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Journal Abstract Search

329 related items for PubMed ID: 26678010

  • 1. Association of four new candidate genetic variants with Parkinson's disease in a Han Chinese population.
    Wang L, Cheng L, Li NN, Yu WJ, Sun XY, Peng R.
    Am J Med Genet B Neuropsychiatr Genet; 2016 Apr; 171B(3):342-7. PubMed ID: 26678010
    [Abstract] [Full Text] [Related]

  • 2. Association analyses of variants of SIPA1L2, MIR4697, GCH1, VPS13C, and DDRGK1 with Parkinson's disease in East Asians.
    Zou M, Li R, Wang JY, Wang K, Wang YN, Li Y, Ji FX, Sun SN, Huang SS, Fan HH, Huang CP, Zhang X, Zhu JH.
    Neurobiol Aging; 2018 Aug; 68():159.e7-159.e14. PubMed ID: 29622492
    [Abstract] [Full Text] [Related]

  • 3. 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; 39():221.e1-5. PubMed ID: 26804608
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Polymorphism in MIR4697 but not VPS13C, GCH1, or SIPA1L2 is associated with risk of Parkinson's disease in a Han Chinese population.
    Yang X, Zheng J, An R, Tian S, Zhao Q, Chen Y, Huang H, Ning PP, Song Y, Xu Y.
    Neurosci Lett; 2017 May 22; 650():8-11. PubMed ID: 28380328
    [Abstract] [Full Text] [Related]

  • 6. Association of three candidate genetic variants in ACMSD/TMEM163, GPNMB and BCKDK /STX1B with sporadic Parkinson's disease in Han Chinese.
    Wang L, Li NN, Lu ZJ, Li JY, Peng JX, Duan LR, Peng R.
    Neurosci Lett; 2019 Jun 11; 703():45-48. PubMed ID: 30880162
    [Abstract] [Full Text] [Related]

  • 7. Genetic association study between STK39 and CCDC62/HIP1R and Parkinson's disease.
    Li NN, Tan EK, Chang XL, Mao XY, Zhang JH, Zhao DM, Liao Q, Yu WJ, Peng R.
    PLoS One; 2013 Jun 11; 8(11):e79211. PubMed ID: 24312176
    [Abstract] [Full Text] [Related]

  • 8. Association of three candidate genetic variants in RAB7L1/NUCKS1, MCCC1 and STK39 with sporadic Parkinson's disease in Han Chinese.
    Wang L, Cheng L, Lu ZJ, Sun XY, Li JY, Peng R.
    J Neural Transm (Vienna); 2016 Apr 11; 123(4):425-30. PubMed ID: 26914237
    [Abstract] [Full Text] [Related]

  • 9. Genome-wide association study of Parkinson's disease in East Asians.
    Foo JN, Tan LC, Irwan ID, Au WL, Low HQ, Prakash KM, Ahmad-Annuar A, Bei J, Chan AY, Chen CM, Chen YC, Chung SJ, Deng H, Lim SY, Mok V, Pang H, Pei Z, Peng R, Shang HF, Song K, Tan AH, Wu YR, Aung T, Cheng CY, Chew FT, Chew SH, Chong SA, Ebstein RP, Lee J, Saw SM, Seow A, Subramaniam M, Tai ES, Vithana EN, Wong TY, Heng KK, Meah WY, Khor CC, Liu H, Zhang F, Liu J, Tan EK.
    Hum Mol Genet; 2017 Jan 01; 26(1):226-232. PubMed ID: 28011712
    [Abstract] [Full Text] [Related]

  • 10. HLA-DRB1 alleles are associated with the susceptibility to sporadic Parkinson's disease in Chinese Han population.
    Sun C, Wei L, Luo F, Li Y, Li J, Zhu F, Kang P, Xu R, Xiao L, Liu Z, Xu P.
    PLoS One; 2012 Jan 01; 7(11):e48594. PubMed ID: 23139797
    [Abstract] [Full Text] [Related]

  • 11. Association analysis of NUCKS1 and INPP5K polymorphism with Parkinson's disease.
    Zhu W, Luo X, Adnan A, Yu P, Zhang S, Huo Z, Xu Q, Pang H.
    Genes Genet Syst; 2018 Sep 15; 93(2):59-64. PubMed ID: 29607885
    [Abstract] [Full Text] [Related]

  • 12. Association between VPS13C rs2414739 polymorphism and Parkinson's disease risk: A meta-analysis.
    Bai X, Liu X, Li X, Li W, Xie A.
    Neurosci Lett; 2021 May 29; 754():135879. PubMed ID: 33838259
    [Abstract] [Full Text] [Related]

  • 13. GWAS-linked GAK locus in Parkinson's disease in Han Chinese and meta-analysis.
    Li NN, Chang XL, Mao XY, Zhang JH, Zhao DM, Tan EK, Peng R.
    Hum Genet; 2012 Jul 29; 131(7):1089-93. PubMed ID: 22198721
    [Abstract] [Full Text] [Related]

  • 14. Assessment of RIT2 rs12456492 association with Parkinson's disease in Mainland China.
    Liu ZH, Guo JF, Wang YQ, Li K, Sun QY, Xu Q, Yan XX, Xu CS, Tang BS.
    Neurobiol Aging; 2015 Mar 29; 36(3):1600.e9-11. PubMed ID: 25559334
    [Abstract] [Full Text] [Related]

  • 15. GSK3β reduces risk of sporadic Parkinson's disease in ethnic Chinese.
    Zhao DM, Li NN, Zhang JH, Chang XL, Mao XY, Liao Q, Tan EK, Peng R.
    Am J Med Genet B Neuropsychiatr Genet; 2012 Sep 29; 159B(6):718-21. PubMed ID: 22815195
    [Abstract] [Full Text] [Related]

  • 16. Association analysis of single-nucleotide polymorphisms of USP24 and USP40 with Parkinson's disease in the Han Chinese population.
    Zhao B, Song W, Chen YP, Huang R, Chen K, Cao B, Yang Y, Shang HF.
    Eur Neurol; 2012 Sep 29; 68(3):181-4. PubMed ID: 22923019
    [Abstract] [Full Text] [Related]

  • 17. The Potential Mutation of GAK Gene in the Typical Sporadic Parkinson's Disease from the Han Population of Chinese Mainland.
    Zhang J, Zeng H, Zhu L, Deng L, Fang X, Deng X, Liang H, Tang C, Cao X, Lu Y, Li J, Ren X, Zuo W, Zhang X, Xu R.
    Mol Neurobiol; 2016 Dec 29; 53(10):7119-7136. PubMed ID: 26676575
    [Abstract] [Full Text] [Related]

  • 18. Association of LRRK2 R1628P variant with Parkinson's disease in Ethnic Han-Chinese and subgroup population.
    Zhang P, Wang Q, Jiao F, Yan J, Chen L, He F, Zhang Q, Tian B.
    Sci Rep; 2016 Nov 04; 6():35171. PubMed ID: 27812003
    [Abstract] [Full Text] [Related]

  • 19. Association study between two novel single nucleotide polymorphisms and sporadic Parkinson's disease in Chinese Han population.
    Li K, Tang BS, Yu RL, Lv ZY, Sun QY, Li Q, Xia K, Yan XX, Guo JF.
    Neurosci Lett; 2012 May 23; 517(1):56-9. PubMed ID: 22531747
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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