(Q30531323)

14 August 2017

Common variation in the LRRK2 gene is a risk factor for Parkinson's disease (English)

1 reference

14 August 2017

1 reference

0 references

27

1 reference

PubMed publication ID

23 June 2017

Pilar Gómez-Garre

14

0 references

Ignacio F Mata

Ignacio F Mata

1

0 references

Pablo Mir

Pablo Mir

15

0 references

Joseph Quinn

Joseph F Quinn

21

0 references

Pau Pastor

Pau Pastor

10

0 references

Beate Ritz

16

Beate Ritz

1 reference

14 August 2017

5

John W Roberts

1 reference

María Victoria Alvarez-Sánchez

14 August 2017

8

Victoria Alvarez

1 reference

14 August 2017

9

Renee Ribacoba

1 reference

14 August 2017

22

Dora Yearout

1 reference

14 August 2017

17

Shannon L Rhodes

1 reference

14 August 2017

4

Ali Samii

1 reference

14 August 2017

7

Pinky Agarwal

1 reference

14 August 2017

3

Carolyn M Hutter

1 reference

14 August 2017

23

Erica Martinez

1 reference

14 August 2017

Vivianna M Van Deerlin

19

Vivianna Van Deerlin

1 reference

14 August 2017

20

Kathryn A Chung

1 reference

14 August 2017

24

Federico M Farin

1 reference

14 August 2017

26

Karen L Edwards

1 reference

14 August 2017

Harvey Checkoway

2

1 reference

14 August 2017

Hojoong M Kim

6

1 reference

14 August 2017

Oswaldo Lorenzo-Betancor

11

1 reference

14 August 2017

Jon Infante

12

1 reference

14 August 2017

María Sierra

13

1 reference

14 August 2017

Amy Colcher

18

1 reference

14 August 2017

Jia Y Wan

25

1 reference

14 August 2017

language of work or name

English

0 references

publication date

31 October 2012

1 reference

14 August 2017

1 reference

14 August 2017

27

1 reference

14 August 2017

14

1 reference

14 August 2017

1822-1825

1 reference

Quantitative assessment of the effect of LRRK2 exonic variants on the risk of Parkinson's disease: a meta-analysis

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

Genome-wide association study confirms extant PD risk loci among the Dutch

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

Clinical characteristics in early Parkinson's disease in a central California population-based study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

Parkinson's disease risks associated with cigarette smoking, alcohol consumption, and caffeine intake

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

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

20 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FMDS.25226

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FMDS.25226

Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3536918

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

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23115130

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23115130

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/MDS.25226

1 reference

14 August 2017

1 reference

14 August 2017

PubMed publication ID

23115130

1 reference