Hardy J - Search Results

1

Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets.

Kia DA, Zhang D, Guelfi S, Manzoni C, Hubbard L, Reynolds RH, Botía J, Ryten M, Ferrari R, Lewis PA, Williams N, Trabzuni D, Hardy J, Wood NW; United Kingdom Brain Expression Consortium (UKBEC) and the International Parkinson’s Disease Genomics Consortium (IPDGC). Kia DA, et al. Among authors: hardy j. JAMA Neurol. 2021 Apr 1;78(4):464-472. doi: 10.1001/jamaneurol.2020.5257. JAMA Neurol. 2021. PMID: 33523105 Free PMC article.

2

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: hardy j. Mov Disord. 2002 Jan;17(1):200-2. doi: 10.1002/mds.1263. Mov Disord. 2002. PMID: 11835466

3

The tau locus is not significantly associated with pathologically confirmed sporadic Parkinson's disease.

de Silva R, Hardy J, Crook J, Khan N, Graham EA, Morris CM, Wood NW, Lees AJ. de Silva R, et al. Among authors: hardy j. Neurosci Lett. 2002 Sep 20;330(2):201-3. doi: 10.1016/s0304-3940(02)00742-5. Neurosci Lett. 2002. PMID: 12231446

4

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: hardy j. Mov Disord. 2002 Sep;17(5):1068-71. doi: 10.1002/mds.10241. Mov Disord. 2002. PMID: 12360561

5

Ethnic differences and disease phenotypes.

Hardy J, Singleton A, Gwinn-Hardy K. Hardy J, et al. Science. 2003 May 2;300(5620):739-40. doi: 10.1126/science.300.5620.739. Science. 2003. PMID: 12730580 No abstract available.

6

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.

7

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. Among authors: hardy j. Ann Neurol. 2003 Aug;54(2):271-4. doi: 10.1002/ana.10663. Ann Neurol. 2003. PMID: 12891685

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. 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.

9

The structure of the tau haplotype in controls and in progressive supranuclear palsy.

Pittman AM, Myers AJ, Duckworth J, Bryden L, Hanson M, Abou-Sleiman P, Wood NW, Hardy J, Lees A, de Silva R. Pittman AM, et al. Among authors: hardy j. Hum Mol Genet. 2004 Jun 15;13(12):1267-74. doi: 10.1093/hmg/ddh138. Epub 2004 Apr 28. Hum Mol Genet. 2004. PMID: 15115761

10

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

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