Study to Determine Mutations in the Gaucher Gene in Patients With Idiopathic Parkinson's Disease for Phenotype-genotype Correlation (PadGau)

Clinical Trial ID NCT01272687

Rank	Title	Journal	Year	PubWeight™‹?›
1	Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.	Nature	1998	21.49
2	Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.	N Engl J Med	2009	7.53
3	Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease.	Brain	2009	4.01
4	Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset.	Neurology	2008	3.83
5	Gaucher disease: complexity in a "simple" disorder.	Mol Genet Metab	2004	2.92
6	Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset.	Neurology	2008	2.73
7	Occurrence of Parkinson's syndrome in type I Gaucher disease.	QJM	1996	2.54
8	Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease.	Neurology	2007	2.41
9	Gaucher disease with parkinsonian manifestations: does glucocerebrosidase deficiency contribute to a vulnerability to parkinsonism?	Mol Genet Metab	2003	2.29
10	Parkinsonism among Gaucher disease carriers.	J Med Genet	2004	2.24
11	Mutations for Gaucher disease confer high susceptibility to Parkinson disease.	Arch Neurol	2009	2.00
12	Emerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease.	FEBS J	2008	1.68
13	Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Greece.	Neurosci Lett	2009	1.56