . Reithmann Christopher, Beckmann Britt-Maria, Kääb Stef |
Novel SCN10A variants associated with Brugada 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 . Fukuyama Megumi, Ohno Seiko, Makiyama Takeru, Horie Mino |
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome. Human molecular genetics 2015 May 24 (10): 2757-63. Le Scouarnec Solena, Karakachoff Matilde, Gourraud Jean-Baptiste, Lindenbaum Pierre, Bonnaud Stéphanie, Portero Vincent, Duboscq-Bidot Laëtitia, Daumy Xavier, Simonet Floriane, Teusan Raluca, Baron Estelle, Violleau Jade, Persyn Elodie, Bellanger Lise, Barc Julien, Chatel Stéphanie, Martins Raphaël, Mabo Philippe, Sacher Frédéric, Haïssaguerre Michel, Kyndt Florence, Schmitt Sébastien, Bézieau Stéphane, Le Marec Hervé, Dina Christian, Schott Jean-Jacques, Probst Vincent, Redon Richa |
Prognostic significance of fever-induced Brugada syndrome. Heart rhythm : the official journal of the Heart Rhythm Society 2016 Mar . Mizusawa Yuka, Morita Hiroshi, Adler Arnon, Havakuk Ofer, Thollet Aurélie, Maury Philippe, Wang Dao W, Hong Kui, Gandjbakhch Estelle, Sacher Frédéric, Hu Dan, Amin Ahmad S, Lahrouchi Najim, Tan Hanno L, Antzelevitch Charles, Probst Vincent, Viskin Sami, Wilde Arthur A |
Common Variant Near HEY2 Has a Protective Effect on Ventricular Fibrillation Occurrence in Brugada Syndrome by Regulating the Repolarization Current. Circulation. Arrhythmia and electrophysiology 2016 Jan 9 (1): . Nakano Yukiko, Ochi Hidenori, Onohara Yuko, Toshishige Masaaki, Tokuyama Takehito, Matsumura Hiroya, Kawazoe Hiroshi, Tomomori Shunsuke, Sairaku Akinori, Watanabe Yoshikazu, Ikenaga Hiroki, Motoda Chikaaki, Suenari Kazuyoshi, Hayashida Yasufumi, Miki Daiki, Oda Nozomu, Kishimoto Shinji, Oda Noboru, Yoshida Yukihiko, Tashiro Satoshi, Chayama Kazuaki, Kihara Yasu |
Heritability in a SCN5A-mutation founder population with increased female susceptibility to non-nocturnal ventricular tachyarrhythmia and sudden cardiac death. Heart rhythm 2017 8 14 (12): 1873-1881. Ter Bekke Rachel M A, Isaacs Aaron, Barysenka Andrei, Hoos Marije B, Jongbloed Jan D H, Hoorntje Jan C A, Patelski Alfons S M, Helderman-van den Enden Apollonia T J M, van den Wijngaard Arthur, Stoll Monika, Volders Paul G |
A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction. PloS one 2017 12 (1): e0170193. Jabbari Reza, Glinge Charlotte, Jabbari Javad, Risgaard Bjarke, Winkel Bo Gregers, Terkelsen Christian Juhl, Tilsted Hans-Henrik, Jensen Lisette Okkels, Hougaard Mikkel, Haunsø Stig, Engstrøm Thomas, Albert Christine M, Tfelt-Hansen Jac |
Detection of Variants in Patients with Idiopathic Ventricular Fibrillation by Whole-exome Sequencing. Annals of clinical and laboratory science 2018 8 48 (4): 427-434. Chang Ya-Sian, Lee Chien-Chin, Huang Hsi-Yuan, Lin Kuo-Hung, Chen Jan-Yow, Chang Kuan-Cheng, Chang Jan-Gow |
SCN5A mutation type and topology are associated with the risk of ventricular arrhythmia by sodium channel blockers. International journal of cardiology 2018 5 266 128-132. Amin Ahmad S, Reckman Yolan J, Arbelo Elena, Spanjaart Anne M, Postema Pieter G, Tadros Rafik, Tanck Michael W, Van den Berg Maarten P, Wilde Arthur A M, Tan Hanno |
Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac Diseases. Circulation. Genomic and precision medicine 2018 10 11 (10): e001797. Nannenberg Eline A, van Rijsingen Ingrid A W, van der Zwaag Paul A, van den Berg Maarten P, van Tintelen J Peter, Tanck Michael W T, Ackerman Michael J, Wilde Arthur A M, Christiaans Im |
SCN5A gene mutations and the risk of ventricular fibrillation and syncope in Brugada syndrome patients: A meta-analysis. Journal of arrhythmia 2018 10 34 (5): 473-477. Raharjo Sunu Budhi, Maulana Rido, Maghfirah Irma, Alzahra Fatimah, Putrinarita Agnes Dinar, Hanafy Dicky A, Yuniadi Yo |
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 |
Identification of Novel SCN5A Single Nucleotide Variants in Brugada Syndrome: A Territory-Wide Study From Hong Kong. Frontiers in physiology 2020 11 574590. Tse Gary, Lee Sharen, Liu Tong, Yuen Ho Chuen, Wong Ian Chi Kei, Mak Chloe, Mok Ngai Shing, Wong Wing T |
Novel SCN5A variants identified in a group of Iranian Brugada syndrome patients. Functional & integrative genomics 2021 2 21 (3-4): 331-340. Ghaffari Taraneh, Mirhosseini Motlagh Naser, Daraei Abdolreza, Tafrihi Majid, Saravi Mehrdad, Sabour Davo |
Pregnancy in women with Brugada syndrome: Is there an increased arrhythmia risk? A case-series report. Journal of cardiovascular electrophysiology 2021 10 33 (1): 123-127. van der Crabben Saskia N, Kowsoleea Astra I E, Clur Sally-Ann B, Wilde Arthur A |
Plasma MicroRNAs as noninvasive diagnostic biomarkers in patients with Brugada syndrome. PloS one 2022 5 17 (5): e0261390. Ikeuchi Yoshihiro, Ochi Hidenori, Motoda Chikaaki, Tokuyama Takehito, Okubo Yousaku, Okamura Sho, Miyauchi Syunsuke, Miyamoto Shogo, Uotani Yukimi, Onohara Yuko, Nakashima Mika, Akiyama Rie, Tahara Hidetoshi, Chayama Kazuaki, Kihara Yasuki, Nakano Yuki |
Association Between Deleterious SCN5A Variants and Ventricular Septal Defect in Young Patients With Brugada Syndrome. JACC. Clinical electrophysiology 2022 3 8 (3): 297-305. Suzuki Keisuke, Sonoda Keiko, Aoki Hisaaki, Nakamura Yuko, Watanabe Seiichi, Yoshida Yoko, Hoshino Kenji, Ozawa Junichi, Imamura Tomohiko, Aiba Takeshi, Kato Koichi, Makiyama Takeru, Kusano Kengo, Horie Minoru, Ohno Sei |
Genome sequencing in a genetically elusive multigenerational long QT syndrome pedigree identifies a novel LQT2-causative deeply intronic KCNH2 variant. Heart rhythm 2022 2 19 (6): 998-1007. Tobert Kathryn E, Tester David J, Zhou Wei, Haglund-Turnquist Carla M, Giudicessi John R, Ackerman Michael |
In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome. Molecular genetics & genomic medicine 2023 8 e2263. Hung Manh Pham, Duy Phuong Nguyen, Thanh Dat Ta, Thi Phuong Le, Phong Hai Phan, Hoai An Trinh, Tuan Viet Tran, Thi Lan Anh Luong, Ha Minh Nguyen, The-Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van-Khanh Tr |
The genetic basis of apparently idiopathic ventricular fibrillation: a retrospective overview. 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 2023 11 . Lisa M Verheul, Martijn H van der Ree, Sanne A Groeneveld, Bart A Mulder, Imke Christiaans, Gijs F L Kapel, Marco Alings, Marianne Bootsma, Daniela Q C M Barge-Schaapveld, Jippe C Balt, Sing-Chien Yap, Ingrid P C Krapels, Rachel M A Ter Bekke, Paul G A Volders, Saskia N van der Crabben, Pieter G Postema, Arthur A M Wilde, Dennis Dooijes, Annette F Baas, Rutger J Hassi |
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- Page last updated:May 06, 2024
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