Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humansBehavioral variant frontotemporal lobar degeneration with amyotrophic lateral sclerosis with a chromosome 9p21 hexanucleotide repeatAnalysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTDTREM2 Variants in Alzheimer's DiseaseThe ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic dataThe expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's diseaseAnalysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individualsRare coding variants in the phospholipase D3 gene confer risk for Alzheimer's diseaseThe Parkinson's disease-linked proteins Fbxo7 and Parkin interact to mediate mitophagyPathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levelsA missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaG2019S leucine-rich repeat kinase 2 causes uncoupling protein-mediated mitochondrial depolarizationA scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene familyFrequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyMutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystoniaImputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studiesGenome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's diseaseFrontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological featuresReelin and stk25 have opposing roles in neuronal polarization and dendritic Golgi deploymentA hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDA nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial diseaseGenome-wide association study reveals genetic risk underlying Parkinson's diseaseA two-stage genome-wide association study of sporadic amyotrophic lateral sclerosisCandidate gene polymorphisms for ischemic stroke.GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriersA genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorderGlucocerebrosidase mutations in clinical and pathologically proven Parkinson's diseaseEvolutionary toggling of the MAPT 17q21.31 inversion regionThe Ischemic Stroke Genetics Study (ISGS) Protocol.The Siblings With Ischemic Stroke Study (SWISS) protocolIntracerebral haemorrhage in Down syndrome: protected or predisposed?The amyloid hypothesis of Alzheimer's disease at 25 yearsThe importance of understanding individual differences in Down syndromeA genetic cause of Alzheimer disease: mechanistic insights from Down syndromeTDP-43 pathology in a patient carrying G2019S LRRK2 mutation and a novel p.Q124E MAPTStemBANCC: Governing Access to Material and Data in a Large Stem Cell Research ConsortiumRecursive splicing in long vertebrate genes.Novel genetic loci underlying human intracranial volume identified through genome-wide associationTime to redefine PD? Introductory statement of the MDS Task Force on the definition of Parkinson's disease.
P50
Q21092490-36EE0C7D-3765-41DD-8BED-315F22FF555EQ21129431-BF10E858-9BF1-419C-84A7-456A03B3F113Q21261387-B49F1939-3C04-452A-B43C-61308D896E7FQ22250873-B8B803BC-07FF-4D15-B2C7-F5DE9224466AQ24289484-D532E724-F311-4F26-A9AA-95F3E7CABF56Q24301425-0F1717F6-CCBC-4511-98B8-C639E75740E6Q24305513-EB37344A-0B38-48EF-8082-549AB357FD57Q24312938-83667FCD-A13C-462C-896D-5EF629A8C1DDQ24316726-B48FAC57-2D92-45ED-9A8E-0FB81EE00667Q24336201-6E19ED3E-EA37-476A-B6BC-619E29F6A1FEQ24337555-DC240A29-9B58-4988-9D65-C8F2B8DD8D55Q24339009-EEC723A0-DAB3-4C38-BEDF-19F18E44E1C5Q24540512-46683EC1-8F41-41C0-A0CF-A4235396FB47Q24562672-7EEB1AE3-F25E-486C-80F8-646F96322A49Q24600803-F59A4C7D-B934-40C8-9371-4AF27E797A10Q24605412-272C48E1-8D77-4328-BB9A-00C33D19CC3DQ24606055-F016A73A-4CC3-4D64-B6C1-753F54BAC378Q24612662-BBFEF594-78BF-4E3F-90E9-9D3EDACB3873Q24630410-ECB57869-1BD8-4248-A03F-6367F8AF4C54Q24630634-6B35478E-E561-407A-B0EF-064B4F11742BQ24634583-6467B1AC-3DEB-44D9-BDA2-3774C1BC4969Q24645475-AA1880AC-7A4F-433D-8108-B55BE44F8481Q24646654-CF1981D4-C9FD-4FDD-A35A-A9124E621E37Q24648667-A6DE0E70-272B-4157-86D7-E1B539F84AFAQ24649888-09F2ACBB-48FF-4051-A0D7-10AC180A6268Q24654145-31D27566-7FE9-4DC7-8BD7-92BF0A20CC63Q24655759-F238C093-8B3F-4A11-AA4B-8551614F48D5Q24656668-D41904D0-DBBA-499A-9251-692764F13730Q24658093-505AFE68-00AF-45B0-BE34-AB035CD84355Q24794936-DA16B9E1-1DBC-4BA2-9101-C363255BCD56Q24803218-368DBB40-3062-49D7-A7D5-9B4D12F48A46Q26745369-2E110BD8-20A9-497A-BD33-49334C0712B7Q26749528-51841921-F6C3-4C18-AA04-3F969E220A3CQ26750601-19201064-B564-48D7-AC9D-A657C3FBA2D6Q26798983-1DF3F9C9-4120-46ED-8645-AA0BB1728FDAQ26851112-43A2DB78-8818-4D71-BE20-5BA2BA4A4364Q26864136-E0EF9520-6A15-40BA-8668-24EA938BC0C5Q27316614-8140007F-1AEB-4F9B-8E61-82BB729C002EQ27653381-8EEF342C-C99D-4369-A3FD-E7319C3396B6Q27686808-C46ABBE4-CBF7-41D6-9E2A-CC29C8C9D07B
P50
description
Amerikaans klinische genetica
@nl
British geneticist (b. 1954)
@en
britisch-US-amerikanischer Genetiker, Molekularbiologe und Alzheimer-Forscher
@de
britisk genetiker
@da
généticien
@fr
name
John Anthony Hardy
@en
John Hardy
@ast
John Hardy
@ca
John Hardy
@da
John Hardy
@de
John Hardy
@es
John Hardy
@fo
John Hardy
@fr
John Hardy
@is
John Hardy
@it
type
label
John Anthony Hardy
@en
John Hardy
@ast
John Hardy
@ca
John Hardy
@da
John Hardy
@de
John Hardy
@es
John Hardy
@fo
John Hardy
@fr
John Hardy
@is
John Hardy
@it
altLabel
Hardy J
@en
Hardy J. A.
@en
Hardy J.
@en
Hardy JA
@en
Hardy
@en
J A Hardy
@en
J Hardy
@en
J. A. Hardy
@en
J. Hardy
@en
John A Hardy
@en
prefLabel
John Anthony Hardy
@en
John Hardy
@ast
John Hardy
@ca
John Hardy
@da
John Hardy
@de
John Hardy
@es
John Hardy
@fo
John Hardy
@fr
John Hardy
@is
John Hardy
@it
P108
P166
P1006
P214
P244
P269
P1006
P1153
56210513900
P1207
n2005108398
P1412
P166
P2070
john-hardy-11582
P21
P213
0000 0001 1742 0077
P214
P244
n2006180219