Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study (Q35525896)

8 August 2017

title

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

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Alexis Brice

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John Ioannidis

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John P A Ioannidis

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Enza Maria Valente

Christine Van Broeckhoven

Enza Maria Valente

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12

Christine Van Broeckhoven

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Eugénie Mutez

Eugénie Mutez

38

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Rachel A Gibson

Rachel Gibson

23

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Jessie Theuns

Jessie Theuns

49

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Andreas Puschmann

Andreas Puschmann

42

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Yun J Kim

Yun Joong Kim

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Chin-Hsien Lin

Chin-Hsien Lin

34

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Ruey-Meei Wu

Ruey-Meei Wu

Marie-Christine Chartier-Harlin

59

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Marie-Christine Chartier-Harlin

14

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George D. Mellick

George D Mellick

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Sung Wook Park

Sung Sup Park

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Matthew J. Farrer

Matthew J Farrer

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Aldo Quattrone

Aldo Quattrone

43

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Suzanne Lesage

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Suzanne Lesage

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Ryan J Uitti

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Zbigniew K Wszolek

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Nobutaka Hattori

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Christine Klein

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Owen A Ross

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Beom S Jeon

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Peter A Silburn

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Rejko Kruger

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Grazia Annesi

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Karin Wirdefeldt

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Laura Brighina

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Barbara Jasinska-Myga

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Barbara Jasinska-Myga

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Carles Vilariño-Güell

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Carles Vilariño-Güell

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Georgios M Hadjigeorgiou

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Georgios M Hadjigeorgiou

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Efthimios Dardiotis

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Soraya Bardien

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40

Grzegorz Opala

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ORCID Public Data File 2021

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Daniela Berg

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ORCID Public Data File 2021

Demetrius M. Maraganore

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Demetrius M Maraganore

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Jonathan Carr

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Hiroyuki Tomiyama

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Vera Tadic

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Michael G Heckman

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Alexandra I Soto-Ortolaza

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Alexandra I Soto-Ortolaza

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Nadine Abahuni

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Justin A Bacon

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Nancy N Diehl

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Elli Kyratzi

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Simone van de Loo

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Demetrios K Vassilatis

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Demetrios K Vassilatis

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Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium

8 August 2017

61

Genetic Epidemiology Of Parkinson's Disease (GEO-PD) Consortium

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35

Timothy Lynch

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Carlo Ferrarese

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Jan O Aasly

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Maria Bozi

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Alexis Elbaz

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Alessandro Ferraris

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Brian Fiske

21

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J Mark Gibson

22

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Christer Nilsson

39

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Manu Sharma

44

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Young Ho Sohn

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Leonidas Stefanis

47

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Linda R White

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8 August 2017

publication date

30 August 2011

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8 August 2017

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8 August 2017

volume

10

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8 August 2017

issue

10

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8 August 2017

page(s)

898-908

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

8 August 2017

cites work

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12 July 2018

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Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review

12 July 2018

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Inhibitors of leucine-rich repeat kinase-2 protect against models of Parkinson's disease

12 July 2018

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Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease

12 July 2018

1 reference

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LRRK2 and Parkinson disease

12 July 2018

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Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

12 July 2018

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LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study

12 July 2018

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

12 July 2018

1 reference

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Genome-wide association studies for complex traits: consensus, uncertainty and challenges

12 July 2018

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Structure of the ROC domain from the Parkinson's disease-associated leucine-rich repeat kinase 2 reveals a dimeric GTPase

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3208320

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3208320

A "silent" polymorphism in the MDR1 gene changes substrate specificity

12 July 2018

1 reference

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3208320

SIFT: Predicting amino acid changes that affect protein function

12 July 2018

1 reference

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Quantifying heterogeneity in a meta-analysis

12 July 2018

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Score tests for association between traits and haplotypes when linkage phase is ambiguous

12 July 2018

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Meta-analysis in clinical trials

12 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3208320

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3208320

Population-wide generalizability of genome-wide discovered associations

26 September 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3208320

Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3208320

Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease

26 September 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3208320

Neurocirculatory and nigrostriatal abnormalities in Parkinson disease from LRRK2 mutation

26 September 2018

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Multiple testing. Part I. Single-step procedures for control of general type I error rates

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3208320

Lrrk2-associated parkinsonism is a major cause of disease in Northern Spain

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3208320

Lrrk2 pathogenic substitutions in Parkinson's disease

15 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3208320

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

15 November 2018

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12 December 2020

Challenges in the clinical application of whole-genome sequencing

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12 December 2020

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

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12 December 2020

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

1 reference

12 December 2020

Diagnostic criteria for Parkinson disease

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Crossref

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970175-2

7 January 2021

inferred from DOI database lookup

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

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970175-2

7 January 2021

inferred from DOI database lookup

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FS1474-4422%2811%2970175-2

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1016/S1474-4422(11)70175-2

1 reference

8 August 2017

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8 August 2017

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