(Q37786653)

23 August 2017

Copy number variation in Parkinson's disease (English)

1 reference

23 August 2017

1 reference

1

Mathias Toft

1 reference

23 August 2017

2

Owen A Ross

1 reference

23 August 2017

6 September 2010

1 reference

23 August 2017

1 reference

23 August 2017

2

1 reference

23 August 2017

9

1 reference

23 August 2017

62

1 reference

https://scigraph.springernature.com/pub.10.1186/gm183

23 August 2017

0 references

cites work

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

Hotspots of large rare deletions in the human genome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

Genome-wide association study reveals genetic risk underlying Parkinson's disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

Mechanisms of change in gene copy number

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

Genomic investigation of alpha-synuclein multiplication and parkinsonism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

Genetics of Parkinson disease: paradigm shifts and future prospects.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

Distribution, type, and origin of Parkin mutations: review and case studies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

Large-scale copy number polymorphism in the human genome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

alpha-Synuclein locus triplication causes Parkinson's disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

Expanding the clinical phenotype of SNCA duplication carriers

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

A new complex homozygous large rearrangement of the PINK1 gene in a Sudanese family with early onset Parkinson's disease

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's disease.

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092113

Whole gene deletion and splicing mutations expand the PINK1 genotypic spectrum

1 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20828427

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genomewide SNP assay reveals mutations underlying Parkinson disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20828427

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/GM183

1 reference

PMC publication ID

3092113

Dimensions Publication ID

23 August 2017

0 references

1 reference

PMC publication ID

3092113

23 August 2017

PubMed publication ID

20828427

1 reference

PMC publication ID

3092113