|
1
|
Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients.
|
BMC Neurol
|
2005
|
1.15
|
|
2
|
No evidence for shorter leukocyte telomere length in Parkinson's disease patients.
|
J Gerontol A Biol Sci Med Sci
|
2010
|
0.98
|
|
3
|
A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample.
|
Arch Neurol
|
2005
|
0.89
|
|
4
|
Tyrosinase exacerbates dopamine toxicity but is not genetically associated with Parkinson's disease.
|
J Neurochem
|
2005
|
0.87
|
|
5
|
Paraoxonase 1 (PON1) gene polymorphisms and Parkinson's disease in a Finnish population.
|
Neurosci Lett
|
2004
|
0.78
|
|
6
|
The human prion gene M129V polymorphism is not associated with idiopathic Parkinson's disease in three distinct populations.
|
Neurosci Lett
|
2005
|
0.77
|
|
7
|
Assessment of PINK1 (PARK6) polymorphisms in Finnish PD.
|
Neurobiol Aging
|
2005
|
0.75
|