Singleton AB - Search Results

1

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.

Holmans P, Moskvina V, Jones L, Sharma M; International Parkinson's Disease Genomics Consortium; Vedernikov A, Buchel F, Saad M, Bras JM, Bettella F, Nicolaou N, Simón-Sánchez J, Mittag F, Gibbs JR, Schulte C, Durr A, Guerreiro R, Hernandez D, Brice A, Stefánsson H, Majamaa K, Gasser T, Heutink P, Wood NW, Martinez M, Singleton AB, Nalls MA, Hardy J, Morris HR, Williams NM. Holmans P, et al. Among authors: singleton ab. Hum Mol Genet. 2013 Mar 1;22(5):1039-49. doi: 10.1093/hmg/dds492. Epub 2012 Dec 7. Hum Mol Genet. 2013. PMID: 23223016 Free PMC article.

2

Case-Control study of the extended tau gene haplotype in Parkinson's disease.

Maraganore DM, Hernandez DG, Singleton AB, Farrer MJ, McDonnell SK, Hutton ML, Hardy JA, Rocca WA. Maraganore DM, et al. Among authors: singleton ab. Ann Neurol. 2001 Nov;50(5):658-61. doi: 10.1002/ana.1228. Ann Neurol. 2001. PMID: 11706972

3

X-linked dystonia ("Lubag") presenting predominantly with parkinsonism: a more benign phenotype?

Evidente VG, Gwinn-Hardy K, Hardy J, Hernandez D, Singleton A. Evidente VG, et al. Mov Disord. 2002 Jan;17(1):200-2. doi: 10.1002/mds.1263. Mov Disord. 2002. PMID: 11835466

4

Genes and parkinsonism.

Hardy J, Cookson MR, Singleton A. Hardy J, et al. Lancet Neurol. 2003 Apr;2(4):221-8. doi: 10.1016/s1474-4422(03)00350-8. Lancet Neurol. 2003. PMID: 12849210 Review.

5

Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.

Hague S, Rogaeva E, Hernandez D, Gulick C, Singleton A, Hanson M, Johnson J, Weiser R, Gallardo M, Ravina B, Gwinn-Hardy K, Crawley A, St George-Hyslop PH, Lang AE, Heutink P, Bonifati V, Hardy J, Singleton A. Hague S, et al. Ann Neurol. 2003 Aug;54(2):271-4. doi: 10.1002/ana.10663. Ann Neurol. 2003. PMID: 12891685

6

X-linked recessive dystonia parkinsonism (XDP; Lubag; DYT3).

Singleton A, Hague S, Hernandez D. Singleton A, et al. Adv Neurol. 2004;94:139-42. Adv Neurol. 2004. PMID: 14509666 Review. No abstract available.

7

Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD.

Eerola J, Hernandez D, Launes J, Hellström O, Hague S, Gulick C, Johnson J, Peuralinna T, Hardy J, Tienari PJ, Singleton AB. Eerola J, et al. Among authors: singleton ab. Neurology. 2003 Oct 14;61(7):1000-2. doi: 10.1212/01.wnl.0000083992.28066.7e. Neurology. 2003. PMID: 14557580

8

Polymorphism in the human DJ-1 gene is not associated with sporadic dementia with Lewy bodies or Parkinson's disease.

Morris CM, O'Brien KK, Gibson AM, Hardy JA, Singleton AB. Morris CM, et al. Among authors: singleton ab. Neurosci Lett. 2003 Dec 4;352(2):151-3. doi: 10.1016/j.neulet.2003.08.037. Neurosci Lett. 2003. PMID: 14625045

9

The law of mass action applied to neurodegenerative disease: a hypothesis concerning the etiology and pathogenesis of complex diseases.

Singleton A, Myers A, Hardy J. Singleton A, et al. Hum Mol Genet. 2004 Apr 1;13 Spec No 1:R123-6. doi: 10.1093/hmg/ddh093. Epub 2004 Feb 19. Hum Mol Genet. 2004. PMID: 14976159 Review.

10

Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease.

Clarimon J, Johnson J, Dogu O, Horta W, Khan N, Lees AJ, Hardy J, Singleton A. Clarimon J, et al. Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):120-3. doi: 10.1002/ajmg.b.30119. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15635662

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