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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Death and ANK2[original query]
Common genetic variants in ANK2 modulate QT interval: results from the KORA study.
Circulation. Cardiovascular genetics 2008 Dec 1 (2): 93-9.
Sedlacek Kamil, Stark Klaus, Cunha Shane R, Pfeufer Arne, Weber Stefan, Berger Iris, Perz Siegfried, Kääb Stefan, Wichmann Hans-Erich, Mohler Peter J, Hengstenberg Christian, Jeron Andre
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
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
Epilepsy-related sudden unexpected death: targeted molecular analysis of inherited heart disease genes using next-generation DNA sequencing.
Brain pathology (Zurich, Switzerland) 2016 May .
Hata Yukiko, Yoshida Koji, Kinoshita Koshi, Nishida Nao
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
Genetic heterogeneity and prognostic impact of recurrent ANK2 and TP53 mutations in mantle cell lymphoma: a multi-centre cohort study.
Scientific reports 2020 Aug 10 (1): 13359.
Jeong Seri, Park Yu Jin, Yun Woobin, Lee Seung-Tae, Choi Jong Rak, Suh Cheolwon, Jo Jae-Cheol, Cha Hee Jeong, Jeong Jee-Yeong, Chang HeeKyung, Cha Yoon Jin, Kim Hyerim, Park Min-Jeong, Song Wonkeun, Cho Eun-Hae, Jeong Eun-Goo, Lee Junnam, Park Yongmin, Lee Yong Seok, Kim Da Jung, Lee Ho S
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
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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