Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Disease and NINJ2[original query] |
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| 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 |
| 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 |
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.
The Lancet. Neurology 2016 Feb 15 (2): 174-184. , |
| 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 |
| 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 |
| 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 |
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