Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 22 (of 22 Records) |
Query Trace: Vogt-koyanagi-harada Disease[original query] |
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Immunogenetics and clinical phenotype of sympathetic ophthalmia in British and Irish patients. The British journal of ophthalmology 2001 Mar 85 (3): 281-6. Kilmartin D J, Wilson D, Liversidge J, Dick A D, Bruce J, Acheson R W, Urbaniak S J, Forrester J |
KIR and HLA gene combinations in Vogt-Koyanagi-Harada disease. Human immunology 2008 Jun 69 (6): 349-53. Levinson Ralph D, Du Zeying, Luo Lihui, Holland Gary N, Rao Narsing A, Reed Elaine F, Rajalingam Ra |
Polymorphism of IFN-gamma gene and Vogt-Koyanagi-Harada disease. Molecular vision 2007 13 2334-8. Horie Yukihiro, Kitaichi Nobuyoshi, Takemoto Yuko, Namba Kenichi, Yoshida Kazuhiko, Hirose Shigeto, Hasumi Yukiko, Ota Masao, Inoko Hidetoshi, Mizuki Nobuhisa, Ohno Shigea |
HLA-DRB1 among patients with Vogt-Koyanagi-Harada disease in Saudi Arabia. Molecular vision 2009 15 1876-80. Iqniebi Alia, Gaafar Ameera, Sheereen Atia, Al-Suliman Abdullah, Mohamed Gamal, Al-Hussein Khaled, Tabbara Khalid |
Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients. Molecular vision 2009 15 1115-9. Horie Yukihiro, Kitaichi Nobuyoshi, Katsuyama Yoshihiko, Yoshida Kazuhiko, Miura Toshie, Ota Masao, Asukata Yuri, Inoko Hidetoshi, Mizuki Nobuhisa, Ishida Susumu, Ohno Shigea |
Elevated serum osteopontin levels and genetic polymorphisms of osteopontin are associated with Vogt-Koyanagi-Harada disease. Investigative ophthalmology & visual science 2011 52 (10): 7084-9. Chu Mingliang, Yang Peizeng, Hu Ranran, Hou Shengping, Li Fuzhen, Chen Yuanyuan, Kijlstra Ai |
Evaluation of NLRP1 gene polymorphisms in Vogt-Koyanagi-Harada disease. Japanese journal of ophthalmology 2011 Jan 55 (1): 57-61. Horie Yukihiro, Saito Wataru, Kitaichi Nobuyoshi, Miura Toshie, Ishida Susumu, Ohno Shigea |
Complement factor H and interleukin gene polymorphisms in patients with non-infectious intermediate and posterior uveitis. Molecular vision 2012 18 1865-72. Yang Ming-ming, Lai Timothy Y Y, Tam Pancy O S, Chiang Sylvia W Y, Chan Carmen K M, Luk Fiona O J, Ng Tsz-Kin, Pang Chi-P |
Association analysis of TGFBR3 gene with Vogt-Koyanagi-Harada disease and Behcet's disease in the Chinese Han population. Current eye research 2012 Apr 37 (4): 312-7. Chen Yuanyuan, Yang Peizeng, Li Fuzhen, Hou Shengping, Jiang Zhengxuan, Shu Qinmeng, Kijlstra Ai |
A study of KIR genes and HLA-C in Vogt-Koyanagi-Harada disease in Saudi Arabia. Molecular vision 2011 17 3523-8. Sheereen Atia, Gaafar Ameera, Iqneibi Alia, Eldali Abdelmoneim, Tabbara Khalid F, Adra Chaker, Al-Hussein Khal |
Association of HLA-DR4/HLA-DRB1*04 with Vogt-Koyanagi-Harada disease: a systematic review and meta-analysis. Scientific reports 2014 4 6887. Shi Tingkun, Lv Wenjuan, Zhang Li, Chen Jianhuan, Chen Hao |
KIR and HLA Genotypes Implicated in Reduced Killer Lymphocytes Immunity Are Associated with Vogt-Koyanagi-Harada Disease. PloS one 2016 11 (8): e0160392. Levinson Ralph D, Yung Madeline, Meguro Akira, Ashouri Elham, Yu Fei, Mizuki Nobuhisa, Ohno Shigeaki, Rajalingam Ra |
Investigation of the association between IL10 gene polymorphisms and Vogt-Koyanagi-Harada disease in a Japanese population. Ophthalmic genetics 2016 Apr 1-3. Higashi Kaori, Meguro Akira, Takeuchi Masaki, Yamane Takahiro, Kitaichi Nobuyoshi, Horie Yukihiro, Namba Kenichi, Ohno Shigeaki, Nakao Kumiko, Sakamoto Taiji, Sakai Tsutomu, Tsuneoka Hiroshi, Keino Hiroshi, Okada Annabelle A, Takeda Atsunobu, Fukuhara Takako, Mashimo Hisashi, Ohguro Nobuyuki, Oono Shinichirou, Enaida Hiroshi, Okinami Satoshi, Mizuki Nobuhi |
Association of Long Noncoding RNAs Polymorphisms With Ankylosing Spondylitis, Vogt-Koyanagi-Harada Disease, and Behcet's Disease. Investigative ophthalmology & visual science 2018 Feb 59 (2): 1158-1166. Yue Yingying, Zhang Jun, Yang Lu, Liu Shengyun, Qi Jian, Cao Qingfeng, Zhou Chunjiang, Wang Yao, Kijlstra Aize, Yang Peizeng, Hou Shengpi |
Association of human leukocyte antigen (HLA)-DQ and HLA-DQA1/DQB1 alleles with Vogt-Koyanagi-Harada disease: A systematic review and meta-analysis. Medicine 2018 Feb 97 (7): e9914. Liu Bing, Deng Tuo, Zhu Linxin, Zhong Jingxia |
Association Study of ARMC9 Gene Variants with Vogt-Koyanagi-Harada Disease in Japanese Patients. Ocular immunology and inflammation 2018 Nov 1-7. Ohno Tomoko, Meguro Akira, Takeuchi Masaki, Yamane Takahiro, Teshigawara Takeshi, Kitaichi Nobuyoshi, Horie Yukihiro, Namba Kenichi, Ohno Shigeaki, Nakao Kumiko, Sakamoto Taiji, Sakai Tsutomu, Nakano Tadashi, Keino Hiroshi, Okada Annabelle A, Takeda Atsunobu, Fukuhara Takako, Mashimo Hisashi, Ohguro Nobuyuki, Oono Shinichirou, Enaida Hiroshi, Okinami Satoshi, Mizuki Nobuhi |
Replication of Genome-Wide Association Analysis Identifies New Susceptibility Loci at Long Noncoding RNA Regions for Vogt-Koyanagi-Harada Disease. Investigative ophthalmology & visual science 2019 Nov 60 (14): 4820-4829. Qi Jian, Du Liping, Deng Jing, Qin Yang, Su Guannan, Hou Shengping, Lv Meng, Zhang Qi, Kijlstra Aize, Yang Peize |
Variants in IL23R-C1orf141 and ADO-ZNF365-EGR2 are associated with susceptibility to Vogt-Koyanagi-Harada disease in Japanese population. PloS one 2020 15 (5): e0233464. Sakono Takuto, Meguro Akira, Takeuchi Masaki, Yamane Takahiro, Teshigawara Takeshi, Kitaichi Nobuyoshi, Horie Yukihiro, Namba Kenichi, Ohno Shigeaki, Nakao Kumiko, Sakamoto Taiji, Sakai Tsutomu, Nakano Tadashi, Keino Hiroshi, Okada Annabelle A, Takeda Atsunobu, Ito Takako, Mashimo Hisashi, Ohguro Nobuyuki, Oono Shinichirou, Enaida Hiroshi, Okinami Satoshi, Horita Nobuyuki, Ota Masao, Mizuki Nobuhi |
Vogt-Koyanagi-Harada Disease: A Case Report With Distinct Brain MRI Enhancement Patterns. Cureus 2020 10 12 (9): e10391. El Beltagi Ahmed, Abdelhady Mohamed, Barakat Nour, Alkailani Yaman, Aboughalia Hass |
Association of ZC3HAV1 single nucleotide polymorphisms with the susceptibility of Vogt-Koyanagi-Harada Disease. BMC medical genomics 2023 5 16 (1): 113. Qiuying Wu, Zhenyu Zhong, Chunya Zhou, Qingfeng Cao, Guannan Su, Peizeng Ya |
Genetic association of PRKCD and CARD9 polymorphisms with Vogt-Koyanagi-Harada disease in the Chinese Han population. Human genomics 2023 2 17 (1): 9. Zhou Chunya, Cai Shiya, Xie Yuhong, Zeng Zhen, Zhang Jun, Su Guannan, Wu Qiuying, Ye Xingsheng, Cao Qingfeng, Yang Peizeng, Hu Jianm |
OR11H1 Missense Variant Confers the Susceptibility to Vogt-Koyanagi-Harada Disease by Mediating Gadd45g Expression. Advanced science (Weinheim, Baden-Wurttemberg, Germany) 2024 1 e2306563. Xingran Li, Guoqing Wang, Xiaotang Wang, Wanqian Li, Na Li, Xianyang Liu, Wei Fan, Siyuan He, Yue Han, Guannan Su, Qingfeng Cao, Peizeng Yang, Shengping H |
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- Page last updated:Apr 22, 2024
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