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Items: 1 to 20 of 99

1.

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.

Fung HC, Scholz S, Matarin M, Simón-Sánchez J, Hernandez D, Britton A, Gibbs JR, Langefeld C, Stiegert ML, Schymick J, Okun MS, Mandel RJ, Fernandez HH, Foote KD, Rodríguez RL, Peckham E, De Vrieze FW, Gwinn-Hardy K, Hardy JA, Singleton A.

Lancet Neurol. 2006 Nov;5(11):911-6.

PMID:
17052657
2.

Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.

Schymick JC, Scholz SW, Fung HC, Britton A, Arepalli S, Gibbs JR, Lombardo F, Matarin M, Kasperaviciute D, Hernandez DG, Crews C, Bruijn L, Rothstein J, Mora G, Restagno G, Chiò A, Singleton A, Hardy J, Traynor BJ.

Lancet Neurol. 2007 Apr;6(4):322-8.

PMID:
17362836
3.

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.

Matarín M, Brown WM, Scholz S, Simón-Sánchez J, Fung HC, Hernandez D, Gibbs JR, De Vrieze FW, Crews C, Britton A, Langefeld CD, Brott TG, Brown RD Jr, Worrall BB, Frankel M, Silliman S, Case LD, Singleton A, Hardy JA, Rich SS, Meschia JF.

Lancet Neurol. 2007 May;6(5):414-20.

4.

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.

5.

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.

6.

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.

7.

SNCA rs356182 variant increases risk of sporadic Parkinson's disease in ethnic Chinese.

Cheng L, Wang L, Li NN, Yu WJ, Sun XY, Li JY, Zhou D, Peng R.

J Neurol Sci. 2016 Sep 15;368:231-4. doi: 10.1016/j.jns.2016.07.032. Epub 2016 Jul 14.

PMID:
27538639
8.

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.

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.

10.

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.

11.

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.

12.

Further delineation of the association signal on chromosome 5 from the first whole genome association study in Parkinson's disease.

Sharma M, Lichtner P, Kruger R, Berg D, Schulte C, Illig T, Riess O, Gasser T.

Neurobiol Aging. 2009 Oct;30(10):1706-9. doi: 10.1016/j.neurobiolaging.2007.12.016. Epub 2008 Feb 15.

PMID:
18280617
13.

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.

14.

Alzheimer's disease and Parkinson's disease genome-wide association study top hits and risk of Parkinson's disease in Korean population.

Chung SJ, Jung Y, Hong M, Kim MJ, You S, Kim YJ, Kim J, Song K.

Neurobiol Aging. 2013 Nov;34(11):2695.e1-7. doi: 10.1016/j.neurobiolaging.2013.05.022. Epub 2013 Jun 29.

PMID:
23820587
15.

P268S in NOD2 associates with susceptibility to Parkinson's disease in Chinese population.

Ma Q, An X, Li Z, Zhang H, Huang W, Cai L, Hu P, Lin Q, Tzeng CM.

Behav Brain Funct. 2013 May 7;9:19. doi: 10.1186/1744-9081-9-19.

16.

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
17.

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. doi: 10.1002/ajmg.b.32410. Epub 2015 Dec 17.

PMID:
26678010
18.

PARK16 polymorphisms, interaction with smoking, and sporadic Parkinson's disease in Japan.

Miyake Y, Tanaka K, Fukushima W, Kiyohara C, Sasaki S, Tsuboi Y, Oeda T, Shimada H, Kawamura N, Sakae N, Fukuyama H, Hirota Y, Nagai M, Nakamura Y; Fukuoka Kinki Parkinson's Disease Study Group.

J Neurol Sci. 2016 Mar 15;362:47-52. doi: 10.1016/j.jns.2016.01.021. Epub 2016 Jan 14.

PMID:
26944116
19.

Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease.

Simón-Sánchez J, Kilarski LL, Nalls MA, Martinez M, Schulte C, Holmans P; International Parkinson's Disease Genomics Consortium; Wellcome Trust Case Control Consortium, Gasser T, Hardy J, Singleton AB, Wood NW, Brice A, Heutink P, Williams N, Morris HR.

PLoS One. 2012;7(3):e28787. doi: 10.1371/journal.pone.0028787. Epub 2012 Mar 12.

20.

Association of DYRK1A polymorphisms with sporadic Parkinson's disease in Chinese Han population.

Cen L, Xiao Y, Wei L, Mo M, Chen X, Li S, Yang X, Huang Q, Qu S, Pei Z, Xu P.

Neurosci Lett. 2016 Oct 6;632:39-43. doi: 10.1016/j.neulet.2016.08.022. Epub 2016 Aug 18.

PMID:
27546826

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