Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: KLF12[original query] |
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Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility.
Arthritis and rheumatism 2008 Aug 58 (8): 2275-86. Julià Antonio, Ballina Javier, Cañete Juan D, Balsa Alejandro, Tornero-Molina Jesus, Naranjo Antonio, Alperi-López Mercedes, Erra Alba, Pascual-Salcedo Dora, Barceló Pere, Camps Jordi, Marsal Sa |
No evidence for association of the KLF12 gene with rheumatoid arthritis in a large UK cohort. Annals of the rheumatic diseases 2010 Jul 69 (7): 1407-8. Eyre Stephen, Flynn Edward, Martin Paul, Hinks Anne, Wilson Anthony G, Morgan Ann W, Emery Paul, Steer Sophia, Hocking Lynne J, Reid David M, Harrison Pille, Wordsworth Paul, Thomson Wendy, Worthington Jane, Barton An |
A functionally relevant IRF5 haplotype is associated with reduced risk to Wegener's granulomatosis. Journal of molecular medicine (Berlin, Germany) 2010 Jan . Wieczorek Stefan, Holle Julia U, Müller Stephanie, Fricke Harald, Gross Wolfgang L, Epplen Jörg |
No evidence of association of the KLF12 gene with rheumatoid arthritis in Spanish and Dutch cohorts and a meta-analysis of published data. Human immunology 2011 Sep 72 (9): 779-82. García-Bermúdez Mercedes, López-Mejias Raquel, Rodriguez-Rodriguez Luis, Fernández-Gutierrez Benjamín, García Antonio, Raya Enrique, Ortiz Ana M, Coenen Marieke J H, van Riel Piet L C M, Radstake Timothy R D J, González-Gay Miguel A, Martín Javi |
Association of protein tyrosine phosphatase non-receptor 22 (PTPN22) rs2476601 and Kruppel-like factor 12 (KLF12) rs1324913 single nucleotide polymorphisms with rheumatoid arthritis in a Latvian population. Scandinavian journal of rheumatology 2011 Nov 40 (6): 491-2. Mihailova A, Mikazane H, Klovins J, Nikitina-Zake |
Genome-wide analysis of esophageal adenocarcinoma yields specific copy number aberrations that correlate with prognosis. Genes, chromosomes & cancer 2014 Apr 53 (4): 324-38. Frankel Adam, Armour Nicola, Nancarrow Derek, Krause Lutz, Hayward Nicholas, Lampe Guy, Smithers B Mark, Barbour Andr |
Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.
Nature communications 2016 7 10605. Zhang Yong-Biao, Hu Jintian, Zhang Jiao, Zhou Xu, Li Xin, Gu Chaohao, Liu Tun, Xie Yangchun, Liu Jiqiang, Gu Mingliang, Wang Panpan, Wu Tingting, Qian Jin, Wang Yue, Dong Xiaoqun, Yu Jun, Zhang Qingg |
Sustained viral response and treatment-induced cytopenia correlate with SLCs and KLF12 genotypes in interferon/ribavirin-treated Chinese chronic hepatitis C patients. Journal of gastroenterology and hepatology 2016 Jan . Mei Ruqi, Chi Xiumei, Wu Ruihong, Xu Hongqin, Wang Xiaomei, Gao Xiuzhu, Sun Haibo, Lv Juan, Yu Ge, Kong Fei, Jiang Jing, Sun Bing, Zhong Jin, Pan Yu, Niu Jun |
Functional characterization of a chr13q22.1 pancreatic cancer risk locus reveals long-range interaction and allele-specific effects on DIS3 expression. Human molecular genetics 2017 (21): 4726-4738. Hoskins Jason W, Ibrahim Abdisamad, Emmanuel Mickey A, Manmiller Sarah M, Wu Yinglun, O'Neill Maura, Jia Jinping, Collins Irene, Zhang Mingfeng, Thomas Janelle V, Rost Lauren M, Das Sudipto, Parikh Hemang, Haake Jefferson M, Matters Gail L, Kurtz Robert C, Bamlet William R, Klein Alison, Stolzenberg-Solomon Rachael, Wolpin Brian M, Yarden Ronit, Wang Zhaoming, Smith Jill, Olson Sara H, Andresson Thorkell, Petersen Gloria M, Amundadottir Laufey |
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
Circulation 2020 Jul 142 (4): 324-338. Lahrouchi Najim, Tadros Rafik, Crotti Lia, Mizusawa Yuka, Postema Pieter G, Beekman Leander, Walsh Roddy, Hasegawa Kanae, Barc Julien, Ernsting Marko, Turkowski Kari L, Mazzanti Andrea, Beckmann Britt M, Shimamoto Keiko, Diamant Ulla-Britt, Wijeyeratne Yanushi D, Kucho Yu, Robyns Tomas, Ishikawa Taisuke, Arbelo Elena, Christiansen Michael, Winbo Annika, Jabbari Reza, Lubitz Steven A, Steinfurt Johannes, Rudic Boris, Loeys Bart, Shoemaker M Ben, Weeke Peter E, Pfeiffer Ryan, Davies Brianna, Andorin Antoine, Hofman Nynke, Dagradi Federica, Pedrazzini Matteo, Tester David J, Bos J Martijn, Sarquella-Brugada Georgia, Campuzano Óscar, Platonov Pyotr G, Stallmeyer Birgit, Zumhagen Sven, Nannenberg Eline A, Veldink Jan H, van den Berg Leonard H, Al-Chalabi Ammar, Shaw Christopher E, Shaw Pamela J, Morrison Karen E, Andersen Peter M, Müller-Nurasyid Martina, Cusi Daniele, Barlassina Cristina, Galan Pilar, Lathrop Mark, Munter Markus, Werge Thomas, Ribasés Marta, Aung Tin, Khor Chiea C, Ozaki Mineo, Lichtner Peter, Meitinger Thomas, van Tintelen J Peter, Hoedemaekers Yvonne, Denjoy Isabelle, Leenhardt Antoine, Napolitano Carlo, Shimizu Wataru, Schott Jean-Jacques, Gourraud Jean-Baptiste, Makiyama Takeru, Ohno Seiko, Itoh Hideki, Krahn Andrew D, Antzelevitch Charles, Roden Dan M, Saenen Johan, Borggrefe Martin, Odening Katja E, Ellinor Patrick T, Tfelt-Hansen Jacob, Skinner Jonathan R, van den Berg Maarten P, Olesen Morten Salling, Brugada Josep, Brugada Ramón, Makita Naomasa, Breckpot Jeroen, Yoshinaga Masao, Behr Elijah R, Rydberg Annika, Aiba Takeshi, Kääb Stefan, Priori Silvia G, Guicheney Pascale, Tan Hanno L, Newton-Cheh Christopher, Ackerman Michael J, Schwartz Peter J, Schulze-Bahr Eric, Probst Vincent, Horie Minoru, Wilde Arthur A, Tanck Michael W T, Bezzina Connie |
Genome-wide association study of prevalent and persistent cervical high-risk human papillomavirus (HPV) infection.
BMC medical genetics 2020 11 21 (1): 231. Adebamowo Sally N, Adeyemo Adebowale A, Rotimi Charles N, Olaniyan Olayinka, Offiong Richard, Adebamowo Clement A, |
Bronchopulmonary dysplasia and wnt pathway-associated single nucleotide polymorphisms. Pediatric research 2021 Dec . Akat Ayberk, Yilmaz Semerci Seda, Ugurel Osman Mutluhan, Erdemir Aysegul, Danhaive Olivier, Cetinkaya Merih, Turgut-Balik Dil |
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