Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and MIR4697[original query] |
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| Association of four new candidate genetic variants with Parkinson's disease in a Han Chinese population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Dec . Wang Ling, Cheng Lan, Li Nan-Nan, Yu Wen-Juan, Sun Xiao-Yi, Peng Ro |
| SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson's diseases in Iranian population: A case-control study. Journal of the neurological sciences 2016 Oct 369 1-4. Safaralizadeh Tannaz, Jamshidi Javad, Esmaili Shandiz Ehsan, Movafagh Abolfazl, Fazeli Atena, Emamalizadeh Babak, Manafi Navid, Taghavi Shaghayegh, Tafakhori Abbas, Darvish Hosse |
| Genome-wide assessment of Parkinson's disease in a Southern Spanish population. Neurobiology of aging 2016 Jun . Bandrés-Ciga Sara, Price Timothy Ryan, Barrero Francisco Javier, Escamilla-Sevilla Francisco, Pelegrina Javier, Arepalli Sampath, Hernández Dena, Gutiérrez Blanca, Cervilla Jorge, Rivera Margarita, Rivera Alberto, Ding Jing-Hui, Vives Francisco, Nalls Michael, Singleton Andrew, Durán Raqu |
| Association of GCH1 and MIR4697, but not SIPA1L2 and VPS13C polymorphisms, with Parkinson's disease in Taiwan. Neurobiology of aging 2016 Mar 39 221.e1-5. Chen Chiung-Mei, Chen Yi-Chun, Chiang Mu-Chun, Fung Hon-Chung, Chang Kuo-Hsuan, Lee-Chen Guey-Jen, Wu Yih- |
| Parkinson's disease susceptibility variants and severity of Lewy body pathology. Parkinsonism & related disorders 2017 Sep . Heckman Michael G, Kasanuki Koji, Diehl Nancy N, Koga Shunsuke, Soto Alexandra, Murray Melissa E, Dickson Dennis W, Ross Owen |
| Polymorphism in MIR4697 but not VPS13C, GCH1, or SIPA1L2 is associated with risk of Parkinson's disease in a Han Chinese population. Neuroscience letters 2017 05 650 8-11. Yang Xinglong, Zheng Jinhua, An Ran, Tian Sijia, Zhao Quanzhen, Chen Yalan, Huang Hongyan, Ning Ping Ping, Song Yi, Xu Yanmi |
| Association analyses of variants of SIPA1L2, MIR4697, GCH1, VPS13C, and DDRGK1 with Parkinson's disease in East Asians. Neurobiology of aging 2018 Mar . Zou Ming, Li Rui, Wang Jian-Yong, Wang Ke, Wang Ya-Nan, Li Yang, Ji Fei-Xue, Sun Sheng-Nan, Huang Shi-Shi, Fan Hui-Hui, Huang Chen-Ping, Zhang Xiong, Zhu Jian-Ho |
| A replication study of GWAS-genetic risk variants associated with Parkinson's disease in a Spanish population. Neuroscience letters 2019 Aug 134425. Tejera-Parrado Cristina, Jesús Silvia, Periñán María Teresa, Buiza-Rueda Dolores, Oliva-Ariza Guillermo, Adarmes-Gómez Astrid D, Macías-García Daniel, Gómez-Garre Pilar, Mir Pab |
| Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications. Clinical genetics 2022 7 102 (5): 391-403. He Guo-Wei, Maslen Cheryl L, Chen Huan-Xin, Hou Hai-Tao, Bai Xiao-Yan, Wang Xiu-Li, Liu Xiao-Cheng, Lu Wan-Li, Chen Xin-Xin, Chen Wei-Dan, Xing Quan-Sheng, Wu Qin, Wang Jun, Yang Q |
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