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Items: 1 to 20 of 42

1.

Investigation of the PARK10 gene in Parkinson disease.

Li YJ, Deng J, Mayhew GM, Grimsley JW, Huo X, Vance JM.

Ann Hum Genet. 2007 Sep;71(Pt 5):639-47. Epub 2007 Mar 27.

2.

Family-based association analysis of the MAPT gene in Parkinson disease.

Wang KS, Mullersman JE, Liu XF.

J Appl Genet. 2010;51(4):509-14.

PMID:
21063069
3.

High-resolution whole-genome association study of Parkinson disease.

Maraganore DM, de Andrade M, Lesnick TG, Strain KJ, Farrer MJ, Rocca WA, Pant PV, Frazer KA, Cox DR, Ballinger DG.

Am J Hum Genet. 2005 Nov;77(5):685-93. Epub 2005 Sep 9.

4.

Association mapping of the PARK10 region for Parkinson's disease susceptibility genes.

Wan JY, Edwards KL, Hutter CM, Mata IF, Samii A, Roberts JW, Agarwal P, Checkoway H, Farin FM, Yearout D, Zabetian CP.

Parkinsonism Relat Disord. 2014 Jan;20(1):93-8. doi: 10.1016/j.parkreldis.2013.10.001. Epub 2013 Oct 11.

5.

Microtubule-associated protein tau (MAPT) influences the risk of Parkinson's disease among Indians.

Das G, Misra AK, Das SK, Ray K, Ray J.

Neurosci Lett. 2009 Aug 21;460(1):16-20. doi: 10.1016/j.neulet.2009.05.031. Epub 2009 May 18.

PMID:
19450659
6.

alpha-Synuclein and Parkinson disease susceptibility.

Winkler S, Hagenah J, Lincoln S, Heckman M, Haugarvoll K, Lohmann-Hedrich K, Kostic V, Farrer M, Klein C.

Neurology. 2007 Oct 30;69(18):1745-50. Epub 2007 Sep 13.

PMID:
17872362
7.

Association study of semaphorin 5A with risk of Parkinson's disease in a Chinese Han population.

Ding H, Wang F, Ding X, Song X, Lu X, Zhang K, Xiao H, Ye M, Chen J, Zhang Q.

Brain Res. 2008 Dec 15;1245:126-9. doi: 10.1016/j.brainres.2008.09.080. Epub 2008 Oct 10.

PMID:
18950607
8.

Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.

Oliveira SA, Li YJ, Noureddine MA, Zuchner S, Qin X, Pericak-Vance MA, Vance JM.

Am J Hum Genet. 2005 Aug;77(2):252-64. Epub 2005 Jun 28.

9.

Progranulin variability has no major role in Parkinson disease genetic etiology.

Nuytemans K, Pals P, Sleegers K, Engelborghs S, Corsmit E, Peeters K, Pickut B, Mattheijssens M, Cras P, De Deyn PP, Theuns J, Van Broeckhoven C.

Neurology. 2008 Oct 7;71(15):1147-51. doi: 10.1212/01.wnl.0000327563.10320.2b.

PMID:
18838661
10.

Genome-wide linkage screen in familial Parkinson disease identifies loci on chromosomes 3 and 18.

Gao X, Martin ER, Liu Y, Mayhew G, Vance JM, Scott WK.

Am J Hum Genet. 2009 Apr;84(4):499-504. doi: 10.1016/j.ajhg.2009.03.005. Epub 2009 Mar 26.

11.

The 5q31 variants associated with psoriasis and Crohn's disease are distinct.

Li Y, Chang M, Schrodi SJ, Callis-Duffin KP, Matsunami N, Civello D, Bui N, Catanese JJ, Leppert MF, Krueger GG, Begovich AB.

Hum Mol Genet. 2008 Oct 1;17(19):2978-85. doi: 10.1093/hmg/ddn196. Epub 2008 Jul 9.

12.

Linkage and association of myocilin (MYOC) polymorphisms with high myopia in a Chinese population.

Tang WC, Yip SP, Lo KK, Ng PW, Choi PS, Lee SY, Yap MK.

Mol Vis. 2007 Apr 4;13:534-44.

13.

Association of a polymorphism in the ABCB1 gene with Parkinson's disease.

Westerlund M, Belin AC, Anvret A, Håkansson A, Nissbrandt H, Lind C, Sydow O, Olson L, Galter D.

Parkinsonism Relat Disord. 2009 Jul;15(6):422-4. doi: 10.1016/j.parkreldis.2008.11.010. Epub 2009 Feb 3.

PMID:
19196542
14.

Fine-mapping and candidate gene investigation within the PARK10 locus.

Haugarvoll K, Toft M, Skipper L, Heckman MG, Crook JE, Soto A, Ross OA, Hulihan MM, Kachergus JM, Sando SB, White LR, Lynch T, Gibson JM, Uitti RJ, Wszolek ZK, Aasly JO, Farrer MJ.

Eur J Hum Genet. 2009 Mar;17(3):336-43. doi: 10.1038/ejhg.2008.187. Epub 2008 Oct 15.

15.

Polymorphism in environment responsive genes and association with Parkinson disease.

Singh M, Khan AJ, Shah PP, Shukla R, Khanna VK, Parmar D.

Mol Cell Biochem. 2008 May;312(1-2):131-8. doi: 10.1007/s11010-008-9728-2. Epub 2008 Mar 9.

PMID:
18327668
16.

Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson's disease.

Refenes N, Bolbrinker J, Tagaris G, Orlacchio A, Drakoulis N, Kreutz R.

BMC Neurol. 2009 Jun 28;9:26. doi: 10.1186/1471-2377-9-26.

17.

Multiple alpha-synuclein gene polymorphisms are associated with Parkinson's disease in a Norwegian population.

Myhre R, Toft M, Kachergus J, Hulihan MM, Aasly JO, Klungland H, Farrer MJ.

Acta Neurol Scand. 2008 Nov;118(5):320-7. doi: 10.1111/j.1600-0404.2008.01019.x. Epub 2008 May 15.

PMID:
18485051
18.
19.

Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's disease.

Belin AC, Björk BF, Westerlund M, Galter D, Sydow O, Lind C, Pernold K, Rosvall L, Håkansson A, Winblad B, Nissbrandt H, Graff C, Olson L.

Neurosci Lett. 2007 Jun 15;420(3):257-62. Epub 2007 May 10.

PMID:
17537576
20.

Mutations for Gaucher disease confer high susceptibility to Parkinson disease.

Mitsui J, Mizuta I, Toyoda A, Ashida R, Takahashi Y, Goto J, Fukuda Y, Date H, Iwata A, Yamamoto M, Hattori N, Murata M, Toda T, Tsuji S.

Arch Neurol. 2009 May;66(5):571-6. doi: 10.1001/archneurol.2009.72.

PMID:
19433656

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