Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Syndrome and GTF2I[original query] |
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Association of GTF2i in the Williams-Beuren syndrome critical region with autism spectrum disorders. Journal of autism and developmental disorders 2012 Jul 42 (7): 1459-69. Malenfant Patrick, Liu Xudong, Hudson Melissa L, Qiao Ying, Hrynchak Monica, Riendeau Noémie, Hildebrand M Jeannette, Cohen Ira L, Chudley Albert E, Forster-Gibson Cynthia, Mickelson Elizabeth C R, Rajcan-Separovic Evica, Lewis M E Suzanne, Holden Jeanette J |
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 |
The GTF2I rs117026326 polymorphism is associated with anti-SSA-positive primary Sjögren's syndrome. Rheumatology (Oxford, England) 2015 Mar 54 (3): 562-4. Zheng Junfeng, Huang Renliang, Huang Qiaoniang, Deng Fengyuan, Chen Yan, Yin Junping, Chen Juan, Wang Ying, Shi Guixiu, Gao Xing, Liu Zuguo, Petersen Frank, Yu Xinh |
Cognitive-behavioral phenotypes of Williams syndrome are associated with genetic variation in the GTF2I gene, in a healthy population. BMC neuroscience 2014 15 127. Crespi Bernard J, Hurd Peter |
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 |
Variation in the Williams syndrome GTF2I gene and anxiety proneness interactively affect prefrontal cortical response to aversive stimuli. Translational psychiatry 2015 5 e622. Jabbi M, Chen Q, Turner N, Kohn P, White M, Kippenhan J S, Dickinson D, Kolachana B, Mattay V, Weinberger D R, Berman K |
Identification of susceptibility gene associated with female primary Sjögren's syndrome in Han Chinese by genome-wide association study.
Human genetics 2016 Aug . Song I-Wen, Chen Hsiang-Cheng, Lin Yuh-Feng, Yang Jenn-Hwai, Chang Chi-Ching, Chou Chung-Tei, Lee Ming-Ta Michael, Chou Yi-Chun, Chen Chien-Hsiun, Chen Yuan-Tsong, Chen Chen-Hung, Wu Jer-Yua |
Common variants near IKZF1 are associated with primary Sjögren's syndrome in Han Chinese. PloS one 2017 12 (5): e0177320. Qu Susu, Du Yang, Chang Suhua, Guo Liyuan, Fang Kechi, Li Yongzhe, Zhang Fengchun, Zhang Kunlin, Wang Ji |
The Williams syndrome prosociality gene GTF2I mediates oxytocin reactivity and social anxiety in a healthy population. Biology letters 2017 Apr 13 (4): . Procyshyn Tanya L, Spence Jason, Read Silven, Watson Neil V, Crespi Bernard |
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 |
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- |
The GTF2I rs117026326 polymorphism is associated with neuromyelitis optica spectrum disorder but not with multiple sclerosis in a Northern Han Chinese population. Journal of neuroimmunology 2019 Aug 337 577045. Liang Hudong, Gao Wenjing, Liu Xianjun, Liu Jingyao, Mao Xijing, Yang Mengge, Long Xixi, Zhou Yang, Zhang Qingxiang, Zhu Jie, Wang Shaofeng, Jin T |
Williams-Beuren syndrome in Mexican patients confirmed by FISH and assessed by aCGH. Journal of genetics 2019 6 98 (2): . Ramírez-Velazco Azubel, Aguayo-Orozco Thania Alejandra, Figuera Luis, Rivera Horacio, Jave-Suárez Luis, Aguilar-Lemarroy Adriana, Torres-Reyes Luis A, Córdova-Fletes Carlos, Barros-Núñez Patricio, Delgadillo-Pérez Saturnino, Dávalos-Rodríguez Ingrid Patricia, García-Ortiz José Elías, Domínguez María |
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 |
Sjögren's syndrome-associated SNPs increase GTF2I expression in salivary gland cells to enhance inflammation development. International immunology 2021 5 33 (8): 423-434. Shimoyama Shuhei, Nakagawa Ikuma, Jiang Jing-Jing, Matsumoto Isao, Chiorini John A, Hasegawa Yoshinori, Ohara Osamu, Hasebe Rie, Ota Mitsutoshi, Uchida Mona, Kamimura Daisuke, Hojyo Shintaro, Tanaka Yuki, Atsumi Tatsuya, Murakami Masaa |
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