Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Disease and WDFY4[original query] |
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Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus.
PLoS genetics 2010 Feb 6 (2): e1000841. Yang Wanling, Shen Nan, Ye Dong-Qing, Liu Qiji, Zhang Yan, Qian Xiao-Xia, Hirankarn Nattiya, Ying Dingge, Pan Hai-Feng, Mok Chi Chiu, Chan Tak Mao, Wong Raymond Woon Sing, Lee Ka Wing, Mok Mo Yin, Wong Sik Nin, Leung Alexander Moon Ho, Li Xiang-Pei, Avihingsanon Yingyos, Wong Chun-Ming, Lee Tsz Leung, Ho Marco Hok Kung, Lee Pamela Pui Wah, Chang Yuk Kwan, Li Philip H, Li Ruo-Jie, Zhang Lu, Wong Wilfred Hing Sang, Ng Irene Oi Lin, Lau Chak Sing, Sham Pak Chung, Lau Yu Lung, |
| Genes identified in Asian SLE GWASs are also associated with SLE in Caucasian populations. European journal of human genetics : EJHG 2012 Dec . Wang C, Ahlford A, Järvinen TM, Nordmark G, Eloranta ML, Gunnarsson I, Svenungsson E, Padyukov L, Sturfelt G, Jönsen A, Bengtsson AA, Truedsson L, Eriksson C, Rantapää-Dahlqvist S, Sjöwall C, Julkunen H, Criswell LA, Graham RR, Behrens TW, Kere J, Rönnblom L, Syvänen AC, Sandling JK |
| Genome-Wide Association Meta-Analysis Reveals Novel Juvenile Idiopathic Arthritis Susceptibility Loci. Arthritis & rheumatology (Hoboken, N.J.) 2017 Jul . McIntosh Laura A, Marion Miranda C, Sudman Marc, Comeau Mary E, Becker Mara L, Bohnsack John F, Fingerlin Tasha E, Griffin Thomas A, Haas J Peter, Lovell Daniel J, Maier Lisa A, Nigrovic Peter A, Prahalad Sampath, Punaro Marilynn, Rosé Carlos D, Wallace Carol A, Wise Carol A, , , , , , , Moncrieffe Halima, Howard Timothy D, Langefeld Carl D, Thompson Susan |
| Mapping eQTLs with RNA-seq reveals novel susceptibility genes, non-coding RNAs and alternative-splicing events in systemic lupus erythematosus. Human molecular genetics 2017 1 26 (5): 1003-1017. Odhams Christopher A, Cortini Andrea, Chen Lingyan, Roberts Amy L, Viñuela Ana, Buil Alfonso, Small Kerrin S, Dermitzakis Emmanouil T, Morris David L, Vyse Timothy J, Cunninghame Graham Deborah |
| Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity. Nature genetics 2018 12 51 (1): 106-116. Coe Bradley P, Stessman Holly A F, Sulovari Arvis, Geisheker Madeleine R, Bakken Trygve E, Lake Allison M, Dougherty Joseph D, Lein Ed S, Hormozdiari Fereydoun, Bernier Raphael A, Eichler Evan |
| Splicing variant of WDFY4 augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis.
Annals of the rheumatic diseases 2018 Jan . Kochi Yuta, Kamatani Yoichiro, Kondo Yuya, Suzuki Akari, Kawakami Eiryo, Hiwa Ryosuke, Momozawa Yukihide, Fujimoto Manabu, Jinnin Masatoshi, Tanaka Yoshiya, Kanda Takashi, Cooper Robert G, Chinoy Hector, Rothwell Simon, Lamb Janine A, Vencovský Ji?í, Mann He?man, Ohmura Koichiro, Myouzen Keiko, Ishigaki Kazuyoshi, Nakashima Ran, Hosono Yuji, Tsuboi Hiroto, Kawasumi Hidenaga, Iwasaki Yukiko, Kajiyama Hiroshi, Horita Tetsuya, Ogawa-Momohara Mariko, Takamura Akito, Tsunoda Shinichiro, Shimizu Jun, Fujio Keishi, Amano Hirofumi, Mimori Akio, Kawakami Atsushi, Umehara Hisanori, Takeuchi Tsutomu, Sano Hajime, Muro Yoshinao, Atsumi Tatsuya, Mimura Toshihide, Kawaguchi Yasushi, Mimori Tsuneyo, Takahashi Atsushi, Kubo Michiaki, Kohsaka Hitoshi, Sumida Takayuki, Yamamoto Kazuhi |
| Trans-ancestry, Bayesian Meta-analysis Discovers 20 Novel Risk Loci for Inflammatory Bowel Disease in an African American, East Asian, and European Cohort. Human molecular genetics 2022 10 . Cordero Roberto Y, Cordero Jennifer B, Stiemke Andrew B, Datta Lisa W, Buyske Steven, Kugathasan Subra, McGovern Dermot P B, Brant Steven R, Simpson Claire |
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