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English
Genetics of parkinsonism
scientific article published on 01 January 2007
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18267242
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18267242%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
review article
1 reference
stated in
Europe PubMed Central
title
Genetics of parkinsonism
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18267242
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18267242%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
main subject
parkinsonian syndrome
1 reference
based on heuristic
inferred from title
author name string
Vincenzo Bonifati
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18267242
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18267242%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
publication date
1 January 2007
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18267242
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18267242%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
published in
Parkinsonism and Related Disorders
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18267242
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18267242%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
volume
13 Suppl 3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18267242
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18267242%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
page(s)
S233-41
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18267242
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18267242%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
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Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
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7 January 2021
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7 January 2021
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alpha-Synuclein locus triplication causes Parkinson's disease
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7 January 2021
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Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease
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7 January 2021
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Multiple regions of alpha-synuclein are associated with Parkinson's disease
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7 January 2021
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Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease
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Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
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7 January 2021
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Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
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7 January 2021
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LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs
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LRRK2 low-penetrance mutations (Gly2019Ser) and risk alleles (Gly2385Arg)-linking familial and sporadic Parkinson's disease
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Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity
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Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
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7 January 2021
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7 January 2021
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7 January 2021
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Deciphering the role of heterozygous mutations in genes associated with parkinsonism
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7 January 2021
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Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers
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7 January 2021
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How much phenotypic variation can be attributed to parkin genotype?
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Hereditary early-onset Parkinson's disease caused by mutations in PINK1
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Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.
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PINK1 protects against oxidative stress by phosphorylating mitochondrial chaperone TRAP1
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7 January 2021
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Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
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7 January 2021
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Linking DJ-1 to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinson's disease
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7 January 2021
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DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex.
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7 January 2021
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Association of PINK1 and DJ-1 confers digenic inheritance of early-onset Parkinson's disease
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7 January 2021
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Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
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7 January 2021
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7 January 2021
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A susceptibility locus for Parkinson's disease maps to chromosome 2p13.
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7 January 2021
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A susceptibility gene for late-onset idiopathic Parkinson's disease
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7 January 2021
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Significant linkage of Parkinson disease to chromosome 2q36-37
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7 January 2021
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Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families
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7 January 2021
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7 January 2021
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The ubiquitin pathway in Parkinson's disease
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Crossref
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7 January 2021
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Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1353-8020%2808%2970008-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in NR4A2 associated with familial Parkinson disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1353-8020%2808%2970008-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1353-8020%2808%2970008-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1353-8020%2808%2970008-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Glucocerebrosidase mutations are an important risk factor for Lewy body disorders.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1353-8020%2808%2970008-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
The genetic basis of Parkinson's disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1353-8020%2808%2970008-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Shaking the tree: mapping complex disease genes with linkage disequilibrium
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS1353-8020%2808%2970008-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
High-resolution whole-genome association study of Parkinson disease.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1353-8020%2808%2970008-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1353-8020%2808%2970008-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic testing in Parkinson's disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1353-8020%2808%2970008-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic testing in Parkinson disease: promises and pitfalls
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS1353-8020%2808%2970008-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
The genetics of Parkinson disease: Implications for neurological care
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1353-8020%2808%2970008-7
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7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1353-8020(08)70008-7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18267242
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18267242%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
PubMed publication ID
18267242
1 reference
stated in
Europe PubMed Central
PubMed publication ID
18267242
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18267242%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
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