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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 5, 2024. (Total: 234082Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Syndrome and CACNB2[original query]
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
High prevalence of genetic variants previously associated with Brugada syndrome in new exome data.
Clinical genetics 2013 Nov 84 (5): 489-95.
Risgaard B, Jabbari R, Refsgaard L, Holst A G, Haunsø S, Sadjadieh A, Winkel B G, Olesen M S, Tfelt-Hansen
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
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
An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation.
Scientific reports 2018 10 8 (1): 14619.
Blancard Malorie, Debbiche Amal, Kato Koichi, Cardin Christelle, Sabrina Guichard, Gandjbakhch Estelle, Probst Vincent, Haissaguerre Michel, Extramiana Fabrice, Hocini Mélèze, Olivier Geoffroy, Leenhardt Antoine, Guicheney Pascale, Rougier Jean-Sébasti
Genetic variants associated with psychotic symptoms across psychiatric disorders.
Neuroscience letters 2020 Jan 134754.
Calabrò Marco, Porcelli Stefano, Crisafulli Concetta, Albani Diego, Kasper Siegfried, Zohar Joseph, Souery Daniel, Montgomery Stuart, Mantovani Vilma, Mendlewicz Julien, Bonassi Stefano, Vieta Eduard, Frustaci Alessandra, Ducci Giuseppe, Landi Stefano, Boccia Stefania, Bellomo Antonello, Di Nicola Marco, Janiri Luigi, Colombo Roberto, Benedetti Francesco, Mandelli Laura, Fabbri Chiara, Serretti Alessand
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