(Q83191880)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16633828%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16633828%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

1

1 reference

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19 January 2020

12

Ben A Oostra

1 reference

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19 January 2020

author name string

Yah-Huei Wu-Chou

2

1 reference

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19 January 2020

Chin-Song Lu

3

1 reference

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19 January 2020

Marina van Doeselaar

4

1 reference

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19 January 2020

Erik J Simons

5

1 reference

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19 January 2020

Christan F Rohé

6

1 reference

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19 January 2020

Hsiu-Chen Chang

7

1 reference

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19 January 2020

Rou-Shayn Chen

8

1 reference

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19 January 2020

Yi-Hsin Weng

9

1 reference

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19 January 2020

Nicola Vanacore

10

1 reference

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19 January 2020

Guido J Breedveld

11

1 reference

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19 January 2020

Vincenzo Bonifati

13

1 reference

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19 January 2020

publication date

22 April 2006

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19 January 2020

1 reference

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19 January 2020

volume

7

1 reference

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19 January 2020

page(s)

133-138

1 reference

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19 January 2020

issue

3

1 reference

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https://scigraph.springernature.com/pub.10.1007/s10048-006-0041-5

19 January 2020

exact match

0 references

cites work

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease

1 reference

12 December 2020

A common LRRK2 mutation in idiopathic Parkinson's disease

1 reference

12 December 2020

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

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Lrrk2 pathogenic substitutions in Parkinson's disease

1 reference

12 December 2020

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

12 December 2020

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

1 reference

12 December 2020

LRRK2 mutations in Parkinson disease

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity

1 reference

12 December 2020

Genetic association studies of complex traits: design and analysis issues

1 reference

12 December 2020

The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease

1 reference

12 December 2020

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

1 reference

12 December 2020

The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.

1 reference

12 December 2020

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

12 December 2020

An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family.

1 reference

12 December 2020

The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S10048-006-0041-5

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16633828%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference