(Q35525896)

8 August 2017

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

1 reference

8 August 2017

1 reference

16

1 reference

8 August 2017

10

Alexis Brice

0 references

John Ioannidis

26

John P A Ioannidis

0 references

Enza Maria Valente

Christine Van Broeckhoven

Enza Maria Valente

0 references

12

Christine Van Broeckhoven

0 references

Eugénie Mutez

Eugénie Mutez

38

0 references

Rachel A Gibson

Rachel Gibson

23

0 references

Jessie Theuns

Jessie Theuns

49

0 references

Andreas Puschmann

Andreas Puschmann

42

0 references

Yun J Kim

Yun Joong Kim

29

0 references

Chin-Hsien Lin

Chin-Hsien Lin

34

0 references

Ruey-Meei Wu

Ruey-Meei Wu

Marie-Christine Chartier-Harlin

59

0 references

Marie-Christine Chartier-Harlin

14

0 references

George D. Mellick

George D Mellick

37

0 references

Sung Wook Park

Sung Sup Park

41

0 references

Matthew J. Farrer

Matthew J Farrer

60

0 references

Aldo Quattrone

Aldo Quattrone

43

0 references

Suzanne Lesage

33

Suzanne Lesage

1 reference

8 August 2017

51

Ryan J Uitti

1 reference

8 August 2017

58

Zbigniew K Wszolek

1 reference

8 August 2017

25

Nobutaka Hattori

1 reference

8 August 2017

30

Christine Klein

1 reference

8 August 2017

1

Owen A Ross

1 reference

8 August 2017

28

Beom S Jeon

1 reference

8 August 2017

45

Peter A Silburn

1 reference

8 August 2017

31

Rejko Kruger

1 reference

8 August 2017

6

Grazia Annesi

1 reference

8 August 2017

57

Karin Wirdefeldt

1 reference

8 August 2017

11

Laura Brighina

1 reference

8 August 2017

Barbara Jasinska-Myga

27

Barbara Jasinska-Myga

1 reference

8 August 2017

Carles Vilariño-Güell

55

Carles Vilariño-Güell

1 reference

8 August 2017

Georgios M Hadjigeorgiou

24

Georgios M Hadjigeorgiou

1 reference

8 August 2017

15

Efthimios Dardiotis

1 reference

8 August 2017

8

Soraya Bardien

1 reference

8 August 2017

40

Grzegorz Opala

1 reference

ORCID Public Data File 2021

8 August 2017

1 reference

Daniela Berg

1 reference

ORCID Public Data File 2021

Demetrius M. Maraganore

36

Demetrius M Maraganore

1 reference

8 August 2017

13

Jonathan Carr

1 reference

8 August 2017

50

Hiroyuki Tomiyama

1 reference

8 August 2017

48

Vera Tadic

1 reference

8 August 2017

3

Michael G Heckman

1 reference

Alexandra I Soto-Ortolaza

8 August 2017

2

Alexandra I Soto-Ortolaza

1 reference

8 August 2017

5

Nadine Abahuni

1 reference

8 August 2017

7

Justin A Bacon

1 reference

8 August 2017

17

Nancy N Diehl

1 reference

8 August 2017

32

Elli Kyratzi

1 reference

8 August 2017

53

Simone van de Loo

1 reference

8 August 2017

Demetrios K Vassilatis

54

Demetrios K Vassilatis

1 reference

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

8 August 2017

61

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

1 reference

8 August 2017

35

Timothy Lynch

1 reference

8 August 2017

19

Carlo Ferrarese

1 reference

8 August 2017

Jan O Aasly

4

1 reference

8 August 2017

Maria Bozi

9

1 reference

8 August 2017

Alexis Elbaz

18

1 reference

8 August 2017

Alessandro Ferraris

20

1 reference

8 August 2017

Brian Fiske

21

1 reference

8 August 2017

J Mark Gibson

22

1 reference

8 August 2017

Christer Nilsson

39

1 reference

8 August 2017

Manu Sharma

44

1 reference

8 August 2017

Young Ho Sohn

46

1 reference

8 August 2017

Leonidas Stefanis

47

1 reference

8 August 2017

Linda R White

56

1 reference

8 August 2017

30 August 2011

1 reference

8 August 2017

1 reference

8 August 2017

10

1 reference

8 August 2017

898-908

1 reference

8 August 2017

10

1 reference

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

8 August 2017

1 reference

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

A map of human genome variation from population-scale sequencing

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

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

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

Inhibitors of leucine-rich repeat kinase-2 protect against models of 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

Novel pathogenic LRRK2 p.Asn1437His substitution in familial 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

LRRK2 and Parkinson 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

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

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

Analysis of Lrrk2 R1628P as a risk factor for 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

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

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

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

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

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

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

Quantifying heterogeneity in a meta-analysis

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

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

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

Meta-analysis in clinical trials

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

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

1 reference

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

1 reference

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

1 reference

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

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

1 reference

12 December 2020

Challenges in the clinical application of whole-genome sequencing

1 reference

12 December 2020

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

1 reference

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

1 reference

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

1 reference

8 August 2017

1 reference