Hardy J - Search Results

1

Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage.

Chen Z, Zhang D, Reynolds RH, Gustavsson EK, García-Ruiz S, D'Sa K, Fairbrother-Browne A, Vandrovcova J; International Parkinson’s Disease Genomics Consortium (IPDGC); Hardy J, Houlden H, Gagliano Taliun SA, Botía J, Ryten M. Chen Z, et al. Among authors: hardy j. Nat Commun. 2021 Apr 6;12(1):2076. doi: 10.1038/s41467-021-22262-5. Nat Commun. 2021. PMID: 33824317 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

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.

8

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

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

Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease.

Martinez M, Brice A, Vaughan JR, Zimprich A, Breteler MM, Meco G, Filla A, Farrer MJ, Bétard C, Singleton A, Hardy J, De Michele G, Bonifati V, Oostra BA, Gasser T, Wood NW, Dürr A. Martinez M, et al. Among authors: hardy j. Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 5;136B(1):72-4. doi: 10.1002/ajmg.b.30196. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15924299

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