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S100B polymorphisms are associated with age of onset of Parkinson's disease.

Fardell C, Zettergren A, Ran C, Carmine Belin A, Ekman A, Sydow O, Bäckman L, Holmberg B, Dizdar N, Söderkvist P, Nissbrandt H.

BMC Med Genet. 2018 Mar 12;19(1):42. doi: 10.1186/s12881-018-0547-3.


Association of S100B polymorphisms and serum S100B with risk of ischemic stroke in a Chinese population.

Lu YL, Wang R, Huang HT, Qin HM, Liu CH, Xiang Y, Wang CF, Luo HC, Wang JL, Lan Y, Wei YS.

Sci Rep. 2018 Jan 17;8(1):971. doi: 10.1038/s41598-018-19156-w.


Association of IL-13, S100B, and TLR-7 Gene Polymorphisms with Enterovirus 71 Infection in Hand, Foot, and Mouth Disease in China.

Zhang Y, Suo X, Zhang Y.

Genet Test Mol Biomarkers. 2019 Mar;23(3):188-196. doi: 10.1089/gtmb.2018.0239. Epub 2019 Feb 26.


No association of the rs9722 C >T in the S100B gene and susceptibility to major depression in a Chinese population.

Yang K, Hu YQ, Xie GR, Mao FQ, Su LY.

Genet Test. 2008 Dec;12(4):487-9. doi: 10.1089/gte.2008.0023.


Association study of astrocyte-derived protein S100B gene polymorphisms with major depressive disorder in Chinese people.

Yang K, Xie GR, Hu YQ, Mao FQ, Su LY.

Can J Psychiatry. 2009 May;54(5):312-9.


Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson's disease - a multicenter study.

von Otter M, Bergström P, Quattrone A, De Marco EV, Annesi G, Söderkvist P, Wettinger SB, Drozdzik M, Bialecka M, Nissbrandt H, Klein C, Nilsson M, Hammarsten O, Nilsson S, Zetterberg H.

BMC Med Genet. 2014 Dec 12;15:131. doi: 10.1186/s12881-014-0131-4.


[Association between S100B gene polymorphisms and hand, foot and mouth disease caused by enterovirus 71 infection].

Li J, Shan RB, Liu RH, Xu YJ, Qu NY, Pan GM, Zhang N, Yang N, Chen ZZ, Zhang WX, Li ZP.

Zhongguo Dang Dai Er Ke Za Zhi. 2017 Aug;19(8):904-907. Chinese.


A search for SNCA 3' UTR variants identified SNP rs356165 as a determinant of disease risk and onset age in Parkinson's disease.

Cardo LF, Coto E, de Mena L, Ribacoba R, Lorenzo-Betancor O, Pastor P, Samaranch L, Mata IF, Díaz M, Moris G, Menéndez M, Corao AI, Alvarez V.

J Mol Neurosci. 2012 Jul;47(3):425-30. doi: 10.1007/s12031-011-9669-1. Epub 2011 Nov 11.


Interaction of polymorphisms in the genes encoding interleukin-6 and estrogen receptor beta on the susceptibility to Parkinson's disease.

Håkansson A, Westberg L, Nilsson S, Buervenich S, Carmine A, Holmberg B, Sydow O, Olson L, Johnels B, Eriksson E, Nissbrandt H.

Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):88-92.


Cytochrome P450 2E1 gene polymorphisms/haplotypes and Parkinson's disease in a Swedish population.

Shahabi HN, Westberg L, Melke J, Håkansson A, Belin AC, Sydow O, Olson L, Holmberg B, Nissbrandt H.

J Neural Transm (Vienna). 2009 May;116(5):567-73. doi: 10.1007/s00702-009-0221-1. Epub 2009 Apr 21.


Genetic analysis of the S100B gene in Chinese patients with Parkinson disease.

Guo Y, Yang H, Deng X, Song Z, Yang Z, Xiong W, Yuan L, Xu H, Deng S, Deng H.

Neurosci Lett. 2013 Oct 25;555:134-6. doi: 10.1016/j.neulet.2013.09.037. Epub 2013 Sep 25.


GLIS1 rs797906: an increased risk factor for late-onset Parkinson's disease in the Han Chinese population.

Song W, Chen YP, Huang R, Chen K, Pan PL, Li J, Yang Y, Shang HF.

Eur Neurol. 2012;68(2):89-92. doi: 10.1159/000337955. Epub 2012 Jul 3.


Association between the estrogen receptor beta gene and age of onset of Parkinson's disease.

Westberg L, Håkansson A, Melke J, Shahabi HN, Nilsson S, Buervenich S, Carmine A, Ahlberg J, Grundell MB, Schulhof B, Klingborg K, Holmberg B, Sydow O, Olson L, Johnels EB, Eriksson E, Nissbrandt H.

Psychoneuroendocrinology. 2004 Sep;29(8):993-8.


Association of PGC-1alpha polymorphisms with age of onset and risk of Parkinson's disease.

Clark J, Reddy S, Zheng K, Betensky RA, Simon DK.

BMC Med Genet. 2011 May 19;12:69. doi: 10.1186/1471-2350-12-69.


S100B gene polymorphisms predict prefrontal spatial function in both schizophrenia patients and healthy individuals.

Zhai J, Cheng L, Dong J, Shen Q, Zhang Q, Chen M, Gao L, Chen X, Wang K, Deng X, Xu Z, Ji F, Liu C, Li J, Dong Q, Chen C.

Schizophr Res. 2012 Jan;134(1):89-94. doi: 10.1016/j.schres.2011.09.029. Epub 2011 Oct 21.


Association of N-acetyl transferase 2 gene polymorphism and slow acetylator phenotype with young onset and late onset Parkinson's disease among Indians.

Chaudhary S, Behari M, Dihana M, Swaminath PV, Govindappa ST, Jayaram S, Singh S, Muthane UB, Juyal RC, B K T.

Pharmacogenet Genomics. 2005 Oct;15(10):731-5.


The single nucleotide polymorphism Rs12817488 is associated with Parkinson's disease in the Chinese population.

Yu RL, Guo JF, Wang YQ, Liu ZH, Sun ZF, Su L, Zhang Y, Yan XX, Tang BS.

J Clin Neurosci. 2015 Jun;22(6):1002-4. doi: 10.1016/j.jocn.2014.11.024. Epub 2015 Mar 26.


Risk variants in the S100B gene, associated with elevated S100B levels, are also associated with visuospatial disability of schizophrenia.

Zhai J, Zhang Q, Cheng L, Chen M, Wang K, Liu Y, Deng X, Chen X, Shen Q, Xu Z, Ji F, Liu C, Dong Q, Chen C, Li J.

Behav Brain Res. 2011 Mar 1;217(2):363-8. doi: 10.1016/j.bbr.2010.11.004. Epub 2010 Nov 9.


Genetic association study of synphilin-1 in idiopathic Parkinson's disease.

Myhre R, Klungland H, Farrer MJ, Aasly JO.

BMC Med Genet. 2008 Mar 21;9:19. doi: 10.1186/1471-2350-9-19.


Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population.

Chen Y, Wei QQ, Ou R, Cao B, Chen X, Zhao B, Guo X, Yang Y, Chen K, Wu Y, Song W, Shang HF.

PLoS One. 2015 Jul 24;10(7):e0133776. doi: 10.1371/journal.pone.0133776. eCollection 2015.

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