Prasanta Kumar Gangopadhyay

Author

Also Known As

Gangopadhyay, P.K., P Gangopadhyay, P K Gangopadhyay, P. K. Gangopadhyay, P.K Gangopadhyay, P.K. GANGOPADHYAY, P.K. Gangopadhyay, Prasanta K Gangopadhyay, Prasanta K. Gangopadhyay, Prasanta Kumar Gangopadhyay

Publications

Citations

H-Index

Concepts

All Affiliations

Bangur Institute of Neurosciences Indian Institute of Chemical Biology Calcutta National Medical College and Hospital Manovikas Kendra Rehabilitation and Research Institute Medical College and Hospital, Kolkata

About

Prasanta Kumar Gangopadhyay is an author at Bangur Institute of Neurosciences specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	14	529
2	Public Health	4	4	168
3	Social Sciences	2	2	71
4	Engineering	1	1	15
5	Biochemistry	1	1	26

Prasanta Kumar Gangopadhyay

Publications

946

Citations

H-Index

Page 1

	Year	Citations
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, Journal of Neurochemistry	2009	105
Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations and genotype–phenotype correlation in Indian patients Arnab Gupta, D. Aikath, Rajarshi Neogi, Human Genetics Indian PatientsMolecular PathogenesisGenetic DisorderGeneticsPathogenesis	2005	87
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, Neuroscience Letters Alzheimer's DiseaseEastern IndiaDegenerative DiseaseRehabilitationNeurology	2003	65
Serotonin transporter promoter variants: Analysis in Indian autistic and control population Subhrangshu Guhathakurta, Sagarmoy Ghosh, Swagata Sinha, Brain Research PsychiatryGenetic DisorderGeneticsNeurotransmitterPsychiatric Genetics	2006	56
Genetic defects in Indian Wilson disease patients and genotype–phenotype correlation Shashwata Mukherjee, Shruti Dutta, Sulagna Majumdar, Parkinsonism & Related Disorders Genetic DisorderGeneticsInherited Metabolic DiseaseGenetic EpidemiologyGenotype–phenotype Correlation	2013	53
A family‐based study of Indian subjects from Kolkata reveals allelic association of the serotonin transporter intron‐2 (STin2) polymorphism and attention‐deficit‐hyperactivity disorder (ADHD) Emili Banerjee, Swagata Sinha, Anindita Chatterjee, American Journal of Medical Genetics Part B Neuropsychiatric Genetics Psychiatric DisordersGeneticsGenetic EpidemiologyHuman PolymorphismSerotonin Transporter Intron‐2	2006	48
Cystathionine β-synthase T833C/844INS68 polymorphism: a family-based study on mentally retarded children Samikshan Dutta, Swagata Sinha, Anindita Chattopadhyay, Behavioral and Brain Functions	2005	43
Molecular Pathogenesis of Wilson Disease Among Indians: A Perspective on Mutation Spectrum in ATP7B gene, Prevalent Defects, Clinical Heterogeneity and Implication Towards Diagnosis Arnab Gupta, Ishita Chattopadhyay, Sumit Dey, Cellular and Molecular Neurobiology Mendelian DisorderDisease MechanismMolecular PathogenesisGenetic DisorderGenetics	2007	43
Association of dopamine D4 receptor (DRD4) polymorphisms with attention deficit hyperactivity disorder in Indian population Nipa Bhaduri, Manali Das, Swagata Sinha, American Journal of Medical Genetics Part B Neuropsychiatric Genetics	2005	41
Molecular Diagnosis of Wilson Disease Using Prevalent Mutations and Informative Single-Nucleotide Polymorphism Markers Aakriti Gupta, Mahua Maulik, Poonam Nasipuri, Clinical Chemistry	2007	41

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