Human Genome Epidemiology Literature Finder
Records 1 - 26 (of 26 Records) |
Query Trace: ANK2[original query] |
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Association of torsades de pointes with novel and known single nucleotide polymorphisms in long QT syndrome genes. American heart journal 2006 Dec 152 (6): 1116-22. Mank-Seymour Amy R, Richmond Jodi L, Wood Linda S, Reynolds Jennifer M, Fan Yu-Ti, Warnes Gregory R, Milos Patrice M, Thompson John |
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 |
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 |
Bipolar disorder with comorbid binge eating history: a genome-wide association study implicates APOB.
Journal of affective disorders 2014 Aug 165 151-8. Winham Stacey J, Cuellar-Barboza Alfredo B, McElroy Susan L, Oliveros Alfredo, Crow Scott, Colby Colin L, Choi Doo-Sup, Chauhan Mohit, Frye Mark A, Biernacka Joanna |
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 |
Expression and replication studies to identify new candidate genes involved in normal hearing function. PloS one 2014 9 (1): e85352. Girotto Giorgia, Vuckovic Dragana, Buniello Annalisa, Lorente-Cánovas Beatriz, Lewis Morag, Gasparini Paolo, Steel Karen |
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 |
Integrated Genetic, Epigenetic, and Transcriptional Profiling Identifies Molecular Pathways in the Development of Laterally Spreading Tumors. Molecular cancer research : MCR 2016 Sep . Hesson Luke B, Ng Benedict, Zarzour Peter, Srivastava Sameer, Kwok Chau-To, Packham Deborah, Nunez Andrea C, Beck Dominik, Ryan Regina, Dower Ashraf, Ford Caroline E, Pimanda John, Sloane Mathew A, Hawkins Nicholas J, Bourke Michael J, Wong Jason W H, Ward Robyn |
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 |
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 |
Novel polymorphisms associated with hyperalphalipoproteinemia and apparent cardioprotection. Journal of clinical lipidology 2017 Nov . Oates Connor P, Koenig Darya, Rhyne Jeffrey, Bogush Nikolay, O'Connell Jeffrey, Mitchell Braxton D, Miller Micha |
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 |
ITPKB and ZNF184 are associated with Parkinson's disease risk in East Asians. Neurobiology of aging 2019 Feb . Chew Elaine Guo Yan, Tan Louis C S, Au Wing-Lok, Prakash Kumar-M, Liu Jianjun, Foo Jia Nee, Tan Eng-Ki |
Host Genetic and Gut Microbial Signatures in Familial Inflammatory Bowel Disease. Clinical and translational gastroenterology 2020 8 11 (7): e00213. Park Yoo Min, Ha Eunji, Gu Ki-Nam, Shin Ga Young, Lee Chang Kyun, Kim Kwangwoo, Kim Hyo Jo |
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 |
The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci. Frontiers in neurology 2020 1 10 1284. Germer Elisabeth Luisa, Imhoff Sophie, Vilariño-Güell Carles, Kasten Meike, Seibler Philip, Brüggemann Norbert, , Klein Christine, Trinh Joan |
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 |
Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study. EBioMedicine 2021 Apr 66 103309. Amanat Sana, Gallego-Martinez Alvaro, Sollini Joseph, Perez-Carpena Patricia, Espinosa-Sanchez Juan M, Aran Ismael, Soto-Varela Andres, Batuecas-Caletrio Angel, Canlon Barbara, May Patrick, Cederroth Christopher R, Lopez-Escamez Jose |
Evaluation of IL1B rs1143634 and IL6 rs1800796 Polymorphisms with Autism Spectrum Disorder in the Turkish Children. Immunological investigations 2021 1 51 (4): 766-777. Pekkoc Uyanik Kubra Cigdem, Kalayci Yigin Aysel, Dogangun Burak, Seven Mehm |
ANK2 as a novel predictive biomarker for immune checkpoint inhibitors and its correlation with antitumor immunity in lung adenocarcinoma. BMC pulmonary medicine 2022 12 22 (1): 483. Zhang Wengang, Shang Xiaoling, Liu Ni, Ma Xinchun, Yang Rui, Xia Handai, Zhang Yuqing, Zheng Qi, Wang Xiuwen, Liu Yang |
The Genetic Basis of Probable REM Sleep Behavior Disorder in Parkinson's Disease. Brain sciences 2023 8 13 (8): . Santiago Perez-Lloret, Guenson Chevalier, Sofia Bordet, Hanny Barbar, Francisco Capani, Lucas Udovin, Matilde Otero-Losa |
Clinical Exome Gene Panel Analysis of a Cohort of Urothelial Bladder Cancer Patients from Sri Lanka. Asian Pacific journal of cancer prevention : APJCP 2023 5 24 (5): 1533-1542. Ajith Malalasekera, Nilaksha Neththikumara, Praveenan Somasundaram, Sajeewani Pathirana, Chathumadavi Ediriweera, Dileepa Ediriweera, Serozsha As Goonewardena, Neville D Perera, Anuruddha Abeygunasekara, Rohan W Jayasekara, Kalum Wettasinghe, M Dilani S Lokuhetty, Vajira H W Dissanaye |
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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- Page last updated:Mar 25, 2024
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