Singleton AB - Search Results

1

Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease.

Hudson G, Nalls M, Evans JR, Breen DP, Winder-Rhodes S, Morrison KE, Morris HR, Williams-Gray CH, Barker RA, Singleton AB, Hardy J, Wood NE, Burn DJ, Chinnery PF. Hudson G, et al. Among authors: singleton ab. Neurology. 2013 May 28;80(22):2042-8. doi: 10.1212/WNL.0b013e318294b434. Epub 2013 May 3. Neurology. 2013. PMID: 23645593 Free PMC article.

2

Case-control study of dopamine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's disease.

Goudreau JL, Maraganore DM, Farrer MJ, Lesnick TG, Singleton AB, Bower JH, Hardy JA, Rocca WA. Goudreau JL, et al. Among authors: singleton ab. Mov Disord. 2002 Nov;17(6):1305-11. doi: 10.1002/mds.10268. Mov Disord. 2002. PMID: 12465073

3

Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients.

Clarimon J, Xiromerisiou G, Eerola J, Gourbali V, Hellström O, Dardiotis E, Peuralinna T, Papadimitriou A, Hadjigeorgiou GM, Tienari PJ, Singleton AB. Clarimon J, et al. Among authors: singleton ab. BMC Neurol. 2005 Jun 20;5:11. doi: 10.1186/1471-2377-5-11. BMC Neurol. 2005. PMID: 15967032 Free PMC article.

4

Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosis.

Garcia ML, Singleton AB, Hernandez D, Ward CM, Evey C, Sapp PA, Hardy J, Brown RH Jr, Cleveland DW. Garcia ML, et al. Among authors: singleton ab. Neurobiol Dis. 2006 Jan;21(1):102-9. doi: 10.1016/j.nbd.2005.06.016. Epub 2005 Aug 3. Neurobiol Dis. 2006. PMID: 16084104

5

Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in Taiwan.

Fung HC, Chen CM, Hardy J, Singleton AB, Lee-Chen GJ, Wu YR. Fung HC, et al. Among authors: singleton ab. Neurosci Lett. 2006 Feb 6;394(1):33-6. doi: 10.1016/j.neulet.2005.10.005. Epub 2005 Oct 27. Neurosci Lett. 2006. PMID: 16257123

6

Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23.

Shatunov A, Sambuughin N, Jankovic J, Elble R, Lee HS, Singleton AB, Dagvadorj A, Ji J, Zhang Y, Kimonis VE, Hardy J, Hallett M, Goldfarb LG. Shatunov A, et al. Among authors: singleton ab. Brain. 2006 Sep;129(Pt 9):2318-31. doi: 10.1093/brain/awl120. Epub 2006 May 15. Brain. 2006. PMID: 16702189 Free article.

7

A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan.

Fung HC, Chen CM, Hardy J, Singleton AB, Wu YR. Fung HC, et al. Among authors: singleton ab. BMC Neurol. 2006 Dec 22;6:47. doi: 10.1186/1471-2377-6-47. BMC Neurol. 2006. PMID: 17187665 Free PMC article.

8

IL1RN VNTR polymorphism in ischemic stroke: analysis in 3 populations.

Worrall BB, Brott TG, Brown RD Jr, Brown WM, Rich SS, Arepalli S, Wavrant-De Vrièze F, Duckworth J, Singleton AB, Hardy J, Meschia JF; SWISS, ISGS, and MSGD Investigators. Worrall BB, et al. Among authors: singleton ab. Stroke. 2007 Apr;38(4):1189-96. doi: 10.1161/01.STR.0000260099.42744.b0. Epub 2007 Mar 1. Stroke. 2007. PMID: 17332449 Free PMC article.

9

DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA.

Camargos S, Scholz S, Simón-Sánchez J, Paisán-Ruiz C, Lewis P, Hernandez D, Ding J, Gibbs JR, Cookson MR, Bras J, Guerreiro R, Oliveira CR, Lees A, Hardy J, Cardoso F, Singleton AB. Camargos S, et al. Among authors: singleton ab. Lancet Neurol. 2008 Mar;7(3):207-15. doi: 10.1016/S1474-4422(08)70022-X. Epub 2008 Feb 1. Lancet Neurol. 2008. PMID: 18243799

10

Genotype-imputation accuracy across worldwide human populations.

Huang L, Li Y, Singleton AB, Hardy JA, Abecasis G, Rosenberg NA, Scheet P. Huang L, et al. Among authors: singleton ab. Am J Hum Genet. 2009 Feb;84(2):235-50. doi: 10.1016/j.ajhg.2009.01.013. Am J Hum Genet. 2009. PMID: 19215730 Free PMC article.

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