(Q43112212)

14 November 2017

0 references

Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibrium (English)

1 reference

14 November 2017

1 reference

linkage disequilibrium

1 reference

1

C Paisán-Ruíz

0 references

Georgios M Hadjigeorgiou

12

object named as

G M Hadjigeorgiou

1 reference

14 November 2017

4

G Xiromerisiou

1 reference

14 November 2017

E W Evans

2

1 reference

14 November 2017

S Jain

3

1 reference

14 November 2017

J R Gibbs

5

1 reference

14 November 2017

J Eerola

6

1 reference

14 November 2017

V Gourbali

7

1 reference

14 November 2017

O Hellström

8

1 reference

14 November 2017

J Duckworth

9

1 reference

14 November 2017

A Papadimitriou

10

1 reference

14 November 2017

P J Tienari

11

1 reference

14 November 2017

A B Singleton

13

1 reference

14 November 2017

language of work or name

English

0 references

publication date

1 February 2006

1 reference

Journal of Medical Genetics

14 November 2017

1 reference

14 November 2017

43

1 reference

14 November 2017

e9

1 reference

14 November 2017

2

1 reference

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

14 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564648

A common LRRK2 mutation in idiopathic Parkinson's disease

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564648

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564648

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564648

Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564648

A human genome diversity cell line panel

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564648

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564648

G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564648

Clinical features of LRRK2-associated Parkinson's disease in central Norway

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564648

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

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564648

Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564648

GENECOUNTING: haplotype analysis with missing genotypes.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564648

GOLD--graphical overview of linkage disequilibrium

15 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16467219

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16467219

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16467219

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.2005.036889

1 reference

14 November 2017

1 reference

14 November 2017

1 reference