LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease (Q33682480)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19343804%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

title

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

1 reference

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25 January 2020

1 reference

1

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25 January 2020

Hirofumi Maruyama

8

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25 January 2020

Hiroyuki Morino

9

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25 January 2020

Debby W Tsuang

14

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25 January 2020

Hideshi Kawakami

17

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25 January 2020

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12

Karen L Edwards

1 reference

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25 January 2020

author name string

Mitsutoshi Yamamoto

2

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25 January 2020

Alexis N Lopez

3

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25 January 2020

Hiroshi Ujike

4

1 reference

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25 January 2020

Yuishin Izumi

6

1 reference

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25 January 2020

Ryuji Kaji

7

1 reference

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25 January 2020

Masaya Oda

10

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25 January 2020

Carolyn M Hutter

11

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25 January 2020

Gerard D Schellenberg

13

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25 January 2020

Dora Yearout

15

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25 January 2020

Eric B Larson

16

1 reference

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25 January 2020

Ignacio F Mata

5

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25 January 2020

language of work or name

English

0 references

publication date

1 May 2009

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25 January 2020

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25 January 2020

volume

24

1 reference

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25 January 2020

issue

7

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25 January 2020

page(s)

1034-1041

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

25 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=2827255

LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

Genetics of Parkinson disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

Tau and alpha-synuclein in susceptibility to, and dementia in, Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

LRRK2 low-penetrance mutations (Gly2019Ser) and risk alleles (Gly2385Arg)-linking familial and sporadic Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

Pathogenic mutations in Parkinson disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

High-resolution whole-genome association study of Parkinson disease.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

A New Statistical Method for Haplotype Reconstruction from Population Data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

Prevalence of dementia and its subtypes in the Japanese American population of King County, Washington state. The Kame Project.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

Criteria for diagnosing Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

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

21 June 2018

1 reference

The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease.

21 January 2018

1 reference

Analysis of LRRK2 functional domains in nondominant Parkinson disease.

21 January 2018

1 reference

Comprehensive screening of a North American Parkinson's disease cohort for LRRK2 mutation.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Implications of small effect sizes of individual genetic variants on the design and interpretation of genetic association studies of complex diseases.

21 January 2018

1 reference

Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease

21 January 2018

1 reference

Lrrk2 pathogenic substitutions in Parkinson's disease

21 January 2018

1 reference

Collaborative Analysis of α-Synuclein Gene Promoter Variability and Parkinson Disease

21 January 2018

1 reference

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

21 January 2018

1 reference

Genetic association between α-synuclein and idiopathic parkinson's disease

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2827255

Analysis of LRRK2 Gly2385Arg genetic variant in non-Chinese Asians

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19343804

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19343804

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/MDS.22514

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19343804%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19343804%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19343804%20AND%20SRC:MED&resulttype=core&format=json