PLA2G6 variant in Parkinson's disease (Q83517580)

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scientific article published on 03 March 2011

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Language	Label	Description	Also known as
English	PLA2G6 variant in Parkinson's disease	scientific article published on 03 March 2011

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

title

PLA2G6 variant in Parkinson's disease (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

main subject

Parkinson's disease

1 reference

based on heuristic

inferred from title

author

Manabu Funayama

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

Nobutaka Hattori

series ordinal

11

object named as

Nobutaka Hattori

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

author name string

Hiroyuki Tomiyama

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

Hiroyo Yoshino

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

Kotaro Ogaki

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

Lin Li

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

Chikara Yamashita

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

Yuanzhe Li

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

Ryogen Sasaki

series ordinal

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

Yasumasa Kokubo

series ordinal

9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

Shigeki Kuzuhara

series ordinal

10

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

publication date

3 March 2011

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

published in

Journal of Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

volume

56

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

issue

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

page(s)

401-403

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

cites work

Multiple regions of alpha-synuclein are associated with Parkinson's disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations for Gaucher disease confer high susceptibility to Parkinson disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Characterization of PLA2G6 as a locus for dystonia-parkinsonism

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Infantile neuroaxonal dystrophy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

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7 January 2021

based on heuristic

inferred from DOI database lookup

Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Phenotypic spectrum of patients with PLA2G6 mutation and PARK14 -linked parkinsonism

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

PLA2G6 mutations and Parkinson's disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN).

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

R632W mutation in PLA2G6 segregates with dystonia-parkinsonism in a consanguineous Iranian family

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2011.22

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1038/JHG.2011.22

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

PubMed publication ID

21368765

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21368765

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21368765%20AND%20SRC:MED&resulttype=core&format=json

retrieved

24 January 2020

 

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