Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 32 Records) |
Query Trace: NINJ2[original query] |
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NINJ2 polymorphism is associated with ischemic stroke in Chinese Han population. Journal of the neurological sciences 2011 Sep 308 (1-2): 67-71. Wan Xin-hong, Li Shu-juan, Cheng Ping, Zhang Qi, Yang Xin-chun, Zhong Guang-zhen, Hu Wen-li, Jin Li, Wang Xiao-fe |
Genetic polymorphisms of a novel vascular susceptibility gene, Ninjurin2 (NINJ2), are associated with a decreased risk of Alzheimer's disease. PloS one 2011 6 (6): e20573. Lin Kun-Pei, Chen Shih-Yuan, Lai Liang-Chuan, Huang Yi-Ling, Chen Jen-Hau, Chen Ta-Fu, Sun Yu, Wen Li-Li, Yip Ping-Keung, Chu Yi-Min, Chen Wei J, Chen Yen-Chi |
No evidence for association of 12p13 SNPs rs11833579 and rs12425791 within NINJ2 gene with ischemic stroke in Chinese Han population. Atherosclerosis 2011 Jun 216 (2): 381-2. Ding Hu, Tu Xin, Xu Yujun, Xu Chenqi, Wang Xiaojing, Cui Guanglin, Bao Xunna, Hui Rutai, Wang Qing K, Wang Dao W |
The rs11833579 and rs12425791 polymorphisms and risk of ischemic stroke in an Asian population: a meta-analysis. Thrombosis research 2012 Jul . Lian G, Yan Y, Jianxiong L, Juanjuan X, Qing C, Guangliang W, Li S |
Heterozygote genotypes at rs2222823 and rs2811712 SNP loci are associated with cerebral small vessel disease in Han Chinese population. CNS neuroscience & therapeutics 2012 Jul 18 (7): 558-65. Li Wei, Hu Bo, Li Gui-Lin, Zhao Xing-Quan, Xin Bao-Zhong, Lin Jin-Xi, Shen Yuan, Liang Xian-Hong, Liu Gai-Fen, Gao Han-Qing, Liao Xiao-Ling, Liang Zhi-Gang, Wang Yong-J |
NINJ2 SNP may affect the onset age of first-ever ischemic stroke without increasing silent cerebrovascular lesions. BMC research notes 2012 5 (1): 155. Kim Dong-Eog, Noh Sang-Mi, Jeong Sang-Wuk, Cha Min- |
Association between 12p13 SNPs rs11833579/rs12425791 near NINJ2 gene and ischemic stroke in East Asian population: evidence from a meta-analysis. Journal of the neurological sciences 2012 May 316 (1-2): 116-21. Li Bing-Hu, Zhang Li-Li, Yin Yan-Wei, Pi Yan, Guo Lu, Yang Qing-Wu, Gao Chang-Yue, Fang Chuan-Qin, Wang Jing-Zhou, Li Jing-Che |
Association between 12p13 SNP rs11833579 and ischemic stroke in Asian population: An updated meta-analysis. Journal of the neurological sciences 2014 Oct 345 (1-2): 198-201. Wang Ling, Zhao Chi, Xia Qing-Xin, Qiao Si-J |
Pharmacogenetic effects of 'candidate gene complexes' on stroke in the GenHAT study. Pharmacogenetics and genomics 2014 Nov 24 (11): 556-63. Sørensen Izel F, Vazquez Ana I, Irvin Marguerite R, Sørensen Peter, Davis Barry R, Ford Charles E, Boerwinkle Eric, Eckfeldt John H, Arnett Donna |
Associations of NINJ2 sequence variants with incident ischemic stroke in the Cohorts for Heart and Aging in Genomic Epidemiology (CHARGE) consortium. PloS one 2014 9 (6): e99798. Bis Joshua C, DeStefano Anita, Liu Xiaoming, Brody Jennifer A, Choi Seung Hoan, Verhaaren Benjamin F J, Debette Stéphanie, Ikram M Arfan, Shahar Eyal, Butler Kenneth R, Gottesman Rebecca F, Muzny Donna, Kovar Christie L, Psaty Bruce M, Hofman Albert, Lumley Thomas, Gupta Mayetri, Wolf Philip A, van Duijn Cornelia, Gibbs Richard A, Mosley Thomas H, Longstreth W T, Boerwinkle Eric, Seshadri Sudha, Fornage Myri |
Association between NINJ2 gene polymorphisms and ischemic stroke: a family-based case-control study. Journal of thrombosis and thrombolysis 2014 Nov 38 (4): 470-6. Zhu Yanping, Liu Kuo, Tang Xun, Wang Jinwei, Yu Zhiping, Wu Yiqun, Chen Dafang, Wang Xueyin, Fang Kai, Li Na, Huang Shaoping, Hu Yongh |
Impact of chromosome 12p13 variants on ischemic stroke risk. The International journal of neuroscience 2015 Aug 1-7. Zhang Zhizhong, Xu Gelin, Wei Yongyue, Zhu Wusheng, Fan Xiaobing, Liu Xinfe |
Chromosome 12p13 variants contribute to large artery atherosclerotic stroke risk in a Chinese population. Journal of the neurological sciences 2015 Oct 357 (1-2): 58-62. Zhang Zhizhong, Xu Gelin, Zhu Wusheng, Bai Wen, Cao Liping, Xiong Yunyun, Li Min, Fan Xiaobing, Li Hua, Ma Minmin, Liu Wenhua, Zhang Renliang, Liu George, Liu Xinfe |
Pharmacogenetic study of long-term response to interferon-ß treatment in multiple sclerosis.
The pharmacogenomics journal 2017 Jan 17 (1): 84-91. Clarelli F, Liberatore G, Sorosina M, Osiceanu A M, Esposito F, Mascia E, Santoro S, Pavan G, Colombo B, Moiola L, Martinelli V, Comi G, Martinelli-Boneschi |
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
The Lancet. Neurology 2016 Feb 15 (2): 174-184. , |
A Novel Functional Polymorphism in the NINJ2 Promoter Predicts Risk of Large Artery Atherosclerotic Stroke. Molecular neurobiology 2015 Dec . Zhang Zhizhong, Ni Guihua, Xu Gelin, Xu Jian, Liu Xinfe |
Genetic variants within Ninjurin 2 gene are associated with risk of ischemic stroke in Iranian population. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2019 Aug . Malekzadeh Vadoud, Azari Iman, Noroozi Rezvan, Shams Roshanak, Farzaneh Mina, Taheri Mohammad, Ghafouri-Fard Soud |
NINJ2 Gene Polymorphisms and Susceptibility to Ischemic Stroke: An Updated Meta-Analysis. Current neurovascular research 2019 7 16 (3): 273-287. Nie Fangfang, Yu Mingli, Liu Mengwei, Shang Mengke, Zeng Fanxin, Liu Wanya |
A single nucleotide polymorphism within Ninjurin 2 is associated with risk of multiple sclerosis. Metabolic brain disease 2019 Jul . Noroozi Rezvan, Azari Iman, Taheri Mohammad, Omrani Mir Davood, Ghafouri-Fard Soud |
A pharmacogenetic study implicates NINJ2 in the response to Interferon-? in multiple sclerosis. Multiple sclerosis (Houndmills, Basingstoke, England) 2019 Jun 1352458519851428. Peroni Silvia, Sorosina Melissa, Malhotra Sunny, Clarelli Ferdinando, Osiceanu Ana Maria, Ferrè Laura, Roostaei Tina, Rio Jordi, Midaglia Luciana, Villar Luisa María, Álvarez-Cermeño José Carlos, Guaschino Clara, Radaelli Marta, Citterio Lorena, Lechner-Scott Jeannette, Spataro Nino, Navarro Arcadi, Martinelli Vittorio, Montalban Xavier, Weiner Howard L, de Jager Philip, Comi Giancarlo, Esposito Federica, Comabella Manuel, Martinelli-Boneschi Filip |
Associations Between Two Single-Nucleotide Polymorphisms in NINJ2 Gene and Risk of Psychiatric Disorders. Journal of molecular neuroscience : MN 2019 Dec . Sayad Arezou, Ghafouri-Fard Soudeh, Omrani Mir Davood, Taheri Mohamm |
The relationship between the prognosis of children with acute arterial stroke and polymorphisms of CDKN2B, HDAC9, NINJ2, NAA25 genes. Journal of thrombosis and thrombolysis 2019 Jan . Bozpolat Adil, Unal Ekrem, Topaloglu Tugba, Taheri Serpil, Bayram Ayse Kacar, Ozcan Alper, Karakukcu Musa, Ozdemir Mehmet Akif, Per Husey |
Assessment of Association between NINJ2 Polymorphisms and Suicide Attempts in an Iranian Population. Journal of molecular neuroscience : MN 2020 May . Safa Amin, Omrani Mir Davood, Nicknafs Fwad, Oskooei Vahid Kholghi, Taheri Mohammad, Ghafouri-Fard Soud |
Application of Artificial Neural Network for Prediction of Risk of Multiple Sclerosis Based on Single Nucleotide Polymorphism Genotypes. Journal of molecular neuroscience : MN 2020 3 70 (7): 1081-1087. Ghafouri-Fard Soudeh, Taheri Mohammad, Omrani Mir Davood, Daaee Amir, Mohammad-Rahimi Hosse |
SLC17A3 rs9379800 and Ischemic Stroke Susceptibility at the Northern Region of Malaysia. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2021 Aug 105908. Ching Shu Chai, Wen Lim Jing, Ismail Nor Ismaliza Mohd, Looi Irene, Kooi Cheah Wee, Peng Long Soo, Mui Lee Soon, Tamibmaniam Jayashamani, Muninathan Prema, Hooi Ong Beng, Ali Siti Maisarah Md, Hassan Muhammad Radzi Abu, Mohamad Mohd Saberi, Griffiths Lyn R, Wei Loo Ke |
Functional rare variant in a C/EBPbeta binding site in NINJ2 gene increases the risk of coronary artery disease. Aging 2021 12 13 (23): 25393-25407. Wang Pengyun, Wang Yifan, Peng Huixin, Wang Jingjing, Zheng Qian, Wang Pengxia, Wang Jing, Zhang Hongfu, Huang Yufeng, Xiong Liang, Zhang Rongfeng, Xia Yunlong, Wang Qing K, Xu Cheng |
Association between genetic variants and risk of obsessive-compulsive disorder. Metabolic brain disease 2021 Nov . Taheri Mohammad, Badrlou Elham, Hussen Bashdar Mahmud, Oskooei Vahid Kholghi, Neishabouri Seyedeh Morvarid, Ghafouri-Fard Soud |
Ninjurin 2 rs118050317 gene polymorphism and endometrial cancer risk. Cancer cell international 2021 Jan 21 (1): 1. Cheng Yimin, Yang Liting, Shi Guangyao, Chen Peng, Li Liang, Fang Hangrong, Chen Ch |
Interdependency of NINJ2 gene expression and polymorphism with susceptibility and response to interferon beta in patients with multiple sclerosis. The International journal of neuroscience 2022 8 1-6. Khorrami Mehdi, Saneipour Maryam, Moridnia Abbas, Shaygannejad Vahid, Sadeghi Erfan, Kassani Aziz, Sarmadi Akram, Mirmosayyeb Om |
Genetic polymorphisms of MRPS30-DT and NINJ2 may influence lung cancer risk. Open medicine (Warsaw, Poland) 2023 3 18 (1): 20230655. Yan Shouchun, Wu Shouzhen, Wu Jia, Zhang Qinlu, He Yongjun, Jiang Chao, Jin Tian |
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- Page last updated:Apr 16, 2024
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