Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 33 Records) |
Query Trace: CYP4V2[original query] |
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New gene variants associated with venous thrombosis: a replication study in White and Black Americans. Journal of thrombosis and haemostasis : JTH 2011 Mar 9 (3): 489-95. Austin H, De Staercke C, Lally C, Bezemer I D, Rosendaal F R, Hooper W |
Tamoxifen-induced venothromboembolic events: exploring validation of putative genetic association. Clinical medicine & research 2013 Feb 11 (1): 16-25. Glurich Ingrid, Chyou Po-Huang, Engel Jessica M, Cross Deanna S, Onitilo Adedayo |
Association of F11 polymorphism rs2289252 with deep vein thrombosis and related phenotypes in population of Latvia. Thrombosis research 2014 Sep 134 (3): 659-63. Rovite Vita, Maurins Uidis, Megnis Kaspars, Vaivade Iveta, Pe?ulis Raitis, Rits Juris, Prave Sandra, Klovins Jan |
Identification of novel CYP4V2 gene mutations in 92 Chinese families with Bietti's crystalline corneoretinal dystrophy. Molecular vision 2015 1 20 1806-14. Meng Xiao Hong, Guo Hong, Xu Hai Wei, Li Qi You, Jin Xin, Bai Yun, Li Shi Ying, Yin Zheng Q |
Identification of CYP4V2 mutation in 36 Chinese families with Bietti crystalline corneoretinal dystrophy. Experimental eye research 2016 Mar . Yin Xiaobei, Yang Liping, Chen Ningning, Cui Hui, Zhao Lin, Feng Lina, Li Aijun, Zhang Huirong, Ma Zhizhong, Li Genl |
Choroidal Vasculature in Bietti Crystalline Dystrophy With CYP4V2 Mutations and in Retinitis Pigmentosa With EYS Mutations. Investigative ophthalmology & visual science 2017 8 58 (10): 3871-3878. Hirashima Takako, Miyata Manabu, Ishihara Kenji, Hasegawa Tomoko, Sugahara Masako, Ogino Ken, Yoshikawa Munemitsu, Hata Masayuki, Kuroda Yoshimasa, Muraoka Yuki, Ooto Sotaro, Yoshimura Nagahi |
Associations between polymorphisms in coagulation-related genes and venous thromboembolism: A meta-analysis with trial sequential analysis. Medicine 2017 Mar 96 (13): e6537. Jiang Jun, Liu Kang, Zou Junjie, Ma Hao, Yang Hongyu, Zhang Xiwei, Jiao Yuanyo |
Choriocapillaris flow deficit in Bietti crystalline dystrophy detected using optical coherence tomography angiography. The British journal of ophthalmology 2017 12 102 (9): 1208-1212. Miyata Manabu, Oishi Akio, Hasegawa Tomoko, Ishihara Kenji, Oishi Maho, Ogino Ken, Sugahara Masako, Hirashima Takako, Hata Masayuki, Yoshikawa Munemitsu, Tsujikawa Akita |
Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes. Journal of thrombosis and haemostasis : JTH 2018 Aug . de Haan H G, van Hylckama Vlieg A, Lotta L A, Gorski M M, Bucciarelli P, Martinelli I, Baglin T P, Peyvandi F, Rosendaal F R, |
Identification of novel CYP4V2 genotypes associated with Bietti crystalline dystrophy and atypical anterior segment phenotypes in Spanish patients. Acta ophthalmologica 2018 4 96 (7): e865-e873. García-García Gerardo Pedro, Martínez-Rubio Magdalena, Moya-Moya Medina-Azahara, Pérez-Santonja Juan José, Escribano Jul |
Comprehensive screening of CYP4V2 in a cohort of Chinese patients with Bietti crystalline dystrophy. Molecular vision 2018 11 24 700-711. Zhang Xiaohui, Xu Ke, Dong Bing, Peng Xiaoyan, Li Qian, Jiang Feng, Xie Yue, Tian Lu, Li Ya |
Association of the CYP4V2 polymorphism rs13146272 with venous thromboembolism in a Chinese population. Clinical and experimental medicine 2019 Feb 19 (1): 159-166. Yue Yongjian, Sun Qing, Man Chiwai, Fu Yingy |
Molecular Functionality of Cytochrome P450 4 (CYP4) Genetic Polymorphisms and Their Clinical Implications. International journal of molecular sciences 2019 Aug 20 (17): . Jarrar Yazun Bashir, Lee Su-J |
Genetic profiling revealed an increased risk of venous thrombosis in the Hungarian Roma population. Thrombosis research 2019 5 179 37-44. Fiatal Szilvia, Pikó Péter, Kósa Zsigmond, Sándor János, Ádány Ró |
Mutation spectrum and genotype-phenotype correlation of inherited retinal dystrophy in Taiwan. Clinical & experimental ophthalmology 2019 Dec . Chen Zhen-Ji, Lin Keng-Hung, Lee Shi-Huang, Shen Ren-Juan, Feng Zhuo-Kun, Wang Xiao-Fang, Huang Xiu-Feng, Huang Zhi-Qin, Jin Zi-Bi |
Novel mutations in CYP4V2 in Bietti corneoretinal crystalline dystrophy: Next-generation sequencing technology and genotype-phenotype correlations. Molecular vision 2019 11 25 654-662. Meng Xiao Hong, He Yan, Zhao Tong Tao, Li Shi Ying, Liu Yong, Yin Zheng Q |
The Correlation Between Abnormal Uterine Artery Flow in the First Trimester and Genetic Thrombophilic Alteration: A Prospective Case-Controlled Pilot Study. Diagnostics (Basel, Switzerland) 2020 Aug 10 (9): . Vedmedovska Natalija, Bokucava Diana, Kivite-Urtane Anda, Rovite Vita, Zake-Nikitina Liene, Klovins Janis, Fodina Violeta, Donders Gilbert G |
[Analysis of phenotype and CYP4V2 gene variants in two pedigrees affected with Bietti crystalline corneoretinal dystrophy]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 12 37 (12): 1340-1343. Xie Yanchuan, Bai Zhouxian, Sun Zongli, Gu Lei, Zhang Xinyuan, Kong Xiangdo |
Diverse Genetic Landscape of Suspected Retinitis Pigmentosa in a Large Korean Cohort. Genes 2021 5 12 (5): . Kim Yoon-Jeon, Kim You-Na, Yoon Young-Hee, Seo Eul-Ju, Seo Go-Hun, Keum Changwon, Lee Beom-Hee, Lee Joo-Yo |
Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese Patients. Ophthalmology. Retina 2021 2 5 (12): 1269-1279. Murakami Yusuke, Koyanagi Yoshito, Fukushima Masatoshi, Yoshimura Marika, Fujiwara Kohta, Akiyama Masato, Momozawa Yukihide, Ueno Shinji, Terasaki Hiroko, Oishi Akio, Miyata Manabu, Ikeda Hanako, Tsujikawa Akitaka, Mizobuchi Kei, Hayashi Takaaki, Fujinami Kaoru, Tsunoda Kazushige, Park Jun Young, Han Jinu, Kim Min, Lee Christopher Seungkyu, Kim Sang Jin, Park Tae Kwann, Joo Kwangsic, Woo Se Joon, Ikeda Yasuhiro, Sonoda Koh-H |
Genetic characteristics and epidemiology of inherited retinal degeneration in Taiwan. NPJ genomic medicine 2021 2 6 (1): 16. Chen Ta-Ching, Huang Ding-Siang, Lin Chao-Wen, Yang Chang-Hao, Yang Chung-May, Wang Victoria Y, Lin Jou-Wei, Luo Allen Chilun, Hu Fung-Rong, Chen Pei-Lu |
Structural and functional phenotypic features and molecular analysis of Indian patients with Bietti crystalline dystrophy. Indian journal of ophthalmology 2022 7 70 (7): 2526-2532. Ratra Dhanashree, Chattree Surabhi, Raviselvan Munispriyan, Pradhan Arkaprava, Giridhar Sne |
Genetic characteristics of suspected retinitis pigmentosa in a cohort of Chinese patients. Gene 2022 12 853 147087. Jin Bingyu, Li Jing, Yang Qiaodan, Tang Xinyu, Wang Chen, Zhao Yue, Zheng Fang, Zhang Yuanzhen, Ma Jianhong, Yan Mi |
CYP4 subfamily V member 2 (CYP4V2) polymorphisms were associated with ischemic stroke in Chinese Han population. BMC medical genomics 2022 11 15 (1): 246. Long Faqing, Wang Desheng, Su Qingjie, Zhang Yuhui, Li Jianhong, Xia Shiliang, Wang Hailun, Wu Yongping, Qu Qium |
Cryptogenic Stroke in the Young: Role of Candidate Gene Polymorphisms in Indian Patients with Ischemic Etiology. Neurology India 2022 1 69 (6): 1655-1662. Salomi Bodda S B, Solomon Raja, Turaka Vijay Prakash, Aaron Sanjith, Christudass Christhunesa |
Clinical and genetic characterization of a large cohort of Chinese patients with Bietti crystalline retinopathy. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 2023 8 . Huajin Li, Xing Wei, Shijing Wu, Tian Zhu, Zixi Sun, Hui Li, Xiaoxu Han, Xuan Zou, Fengxia Yao, Ruifang S |
Outer retinal tubulation in Bietti crystalline dystrophy associated with the retinal pigment epithelium atrophy. Retina (Philadelphia, Pa.) 2023 2 . Wang Yusong, Chen Jieqiong, Sun Junran, Li Tong, Yu Suqin, Gong Yuanyuan, Yu Yang, Wan Xiaoling, Jia Huixun, Wu Jihong, Yuan Fei, Shen Xi, Wang Zhiliang, Qiao Tong, Wu Qiang, Xu Yu, Wang Zhaoyang, Yang Chenhao, Qu Jifang, Chen Jianjun, Sun Xiaodong, |
An In-Depth Single-Gene Worldwide Carrier Frequency and Genetic Prevalence Analysis of CYP4V2 as the Cause of Bietti Crystalline Dystrophy. Translational vision science & technology 2023 2 12 (2): 27. Hanany Mor, Yang Richard Rui, Lam Chun Man, Beryozkin Avigail, Sundaresan Yogapriya, Sharon Dr |
CYP4V2 rs56413992 C?>?T was associated with the risk of coronary heart disease in the Chinese Han population: a case-control study. BMC medical genomics 2023 12 16 (1): 322. Kang Huang, Tianyi Ma, Qiang Li, Zanrui Zhong, Yilei Zhou, Wei Zhang, Ting Qin, Shilin Tang, Jianghua Zhong, Shijuan |
Bietti's crystalline dystrophy: genotyping and deep qualitative and quantitative phenotyping in preparation for clinical trials. The British journal of ophthalmology 2023 11 . Qian Li, Cong Wang, Shengjuan Zhang, Zhongjie Fu, Xiaodong Jiao, Zi-Bing Jin, James Fielding Hejtmancik, Xiaoyan Pe |
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- Page last updated:Apr 16, 2024
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