HuGE Literature Finder
Records 1-30
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Single nucleotide polymorphisms of SCN5A and SCN10A genes increase the risk of ventricular arrhythmias during myocardial infarction.
Advances in clinical and experimental medicine : official organ Wroclaw Medical University 2020 Apr . Foddha Hajer, Bouzidi Nadia, Foddha Abdelhak, Chouchene Saoussen, Touhami Rahma, Leban Nadia, Maatoug Mohamed Faouzi, Gamra Habib, Ferchichi Salima, Chibani Jemni Ben, Khelil Amel H |
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Systematic Meta-Analysis of the Association Between a Common NOS1AP Genetic Polymorphism, the QTc Interval, and Sudden Death.
International heart journal 2019 Aug . Zang Xiaobiao, Li Sisi, Zhao Yonghui, Chen Ke, Wang Xianqing, Song Weifeng, Ma Jifang, Tu Xin, Xia Yunlong, Zhang Shulong, Gao Chuan |
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Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths.
Forensic science international. Genetics 2019 Jul 42 203-212. Martinez-Matilla M, Blanco-Verea A, Santori M, Ansede-Bermejo J, Ramos-Luis E, Gil R, Bermejo A M, Lotufo-Neto F, Hirata M H, Brisighelli F, Paramo M, Carracedo A, Brion |
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A common indel polymorphism of the Desmoglein-2 (DSG2) is associated with sudden cardiac death in Chinese populations.
Forensic science international 2019 Jun 301 382-387. Zou Yan, Zhang Qing, Zhang Jianhua, Chen Xuekun, Zhou Wei, Yang Zhenzhen, Yang Qi, Yu Huan, Li Lijuan, He Yan, Li Chengtao, Zhang Suhua, Zhu Shaohua, Luo Bin, Gao Yuzh |
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Usefulness of Genetic Testing in Sudden Cardiac Arrest Survivors With or Without Previous Clinical Evidence of Heart Disease.
The American journal of cardiology 2019 Mar . Asatryan Babken, Schaller André, Seiler Jens, Servatius Helge, Noti Fabian, Baldinger Samuel H, Tanner Hildegard, Roten Laurent, Dillier Roger, Lam Anna, Haeberlin Andreas, Conte Giulio, Saguner Ardan M, Müller Stephan Andreas, Duru Firat, Auricchio Angelo, Ammann Peter, Sticherling Christian, Burri Haran, Reichlin Tobias, Wilhelm Matthias, Medeiros-Domingo Argel |
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Usefulness of Single Nucleotide Polymorphisms as Predictors of Sudden Cardiac Death.
The American journal of cardiology 2019 Mar . Tamariz Leonardo, Balda Javier, Pareja Dennise, Palacio Ana, Myerburg Robert J, Conway Douglas, Davis Lea, Goldberger Jeffrey |
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Genetic characterization and genotype-phenotype associations in a large cohort of patients with hypertrophic cardiomyopathy - An ancillary study of the Portuguese registry of hypertrophic cardiomyopathy.
International journal of cardiology 2018 Dec . Lopes Luis Rocha, Brito Dulce, Belo Adriana, Cardim Nuno, |
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The narrow-sense and common single nucleotide polymorphism heritability of early repolarization.
International journal of cardiology 2018 Oct . Bastiaenen Rachel, Nolte Ilja M, Munroe Patricia B, Riese Harriëtte, Nelson Christopher, O'Connor Henry, Gang Yi, Warren Helen R, Cabrera Claudia, Reinhard Wibke, Hengstenberg Christian, Rijsdijk Frühling V, Spector Tim, Snieder Harold, Samani Nilesh J, Jamshidi Yalda, Behr Elijah |
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Associations between common ion channel single nucleotide polymorphisms and sudden cardiac death in adults: A MOOSE-compliant meta-analysis.
Medicine 2018 Sep 97 (38): e12428. Liu Xiaoli, Shi Jianli, Xiao Peil |
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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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SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups.
European heart journal 2018 Jul . Baruteau Alban-Elouen, Kyndt Florence, Behr Elijah R, Vink Arja S, Lachaud Matthias, Joong Anna, Schott Jean-Jacques, Horie Minoru, Denjoy Isabelle, Crotti Lia, Shimizu Wataru, Bos Johan M, Stephenson Elizabeth A, Wong Leonie, Abrams Dominic J, Davis Andrew M, Winbo Annika, Dubin Anne M, Sanatani Shubhayan, Liberman Leonardo, Kaski Juan Pablo, Rudic Boris, Kwok Sit Yee, Rieubland Claudine, Tfelt-Hansen Jacob, Van Hare George F, Guyomarc'h-Delasalle Béatrice, Blom Nico A, Wijeyeratne Yanushi D, Gourraud Jean-Baptiste, Le Marec Hervé, Ozawa Junichi, Fressart Véronique, Lupoglazoff Jean-Marc, Dagradi Federica, Spazzolini Carla, Aiba Takeshi, Tester David J, Zahavich Laura A, Beauséjour-Ladouceur Virginie, Jadhav Mangesh, Skinner Jonathan R, Franciosi Sonia, Krahn Andrew D, Abdelsayed Mena, Ruben Peter C, Yung Tak-Cheung, Ackerman Michael J, Wilde Arthur A, Schwartz Peter J, Probst Vince |
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A SNaPshot assay for detection of 45 mutations in the SCN5A gene in the Chinese Han Population.
Electrophoresis 2018 Jun . Wang Jiaqi, Wang Xudong, Ma Zhihua, Yun Keming, Liu Jinding, Chen Deqing, Liu Zidong, Shi Jie, Li Zeqin, Gao Cairong, Du Qiuxiang, Zhang Gengqi |
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Importance of Variant Interpretation in Whole-Exome Molecular Autopsy: Population-Based Case Series.
Circulation 2018 Jun 137 (25): 2705-2715. Shanks Garrett W, Tester David J, Ackerman Jaeger P, Simpson Michael A, Behr Elijah R, White Steven M, Ackerman Michael |
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Primary Myocardial Fibrosis as an Alternative Phenotype Pathway of Inherited Cardiac Structural Disorders.
Circulation 2018 Jun 137 (25): 2716-2726. Junttila M Juhani, Holmström Lauri, Pylkäs Katri, Mantere Tuomo, Kaikkonen Kari, Porvari Katja, Kortelainen Marja-Leena, Pakanen Lasse, Kerkelä Risto, Myerburg Robert J, Huikuri Heikki |
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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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Genome-Wide Associations of Global Electrical Heterogeneity ECG Phenotype: The ARIC (Atherosclerosis Risk in Communities) Study and CHS (Cardiovascular Health Study).
Journal of the American Heart Association 2018 Apr 7 (8): . Tereshchenko Larisa G, Sotoodehnia Nona, Sitlani Colleen M, Ashar Foram N, Kabir Muammar, Biggs Mary L, Morley Michael P, Waks Jonathan W, Soliman Elsayed Z, Buxton Alfred E, Biering-Sørensen Tor, Solomon Scott D, Post Wendy S, Cappola Thomas P, Siscovick David S, Arking Dan |
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Critical Roles of Xirp Proteins in Cardiac Conduction and Their Rare Variants Identified in Sudden Unexplained Nocturnal Death Syndrome and Brugada Syndrome in Chinese Han Population.
Journal of the American Heart Association 2018 01 7 (1): . Huang Lei, Wu Kuo-Ho, Zhang Liyong, Wang Qinchuan, Tang Shuangbo, Wu Qiuping, Jiang Pei-Hsiu, Lin Jim Jung-Ching, Guo Jian, Wang Lin, Loh Shih-Hurng, Cheng Jiandi |
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Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome.
PloS one 2018 13 (4): e0195594. Gray Belinda, Gnanappa Ganesh Kumar, Bagnall Richard D, Femia Giuseppe, Yeates Laura, Ingles Jodie, Burns Charlotte, Puranik Rajesh, Grieve Stuart M, Semsarian Christopher, Sy Raymond |
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Sudden cardiac arrest in patients without overt heart disease: a limited value of next generation sequencing.
Polish archives of internal medicine 2018 12 128 (12): 721-730. Stepien-Wojno Malgorzata, Poninska Joanna, Rydzanicz Malgorzata, Bilinska Maria, Truszkowska Grazyna, Baranowski Rafal, Lutynska Anna, Biernacka Elzbieta K, Stepinska Janina, Kowalik Ilona, Ploski Rafal, Bilinska Zofia |
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Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death.
Circulation. Genomic and precision medicine 2018 08 11 (8): e002151. Sveinbjornsson Gardar, Olafsdottir Eva F, Thorolfsdottir Rosa B, Davidsson Olafur B, Helgadottir Anna, Jonasdottir Adalbjorg, Jonasdottir Aslaug, Bjornsson Eythor, Jensson Brynjar O, Arnadottir Gudny A, Kristinsdottir Hallfridur, Stephensen Sigurdur S, Oskarsson Gylfi, Gudbjartsson Tomas, Sigurdsson Emil L, Andersen Karl, Danielsen Ragnar, Arnar David O, Jonsdottir Ingileif, Thorsteinsdottir Unnur, Sulem Patrick, Thorgeirsson Gudmundur, Gudbjartsson Daniel F, Holm Hilma, Stefansson Ka |
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H558R, a common SCN5A polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of SCN5A promoters.
Journal of biomedical science 2017 Dec 24 (1): 91. Matsumura Hiroya, Nakano Yukiko, Ochi Hidenori, Onohara Yuko, Sairaku Akinori, Tokuyama Takehito, Tomomori Shunsuke, Motoda Chikaaki, Amioka Michitaka, Hironobe Naoya, Toshishige Masaaki, Takahashi Shinya, Imai Katsuhiko, Sueda Taijiro, Chayama Kazuaki, Kihara Yasu |
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Yield and Pitfalls of Ajmaline Testing in the Evaluation of Unexplained Cardiac Arrest and Sudden Unexplained Death: Single-Center Experience With 482 Families.
JACC. Clinical electrophysiology 2017 Dec 3 (12): 1400-1408. Tadros Rafik, Nannenberg Eline A, Lieve Krystien V, Škori?-Milosavljevi? Doris, Lahrouchi Najim, Lekanne Deprez Ronald H, Vendrik Jeroen, Reckman Yolan J, Postema Pieter G, Amin Ahmad S, Bezzina Connie R, Wilde Arthur A M, Tan Hanno |
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Utility of Genetics for Risk Stratification in Pediatric Hypertrophic Cardiomyopathy.
Clinical genetics 2017 Oct . Mathew J, Zahavich L, Lafreniere-Roula M, Wilson J, George K, Benson L, Bowdin S, Mital |
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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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Multiple Gene Variants in Hypertrophic Cardiomyopathy in the Era of Next-Generation Sequencing.
Circulation. Cardiovascular genetics 2017 Aug 10 (4): . Burns Charlotte, Bagnall Richard D, Lam Lien, Semsarian Christopher, Ingles Jod |
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The Brugada Syndrome Susceptibility Gene
Circulation research 2017 Aug 121 (5): 537-548. Veerman Christiaan C, Podliesna Svitlana, Tadros Rafik, Lodder Elisabeth M, Mengarelli Isabella, de Jonge Berend, Beekman Leander, Barc Julien, Wilders Ronald, Wilde Arthur A M, Boukens Bastiaan J, Coronel Ruben, Verkerk Arie O, Remme Carol Ann, Bezzina Connie |
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Association between an indel polymorphism in the 3'UTR of COL1A2 and the risk of sudden cardiac death in Chinese populations.
Legal medicine (Tokyo, Japan) 2017 Jul 28 22-26. Yin Zhixia, Guo Yadong, Zhang Jianhua, Zhang Qing, Li Lijuan, Wang Shouyu, Wang Chaoqun, He Yan, Zhu Shaohua, Li Chengtao, Zhang Suhua, Zha Lagabaiyila, Cai Jifeng, Luo Bin, Gao Yuzh |
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Association of Polymorphism in SCN5A, GJA5, and KCNN3 Gene with Sudden Cardiac Death.
Bulletin of experimental biology and medicine 2017 Jun . Ivanova A A, Maksimov V N, Ivanoshchuk D E, Orlov P S, Novoselov V P, Savchenko S V, Voevoda M |
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Identification of pathogenic variants in genes related to channelopathy and cardiomyopathy in Korean sudden cardiac arrest survivors.
Journal of human genetics 2017 Jun 62 (6): 615-620. Song Ju Sun, Kang Jong-Sun, Kim Young-Eun, Park Seung-Jung, Park Kyoung-Min, Huh June, Kim June Soo, Cho Hana, Ki Chang-Seok, On Young Ke |
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An East Asian Common Variant Vinculin P.Asp841His Was Associated With Sudden Unexplained Nocturnal Death Syndrome in the Chinese Han Population.
Journal of the American Heart Association 2017 Apr 6 (4): . Cheng Jianding, Kyle John W, Lang Di, Wiedmeyer Brandi, Guo Jian, Yin Kun, Huang Lei, Vaidyanathan Ravi, Su Terry, Makielski Jonathan |
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Genetic anticipation in a special form of hypertrophic cardiomyopathy with sudden cardiac death in a family with 74 members across 5 generations.
Medicine 2017 Mar 96 (11): e6249. Guo Xiying, Fan Chaomei, Wang Yanping, Wang Miao, Cai Chi, Yang Yinjian, Zhao Shihua, Duan Fujian, Li Yis |
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An insertion/deletion polymorphism within 3'UTR of RYR2 modulates sudden unexplained death risk in Chinese populations.
Forensic science international 2017 Jan 270 165-172. Wang Shouyu, Zhang Zhixiang, Yang Ya, Wang Chaoqun, Tao Ruiyang, Hu Shuxiang, Yin Zhixia, Zhang Qing, Li Lijuan, He Yan, Zhu Shaohua, Li Chengtao, Zhang Suhua, Zhang Jianhua, Sheng Lihui, Wu Fangyu, Luo Bin, Gao Yuzh |
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Genetic analysis in post-mortem samples with micro-ischemic alterations.
Forensic science international 2017 Jan 271 120-125. Campuzano Oscar, Sanchez-Molero Olallo, Mademont-Soler Irene, Coll Monica, Allegue Catarina, Ferrer-Costa Carles, Mates Jesus, Perez-Serra Alexandra, Del Olmo Bernat, Iglesias Anna, Sarquella-Brugada Georgia, Brugada Josep, Borondo Juan Carlos, Castella Josep, Medallo Jordi, Brugada Ram |
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A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.
European heart journal 2017 01 38 (1): 27-34. Gudbjartsson Daniel F, Holm Hilma, Sulem Patrick, Masson Gisli, Oddsson Asmundur, Magnusson Olafur Th, Saemundsdottir Jona, Helgadottir Hafdis Th, Helgason Hannes, Johannsdottir Hrefna, Gretarsdottir Solveig, Gudjonsson Sigurjon A, Njølstad Inger, Løchen Maja-Lisa, Baum Larry, Ma Ronald C W, Sigfusson Gunnlaugur, Kong Augustine, Thorgeirsson Guðmundur, Sverrisson Jon Th, Thorsteinsdottir Unnur, Stefansson Kari, Arnar David |
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Polymorphisms in the GNAS Gene as Predictors of Ventricular Tachyarrhythmias and Sudden Cardiac Death: Results From the DISCOVERY Trial and Oregon Sudden Unexpected Death Study.
Journal of the American Heart Association 2016 Nov 5 (12): . Wieneke Heinrich, Svendsen Jesper Hastrup, Lande Jeffrey, Spencker Sebastian, Martinez Juan Gabriel, Strohmer Bernhard, Toivonen Lauri, Le Marec Hervé, Garcia-Fernandez F Javier, Corrado Domenico, Huertas-Vazquez Adriana, Uy-Evanado Audrey, Rusinaru Carmen, Reinier Kyndaron, Foldesi Csaba, Hulak Wieslaw, Chugh Sumeet S, Siffert Winfri |
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Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality.
Genetics in medicine : official journal of the American College of Medical Genetics 2016 Oct . Ghouse Jonas, Have Christian T, Skov Morten W, Andreasen Laura, Ahlberg Gustav, Nielsen Jonas B, Skaaby Tea, Olesen Søren-Peter, Grarup Niels, Linneberg Allan, Pedersen Oluf, Vestergaard Henrik, Haunsø Stig, Svendsen Jesper H, Hansen Torben, Kanters Jørgen K, Olesen Morten |
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Comparison of Long-Term Outcome between Apical and Asymmetric Septal Hypertrophic Cardiomyopathy.
Cardiology 2016 Sep 136 (2): 108-114. An Shuoyan, Fan Chaomei, Yan Lirong, Cai Chi, Yang Yinjian, Zhai Shanshan, Zhao Shihua, Liu Yanling, Duan Fujian, Wang Zhimin, Li Yis |
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Prevalence and Phenotypic Expression of Mutations in the MYH7, MYBPC3 and TNNT2 Genes in Families with Hypertrophic Cardiomyopathy in the South of Brazil: A Cross-Sectional Study.
Arquivos brasileiros de cardiologia 2016 Sep 107 (3): 257-265. Mattos Beatriz Piva E, Scolari Fernando Luís, Torres Marco Antonio Rodrigues, Simon Laura, Freitas Valéria Centeno de, Giugliani Roberto, Matte Úrsu |
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KCNN2 polymorphisms and cardiac tachyarrhythmias.
Medicine 2016 Jul 95 (29): e4312. Yu Chih-Chieh, Chia-Ti Tsai, Chen Pei-Lung, Wu Cho-Kai, Chiu Fu-Chun, Chiang Fu-Tien, Chen Peng-Sheng, Chen Chi-Ling, Lin Lian-Yu, Juang Jyh-Ming, Ho Li-Ting, Lai Ling-Ping, Yang Wei-Shiung, Lin Jiunn-L |
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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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Association of common and rare variants of SCN10A gene with sudden unexplained nocturnal death syndrome in Chinese Han population.
International journal of legal medicine 2016 Jun . Zhang Liyong, Zhou Feng, Huang Lei, Wu Qiuping, Zheng Jinxiang, Wu Yeda, Yin Kun, Cheng Jiandi |
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Surveillance after cardiac arrest in patients with Brugada syndrome without an implantable defibrillator: An alarm effect of the previous syncope.
International journal of cardiology 2016 May 218 69-74. Calvo David, Flórez Juan Pablo, Valverde Irene, Rubín José, Pérez Diego, Vasserot Mar Gonzalez, Rodríguez-Reguero Julián, Avanzas Pablo, de la Hera Jesús María, Gómez Juan, Coto Eliecer, Martínez-Camblor Pablo, Morís Cés |
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An R1632C variant in the SCN5A gene causing Brugada syndrome.
Molecular medicine reports 2016 Apr . García-Molina Esperanza, Sabater-Molina María, Muñoz Carmen, Ruiz-Espejo Francisco, Gimeno Juan |
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Brugada Syndrome and PKP2: Evidences and uncertainties.
International journal of cardiology 2016 Apr 214 403-405. Campuzano Oscar, Fernández-Falgueras Anna, Iglesias Anna, Brugada Ram |
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The Canadian Arrhythmogenic Right Ventricular Cardiomyopathy Registry: Rationale, Design, and Preliminary Recruitment.
The Canadian journal of cardiology 2016 Apr . Krahn Andrew D, Healey Jeffrey S, Gerull Brenda, Angaran Paul, Chakrabarti Santabhanu, Sanatani Shubhayan, Arbour Laura, Laksman Zachary W M, Carroll Sandra L, Seifer Colette, Green Martin, Roberts Jason D, Talajic Mario, Hamilton Robert, Gardner Mart |
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The 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 |
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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 |
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Sudden Cardiac Arrest and Rare Genetic Variants in the Community.
Circulation. Cardiovascular genetics 2016 Jan . Milano Annalisa, Blom Marieke T, Lodder Elisabeth M, van Hoeijen Daniel A, Barc Julien, Koopmann Tamara T, Bardai Abdennasser, Beekman Leander, Lichtner Peter, van den Berg Maarten P, Wilde Arthur A M, Bezzina Connie R, Tan Hanno |
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Associations of Prolonged QTc in Sickle Cell Disease.
PloS one 2016 11 (10): e0164526. Indik Julia H, Nair Vineet, Rafikov Ruslan, Nyotowidjojo Iwan S, Bisla Jaskanwal, Kansal Mayank, Parikh Devang S, Robinson Melissa, Desai Anand, Oberoi Megha, Gupta Akash, Abbasi Taimur, Khalpey Zain, Patel Amit R, Lang Roberto M, Dudley Samuel C, Choi Bum-Rak, Garcia Joe G N, Machado Roberto F, Desai Ankit |
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Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect.
Journal of the American Heart Association 2016 5 (7): . Veltmann Christian, Barajas-Martinez Hector, Wolpert Christian, Borggrefe Martin, Schimpf Rainer, Pfeiffer Ryan, Cáceres Gabriel, Burashnikov Elena, Antzelevitch Charles, Hu D |
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Rare coding TTN variants are associated with electrocardiographic QT interval in the general population.
Scientific reports 2016 6 28356. Kapoor Ashish, Bakshy Kiranmayee, Xu Linda, Nandakumar Priyanka, Lee Dongwon, Boerwinkle Eric, Grove Megan L, Arking Dan E, Chakravarti Aravin |
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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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ABCB1 gene variants, digoxin and risk of sudden cardiac death in a general population.
Heart (British Cardiac Society) 2015 Nov . Niemeijer Maartje N, van den Berg Marten E, Deckers Jaap W, Aarnoudse Adrianus L H J, Hofman Albert, Franco Oscar H, Uitterlinden André G, Rijnbeek Peter R, Eijgelsheim Mark, Stricker Bruno |
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Identification of rare variants of DSP gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han population.
International journal of legal medicine 2015 Nov . Zhao Qianhao, Chen Yili, Peng Longlun, Gao Rui, Liu Nian, Jiang Pingping, Liu Chao, Tang Shuangbo, Quan Li, Makielski Jonathan C, Cheng Jiandi |
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Clinical and Prognostic Profiles of Cardiomyopathies Caused by Mutations in the Troponin T Gene.
Revista espanola de cardiologia (English ed.) 2015 Oct . Ripoll-Vera Tomás, Gámez José María, Govea Nancy, Gómez Yolanda, Núñez Juana, Socías Lorenzo, Escandell Ángela, Rosell Jor |
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High-throughput genetic characterization of a cohort of Brugada syndrome patients.
Human molecular genetics 2015 Oct 24 (20): 5828-35. Di Resta Chiara, Pietrelli Alessandro, Sala Simone, Della Bella Paolo, De Bellis Gianluca, Ferrari Maurizio, Bordoni Roberta, Benedetti Sa |
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Mutational analysis of mitochondrial DNA in Brugada syndrome.
Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology 2015 Oct . Stocchi Laura, Polidori Emanuela, Potenza Lucia, Rocchi Marco Bruno Luigi, Calcabrini Cinzia, Busacca Paolo, Capalbo Maria, Potenza Domenico, Amati Francesca, Mango Ruggiero, Romeo Francesco, Novelli Giuseppe, Stocchi Vilber |
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Genetics of inherited arrhythmias in pediatrics.
Current opinion in pediatrics 2015 Sep . Campuzano Oscar, Sarquella-Brugada Georgia, Cesar Sergi, Iglesias Anna, Arbelo Elena, Brugada Josep, Brugada Ram |
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NOS1AP polymorphisms modify QTc interval duration but not cardiac arrest risk in hypertrophic cardiomyopathy.
Journal of cardiovascular electrophysiology 2015 Sep . Earle Nikki, Ingles Jodie, Bagnall Richard D, Gray Belinda, Crawford Jackie, Smith Warren, Shelling Andrew N, Love Donald R, Semsarian Chris, Skinner Jonathan |
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[Mutation and clinical relevance in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy].
Zhonghua xin xue guan bing za zhi 2015 Aug 43 (8): 682-9. Jie Liu, Wenling Liu, Dayi Hu, Tiangang Zhu, Wen Liu, Zhanfeng Ma, Jie Yang, Wenli Xie, Cuilan Li, Lei Li, Guozhong P |
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Enhanced Classification of Brugada Syndrome-Associated and Long-QT Syndrome-Associated Genetic Variants in the SCN5A-Encoded Nav1.5 Cardiac Sodium Channel.
Circulation. Cardiovascular genetics 2015 Aug 8 (4): 582-95. Kapplinger Jamie D, Giudicessi John R, Ye Dan, Tester David J, Callis Thomas E, Valdivia Carmen R, Makielski Jonathan C, Wilde Arthur A, Ackerman Michael |
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Chronic obstructive pulmonary disease and sudden cardiac death: the Rotterdam study.
European heart journal 2015 Jul 36 (27): 1754-61. Lahousse Lies, Niemeijer Maartje N, van den Berg Marten E, Rijnbeek Peter R, Joos Guy F, Hofman Albert, Franco Oscar H, Deckers Jaap W, Eijgelsheim Mark, Stricker Bruno H, Brusselle Guy |
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Contribution of Cardiac Sodium Channel ?-Subunit Variants to Brugada Syndrome.
Circulation journal : official journal of the Japanese Circulation Society 2015 Jul . Peeters Uschi, Scornik Fabiana, Riuró Helena, Pérez Guillermo, Komurcu-Bayrak Evrim, Van Malderen Sophie, Pappaert Gudrun, Tarradas Anna, Pagans Sara, Daneels Dorien, Breckpot Karine, Brugada Pedro, Bonduelle Maryse, Brugada Ramon, Van Dooren Son |
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Genetics of Brugada syndrome.
Journal of human genetics 2015 Jul . Watanabe Hiroshi, Minamino Toh |
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Next-generation sequencing of 34 genes in sudden unexplained death victims in forensics and in patients with channelopathic cardiac diseases.
International journal of legal medicine 2015 Jul 129 (4): 793-800. Hertz C L, Christiansen S L, Ferrero-Miliani L, Fordyce S L, Dahl M, Holst A G, Ottesen G L, Frank-Hansen R, Bundgaard H, Morling |
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Phenotypic expression is a prerequisite for malignant arrhythmic events and sudden cardiac death in arrhythmogenic right ventricular cardiomyopathy.
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 Jul . Zorzi Alessandro, Rigato Ilaria, Pilichou Kalliopi, Perazzolo Marra Martina, Migliore Federico, Mazzotti Elisa, Gregori Dario, Thiene Gaetano, Daliento Luciano, Iliceto Sabino, Rampazzo Alessandra, Basso Cristina, Bauce Barbara, Corrado Domeni |
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Prolonged QT: A rare cause of cardiac arrest.
JAAPA : official journal of the American Academy of Physician Assistants 2015 Jul 28 (7): 1-4. Carlquist Jennif |
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The global distribution of the p.R1193Q polymorphism in the SCN5A gene.
Legal medicine (Tokyo, Japan) 2015 Jul . Matsusue Aya, Yuasa Isao, Umetsu Kazuo, Nakayashiki Nori, Dewa Koji, Nishimukai Hiroaki, Kashiwagi Masayuki, Hara Kenji, Waters Brian, Takayama Mio, Ikematsu Natsuki, Kubo Shin-Ic |
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Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.
Cardiovascular research 2015 Jun 106 (3): 520-9. Behr Elijah R, Savio-Galimberti Eleonora, Barc Julien, Holst Anders G, Petropoulou Evmorfia, Prins Bram P, Jabbari Javad, Torchio Margherita, Berthet Myriam, Mizusawa Yuka, Yang Tao, Nannenberg Eline A, Dagradi Federica, Weeke Peter, Bastiaenan Rachel, Ackerman Michael J, Haunso Stig, Leenhardt Antoine, Kääb Stefan, Probst Vincent, Redon Richard, Sharma Sanjay, Wilde Arthur, Tfelt-Hansen Jacob, Schwartz Peter, Roden Dan M, Bezzina Connie R, Olesen Morten, Darbar Dawood, Guicheney Pascale, Crotti Lia, , Jamshidi Yal |
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RyR2 Common Gene Variant G1886S and the Risk of Ventricular Arrhythmias in ICD Patients with Heart Failure.
Journal of cardiovascular electrophysiology 2015 Jun 26 (6): 656-61. Francia Pietro, Adduci Carmen, Semprini Lorenzo, Stanzione Rosita, Serdoz Andrea, Caprinozzi Massimo, Santini Daria, Cotugno Maria, Palano Francesca, Musumeci Maria Beatrice, Rubattu Speranza, Volpe Massi |
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SCN4A variants and Brugada syndrome: phenotypic and genotypic overlap between cardiac and skeletal muscle sodium channelopathies.
European journal of human genetics : EJHG 2015 Jun . Bissay Véronique, Van Malderen Sophie C H, Keymolen Kathelijn, Lissens Willy, Peeters Uschi, Daneels Dorien, Jansen Anna C, Pappaert Gudrun, Brugada Pedro, De Keyser Jacques, Van Dooren Son |
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Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series.
International journal of legal medicine 2015 May 129 (3): 495-504. Partemi Sara, Vidal Monica Coll, Striano Pasquale, Campuzano Oscar, Allegue Catarina, Pezzella Marianna, Elia Maurizio, Parisi Pasquale, Belcastro Vincenzo, Casellato Susanna, Giordano Lucio, Mastrangelo Massimo, Pietrafusa Nicola, Striano Salvatore, Zara Federico, Bianchi Amedeo, Buti Daniela, La Neve Angela, Tassinari Carlo Alberto, Oliva Antonio, Brugada Ram |
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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 |
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Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers.
European heart journal 2015 Apr 36 (14): 847-55. Bhonsale Aditya, Groeneweg Judith A, James Cynthia A, Dooijes Dennis, Tichnell Crystal, Jongbloed Jan D H, Murray Brittney, te Riele Anneline S J M, van den Berg Maarten P, Bikker Hennie, Atsma Douwe E, de Groot Natasja M, Houweling Arjan C, van der Heijden Jeroen F, Russell Stuart D, Doevendans Pieter A, van Veen Toon A, Tandri Harikrishna, Wilde Arthur A, Judge Daniel P, van Tintelen J Peter, Calkins Hugh, Hauer Richard |
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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 |
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A founder MYBPC3 mutation results in HCM with a high risk of sudden death after the fourth decade of life.
Journal of medical genetics 2015 Mar . Calore Chiara, De Bortoli Marzia, Romualdi Chiara, Lorenzon Alessandra, Angelini Annalisa, Basso Cristina, Thiene Gaetano, Iliceto Sabino, Rampazzo Alessandra, Melacini Pao |
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Arrhythmic risk assessment in genotyped families with arrhythmogenic right ventricular cardiomyopathy.
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 Mar . Protonotarios Alexandros, Anastasakis Aris, Panagiotakos Demosthenes B, Antoniades Loizos, Syrris Petros, Vouliotis Apostolos, Stefanadis Christodoulos, Tsatsopoulou Adalena, McKenna William J, Protonotarios Nik |
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Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy.
Heart (British Cardiac Society) 2015 Feb 101 (4): 294-301. Lopes Luis R, Syrris Petros, Guttmann Oliver P, O'Mahony Constantinos, Tang Hak Chiaw, Dalageorgou Chrysoula, Jenkins Sharon, Hubank Mike, Monserrat Lorenzo, McKenna William J, Plagnol Vincent, Elliott Perry |
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Electromechanical window negativity in genotyped long-QT syndrome patients: relation to arrhythmia risk.
European heart journal 2015 Jan 36 (3): 179-86. ter Bekke Rachel M A, Haugaa Kristina H, van den Wijngaard Arthur, Bos J Martijn, Ackerman Michael J, Edvardsen Thor, Volders Paul G |
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A Common Polymorphism of the Human Cardiac Sodium Channel Alpha Subunit (SCN5A) Gene Is Associated with Sudden Cardiac Death in Chronic Ischemic Heart Disease.
PloS one 2015 10 (7): e0132137. Marcsa Boglárka, Dénes Réka, Vörös Krisztina, Rácz Gergely, Sasvári-Székely Mária, Rónai Zsolt, Tör? Klára, Keszler Gerge |
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Analysis of SNP (single nucleotide polymorphism) multiplex markers related to sudden cardiac death in Brazilian families.
Genetics and molecular research : GMR 2015 14 (4): 14348. Braganholi D F, Cicarelli R M |
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Common Variants in TRDN and CALM1 Are Associated with Risk of Sudden Cardiac Death in Chronic Heart Failure Patients in Chinese Han Population.
PloS one 2015 10 (7): e0132459. Liu Zhouying, Liu Xiaoyan, Yu Haiyun, Pei Juanhui, Zhang Yinhui, Gong Jing, Pu Jiel |
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Determining the pathogenicity of genetic variants associated with cardiac channelopathies.
Scientific reports 2015 5 7953. Campuzano Oscar, Allegue Catarina, Fernandez Anna, Iglesias Anna, Brugada Ram |
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Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients.
PloS one 2015 10 (6): e0131517. Ohno Seiko, Hasegawa Kanae, Horie Mino |
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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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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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Brugada syndrome risk loci seem protective against atrial fibrillation.
European journal of human genetics : EJHG 2014 Dec 22 (12): 1357-61. Andreasen Laura, Nielsen Jonas B, Darkner Stine, Christophersen Ingrid E, Jabbari Javad, Refsgaard Lena, Thiis Jens J, Sajadieh Ahmad, Tveit Arnljot, Haunsø Stig, Svendsen Jesper H, Schmitt Nicole, Olesen Morten |
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Evaluation of genes encoding for the transient outward current (Ito) identifies the KCND2 gene as a cause of J-wave syndrome associated with sudden cardiac death.
Circulation. Cardiovascular genetics 2014 Dec 7 (6): 782-9. Perrin Mark J, Adler Arnon, Green Sharon, Al-Zoughool Foad, Doroshenko Petro, Orr Nathan, Uppal Shaheen, Healey Jeff S, Birnie David, Sanatani Shubhayan, Gardner Martin, Champagne Jean, Simpson Chris, Ahmad Kamran, van den Berg Maarten P, Chauhan Vijay, Backx Peter H, van Tintelen J Peter, Krahn Andrew D, Gollob Michael |
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A common SCN5A variant is associated with PR interval and atrial fibrillation among African Americans.
Journal of cardiovascular electrophysiology 2014 Nov 25 (11): 1150-7. Ilkhanoff Leonard, Arking Dan E, Lemaitre Rozenn N, Alonso Alvaro, Chen Lin Y, Durda Peter, Hesselson Stephanie E, Kerr Kathleen F, Magnani Jared W, Marcus Gregory M, Schnabel Renate B, Smith J Gustav, Soliman Elsayed Z, Reiner Alexander P, Sotoodehnia Nona, |
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Merits and pitfalls of genetic testing in a hypertrophic cardiomyopathy clinic.
The Israel Medical Association journal : IMAJ 2014 Nov 16 (11): 707-13. Arad Michael, Monserrat Lorenzo, Haron-Khun Shiraz, Seidman Jonathan G, Seidman Christine E, Arbustini Eloisa, Glikson Michael, Freimark D |
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
Nature genetics 2014 Aug 46 (8): 826-36. Arking Dan E, Pulit Sara L, Crotti Lia, van der Harst Pim, Munroe Patricia B, Koopmann Tamara T, Sotoodehnia Nona, Rossin Elizabeth J, Morley Michael, Wang Xinchen, Johnson Andrew D, Lundby Alicia, Gudbjartsson Daníel F, Noseworthy Peter A, Eijgelsheim Mark, Bradford Yuki, Tarasov Kirill V, Dörr Marcus, Müller-Nurasyid Martina, Lahtinen Annukka M, Nolte Ilja M, Smith Albert Vernon, Bis Joshua C, Isaacs Aaron, Newhouse Stephen J, Evans Daniel S, Post Wendy S, Waggott Daryl, Lyytikäinen Leo-Pekka, Hicks Andrew A, Eisele Lewin, Ellinghaus David, Hayward Caroline, Navarro Pau, Ulivi Sheila, Tanaka Toshiko, Tester David J, Chatel Stéphanie, Gustafsson Stefan, Kumari Meena, Morris Richard W, Naluai Åsa T, Padmanabhan Sandosh, Kluttig Alexander, Strohmer Bernhard, Panayiotou Andrie G, Torres Maria, Knoflach Michael, Hubacek Jaroslav A, Slowikowski Kamil, Raychaudhuri Soumya, Kumar Runjun D, Harris Tamara B, Launer Lenore J, Shuldiner Alan R, Alonso Alvaro, Bader Joel S, Ehret Georg, Huang Hailiang, Kao W H Linda, Strait James B, Macfarlane Peter W, Brown Morris, Caulfield Mark J, Samani Nilesh J, Kronenberg Florian, Willeit Johann, , , Smith J Gustav, Greiser Karin H, Meyer Zu Schwabedissen Henriette, Werdan Karl, Carella Massimo, Zelante Leopoldo, Heckbert Susan R, Psaty Bruce M, Rotter Jerome I, Kolcic Ivana, Polašek Ozren, Wright Alan F, Griffin Maura, Daly Mark J, , Arnar David O, Hólm Hilma, Thorsteinsdottir Unnur, , Denny Joshua C, Roden Dan M, Zuvich Rebecca L, Emilsson Valur, Plump Andrew S, Larson Martin G, O'Donnell Christopher J, Yin Xiaoyan, Bobbo Marco, D'Adamo Adamo P, Iorio Annamaria, Sinagra Gianfranco, Carracedo Angel, Cummings Steven R, Nalls Michael A, Jula Antti, Kontula Kimmo K, Marjamaa Annukka, Oikarinen Lasse, Perola Markus, Porthan Kimmo, Erbel Raimund, Hoffmann Per, Jöckel Karl-Heinz, Kälsch Hagen, Nöthen Markus M, , den Hoed Marcel, Loos Ruth J F, Thelle Dag S, Gieger Christian, Meitinger Thomas, Perz Siegfried, Peters Annette, Prucha Hanna, Sinner Moritz F, Waldenberger Melanie, de Boer Rudolf A, Franke Lude, van der Vleuten Pieter A, Beckmann Britt Maria, Martens Eimo, Bardai Abdennasser, Hofman Nynke, Wilde Arthur A M, Behr Elijah R, Dalageorgou Chrysoula, Giudicessi John R, Medeiros-Domingo Argelia, Barc Julien, Kyndt Florence, Probst Vincent, Ghidoni Alice, Insolia Roberto, Hamilton Robert M, Scherer Stephen W, Brandimarto Jeffrey, Margulies Kenneth, Moravec Christine E, del Greco M Fabiola, Fuchsberger Christian, O'Connell Jeffrey R, Lee Wai K, Watt Graham C M, Campbell Harry, Wild Sarah H, El Mokhtari Nour E, Frey Norbert, Asselbergs Folkert W, Mateo Leach Irene, Navis Gerjan, van den Berg Maarten P, van Veldhuisen Dirk J, Kellis Manolis, Krijthe Bouwe P, Franco Oscar H, Hofman Albert, Kors Jan A, Uitterlinden André G, Witteman Jacqueline C M, Kedenko Lyudmyla, Lamina Claudia, Oostra Ben A, Abecasis Gonçalo R, Lakatta Edward G, Mulas Antonella, Orrú Marco, Schlessinger David, Uda Manuela, Markus Marcello R P, Völker Uwe, Snieder Harold, Spector Timothy D, Ärnlöv Johan, Lind Lars, Sundström Johan, Syvänen Ann-Christine, Kivimaki Mika, Kähönen Mika, Mononen Nina, Raitakari Olli T, Viikari Jorma S, Adamkova Vera, Kiechl Stefan, Brion Maria, Nicolaides Andrew N, Paulweber Bernhard, Haerting Johannes, Dominiczak Anna F, Nyberg Fredrik, Whincup Peter H, Hingorani Aroon D, Schott Jean-Jacques, Bezzina Connie R, Ingelsson Erik, Ferrucci Luigi, Gasparini Paolo, Wilson James F, Rudan Igor, Franke Andre, Mühleisen Thomas W, Pramstaller Peter P, Lehtimäki Terho J, Paterson Andrew D, Parsa Afshin, Liu Yongmei, van Duijn Cornelia M, Siscovick David S, Gudnason Vilmundur, Jamshidi Yalda, Salomaa Veikko, Felix Stephan B, Sanna Serena, Ritchie Marylyn D, Stricker Bruno H, Stefansson Kari, Boyer Laurie A, Cappola Thomas P, Olsen Jesper V, Lage Kasper, Schwartz Peter J, Kääb Stefan, Chakravarti Aravinda, Ackerman Michael J, Pfeufer Arne, de Bakker Paul I W, Newton-Cheh Christoph |
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Genotype-positive status in patients with hypertrophic cardiomyopathy is associated with higher rates of heart failure events.
Circulation. Cardiovascular genetics 2014 Aug 7 (4): 416-22. Li Qin, Gruner Christiane, Chan Raymond H, Care Melanie, Siminovitch Katherine, Williams Lynne, Woo Anna, Rakowski Har |
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Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome.
Journal of the American College of Cardiology 2014 Jul 64 (1): 66-79. Hu Dan, Barajas-Martínez Hector, Pfeiffer Ryan, Dezi Fabio, Pfeiffer Jenna, Buch Tapan, Betzenhauser Matthew J, Belardinelli Luiz, Kahlig Kristopher M, Rajamani Sridharan, DeAntonio Harry J, Myerburg Robert J, Ito Hiroyuki, Deshmukh Pramod, Marieb Mark, Nam Gi-Byoung, Bhatia Atul, Hasdemir Can, Haïssaguerre Michel, Veltmann Christian, Schimpf Rainer, Borggrefe Martin, Viskin Sami, Antzelevitch Charl |
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Association of CASQ2 polymorphisms with sudden cardiac arrest and heart failure in patients with coronary artery disease.
Heart rhythm : the official journal of the Heart Rhythm Society 2014 Apr 11 (4): 646-52. Refaat Marwan M, Aouizerat Bradley E, Pullinger Clive R, Malloy Mary, Kane John, Tseng Zian |
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Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrest.
Heart rhythm : the official journal of the Heart Rhythm Society 2014 Mar 11 (3): 471-7. Lemaitre Rozenn N, Johnson Catherine O, Hesselson Stephanie, Sotoodehnia Nona, Sotoodhenia Nona, McKnight Barbara, Sitlani Colleen M, Rea Thomas D, King Irena B, Kwok Pui-Yan, Mak Angel, Li Guo, Brody Jennifer, Larson Eric, Mozaffarian Dariush, Psaty Bruce M, Huertas-Vazquez Adriana, Tardif Jean-Claude, Albert Christine M, Lyytikäinen Leo-Pekka, Arking Dan E, Kääb Stefan, Huikuri Heikki V, Krijthe Bouwe P, Eijgelsheim Mark, Wang Ying A, Reinier Kyndaron, Lehtimäki Terho, Pulit Sara L, Brugada Ramon, Müller-Nurasyid Martina, Newton-Cheh Chris H, Karhunen Pekka J, Stricker Bruno H, Goyette Philippe, Rotter Jerome I, Chugh Sumeet S, Chakravarti Aravinda, Jouven Xavier, Siscovick David |
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Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.
European heart journal 2014 Feb 35 (8): 524-31. Seppälä Ilkka, Kleber Marcus E, Lyytikäinen Leo-Pekka, Hernesniemi Jussi A, Mäkelä Kari-Matti, Oksala Niku, Laaksonen Reijo, Pilz Stefan, Tomaschitz Andreas, Silbernagel Günther, Boehm Bernhard O, Grammer Tanja B, Koskinen Tuomas, Juonala Markus, Hutri-Kähönen Nina, Alfthan Georg, Viikari Jorma S A, Kähonen Mika, Raitakari Olli T, März Winfried, Meinitzer Andreas, Lehtimäki Terho, |
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Gene-environment interaction between SCN5A-1103Y and hypokalemia influences QT interval prolongation in African Americans: the Jackson Heart Study.
American heart journal 2014 Jan 167 (1): 116-122.e1. Akylbekova Ermeg L, Payne John P, Newton-Cheh Christopher, May Warren L, Fox Ervin R, Wilson James G, Sarpong Daniel F, Taylor Herman A, Maher Joseph |
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Single nucleotide polymorphisms in arrhythmia genes modify the risk of cardiac events and sudden death in long QT syndrome.
Heart rhythm : the official journal of the Heart Rhythm Society 2014 Jan 11 (1): 76-82. Earle Nikki, Yeo Han Dug, Pilbrow Anna, Crawford Jackie, Smith Warren, Shelling Andrew N, Cameron Vicky, Love Donald R, Skinner Jonathan |
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The KCNJ8-S422L variant previously associated with J-wave syndromes is found at an increased frequency in Ashkenazi Jews.
European journal of human genetics : EJHG 2014 Jan 22 (1): 94-8. Veeramah Krishna R, Karafet Tatiana M, Wolf Daniel, Samson Ricardo A, Hammer Michael |
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Associations of GSTM1*0 and GSTA1*A genotypes with the risk of cardiovascular death among hemodialyses patients.
BMC nephrology 2014 15 12. Suvakov Sonja, Damjanovic Tatjana, Pekmezovic Tatjana, Jakovljevic Jovana, Savic-Radojevic Ana, Pljesa-Ercegovac Marija, Radovanovic Slavica, Simic Dragan V, Pljesa Steva, Zarkovic Milos, Mimic-Oka Jasmina, Dimkovic Nada, Simic Tatja |
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