Singleton AB - Search Results

1

Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2).

Towns C, Richer M, Jasaityte S, Stafford EJ, Joubert J, Antar T, Martinez-Carrasco A, Makarious MB, Casey B, Vitale D, Levine K, Leonard H, Pantazis CB, Screven LA, Hernandez DG, Wegel CE, Solle J, Nalls MA, Blauwendraat C, Singleton AB, Tan MMX, Iwaki H, Morris HR; Global Parkinson’s Genetics Program (GP2). Towns C, et al. Among authors: singleton ab. NPJ Parkinsons Dis. 2023 Sep 12;9(1):131. doi: 10.1038/s41531-023-00533-w. NPJ Parkinsons Dis. 2023. PMID: 37699923 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

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.

4

Mutation at the SCA17 locus is not a common cause of parkinsonism.

Hernandez D, Hanson M, Singleton A, Gwinn-Hardy K, Freeman J, Ravina B, Doheny D, Gallardo M, Weiser R, Hardy J, Singleton A. Hernandez D, et al. Parkinsonism Relat Disord. 2003 Aug;9(6):317-20. doi: 10.1016/s1353-8020(03)00027-0. Parkinsonism Relat Disord. 2003. PMID: 12853230

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

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

8

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.

9

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

10

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

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