Hardy J - Search Results

1

Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at 16q11.2 and MAPT H1 loci.

Soutar MPM, Melandri D, O'Callaghan B, Annuario E, Monaghan AE, Welsh NJ, D'Sa K, Guelfi S, Zhang D, Pittman A, Trabzuni D, Verboven AHA, Pan KS, Kia DA, Bictash M, Gandhi S, Houlden H, Cookson MR, Kasri NN, Wood NW, Singleton AB, Hardy J, Whiting PJ, Blauwendraat C, Whitworth AJ, Manzoni C, Ryten M, Lewis PA, Plun-Favreau H. Soutar MPM, et al. Among authors: hardy j. Brain. 2022 Dec 19;145(12):4349-4367. doi: 10.1093/brain/awac325. Brain. 2022. PMID: 36074904 Free PMC article.

2

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

3

Presenilin 1 mutation in an african american family presenting with atypical Alzheimer dementia.

Rippon GA, Crook R, Baker M, Halvorsen E, Chin S, Hutton M, Houlden H, Hardy J, Lynch T. Rippon GA, et al. Among authors: hardy j. Arch Neurol. 2003 Jun;60(6):884-8. doi: 10.1001/archneur.60.6.884. Arch Neurol. 2003. PMID: 12810495

4

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.

5

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

6

Association between cardiac denervation and parkinsonism caused by alpha-synuclein gene triplication.

Singleton A, Gwinn-Hardy K, Sharabi Y, Li ST, Holmes C, Dendi R, Hardy J, Singleton A, Crawley A, Goldstein DS. Singleton A, et al. Among authors: hardy j. Brain. 2004 Apr;127(Pt 4):768-72. doi: 10.1093/brain/awh081. Epub 2004 Jan 21. Brain. 2004. PMID: 14736756

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

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

10

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

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