Virtual International Authority File


John Anthony Hardy British geneticist (b. 1954) Wikidata

Hardy, John A. National Library of the Netherlands ISNI

Hardy, John, 1954- National Library of Israel Library of Congress/NACO NUKAT Center of Warsaw University Library

Hardy, John Sudoc [ABES], France

Hardy, John E. R. National Library of Spain

VIAF ID: 9285947 (Personal)


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Title Sources
Animated tales of the world National Library of Spain
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data. Wikidata
Dense-core plaques in Tg2576 and PSAPP mouse models of Alzheimer's disease are centered on vessel walls Wikidata
Differential DJ-1 gene expression in Parkinson's disease. Wikidata
Disentangling the role of the tau gene locus in sporadic tauopathies. Wikidata
Disintegrating brain networks: from syndromes to molecular nexopathies. Wikidata
Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation Wikidata
DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkers. Wikidata
Does the difference between PART and Alzheimer's disease lie in the age-related changes in cerebral arteries that trigger the accumulation of Aβ and propagation of tau? Wikidata
Dopamine and apomorphine do not modulate the uptake of [3H]D-aspartate in the rat striatum in-vitro. Wikidata
Egiptomanía : el fascinante mundo del antiguo Egipto = Egyptomania National Library of Spain
Egypte, splendeurs de l'âge d'or : l'or et les dieux Sudoc [ABES], France
Egypte, voyage au pays des pharaons Sudoc [ABES], France
Egyptomania (Planeta-DeAgustini) National Library of Spain
Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease. Wikidata
Epigenetic mechanisms in Alzheimer's disease: progress but much to do. Wikidata
Erratum: correction: Aβ peptide vaccination prevents memory loss in an animal model of Alzheimer's disease Wikidata
Erratum to "Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome" [Neurobiol. Aging 35 (2014) 1513.e1-1513.e5]. Wikidata
Establishing the role of rare coding variants in known Parkinson's disease risk loci. Wikidata
European voyaging towards Australia : [papers presented at an international colloquium held at the Chateau d'Entrecasteaux, 1987] Sudoc [ABES], France
Evolutionary toggling of the MAPT 17q21.31 inversion region Wikidata
Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to L-DOPA treatment. Wikidata
Exome sequencing in a consanguineous family clinically diagnosed with early-onset Alzheimer's disease identifies a homozygous CTSF mutation Wikidata
Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases Wikidata
Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA. Wikidata
Expression of BRI-amyloid beta peptide fusion proteins: a novel method for specific high-level expression of amyloid beta peptides. Wikidata
Expression of mBRI2 in mice. Wikidata
Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer's disease. Wikidata
Familial clustering of stroke according to proband age at onset of presenting ischemic stroke. Wikidata
Familial frontotemporal dementia associated with a novel presenilin-1 mutation. Wikidata
Familial non-specific dementia maps to chromosome 3 Wikidata
Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations Wikidata
Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus. Wikidata
Frontal temporal dementia: dissecting the aetiology and pathogenesis. Wikidata
Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysis Wikidata
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features Wikidata
Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosis. Wikidata
Full genome screen for Alzheimer disease: Stage II analysis Wikidata
Functional characterization of three single-nucleotide polymorphisms present in the human APOE promoter sequence: Differential effects in neuronal cells and on DNA-protein interactions. Wikidata
Functional Studies of Missense TREM2 Mutations in Human Stem Cell-Derived Microglia. Wikidata
Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs. Wikidata
FUS and TDP43 genetic variability in FTD and CBS Wikidata
G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort. Wikidata
G2019S leucine-rich repeat kinase 2 causes uncoupling protein-mediated mitochondrial depolarization Wikidata
GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers Wikidata
GBA-Associated Parkinson's Disease: Progression in a Deep Brain Stimulation Cohort. Wikidata
Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia. Wikidata
Gene co-expression networks shed light into diseases of brain iron accumulation. Wikidata
Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease. Wikidata
Genes and parkinsonism. Wikidata
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies. Wikidata
Genetic analysis in neurology: the next 10 years. Wikidata
Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R gene. Wikidata
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk Wikidata
Jane Austen's heroines : Intimacy in human relationships Sudoc [ABES], France
L'Egypt National Library of Spain
Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation. Wikidata
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics. Wikidata
Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3. Wikidata
Merlí i els dracs un conte del País de Gal·les National Library of Spain
Neurodegeneration, 2005: Sudoc [ABES], France Library of Congress/NACO National Library of Israel NUKAT Center of Warsaw University Library National Library of the Netherlands Wikidata
De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions Wikidata
A phenotype of atypical apraxia of speech in a family carrying SQSTM1 mutation. Wikidata
A presenilin-1 mutation (T245P) in transmembrane domain 6 causes early onset Alzheimer's disease. Wikidata
Rancid aluminium National Library of Spain
A rapid method for preparing synaptosomes: comparison, with alternative procedures. Wikidata
Studies from Terra Australis to Australia Sudoc [ABES], France
Whole genome association analysis shows that ACE is a risk factor for Alzheimer's disease and fails to replicate most candidates from Meta-analysis Wikidata
Whole genome association studies: deciding when persistence becomes perseveration. Wikidata
Widespread alterations of alpha-synuclein in multiple system atrophy Wikidata
Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations. Wikidata
Widespread sex differences in gene expression and splicing in the adult human brain. Wikidata
Zespoły neurozwyrodnieniowe spowodowane gromadzeniem się żelaza w mózgu - aktualne dane dotyczące objawów klinicznych, podstaw histologicznych i genetycznych oraz możliwości leczenia = Syndromes of Neurodegeneration with Brain Iron Accumulation (NBIA) NUKAT Center of Warsaw University Library
α-Synuclein mutations cluster around a putative protein loop. Wikidata
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy? Wikidata

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