Genomewide SNP assay reveals mutations underlying Parkinson disease (Q60532590)

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10 January 2020

title

Genomewide SNP assay reveals mutations underlying Parkinson disease (English)

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10 January 2020

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1

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10 January 2020

Sonja W. Scholz

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10 January 2020

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Dena Hernandez

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10 January 2020

author name string

Maria del Mar Matarin

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10 January 2020

Hon-Chung Fung

4

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10 January 2020

J Raphael Gibbs

6

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10 January 2020

Angela Britton

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10 January 2020

John Hardy

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10 January 2020

Andrew Singleton

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publication date

1 February 2008

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10 January 2020

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10 January 2020

volume

29

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10 January 2020

issue

2

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10 January 2020

page(s)

315-322

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

10 January 2020

cites work

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https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

Structural variation in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

Application of genome-wide single nucleotide polymorphism typing: simple association and beyond

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

Epstein-Barr virus: transformation, cytopathic changes, and viral antigens in squirrel monkey and marmoset leukocytes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

Large-scale copy number polymorphism in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

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https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

alpha-Synuclein locus triplication causes Parkinson's disease

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https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

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https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20626

7 January 2021

Identifiers

DOI

10.1002/HUMU.20626

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17994548%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

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