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Items: 13

1.

Is the Enzyme ACMSD a Novel Therapeutic Target in Parkinson's Disease?

Thirtamara-Rajamani K, Li P, Escobar Galvis ML, Labrie V, Brundin P, Brundin L.

J Parkinsons Dis. 2017;7(4):577-587. doi: 10.3233/JPD-171240. Review.

2.

A Novel p.Glu298Lys Mutation in the ACMSD Gene in Sporadic Parkinson's Disease.

Vilas D, Fernández-Santiago R, Sanchez E, Azcona LJ, Santos-Montes M, Casquero P, Argandoña L, Tolosa E, Paisán-Ruiz C.

J Parkinsons Dis. 2017;7(3):459-463. doi: 10.3233/JPD-171146.

PMID:
28671144
3.

Genome-wide assessment of Parkinson's disease in a Southern Spanish population.

Bandrés-Ciga S, Price TR, Barrero FJ, Escamilla-Sevilla F, Pelegrina J, Arepalli S, Hernández D, Gutiérrez B, Cervilla J, Rivera M, Rivera A, Ding JH, Vives F, Nalls M, Singleton A, Durán R.

Neurobiol Aging. 2016 Sep;45:213.e3-213.e9. doi: 10.1016/j.neurobiolaging.2016.06.001. Epub 2016 Jun 11.

4.

Genetic Mutation Analysis of Parkinson's Disease Patients Using Multigene Next-Generation Sequencing Panels.

Gorostidi A, Martí-Massó JF, Bergareche A, Rodríguez-Oroz MC, López de Munain A, Ruiz-Martínez J.

Mol Diagn Ther. 2016 Oct;20(5):481-91. doi: 10.1007/s40291-016-0216-1.

PMID:
27294386
5.

Association of Parkinson's Disease GWAS-Linked Loci with Alzheimer's Disease in Han Chinese.

Zhu XC, Cao L, Tan MS, Jiang T, Wang HF, Lu H, Tan CC, Zhang W, Tan L, Yu JT.

Mol Neurobiol. 2017 Jan;54(1):308-318. doi: 10.1007/s12035-015-9649-5. Epub 2016 Jan 6.

PMID:
26738859
6.

Variants in GBA, SNCA, and MAPT influence Parkinson disease risk, age at onset, and progression.

Davis AA, Andruska KM, Benitez BA, Racette BA, Perlmutter JS, Cruchaga C.

Neurobiol Aging. 2016 Jan;37:209.e1-209.e7. doi: 10.1016/j.neurobiolaging.2015.09.014. Epub 2015 Sep 30.

7.

Association analysis of STK39, MCCC1/LAMP3 and sporadic PD in the Chinese Han population.

Wang YQ, Tang BS, Yu RL, Li K, Liu ZH, Xu Q, Sun QY, Yan XX, Guo JF.

Neurosci Lett. 2014 Apr 30;566:206-9. doi: 10.1016/j.neulet.2014.03.007. Epub 2014 Mar 12.

PMID:
24631562
8.

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 Nov 27;8(11):e79211. doi: 10.1371/journal.pone.0079211. eCollection 2013.

9.

Meta-analysis supports association of a functional SNP (rs1801133) in the MTHFR gene with Parkinson's disease.

Zhu ZG, Ai QL, Wang WM, Xiao ZC.

Gene. 2013 Nov 15;531(1):78-83. doi: 10.1016/j.gene.2013.07.034. Epub 2013 Aug 3.

PMID:
23916622
10.

Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease.

Pihlstrøm L, Axelsson G, Bjørnarå KA, Dizdar N, Fardell C, Forsgren L, Holmberg B, Larsen JP, Linder J, Nissbrandt H, Tysnes OB, Ohman E, Dietrichs E, Toft M.

Neurobiol Aging. 2013 Jun;34(6):1708.e7-13. doi: 10.1016/j.neurobiolaging.2012.10.019. Epub 2012 Nov 13.

PMID:
23153929
11.

Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.

Liu X, Cheng R, Verbitsky M, Kisselev S, Browne A, Mejia-Sanatana H, Louis ED, Cote LJ, Andrews H, Waters C, Ford B, Frucht S, Fahn S, Marder K, Clark LN, Lee JH.

BMC Med Genet. 2011 Aug 3;12:104. doi: 10.1186/1471-2350-12-104.

12.

Genetics of Parkinson's disease and essential tremor.

Zimprich A.

Curr Opin Neurol. 2011 Aug;24(4):318-23. doi: 10.1097/WCO.0b013e3283484b87. Review.

PMID:
21734494
13.

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.

International Parkinson Disease Genomics Consortium, Nalls MA, Plagnol V, Hernandez DG, Sharma M, Sheerin UM, Saad M, Simón-Sánchez J, Schulte C, Lesage S, Sveinbjörnsdóttir S, Stefánsson K, Martinez M, Hardy J, Heutink P, Brice A, Gasser T, Singleton AB, Wood NW.

Lancet. 2011 Feb 19;377(9766):641-9. doi: 10.1016/S0140-6736(10)62345-8. Epub 2011 Feb 1.

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