Singleton A - Search Results

1

Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies.

Bras J, Guerreiro R, Darwent L, Parkkinen L, Ansorge O, Escott-Price V, Hernandez DG, Nalls MA, Clark LN, Honig LS, Marder K, Van Der Flier WM, Lemstra A, Scheltens P, Rogaeva E, St George-Hyslop P, Londos E, Zetterberg H, Ortega-Cubero S, Pastor P, Ferman TJ, Graff-Radford NR, Ross OA, Barber I, Braae A, Brown K, Morgan K, Maetzler W, Berg D, Troakes C, Al-Sarraj S, Lashley T, Compta Y, Revesz T, Lees A, Cairns N, Halliday GM, Mann D, Pickering-Brown S, Dickson DW, Singleton A, Hardy J. Bras J, et al. Among authors: singleton a. Hum Mol Genet. 2014 Dec 1;23(23):6139-46. doi: 10.1093/hmg/ddu334. Epub 2014 Jun 27. Hum Mol Genet. 2014. PMID: 24973356 Free PMC article.

2

No association between a polymorphism in the presenilin 1 gene and dementia with Lewy bodies.

Singleton AB, Lamb H, Leake A, McKeith IG, Ince PG, Perry RH, Morris CM. Singleton AB, et al. Neuroreport. 1997 Nov 10;8(16):3637-9. doi: 10.1097/00001756-199711100-00042. Neuroreport. 1997. PMID: 9427340

3

Apolipoprotein E and alpha-1 antichymotrypsin polymorphism genotyping in Alzheimer's disease and in dementia with Lewy bodies. Distinctions between diseases.

Lamb H, Christie J, Singleton AB, Leake A, Perry RH, Ince PG, McKeith IG, Melton LM, Edwardson JA, Morris CM. Lamb H, et al. Among authors: singleton ab. Neurology. 1998 Feb;50(2):388-91. doi: 10.1212/wnl.50.2.388. Neurology. 1998. PMID: 9484359

4

No association between the K variant of the butyrylcholinesterase gene and pathologically confirmed Alzheimer's disease.

Singleton AB, Smith G, Gibson AM, Woodward R, Perry RH, Ince PG, Edwardson JA, Morris CM. Singleton AB, et al. Hum Mol Genet. 1998 May;7(5):937-9. doi: 10.1093/hmg/7.5.937. Hum Mol Genet. 1998. PMID: 9536100

5

Alpha2-macroglobulin polymorphisms in Alzheimer's disease and dementia with Lewy bodies.

Singleton AB, Gibson AM, McKeith IG, Ballard CA, Perry RH, Ince PG, Edwardson JA, Morris CM. Singleton AB, et al. Neuroreport. 1999 May 14;10(7):1507-10. doi: 10.1097/00001756-199905140-00021. Neuroreport. 1999. PMID: 10380971

6

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

7

Transfected synphilin-1 forms cytoplasmic inclusions in HEK293 cells.

O'Farrell C, Murphy DD, Petrucelli L, Singleton AB, Hussey J, Farrer M, Hardy J, Dickson DW, Cookson MR. O'Farrell C, et al. Among authors: singleton ab. Brain Res Mol Brain Res. 2001 Dec 16;97(1):94-102. doi: 10.1016/s0169-328x(01)00292-3. Brain Res Mol Brain Res. 2001. PMID: 11744167

8

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. Among authors: singleton a. Mov Disord. 2002 Jan;17(1):200-2. doi: 10.1002/mds.1263. Mov Disord. 2002. PMID: 11835466

9

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. Among authors: singleton a. Mov Disord. 2002 Sep;17(5):1068-71. doi: 10.1002/mds.10241. Mov Disord. 2002. PMID: 12360561

10

Clinical and neuropathological correlates of apolipoprotein E genotype in dementia with Lewy bodies.

Singleton AB, Wharton A, O'Brien KK, Walker MP, McKeith IG, Ballard CG, O'Brien J, Perry RH, Ince PG, Edwardson JA, Morris CM. Singleton AB, et al. Dement Geriatr Cogn Disord. 2002;14(4):167-75. doi: 10.1159/000066022. Dement Geriatr Cogn Disord. 2002. PMID: 12411758

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