Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 15, 2024. (Total: 231458Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 5 (of 5 Records)

Query Trace: Arrhythmia and AKAP9[original query]
Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.
Journal of the American College of Cardiology 2010 12 57 (1): 40-7.
Barc Julien, Briec François, Schmitt Sébastien, Kyndt Florence, Le Cunff Martine, Baron Estelle, Vieyres Claude, Sacher Frédéric, Redon Richard, Le Caignec Cédric, Le Marec Hervé, Probst Vincent, Schott Jean-Jacqu
AKAP9 is a genetic modifier of congenital long-QT syndrome type 1.
Circulation. Cardiovascular genetics 2014 Oct 7 (5): 599-606.
de Villiers Carin P, van der Merwe Lize, Crotti Lia, Goosen Althea, George Alfred L, Schwartz Peter J, Brink Paul A, Moolman-Smook Johanna C, Corfield Valerie
Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndrome.
Journal of the American College of Cardiology 2014 Apr 63 (14): 1430-7.
Weeke Peter, Mosley Jonathan D, Hanna David, Delaney Jessica T, Shaffer Christian, Wells Quinn S, Van Driest Sara, Karnes Jason H, Ingram Christie, Guo Yan, Shyr Yu, Norris Kris, Kannankeril Prince J, Ramirez Andrea H, Smith Joshua D, Mardis Elaine R, Nickerson Deborah, George Alfred L, Roden Dan
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
Targeted next-generation sequencing detects novel gene-phenotype associations and expands the mutational spectrum in cardiomyopathies.
PloS one 2017 7 12 (7): e0181842.
Forleo Cinzia, D'Erchia Anna Maria, Sorrentino Sandro, Manzari Caterina, Chiara Matteo, Iacoviello Massimo, Guaricci Andrea Igoren, De Santis Delia, Musci Rita Leonarda, La Spada Antonino, Marangelli Vito, Pesole Graziano, Favale Stefa
TOP