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English
Considerations for genomewide association studies in Parkinson disease
scientific article published on June 2006
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1474090
retrieved
30 October 2017
title
Considerations for genomewide association studies in Parkinson disease
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1474090
retrieved
30 October 2017
main subject
Parkinson's disease
1 reference
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inferred from title
author
Richard H Myers
object named as
Richard H Myers
series ordinal
1
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language of work or name
English
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publication date
1 June 2006
1 reference
stated in
Europe PubMed Central
PMCID
1474090
retrieved
30 October 2017
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1474090
retrieved
30 October 2017
volume
78
1 reference
stated in
Europe PubMed Central
PMCID
1474090
retrieved
30 October 2017
page(s)
1081-1082
1 reference
stated in
Europe PubMed Central
PMCID
1474090
retrieved
30 October 2017
issue
6
1 reference
stated in
Europe PubMed Central
PMCID
1474090
retrieved
30 October 2017
cites work
Genomewide association, Parkinson disease, and PARK10
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474090
retrieved
28 May 2018
Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474090
retrieved
28 May 2018
High-resolution whole-genome association study of Parkinson disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474090
retrieved
28 May 2018
Blood is thicker than water: the strengths of family-based case-control studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474090
retrieved
28 May 2018
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474090
retrieved
28 May 2018
Parkinson's disease: piecing together a genetic jigsaw
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474090
retrieved
28 May 2018
Segregation analysis of Parkinson disease revealing evidence for a major causative gene.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474090
retrieved
28 May 2018
A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474090
retrieved
16 August 2018
No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1474090
retrieved
16 August 2018
Identifiers
DOI
10.1086/504730
1 reference
stated in
Europe PubMed Central
PMCID
1474090
retrieved
30 October 2017
PMCID
1474090
1 reference
stated in
Europe PubMed Central
PMCID
1474090
retrieved
30 October 2017
PubMed ID
16685659
1 reference
stated in
Europe PubMed Central
PMCID
1474090
retrieved
30 October 2017
ResearchGate publication ID
7094888
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