Prasanta Kumar Gangopadhyay

Single‐nucleotide polymorphism (A118G) in exon 1 of<i>OPRM1</i>gene causes alteration in downstream signaling by mu‐opioid receptor and may contribute to the genetic risk for addiction

Ishani Deb, Japashish Chakraborty, Prasanta Kumar Gangopadhyay et al. · Journal of Neurochemistry · 2009 · 105 citations · Full text

Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations and genotype–phenotype correlation in Indian patients

Arnab Gupta, D. Aikath, Rajarshi Neogi et al. · Human Genetics · 2005 · 87 citations

Indian Patients, Molecular Pathogenesis, Genetic Disorder +10

Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India

Biswanath Chattopadhyay, Subho Ghosh, Prasanta Kumar Gangopadhyay et al. · Neuroscience Letters · 2003 · 65 citations

Alzheimer's Disease, Eastern India, Degenerative Disease +7

Serotonin transporter promoter variants: Analysis in Indian autistic and control population

Subhrangshu Guhathakurta, Sagarmoy Ghosh, Swagata Sinha et al. · Brain Research · 2006 · 56 citations

Psychiatry, Genetic Disorder, Genetics +5

Genetic defects in Indian Wilson disease patients and genotype–phenotype correlation

Shashwata Mukherjee, Shruti Dutta, Sulagna Majumdar et al. · Parkinsonism & Related Disorders · 2013 · 53 citations · Full text

Genetic Disorder, Genetics, Inherited Metabolic Disease +7