Singleton AB - Search Results

1

Multi-ancestry genome-wide association meta-analysis of Parkinson's disease.

Kim JJ, Vitale D, Otani DV, Lian MM, Heilbron K; 23andMe Research Team; Iwaki H, Lake J, Solsberg CW, Leonard H, Makarious MB, Tan EK, Singleton AB, Bandres-Ciga S, Noyce AJ; Global Parkinson’s Genetics Program (GP2); Blauwendraat C, Nalls MA, Foo JN, Mata I. Kim JJ, et al. Among authors: singleton ab. Nat Genet. 2024 Jan;56(1):27-36. doi: 10.1038/s41588-023-01584-8. Epub 2023 Dec 28. Nat Genet. 2024. PMID: 38155330 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

Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians.

Subramony SH, Hernandez D, Adam A, Smith-Jefferson S, Hussey J, Gwinn-Hardy K, Lynch T, McDaniel O, Hardy J, Farrer M, Singleton A. Subramony SH, et al. Mov Disord. 2002 Sep;17(5):1068-71. doi: 10.1002/mds.10241. Mov Disord. 2002. PMID: 12360561

5

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.

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

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.

8

A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion.

Dogu O, Johnson J, Hernandez D, Hanson M, Hardy J, Apaydin H, Özekmekçi S, Sevim S, Gwinn-Hardy K, Singleton A. Dogu O, et al. Mov Disord. 2004 Jul;19(7):812-816. doi: 10.1002/mds.20028. Mov Disord. 2004. PMID: 15254940

9

Analysis of familial and sporadic restless legs syndrome in age of onset, gender, and severity features.

Hanson M, Honour M, Singleton A, Crawley A, Singleton A, Hardy J, Gwinn-Hardy K. Hanson M, et al. J Neurol. 2004 Nov;251(11):1398-401. doi: 10.1007/s00415-004-0552-7. J Neurol. 2004. PMID: 15592737

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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