HuGE Literature Finder
Records 1-13
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Association between CACNA1C gene polymorphisms and ritodrine-induced adverse events in preterm labor patients.
European journal of clinical pharmacology 2017 Apr . Baek Min Young, Hwang Han Sung, Park Jin Young, Chung Jee Eun, Lee Kyung Eun, Lee Gwan Yung, Seong Jin Won, Yee Jeong, Kim Young Ju, Gwak Hye S |
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Electrocardiogram Alterations Associated With Psychotropic Drug Use and CACNA1C Gene Variants in Three Independent Samples.
Basic & clinical pharmacology & toxicology 2016 Nov . Fabbri Chiara, Boriani Giuseppe, Diemberger Igor, Filippi Maria Giulia, Ravegnini Gloria, Hrelia Patrizia, Minarini Alessandro, Albani Diego, Forloni Gianluigi, Angelini Sabrina, Serretti Alessand |
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Genomic contributors to atrial electroanatomical remodeling and atrial fibrillation progression: Pathway enrichment analysis of GWAS data.
Scientific reports 2016 Nov 6 36630. Husser Daniela, Ueberham Laura, Dinov Borislav, Kosiuk Jedrzej, Kornej Jelena, Hindricks Gerhard, Shoemaker M Benjamin, Roden Dan M, Bollmann Andreas, Büttner Pet |
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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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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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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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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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Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation and variant phenotypes.
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 2014 Dec 16 (12): 1828-37. Fukuyama Megumi, Wang Qi, Kato Koichi, Ohno Seiko, Ding Wei-Guang, Toyoda Futoshi, Itoh Hideki, Kimura Hiromi, Makiyama Takeru, Ito Makoto, Matsuura Hiroshi, Horie Mino |
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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 |
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Exome sequencing and systems biology converge to identify novel mutations in the L-type calcium channel, CACNA1C, linked to autosomal dominant long QT syndrome.
Circulation. Cardiovascular genetics 2013 Jun 6 (3): 279-89. Boczek Nicole J, Best Jabe M, Tester David J, Giudicessi John R, Middha Sumit, Evans Jared M, Kamp Timothy J, Ackerman Michael |
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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 |
GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.
BMC cardiovascular disorders 2011 11 (1): 29. Aouizerat Bradley E, Vittinghoff Eric, Musone Stacy L, Pawlikowska Ludmila, Kwok Pui-Yan, Olgin Jeffrey E, Tseng Zian |
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Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.
Heart rhythm : the official journal of the Heart Rhythm Society 2010 Dec 7 (12): 1872-82. Burashnikov Elena, Pfeiffer Ryan, Barajas-Martinez Héctor, Delpón Eva, Hu Dan, Desai Mayurika, Borggrefe Martin, Häissaguerre Michel, Kanter Ronald, Pollevick Guido D, Guerchicoff Alejandra, Laiño Ruben, Marieb Mark, Nademanee Koonlawee, Nam Gi-Byoung, Robles Roberto, Schimpf Rainer, Stapleton Dwight D, Viskin Sami, Winters Stephen, Wolpert Christian, Zimmern Samuel, Veltmann Christian, Antzelevitch Charl |
- Page last reviewed:Mar 16, 2019
- Page last updated:May 30, 2020
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