Non-synonymous GIGYF2 variants in Parkinson's disease from two Asian populations. (Q46239598)

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scientific article published on 16 May 2009

Non-synonymous GIGYF2 variants in Parkinson’s disease from two Asian populations

Language	Label	Description	Also known as
English	Non-synonymous GIGYF2 variants in Parkinson's disease from two Asian populations.	scientific article published on 16 May 2009	Non-synonymous GIGYF2 variants in Parkinson’s disease from two Asian populations

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19449032%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Non-synonymous GIGYF2 variants in Parkinson's disease from two Asian populations (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19449032%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Parkinson's disease

1 reference

based on heuristic

inferred from title

12

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19449032%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19449032%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

5

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19449032%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

author name string

Chin-Hslen Lin

2

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28 January 2020

Louis C Tan

4

1 reference

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19449032%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

R Li

6

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19449032%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Hui-Qin Lim

7

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19449032%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Ratnagopal Pavanni

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19449032%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

Yih Yuen

9

1 reference

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28 January 2020

K M Prakash

10

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28 January 2020

Yi Zhao

11

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28 January 2020

Eng-King Tan

1

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28 January 2020

publication date

16 May 2009

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28 January 2020

1 reference

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PubMed publication ID

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28 January 2020

126

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28 January 2020

3

1 reference

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PubMed publication ID

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28 January 2020

425-430

1 reference

Europe PubMed Central

PubMed publication ID

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28 January 2020

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PARK11 gene (GIGYF2) variants Asn56Ser and Asn457Thr are not pathogenic for Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deciphering the role of heterozygous mutations in genes associated with parkinsonism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two novel proteins that are linked to insulin-like growth factor (IGF-I) receptors by the Grb10 adapter and modulate IGF-I signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathogenic mutations in Parkinson disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucocerebrosidase mutations and risk of Parkinson disease in Chinese patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reported mutations inGIGYF2are not a common cause of Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic testing in Parkinson disease: promises and pitfalls

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype analysis of the PARK 11 gene, GIGYF2, in sporadic Parkinson's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The ubiquitin pathway in Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of replication of association between GIGYF2 variants and Parkinson disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in NR4A2 associated with familial Parkinson disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation in GIGYF2 is not associated with Parkinson disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of PLA2G6 as a locus for dystonia-parkinsonism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19449032

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-009-0678-X

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19449032%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19449032%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

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