(Q33352050)

26 July 2017

Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's disease (English)

1 reference

26 July 2017

1 reference

Steven J Schrodi

5

0 references

Yonghong Li

object named as

Yonghong Li

1 reference

26 July 2017

Georgios M Hadjigeorgiou

12

object named as

Georgios Hadjigeorgiou

1 reference

26 July 2017

3

Georgia Xiromerisiou

1 reference

26 July 2017

Charles Rowland

2

1 reference

26 July 2017

Robert J Lagier

4

1 reference

26 July 2017

Efthimios Dradiotis

6

1 reference

26 July 2017

David Ross

7

1 reference

26 July 2017

Nam Bui

8

1 reference

26 July 2017

Joseph Catanese

9

1 reference

26 July 2017

Konstantinos Aggelakis

10

1 reference

26 July 2017

Andrew Grupe

11

1 reference

26 July 2017

language of work or name

English

0 references

publication date

16 July 2008

1 reference

26 July 2017

1 reference

26 July 2017

3

1 reference

26 July 2017

e2707

1 reference

26 July 2017

7

1 reference

Creative Commons Attribution 4.0 International

26 July 2017

start time

16 July 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Beyond Parkinson disease: amyotrophic lateral sclerosis and the axon guidance pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

Pathway-based approaches for analysis of genomewide association studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

SORL1 variants and risk of late-onset Alzheimer's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

A genomic pathway approach to a complex disease: axon guidance and Parkinson disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

Replicating genotype-phenotype associations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

Polymorphisms associated with coronary heart disease: better by the score

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

Understanding the molecular causes of Parkinson's disease.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

Genetic evidence for ubiquitin-specific proteases USP24 and USP40 as candidate genes for late-onset Parkinson disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

Genomewide association, Parkinson disease, and PARK10

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

High-resolution whole-genome association study of Parkinson disease.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

A common LRRK2 mutation in idiopathic Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

Molecular Pathways of Neurodegeneration in Parkinson's Disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

High-throughput SNP allele-frequency determination in pooled DNA samples by kinetic PCR.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2442653

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

21 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002707

No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002707

A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002707

BDNF tagging polymorphisms and haplotype analysis in sporadic Parkinson's disease in diverse ethnic groups

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002707

The Tau Gene Haplotype H1 Confers a Susceptibility to Parkinson’s Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002707

Collaborative Analysis of α-Synuclein Gene Promoter Variability and Parkinson Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002707

LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002707

Problems with genome-wide association studies

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18628988

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variants

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18628988

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Polymorphism in semaphorin 5A (Sema5A) gene is not a marker of Parkinson's disease risk

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18628988

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0002707

1 reference

26 July 2017

0 references

1 reference

26 July 2017

1 reference