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836 results
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Application of genome-wide single nucleotide polymorphism typing: simple association and beyond.
Gibbs JR, Singleton A. Gibbs JR, et al. Among authors: singleton a. PLoS Genet. 2006 Oct 6;2(10):e150. doi: 10.1371/journal.pgen.0020150. PLoS Genet. 2006. PMID: 17029559 Free PMC article. Review.
Familiality in simple and complex disease.
Singleton A. Singleton A. Clin Auton Res. 2003 Apr;13(2):88-90. doi: 10.1007/s10286-003-0091-9. Clin Auton Res. 2003. PMID: 12720091 Review.
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.
alpha-Synuclein locus triplication causes Parkinson's disease.
Singleton AB, Farrer M, Johnson J, Singleton A, Hague S, Kachergus J, Hulihan M, Peuralinna T, Dutra A, Nussbaum R, Lincoln S, Crawley A, Hanson M, Maraganore D, Adler C, Cookson MR, Muenter M, Baptista M, Miller D, Blancato J, Hardy J, Gwinn-Hardy K. Singleton AB, et al. Among authors: singleton a. Science. 2003 Oct 31;302(5646):841. doi: 10.1126/science.1090278. Science. 2003. PMID: 14593171 No abstract available.
Confirmation of the protective effect of iNOS in an independent cohort of Parkinson disease.
Hague S, Peuralinna T, Eerola J, Hellström O, Tienari PJ, Singleton AB. Hague S, et al. Among authors: singleton ab. Neurology. 2004 Feb 24;62(4):635-6. doi: 10.1212/01.wnl.0000110191.38152.29. Neurology. 2004. PMID: 14981185
No evidence for tau duplications in frontal temporal dementia families showing genetic linkage to the tau locus in which tau mutations have not been found.
Johnson J, Ostojic J, Lannfelt L, Glaser A, Basun H, Rogaeva E, Kawarai T, Bruni A, St George Hyslop PH, Goate A, Pastor P, Chakraverty S, Norton J, Morris JC, Hardy J, Singleton A. Johnson J, et al. Among authors: singleton a. Neurosci Lett. 2004 Jun 10;363(2):99-101. doi: 10.1016/j.neulet.2004.03.070. Neurosci Lett. 2004. PMID: 15172093
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. Among authors: singleton a. Mov Disord. 2004 Jul;19(7):812-816. doi: 10.1002/mds.20028. Mov Disord. 2004. PMID: 15254940
The tau H2 haplotype is almost exclusively Caucasian in origin.
Evans W, Fung HC, Steele J, Eerola J, Tienari P, Pittman A, Silva Rd, Myers A, Vrieze FW, Singleton A, Hardy J. Evans W, et al. Among authors: singleton a. Neurosci Lett. 2004 Oct 21;369(3):183-5. doi: 10.1016/j.neulet.2004.05.119. Neurosci Lett. 2004. PMID: 15464261
Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.
Hernandez DG, Paisán-Ruíz C, McInerney-Leo A, Jain S, Meyer-Lindenberg A, Evans EW, Berman KF, Johnson J, Auburger G, Schäffer AA, Lopez GJ, Nussbaum RL, Singleton AB. Hernandez DG, et al. Among authors: singleton ab. Ann Neurol. 2005 Mar;57(3):453-6. doi: 10.1002/ana.20401. Ann Neurol. 2005. PMID: 15732108
Torsin A haplotype predisposes to idiopathic dystonia.
Clarimon J, Asgeirsson H, Singleton A, Jakobsson F, Hjaltason H, Hardy J, Sveinbjornsdottir S. Clarimon J, et al. Among authors: singleton a. Ann Neurol. 2005 May;57(5):765-7. doi: 10.1002/ana.20485. Ann Neurol. 2005. PMID: 15852391
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