Prasanta K Gangopadhyay

Author PubWeight™ 5.04^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Molecular diagnosis of Wilson disease using prevalent mutations and informative single-nucleotide polymorphism markers.	Clin Chem	2007	1.50
2	Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India.	Neurosci Lett	2003	1.12
3	Molecular pathogenesis of Wilson disease among Indians: a perspective on mutation spectrum in ATP7B gene, prevalent defects, clinical heterogeneity and implication towards diagnosis.	Cell Mol Neurobiol	2007	0.84
4	An association analysis of reelin gene (RELN) polymorphisms with childhood epilepsy in eastern Indian population from West Bengal.	Cell Mol Neurobiol	2010	0.78
5	Reelin gene polymorphisms in the Indian population: a possible paternal 5'UTR-CGG-repeat-allele effect on autism.	Am J Med Genet B Neuropsychiatr Genet	2007	0.77
6	Acute intranigral homocysteine administration produces stereotypic behavioral changes and striatal dopamine depletion in Sprague-Dawley rats.	Brain Res	2006	0.76