Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: GTF2IRD1[original query] |
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Human gene copy number spectra analysis in congenital heart malformations. Physiological genomics 2012 Feb . Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME |
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23.
Nature genetics 2013 Nov 45 (11): 1361-5. Li Yongzhe, Zhang Kunlin, Chen Hua, Sun Fei, Xu Juanjuan, Wu Ziyan, Li Ping, Zhang Liuyan, Du Yang, Luan Haixia, Li Xi, Wu Lijun, Li Hongbin, Wu Huaxiang, Li Xiangpei, Li Xiaomei, Zhang Xiao, Gong Lu, Dai Lie, Sun Lingyun, Zuo Xiaoxia, Xu Jianhua, Gong Huiping, Li Zhijun, Tong Shengquan, Wu Min, Li Xiaofeng, Xiao Weiguo, Wang Guochun, Zhu Ping, Shen Min, Liu Shengyun, Zhao Dongbao, Liu Wei, Wang Yi, Huang Cibo, Jiang Quan, Liu Guijian, Liu Bin, Hu Shaoxian, Zhang Wen, Zhang Zhuoli, You Xin, Li Mengtao, Hao Weixin, Zhao Cheng, Leng Xiaomei, Bi Liqi, Wang Yongfu, Zhang Fengxiao, Shi Qun, Qi Wencheng, Zhang Xuewu, Jia Yuan, Su Jinmei, Li Qin, Hou Yong, Wu Qingjun, Xu Dong, Zheng Wenjie, Zhang Miaojia, Wang Qian, Fei Yunyun, Zhang Xuan, Li Jing, Jiang Ying, Tian Xinping, Zhao Lidan, Wang Li, Zhou Bin, Li Yang, Zhao Yan, Zeng Xiaofeng, Ott Jurg, Wang Jing, Zhang Fengch |
Association of GTF2I and GTF2IRD1 polymorphisms with systemic lupus erythematosus in a Chinese Han population. Clinical and experimental rheumatology 2015 Aug . Li Yuan, Li Ping, Chen Si, Wu Ziyan, Li Jing, Zhang Shulan, Cao Chunwei, Wang Li, Liu Bin, Zhang Fengchun, Li Yong Z |
High-density genotyping of immune-related loci identifies new SLE risk variants in individuals with Asian ancestry. Nature genetics 2016 Mar 48 (3): 323-30. Sun Celi, Molineros Julio E, Looger Loren L, Zhou Xu-Jie, Kim Kwangwoo, Okada Yukinori, Ma Jianyang, Qi Yuan-Yuan, Kim-Howard Xana, Motghare Prasenjeet, Bhattarai Krishna, Adler Adam, Bang So-Young, Lee Hye-Soon, Kim Tae-Hwan, Kang Young Mo, Suh Chang-Hee, Chung Won Tae, Park Yong-Beom, Choe Jung-Yoon, Shim Seung Cheol, Kochi Yuta, Suzuki Akari, Kubo Michiaki, Sumida Takayuki, Yamamoto Kazuhiko, Lee Shin-Seok, Kim Young Jin, Han Bok-Ghee, Dozmorov Mikhail, Kaufman Kenneth M, Wren Jonathan D, Harley John B, Shen Nan, Chua Kek Heng, Zhang Hong, Bae Sang-Cheol, Nath Swapan |
A missense variant in NCF1 is associated with susceptibility to multiple autoimmune diseases. Nature genetics 2017 Mar 49 (3): 433-437. Zhao Jian, Ma Jianyang, Deng Yun, Kelly Jennifer A, Kim Kwangwoo, Bang So-Young, Lee Hye-Soon, Li Quan-Zhen, Wakeland Edward K, Qiu Rong, Liu Mengru, Guo Jianping, Li Zhanguo, Tan Wenfeng, Rasmussen Astrid, Lessard Christopher J, Sivils Kathy L, Hahn Bevra H, Grossman Jennifer M, Kamen Diane L, Gilkeson Gary S, Bae Sang-Cheol, Gaffney Patrick M, Shen Nan, Tsao Betty |
Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior. Molecular genetics & genomic medicine 2018 7 6 (5): 749-765. Kopp Nathan D, Parrish Phoebe C R, Lugo Michael, Dougherty Joseph D, Kozel Beth |
Williams Syndrome neuroanatomical score associates with GTF2IRD1 in large-scale magnetic resonance imaging cohorts: a proof of concept for multivariate endophenotypes. Translational psychiatry 2018 6 8 (1): 114. Fan Chun Chieh, Schork Andrew J, Brown Timothy T, Spencer Barbara E, Akshoomoff Natacha, Chen Chi-Hua, Kuperman Joshua M, Hagler Donald J, Steen Vidar M, Le Hellard Stephanie, Håberg Asta Kristine, Espeseth Thomas, Andreassen Ole A, Dale Anders M, Jernigan Terry L, Halgren Eric, |
Association of GTF2IRD1-GTF2I polymorphisms with neuromyelitis optica spectrum disorders in Han Chinese patients. Neural regeneration research 2019 Feb 14 (2): 346-353. Xie Jing-Lu, Liu Ju, Lian Zhi-Yun, Chen Hong-Xi, Shi Zi-Yan, Zhang Qin, Feng Hui-Ru, Du Qin, Miao Xiao-Hui, Zhou Hong- |
GTF2IRD1 on chromosome 7 is a novel oncogene regulating the tumor-suppressor gene TGF?R2 in colorectal cancer. Cancer science 2019 11 111 (2): 343-355. Nambara Sho, Masuda Takaaki, Kobayashi Yuta, Sato Kuniaki, Tobo Taro, Koike Kensuke, Noda Miwa, Ogawa Yushi, Kuroda Yousuke, Ito Shuhei, Eguchi Hidetoshi, Sugimachi Keishi, Mimori Kos |
Association of NCF1 polymorphism with systemic lupus erythematosus and systemic sclerosis but not with ANCA-associated vasculitis in a Japanese population. Scientific reports 2019 Nov 9 (1): 16366. Yokoyama Nozomi, Kawasaki Aya, Matsushita Takashi, Furukawa Hiroshi, Kondo Yuya, Hirano Fumio, Sada Ken-Ei, Matsumoto Isao, Kusaoi Makio, Amano Hirofumi, Nagaoka Shouhei, Setoguchi Keigo, Nagai Tatsuo, Shimada Kota, Sugii Shoji, Hashimoto Atsushi, Matsui Toshihiro, Okamoto Akira, Chiba Noriyuki, Suematsu Eiichi, Ohno Shigeru, Katayama Masao, Migita Kiyoshi, Kono Hajime, Hasegawa Minoru, Kobayashi Shigeto, Yamada Hidehiro, Nagasaka Kenji, Sugihara Takahiko, Yamagata Kunihiro, Ozaki Shoichi, Tamura Naoto, Takasaki Yoshinari, Hashimoto Hiroshi, Makino Hirofumi, Arimura Yoshihiro, Harigai Masayoshi, Sato Shinichi, Sumida Takayuki, Tohma Shigeto, Takehara Kazuhiko, Tsuchiya Naoyu |
A Dynamic Transcription Factor Signature Along the Colorectal Adenoma-Carcinoma Sequence in Patients With Co-Occurrent Adenoma and Carcinoma. Frontiers in oncology 2021 6 11 597447. Pan Zongfu, He Ying, Zhu Wenjuan, Xu Tong, Hu Xiaoping, Huang Pi |
?-Arrestin 2 (ARRB2) Polymorphism is Associated With Adverse Consequences of Chronic Heroin Use. The American journal on addictions 2021 Mar . Karavidha Klevis K, Burmeister Margit, Greenwald Mark |
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