Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
These results indicate that the GIGYF2 indel may be associated with increased risk of PD in northern China.
|
28873462 |
2017 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Although further research is still required, this finding may shed light on the GIGYF2-associated mechanisms that lead to PD and suggests insulin dysregulation as a disease-specific mechanism for both PD and cognitive dysfunction.
|
26134514 |
2015 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
To explore the contribution of GIGYF2 to PD at the genetic level, we analyzed the relationship between all reported GIGYF2 variants (including mutations and polymorphisms) and PD through a meta-analysis.
|
26152800 |
2015 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's disease.
|
22503729 |
2012 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Notably, gigyf2 functional abrogation did not increase diencephalic DA neurons susceptibility to the PD-inducing drug MPP+.
|
20060621 |
2011 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
In conclusion, within the Chinese population, the c.297T>C p.Ala99Ala polymorphism of the GIGYF2 gene may be associated with an increased risk of developing PD.
|
22115759 |
2011 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Together, our results do not support a role for GIGYF2 in the genetic etiology of Belgian PD.
|
19321232 |
2011 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Our data suggest that GIGYF2 is unlikely to play a major role in PD in Japanese patients, similar to other populations.
|
20641165 |
2010 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Our data indicate the GIGYF2 variants are not associated with PD in the mainland Chinese Population.
|
20044296 |
2010 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Together, these results do not support a major role of GIGYF2 in PD.
|
20004041 |
2010 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Considering the scarcity of studies on GIGYF2, ATP13A2 and GBA mutation frequency in Latin American countries, we present significant data about the contribution of these genes to PD susceptibility.
|
20816920 |
2010 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
In conclusion, we identified nine novel variants in GIGYF2 gene, which might be associated with PD in the Chinese population.
|
20178831 |
2010 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
However, its location in the highly polymorphic GIGYF2 glutamine/proline-rich region does not support a role in PD.
|
19845746 |
2010 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
PARK11 gene (GIGYF2) variants Asn56Ser and Asn457Thr are not pathogenic for Parkinson's disease.
|
19250854 |
2009 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
By sequencing the whole GIGYF2 coding region in forty-six probands (thirty-seven Italians) with familial Parkinson's disease compatible with an autosomal dominant inheritance, we identified no mutations.
|
19482505 |
2009 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
We conducted a comprehensive genetic analysis of the entire GIGYF2 gene in a cohort of young onset and familial PD patients, followed up with screening of specific variants in a separate group of PD and healthy controls.
|
19449032 |
2009 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
We also did not find a significant increase in risk for PD among those inheriting variants in GIGYF2 (p = 0.28).
|
19279319 |
2009 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Among the most interesting findings of the year was the nomination of GIGYF2 as the gene that is defective at the PARK11 locus and is a potentially frequent cause of typical Parkinson's disease.
|
19348706 |
2009 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The GIGYF2 gene maps to human chromosome 2q37 within a region linked to familial Parkinson's disease (PARK11 locus), and association of GIGYF2 mutations with Parkinson's disease has been described in some but not other recent publications.
|
19744960 |
2009 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
GIGYF2 Asn56Ser mutation is rare in Chinese Parkinson's disease patients.
|
19638301 |
2009 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Our results suggest that the GIGYF2 Asn56Ser and Asn457Thr mutations are a rare cause of PD in North American Caucasian population.
|
19429085 |
2009 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Lack of replication of association between GIGYF2 variants and Parkinson disease.
|
18923002 |
2009 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
LHGDN |
One index case (PD onset age 33) inherited a GIGYF2 mutation (Ile278Val) from her affected father (PD onset age 66) and a previously described PD-linked mutation in the LRRK2 gene (Ile1371Val) from her affected mother (PD onset age 61).
|
18358451 |
2008 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
One index case (PD onset age 33) inherited a GIGYF2 mutation (Ile278Val) from her affected father (PD onset age 66) and a previously described PD-linked mutation in the LRRK2 gene (Ile1371Val) from her affected mother (PD onset age 61).
|
18358451 |
2008 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Therefore, PARK11 does not seem to play a major role for familial PD in the European population.
|
15523496 |
2005 |