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Whole genome analysis in a consanguineous family with early onset Alzheimer's disease.
Clarimón J, Djaldetti R, Lleó A, Guerreiro RJ, Molinuevo JL, Paisán-Ruiz C, Gómez-Isla T, Blesa R, Singleton A, Hardy J. Clarimón J, et al. Among authors: singleton a. Neurobiol Aging. 2009 Dec;30(12):1986-91. doi: 10.1016/j.neurobiolaging.2008.02.008. Epub 2008 Apr 2. Neurobiol Aging. 2009. PMID: 18387709 Free PMC article.
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretion.
De Jonghe C, Cruts M, Rogaeva EA, Tysoe C, Singleton A, Vanderstichele H, Meschino W, Dermaut B, Vanderhoeven I, Backhovens H, Vanmechelen E, Morris CM, Hardy J, Rubinsztein DC, St George-Hyslop PH, Van Broeckhoven C. De Jonghe C, et al. Among authors: singleton a. Hum Mol Genet. 1999 Aug;8(8):1529-40. doi: 10.1093/hmg/8.8.1529. Hum Mol Genet. 1999. PMID: 10401002
Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese.
Gwinn-Hardy K, Chen JY, Liu HC, Liu TY, Boss M, Seltzer W, Adam A, Singleton A, Koroshetz W, Waters C, Hardy J, Farrer M. Gwinn-Hardy K, et al. Among authors: singleton a. Neurology. 2000 Sep 26;55(6):800-5. doi: 10.1212/wnl.55.6.800. Neurology. 2000. PMID: 10993999
Genetic analysis of synphilin-1 in familial Parkinson's disease.
Farrer M, Destée A, Levecque C, Singleton A, Engelender S, Becquet E, Mouroux V, Richard F, Defebvre L, Crook R, Hernandez D, Ross CA, Hardy J, Amouyel P, Chartier-Harlin MC. Farrer M, et al. Among authors: singleton a. Neurobiol Dis. 2001 Apr;8(2):317-23. doi: 10.1006/nbdi.2000.0326. Neurobiol Dis. 2001. PMID: 11300726
The genetics of ischaemic stroke.
Matarin M, Singleton A, Hardy J, Meschia J. Matarin M, et al. Among authors: singleton a. J Intern Med. 2010 Feb;267(2):139-55. doi: 10.1111/j.1365-2796.2009.02202.x. J Intern Med. 2010. PMID: 20175863 Free PMC article. Review.
1,008 results