|
1
|
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
|
Neuron
|
2004
|
14.35
|
|
2
|
Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*.
|
Brain
|
2005
|
1.85
|
|
3
|
Parkin protects mitochondrial genome integrity and supports mitochondrial DNA repair.
|
Hum Mol Genet
|
2009
|
1.59
|
|
4
|
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease.
|
Eur J Hum Genet
|
2006
|
1.56
|
|
5
|
The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval.
|
Am J Hum Genet
|
2003
|
1.30
|
|
6
|
PARK11 is not linked with Parkinson's disease in European families.
|
Eur J Hum Genet
|
2005
|
0.92
|
|
7
|
Transcranial ultrasound in different monogenetic subtypes of Parkinson's disease.
|
J Neurol
|
2007
|
0.83
|
|
8
|
A novel LRRK2 mutation in an Austrian cohort of patients with Parkinson's disease.
|
Mov Disord
|
2007
|
0.80
|
|
9
|
A unique case of coincidence of early onset Parkinson's disease and multiple sclerosis.
|
Mov Disord
|
2007
|
0.80
|
|
10
|
Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's disease.
|
Neurogenetics
|
2003
|
0.78
|
|
11
|
High-throughput homogeneous mass cleave assay technology for the diagnosis of autosomal recessive Parkinson's disease.
|
J Mol Diagn
|
2008
|
0.75
|