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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 - 6 (of 6 Records)

Query Trace: Disease and ETS2[original query]
TERT promoter mutations in bladder cancer affect patient survival and disease recurrence through modification by a common polymorphism.
Proceedings of the National Academy of Sciences of the United States of America 2013 Oct 110 (43): 17426-31.
Rachakonda P Sivaramakrishna, Hosen Ismail, de Verdier Petra J, Fallah Mahdi, Heidenreich Barbara, Ryk Charlotta, Wiklund N Peter, Steineck Gunnar, Schadendorf Dirk, Hemminki Kari, Kumar Raj
Prognostic quality of activating TERT promoter mutations in glioblastoma: interaction with the rs2853669 polymorphism and patient age at diagnosis.
Neuro-oncology 2015 Sep 17 (9): 1231-40.
Spiegl-Kreinecker Sabine, Lötsch Daniela, Ghanim Bahil, Pirker Christine, Mohr Thomas, Laaber Magdalena, Weis Serge, Olschowski Alfred, Webersinke Gerald, Pichler Josef, Berger Walt
Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study. GWAS Catalog
American journal of human genetics 2020 12 108 (1): 84-99.
Ortiz-Fernández Lourdes, Saruhan-Direskeneli Güher, Alibaz-Oner Fatma, Kaymaz-Tahra Sema, Coit Patrick, Kong Xiufang, Kiprianos Allan P, Maughan Robert T, Aydin Sibel Z, Aksu Kenan, Keser Gokhan, Kamali Sevil, Inanc Murat, Springer Jason, Akar Servet, Onen Fatos, Akkoc Nurullah, Khalidi Nader A, Koening Curry, Karadag Omer, Kiraz Sedat, Forbess Lindsy, Langford Carol A, McAlear Carol A, Ozbalkan Zeynep, Yavuz Sule, Çetin Gozde Yildirim, Alpay-Kanitez Nilufer, Chung Sharon, Ates Askin, Karaaslan Yasar, McKinnon-Maksimowicz Kathleen, Monach Paul A, Ozer Hüseyin T E, Seyahi Emire, Fresko Izzet, Cefle Ayse, Seo Philip, Warrington Kenneth J, Ozturk Mehmet A, Ytterberg Steven R, Cobankara Veli, Onat Ahmet Mesut, Duzgun Nur?en, B?cakc?gil Muge, Yentür Sibel P, Lally Lindsay, Manfredi Angelo A, Baldissera Elena, Erken Eren, Yazici Ayten, K?sac?k Bünyamin, Ka?ifo?lu Timuçin, Dalkilic Ediz, Cuthbertson David, Pagnoux Christian, Sreih Antoine, Reales Guillermo, Wallace Chris, Wren Jonathan D, Cunninghame-Graham Deborah S, Vyse Timothy J, Sun Ying, Chen Huiyong, Grayson Peter C, Tombetti Enrico, Jiang Lindi, Mason Justin C, Merkel Peter A, Direskeneli Haner, Sawalha Amr
Multi-omics integration identifies key upstream regulators of pathomechanisms in hypertrophic cardiomyopathy due to truncating MYBPC3 mutations.
Clinical epigenetics 2021 3 13 (1): 61.
Pei J, Schuldt M, Nagyova E, Gu Z, El Bouhaddani S, Yiangou L, Jansen M, Calis J J A, Dorsch L M, Blok C Snijders, van den Dungen N A M, Lansu N, Boukens B J, Efimov I R, Michels M, Verhaar M C, de Weger R, Vink A, van Steenbeek F G, Baas A F, Davis R P, Uh H W, Kuster D W D, Cheng C, Mokry M, van der Velden J, Asselbergs F W, Harakalova
Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology.
EBioMedicine 2022 10 85 104290.
Clark Lorraine N, Gao Yizhe, Wang Gao T, Hernandez Nora, Ashley-Koch Allison, Jankovic Joseph, Ottman Ruth, Leal Suzanne M, Rodriguez Sandra M Barral, Louis Elan
Fine-mapping and molecular characterisation of primary sclerosing cholangitis genetic risk loci.
Nature communications 2024 11 15 (1): 9594.
Elizabeth C Goode, Laura Fachal, Nikolaos Panousis, Loukas Moutsianas, Rebecca E McIntyre, Benjamin Yu Hang Bai, Norihito Kawasaki, Alexandra Wittmann, Tim Raine, Simon M Rushbrook, Carl A Anders
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