Hardy J - Search Results

1

Investigation of the genetic aetiology of Lewy body diseases with and without dementia.

Wu L, Real R, Martinez A, Chia R, Lawton MA, Shoai M, Bresner C, Hubbard L, Blauwendraat C, Singleton AB, Ryten M, Scholz SW, Traynor BJ, Williams N, Hu MTM, Ben-Shlomo Y, Grosset DG, Hardy J, Morris HR; International LBD Genomic Consortium. Wu L, et al. Among authors: hardy j. medRxiv [Preprint]. 2023 Oct 27:2023.10.17.23297157. doi: 10.1101/2023.10.17.23297157. medRxiv. 2023. Update in: Brain Commun. 2024 May 31;6(4):fcae190. doi: 10.1093/braincomms/fcae190 PMID: 37987016 Free PMC article. Updated. Preprint.

2

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.

3

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. Among authors: hardy j. 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.

4

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: hardy j. Mov Disord. 2004 Jul;19(7):812-816. doi: 10.1002/mds.20028. Mov Disord. 2004. PMID: 15254940

5

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: hardy j. Neurosci Lett. 2004 Oct 21;369(3):183-5. doi: 10.1016/j.neulet.2004.05.119. Neurosci Lett. 2004. PMID: 15464261

6

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. Among authors: hardy j. J Neurol. 2004 Nov;251(11):1398-401. doi: 10.1007/s00415-004-0552-7. J Neurol. 2004. PMID: 15592737

7

Genome-wide analysis of the parkinsonism-dementia complex of Guam.

Morris HR, Steele JC, Crook R, Wavrant-De Vrièze F, Onstead-Cardinale L, Gwinn-Hardy K, Wood NW, Farrer M, Lees AJ, McGeer PL, Siddique T, Hardy J, Perez-Tur J. Morris HR, et al. Among authors: hardy j. Arch Neurol. 2004 Dec;61(12):1889-97. doi: 10.1001/archneur.61.12.1889. Arch Neurol. 2004. PMID: 15596609

8

Unaltered alpha-synuclein blood levels in juvenile Parkinsonism with a parkin exon 4 deletion.

Miller DW, Crawley A, Gwinn-Hardy K, Lopez G, Nussbaum R, Cookson MR, Singleton AB, Hardy J, Dogu O. Miller DW, et al. Among authors: hardy j. Neurosci Lett. 2005 Feb 21;374(3):189-91. doi: 10.1016/j.neulet.2004.10.053. Epub 2004 Nov 19. Neurosci Lett. 2005. PMID: 15663960

9

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: hardy j. Ann Neurol. 2005 May;57(5):765-7. doi: 10.1002/ana.20485. Ann Neurol. 2005. PMID: 15852391

10

Mutation analysis of patients with neuronal intermediate filament inclusion disease (NIFID).

Momeni P, Cairns NJ, Perry RH, Bigio EH, Gearing M, Singleton AB, Hardy J. Momeni P, et al. Among authors: hardy j. Neurobiol Aging. 2006 May;27(5):778.e1-778.e6. doi: 10.1016/j.neurobiolaging.2005.03.030. Epub 2005 Jul 7. Neurobiol Aging. 2006. PMID: 16005115

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