(Q37531309)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

title

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

1 reference

parkinsonian syndrome

1 reference

30

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Matthew J. Farrer

33

1 reference

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4 January 2020

Kristoffer Haugarvoll

1

1 reference

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4 January 2020

Stefano Goldwurm

10

1 reference

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4 January 2020

Uwe Walter

14

1 reference

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4 January 2020

Daniela Berg

1 reference

ORCID Public Data File 2021

author name string

R Rademakers

2

1 reference

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4 January 2020

J M Kachergus

3

1 reference

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4 January 2020

K Nuytemans

4

1 reference

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4 January 2020

O A Ross

5

1 reference

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4 January 2020

J M Gibson

6

1 reference

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4 January 2020

E-K Tan

7

1 reference

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4 January 2020

C Gaig

8

1 reference

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4 January 2020

E Tolosa

9

1 reference

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4 January 2020

M Guidi

11

1 reference

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4 January 2020

G Riboldazzi

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

L Brown

13

1 reference

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4 January 2020

R Benecke

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

D Berg

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

T Gasser

17

1 reference

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4 January 2020

J Theuns

18

1 reference

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4 January 2020

P Pals

19

1 reference

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4 January 2020

P Cras

20

1 reference

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4 January 2020

P Paul De Deyn

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

S Engelborghs

22

1 reference

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4 January 2020

B Pickut

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

R J Uitti

24

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

T Foroud

25

1 reference

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4 January 2020

W C Nichols

26

1 reference

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4 January 2020

J Hagenah

27

1 reference

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4 January 2020

C Klein

28

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

A Samii

29

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

V Bonifati

31

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

C Van Broeckhoven

32

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Z K Wszolek

34

1 reference

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4 January 2020

language of work or name

English

0 references

publication date

12 March 2008

1 reference

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4 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

volume

70

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

issue

16 Pt 2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

page(s)

1456-1460

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

LRRK2 phosphorylates moesin at threonine-558: characterization of how Parkinson's disease mutants affect kinase activity

4 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

GTP binding is essential to the protein kinase activity of LRRK2, a causative gene product for familial Parkinson's disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

LRRK2 in Parkinson's disease: protein domains and functional insights

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

A New Statistical Method for Haplotype Reconstruction from Population Data

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

Diagnostic criteria for Parkinson disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

Parkinsonism: onset, progression, and mortality

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

Leucine-rich repeat kinase 2 (LRRK2)/PARK8 possesses GTPase activity that is altered in familial Parkinson's disease R1441C/G mutants

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

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

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease.

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

Leucine-rich repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

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

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

Autosomal dominant parkinsonism associated with variable synuclein and tau pathology

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

Mechanistic insight into the dominant mode of the Parkinson's disease-associated G2019S LRRK2 mutation

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

Global distribution and reduced penetrance: Lrrk2 R1441C in an Irish Parkinson's disease kindred

3 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

Mutations in LRRK2 other than G2019S are rare in a north american–based sample of familial Parkinson's disease

3 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906630

Parkinson disease: handedness predicts asymmetry

3 December 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Analysis of 14 LRRK2 mutations in Parkinson's plus syndromes and late-onset Parkinson's disease

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1212/01.WNL.0000304044.22253.03

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18337586%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

PubMed publication ID

18337586

1 reference