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Journal Abstract Search

519 related items for PubMed ID: 32746945

  • 1. GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control study.
    Pan HX, Zhao YW, Mei JP, Fang ZH, Wang Y, Zhou X, Zhou YJ, Zhang R, Zhang KL, Jiang L, Zeng Q, He Y, Wang Z, Liu ZH, Xu Q, Sun QY, Yang Y, Hu YC, Chen YS, Du J, Lei LF, Zhang HN, Wang CY, Yan XX, Shen L, Jiang H, Tan JQ, Li JC, Tang BS, Guo JF.
    Transl Neurodegener; 2020 Aug 04; 9(1):31. PubMed ID: 32746945
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  • 4. Low frequency of GCH1 and TH mutations in Parkinson's disease.
    Rengmark A, Pihlstrøm L, Linder J, Forsgren L, Toft M.
    Parkinsonism Relat Disord; 2016 Aug 04; 29():109-11. PubMed ID: 27185167
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  • 7. Rare GCH1 heterozygous variants contributing to Parkinson's disease.
    Xu Q, Li K, Sun Q, Ding D, Zhao Y, Yang N, Luo Y, Liu Z, Zhang Y, Wang C, Xia K, Yan X, Jiang H, Shen L, Tang B, Guo J.
    Brain; 2017 Jul 01; 140(7):e41. PubMed ID: 28582483
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  • 9. SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson's diseases in Iranian population: A case-control study.
    Safaralizadeh T, Jamshidi J, Esmaili Shandiz E, Movafagh A, Fazeli A, Emamalizadeh B, Manafi N, Taghavi S, Tafakhori A, Darvish H.
    J Neurol Sci; 2016 Oct 15; 369():1-4. PubMed ID: 27653855
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  • 10. Aging modifies the effect of GCH1 RS11158026 on DAT uptake and Parkinson's disease clinical severity.
    Webb J, Willette AA.
    Neurobiol Aging; 2017 Feb 15; 50():39-46. PubMed ID: 27871051
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  • 12. Association of GCH1 and MIR4697, but not SIPA1L2 and VPS13C polymorphisms, with Parkinson's disease in Taiwan.
    Chen CM, Chen YC, Chiang MC, Fung HC, Chang KH, Lee-Chen GJ, Wu YR.
    Neurobiol Aging; 2016 Mar 15; 39():221.e1-5. PubMed ID: 26804608
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  • 13. Association Analysis of Essential Tremor-Associated Genetic Variants in Sporadic Late-Onset Parkinson's Disease.
    Zeng S, Zhou X, He R, Zhao Y, Liu Z, Xu Q, Guo J, Yan X, Li J, Tang B, Sun Q.
    Tremor Other Hyperkinet Mov (N Y); 2024 Mar 15; 14():25. PubMed ID: 38737298
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  • 14. Genetic Analysis of Neurite Outgrowth Inhibitor-Associated Genes in Parkinson's Disease: A Cross-Sectional Cohort Study.
    Huang X, Wang Y, Xiang Y, Zhao Y, Pan H, Liu Z, Xu Q, Sun Q, Tan J, Yan X, Li J, Tang B, Guo J.
    CNS Neurosci Ther; 2024 Oct 15; 30(10):e70070. PubMed ID: 39354865
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  • 15. Contribution of coding/non-coding variants in NUS1 to late-onset sporadic Parkinson's disease.
    Jiang L, Pan HX, Zhao YW, Zeng Q, Liu ZH, Sun QY, Xu Q, Tan JQ, Yan XX, Li JC, Tang BS, Guo JF.
    Parkinsonism Relat Disord; 2021 Mar 15; 84():29-34. PubMed ID: 33548880
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  • 16. GCH1 in early-onset Parkinson's disease.
    Cobb SA, Wider C, Ross OA, Mata IF, Adler CH, Rajput A, Rajput AH, Wu RM, Hauser R, Josephs KA, Carr J, Gwinn K, Heckman MG, Aasly JO, Lynch T, Uitti RJ, Wszolek ZK, Kapatos G, Farrer MJ.
    Mov Disord; 2009 Oct 30; 24(14):2070-5. PubMed ID: 19735094
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  • 17. The role of genetics in Parkinson's disease: a large cohort study in Chinese mainland population.
    Zhao Y, Qin L, Pan H, Liu Z, Jiang L, He Y, Zeng Q, Zhou X, Zhou X, Zhou Y, Fang Z, Wang Z, Xiang Y, Yang H, Wang Y, Zhang K, Zhang R, He R, Zhou X, Zhou Z, Yang N, Liang D, Chen J, Zhang X, Zhou Y, Liu H, Deng P, Xu K, Xu K, Zhou C, Zhong J, Xu Q, Sun Q, Li B, Zhao G, Wang T, Chen L, Shang H, Liu W, Chan P, Xue Z, Wang Q, Guo L, Wang X, Xu C, Zhang Z, Chen T, Lei L, Zhang H, Wang C, Tan J, Yan X, Shen L, Jiang H, Zhang Z, Hu Z, Xia K, Yue Z, Li J, Guo J, Tang B.
    Brain; 2020 Jul 01; 143(7):2220-2234. PubMed ID: 32613234
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  • 18. GCH1 Deficiency Activates Brain Innate Immune Response and Impairs Tyrosine Hydroxylase Homeostasis.
    Larbalestier H, Keatinge M, Watson L, White E, Gowda S, Wei W, Koler K, Semenova SA, Elkin AM, Rimmer N, Sweeney ST, Mazzolini J, Sieger D, Hide W, McDearmid J, Panula P, MacDonald RB, Bandmann O.
    J Neurosci; 2022 Jan 26; 42(4):702-716. PubMed ID: 34876467
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