Comprehensive analysis of LRRK2 in publicly available Parkinson's disease cases and neurologically normal controls (Q80535570)

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1 January 2020

title

Comprehensive analysis of LRRK2 in publicly available Parkinson's disease cases and neurologically normal controls (English)

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1 January 2020

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Coro Paisán-Ruíz

1

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1 January 2020

Priti Nath

2

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1 January 2020

Nicole Washecka

3

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1 January 2020

J Raphael Gibbs

4

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1 January 2020

Andrew B Singleton

5

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1 January 2020

publication date

1 April 2008

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1 January 2020

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1 January 2020

volume

29

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1 January 2020

issue

4

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1 January 2020

page(s)

485-490

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Haploview: analysis and visualization of LD and haplotype maps

1 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

Common variants of LRRK2 are not associated with sporadic Parkinson's disease

1 reference

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7 January 2021

G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

Frequency of LRRK2 mutations in early- and late-onset Parkinson disease.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

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.20668

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.20668

7 January 2021

The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

Reporting and interpretation of genetic variants in cases and controls

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease

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https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.

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https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

Comprehensive screening of a North American Parkinson's disease cohort for LRRK2 mutation.

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https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations

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https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics

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https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

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.20668

7 January 2021

LRRK2 gene in Parkinson disease: Mutation analysis and case control association study

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibrium

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

Analysis of LRRK2 functional domains in nondominant Parkinson disease.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20668

7 January 2021

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

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7 January 2021

Identifiers

DOI

10.1002/HUMU.20668

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18213618%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference