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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 2, 2023. (Total: 223599Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Arrhythmia and ANK2[original query]
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
Phenotypic Variability of ANK2 Mutations in Patients With Inherited Primary Arrhythmia Syndromes.
Circulation journal : official journal of the Japanese Circulation Society 2016 Oct .
Ichikawa Mari, Aiba Takeshi, Ohno Seiko, Shigemizu Daichi, Ozawa Junichi, Sonoda Keiko, Fukuyama Megumi, Itoh Hideki, Miyamoto Yoshihiro, Tsunoda Tatsuhiko, Makiyama Takeru, Tanaka Toshihiro, Shimizu Wataru, Horie Mino
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
Genotype and clinical characteristics of congenital long QT syndrome in Thailand.
Indian pacing and electrophysiology journal 2018 7 18 (5): 165-171.
Saprungruang Ankavipar, Khongphatthanayothin Apichai, Mauleekoonphairoj John, Wandee Pharawee, Kanjanauthai Supaluck, Bhuiyan Zahurul A, Wilde Arthur A M, Poovorawan Yo
Putative role of Brugada syndrome genes in familial atrial fibrillation.
European review for medical and pharmacological sciences 2019 9 23 (17): 7582-7598.
Maltese P E, Aldanova E, Kriuchkova N, Averianov A, Manara E, Paolacci S, Bruson A, Miotto R, Sartori M, Guerri G, Zuntini M, Marceddu G, Tezzele S, Tadtaeva K, Chernova A, Aksyutina N, Nikulina S, Nodari S, Bertelli
Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation.
American journal of medical genetics. Part A 2020 4 182 (6): 1387-1399.
Coban-Akdemir Zeynep H, Charng Wu-Lin, Azamian Mahshid, Paine Ingrid S, Punetha Jaya, Grochowski Christopher M, Gambin Tomasz, Valdes Santiago O, Cannon Bryan, Zapata Gladys, Hernandez Patricia P, Jhangiani Shalini, Doddapaneni Harsha, Hu Jianhong, Boricha Fatima, Muzny Donna M, Boerwinkle Eric, Yang Yaping, Gibbs Richard A, Posey Jennifer E, Wehrens Xander H T, Belmont John W, Kim Jeffrey J, Miyake Christina Y, Lupski James R, Lalani Seema
Overlap Arrhythmia Syndromes Resulting from Multiple Genetic Variations Studied in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
International journal of molecular sciences 2021 7 22 (13): .
Treat Jacqueline A, Pfeiffer Ryan, Barajas-Martinez Hector, Goodrow Robert J, Bot Corina, Haedo Rodolfo J, Knox Ronald, Cordeiro Jonathan
Clinical Heterogeneity in Patients with Long QT Syndrome and Segregation of Single Nucleotide Variants and Clinical Symptoms in 17 Affected Families.
Molecular syndromology 2023 10 14 (5): 363-374.
Elcin Bora, Ayca Y?ld?z Bulut, Tufan Cankaya, Tayfun Cinleti, Halise Zeynep Genç, Emin Evren Ozcan, Ebru Ozpelit, Ayfer Ulgenalp, Ahmet Okay Caglay
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