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Results: 1 to 20 of 221

1.

A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease.

Krüger R, Sharma M, Riess O, Gasser T, Van Broeckhoven C, Theuns J, Aasly J, Annesi G, Bentivoglio AR, Brice A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, Hadjigeorgiou GM, Hattori N, Ioannidis JP, Jasinska-Myga B, Klein C, Lambert JC, Lesage S, Lin JJ, Lynch T, Mellick GD, de Nigris F, Opala G, Prigione A, Quattrone A, Ross OA, Satake W, Silburn PA, Tan EK, Toda T, Tomiyama H, Wirdefeldt K, Wszolek Z, Xiromerisiou G, Maraganore DM; Genetic Epidemiology of Parkinson's disease consortium.

Neurobiol Aging. 2011 Mar;32(3):548.e9-18. doi: 10.1016/j.neurobiolaging.2009.11.021. Epub 2009 Dec 24.

PMID:
20036034
[PubMed - indexed for MEDLINE]
2.

Genetic variations of Omi/HTRA2 in Chinese patients with Parkinson's disease.

Wang CY, Xu Q, Weng L, Zhang Q, Zhang HN, Guo JF, Tan LM, Tang JG, Yan XX, Tang BS.

Brain Res. 2011 Apr 18;1385:293-7. doi: 10.1016/j.brainres.2011.02.037. Epub 2011 Feb 19.

PMID:
21338583
[PubMed - indexed for MEDLINE]
3.

Genetic variation of Omi/HtrA2 and Parkinson's disease.

Ross OA, Soto AI, Vilariño-Güell C, Heckman MG, Diehl NN, Hulihan MM, Aasly JO, Sando S, Gibson JM, Lynch T, Krygowska-Wajs A, Opala G, Barcikowska M, Czyzewski K, Uitti RJ, Wszolek ZK, Farrer MJ.

Parkinsonism Relat Disord. 2008 Nov;14(7):539-43. doi: 10.1016/j.parkreldis.2008.08.003. Epub 2008 Sep 14.

PMID:
18790661
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Novel variant Pro143Ala in HTRA2 contributes to Parkinson's disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria.

Lin CH, Chen ML, Chen GS, Tai CH, Wu RM.

Hum Genet. 2011 Dec;130(6):817-27. doi: 10.1007/s00439-011-1041-6. Epub 2011 Jun 24.

PMID:
21701785
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controls.

Simón-Sánchez J, Singleton AB.

Hum Mol Genet. 2008 Jul 1;17(13):1988-93. doi: 10.1093/hmg/ddn096. Epub 2008 Mar 25.

PMID:
18364387
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Altered enzymatic activity and allele frequency of OMI/HTRA2 in Alzheimer's disease.

Westerlund M, Behbahani H, Gellhaar S, Forsell C, Belin AC, Anvret A, Zettergren A, Nissbrandt H, Lind C, Sydow O, Graff C, Olson L, Ankarcrona M, Galter D.

FASEB J. 2011 Apr;25(4):1345-52. doi: 10.1096/fj.10-163402. Epub 2010 Dec 16.

PMID:
21163861
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

HtrA2/Omi is involved in 6-OHDA-induced endoplasmic reticulum stress in SH-SY5Y cells.

Luo F, Wei L, Sun C, Chen X, Wang T, Li Y, Liu Z, Chen Z, Xu P.

J Mol Neurosci. 2012 May;47(1):120-7. doi: 10.1007/s12031-011-9694-0. Epub 2012 Jan 13.

PMID:
22246992
[PubMed - indexed for MEDLINE]
8.

PITX3 gene polymorphism is associated with Parkinson's disease in Chinese population.

Liu J, Sun QY, Tang BS, Hu L, Yu RH, Wang L, Shi CH, Yan XX, Pan Q, Xia K, Guo JF.

Brain Res. 2011 May 25;1392:116-20. doi: 10.1016/j.brainres.2011.03.064. Epub 2011 Apr 6.

PMID:
21524731
[PubMed - indexed for MEDLINE]
9.

Large-scale replication and heterogeneity in Parkinson disease genetic loci.

Sharma M, Ioannidis JP, Aasly JO, Annesi G, Brice A, Van Broeckhoven C, Bertram L, Bozi M, Crosiers D, Clarke C, Facheris M, Farrer M, Garraux G, Gispert S, Auburger G, Vilariño-Güell C, Hadjigeorgiou GM, Hicks AA, Hattori N, Jeon B, Lesage S, Lill CM, Lin JJ, Lynch T, Lichtner P, Lang AE, Mok V, Jasinska-Myga B, Mellick GD, Morrison KE, Opala G, Pramstaller PP, Pichler I, Park SS, Quattrone A, Rogaeva E, Ross OA, Stefanis L, Stockton JD, Satake W, Silburn PA, Theuns J, Tan EK, Toda T, Tomiyama H, Uitti RJ, Wirdefeldt K, Wszolek Z, Xiromerisiou G, Yueh KC, Zhao Y, Gasser T, Maraganore D, Krüger R; GEO-PD Consortium.

Neurology. 2012 Aug 14;79(7):659-67. doi: 10.1212/WNL.0b013e318264e353. Epub 2012 Jul 11.

PMID:
22786590
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?

Sutherland GT, Halliday GM, Silburn PA, Mastaglia FL, Rowe DB, Boyle RS, O'Sullivan JD, Ly T, Wilton SD, Mellick GD.

Mov Disord. 2009 Apr 30;24(6):833-8. doi: 10.1002/mds.22214.

PMID:
19224617
[PubMed - indexed for MEDLINE]
11.

Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study.

Elbaz A, Nelson LM, Payami H, Ioannidis JP, Fiske BK, Annesi G, Carmine Belin A, Factor SA, Ferrarese C, Hadjigeorgiou GM, Higgins DS, Kawakami H, Krüger R, Marder KS, Mayeux RP, Mellick GD, Nutt JG, Ritz B, Samii A, Tanner CM, Van Broeckhoven C, Van Den Eeden SK, Wirdefeldt K, Zabetian CP, Dehem M, Montimurro JS, Southwick A, Myers RM, Trikalinos TA.

Lancet Neurol. 2006 Nov;5(11):917-23.

PMID:
17052658
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Common variants in PARK loci and related genes and Parkinson's disease.

Chung SJ, Armasu SM, Biernacka JM, Lesnick TG, Rider DN, Lincoln SJ, Ortolaza AI, Farrer MJ, Cunningham JM, Rocca WA, Maraganore DM.

Mov Disord. 2011 Feb 1;26(2):280-8. doi: 10.1002/mds.23376. Epub 2010 Dec 13.

PMID:
21412835
[PubMed - indexed for MEDLINE]
Free PMC Article
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;131(7):1089-93. doi: 10.1007/s00439-011-1133-3. Epub 2011 Dec 24.

PMID:
22198721
[PubMed - indexed for MEDLINE]
14.

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease.

Strauss KM, Martins LM, Plun-Favreau H, Marx FP, Kautzmann S, Berg D, Gasser T, Wszolek Z, Müller T, Bornemann A, Wolburg H, Downward J, Riess O, Schulz JB, Krüger R.

Hum Mol Genet. 2005 Aug 1;14(15):2099-111. Epub 2005 Jun 16.

PMID:
15961413
[PubMed - indexed for MEDLINE]
Free Article
15.

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study.

Ross OA, Soto-Ortolaza AI, Heckman MG, Aasly JO, Abahuni N, Annesi G, Bacon JA, Bardien S, Bozi M, Brice A, Brighina L, Van Broeckhoven C, Carr J, Chartier-Harlin MC, Dardiotis E, Dickson DW, Diehl NN, Elbaz A, Ferrarese C, Ferraris A, Fiske B, Gibson JM, Gibson R, Hadjigeorgiou GM, Hattori N, Ioannidis JP, Jasinska-Myga B, Jeon BS, Kim YJ, Klein C, Kruger R, Kyratzi E, Lesage S, Lin CH, Lynch T, Maraganore DM, Mellick GD, Mutez E, Nilsson C, Opala G, Park SS, Puschmann A, Quattrone A, Sharma M, Silburn PA, Sohn YH, Stefanis L, Tadic V, Theuns J, Tomiyama H, Uitti RJ, Valente EM, van de Loo S, Vassilatis DK, Vilariño-Güell C, White LR, Wirdefeldt K, Wszolek ZK, Wu RM, Farrer MJ; Genetic Epidemiology Of Parkinson's Disease (GEO-PD) Consortium.

Lancet Neurol. 2011 Oct;10(10):898-908. doi: 10.1016/S1474-4422(11)70175-2. Epub 2011 Aug 30. Erratum in: Lancet Neurol. 2011 Oct;10(10):870.

PMID:
21885347
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Mitochondrial translation initiation factor 3 polymorphism and Parkinson's disease.

Behrouz B, Vilariño-Güell C, Heckman MG, Soto-Ortolaza AI, Aasly JO, Sando S, Lynch T, Craig D, Uitti RJ, Wszolek ZK, Ross OA, Farrer MJ.

Neurosci Lett. 2010 Dec 17;486(3):228-30. doi: 10.1016/j.neulet.2010.09.059. Epub 2010 Sep 29.

PMID:
20887776
[PubMed - indexed for MEDLINE]
17.

Association between PLA2G6 gene polymorphisms and Parkinson's disease in the Chinese Han population.

Lv Z, Guo J, Sun Q, Li K, Yu R, Tian J, Yan X, Tang B.

Parkinsonism Relat Disord. 2012 Jun;18(5):641-4. doi: 10.1016/j.parkreldis.2012.02.015. Epub 2012 Mar 27.

PMID:
22459563
[PubMed - indexed for MEDLINE]
18.

Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease.

Sharma M, Maraganore DM, Ioannidis JP, Riess O, Aasly JO, Annesi G, Abahuni N, Bentivoglio AR, Brice A, Van Broeckhoven C, Chartier-Harlin MC, Destée A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, Gispert S, Hattori N, Jasinska-Myga B, Klein C, Lesage S, Lynch T, Lichtner P, Lambert JC, Lang AE, Mellick GD, De Nigris F, Opala G, Quattrone A, Riva C, Rogaeva E, Ross OA, Satake W, Silburn PA, Theuns J, Toda T, Tomiyama H, Uitti RJ, Wirdefeldt K, Wszolek Z, Gasser T, Krüger R; Genetic Epidemiology of Parkinson's Disease Consortium.

Neurobiol Aging. 2011 Nov;32(11):2108.e1-5. doi: 10.1016/j.neurobiolaging.2011.05.024. Epub 2011 Jul 22.

PMID:
21782285
[PubMed - indexed for MEDLINE]
19.

Association study between the LINGO1 gene and Parkinson's disease in the Italian population.

Annesi F, De Marco EV, Rocca FE, Nicoletti A, Pugliese P, Nicoletti G, Arabia G, Tarantino P, De Mari M, Lamberti P, Gallerini S, Marconi R, Epifanio A, Morgante L, Cozzolino A, Barone P, Torchia G, Zappia M, Annesi G, Quattrone A.

Parkinsonism Relat Disord. 2011 Sep;17(8):638-41. doi: 10.1016/j.parkreldis.2011.06.020. Epub 2011 Jul 12.

PMID:
21752692
[PubMed - indexed for MEDLINE]
20.

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. doi: 10.1016/j.neulet.2012.04.024. Epub 2012 Apr 15.

PMID:
22531747
[PubMed - indexed for MEDLINE]

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