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Prasanta Kumar Gangopadhyay
Observed names:
P Gangopadhyay,
P K Gangopadhyay,
P. K. Gangopadhyay,
P.K Gangopadhyay,
P.K. Gangopadhyay,
Prasanta K Gangopadhyay,
Prasanta K. Gangopadhyay
show all 7
Observed institutions:
Calcutta National Medical College and Hospital,
Bangur Institute of Neurosciences,
Institute of Post Graduate Medical Education and Research,
Chattagram International Medical College,
Medical College and Hospital, Kolkata
OpenAlex ID:
A5113218917
Single‐nucleotide polymorphism (A118G) in exon 1 ofOPRM1gene causes alteration in downstream signaling by mu‐opioid receptor and may contribute to the genetic risk for addiction
2009
·
Ishani Deb
, Japashish Chakraborty
, et al.
·
Journal of Neurochemistry
·
105
Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations and genotype–phenotype correlation in Indian patients
2005
·
A. Gupta
, D. Aikath
, et al.
·
Human Genetics
·
84
Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India
2003
·
Biswanath Chattopadhyay
, Subho Ghosh
, et al.
·
Neuroscience Letters
·
66
Genetic defects in Indian Wilson disease patients and genotype–phenotype correlation
2013
·
Shashwata Mukherjee
, Shruti Dutta
, et al.
·
Parkinsonism & Related Disorders
·
60
PDF
Serotonin transporter promoter variants: Analysis in Indian autistic and control population
2006
·
Subhrangshu Guhathakurta
, Sagarmoy Ghosh
, et al.
·
Brain Research
·
56
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)
2006
·
Emili Banerjee
, Swagata Sinha
, et al.
·
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
·
48
Cystathionine β-synthase T833C/844INS68 polymorphism: a family-based study on mentally retarded children
2005
·
Samikshan Dutta
, Swagata Sinha
, et al.
·
Behavioral and Brain Functions
·
47
PDF
Association of dopamine D4 receptor (DRD4) polymorphisms with attention deficit hyperactivity disorder in Indian population
2005
·
Nipa Bhaduri
, Manali Das
, et al.
·
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
·
43
Molecular Pathogenesis of Wilson Disease Among Indians: A Perspective on Mutation Spectrum in ATP7B gene, Prevalent Defects, Clinical Heterogeneity and Implication Towards Diagnosis
2007
·
Arnab Gupta
, Ishita Chattopadhyay
, et al.
·
Cellular and Molecular Neurobiology
·
42
Molecular Diagnosis of Wilson Disease Using Prevalent Mutations and Informative Single-Nucleotide Polymorphism Markers
2007
·
A. Gupta
, M. Maulik
, et al.
·
Clinical Chemistry
·
41
PDF
Reelin gene polymorphisms in the Indian population: A possible paternal 5′UTR‐CGG‐repeat‐allele effect on autism
2006
·
Shruti Dutta
, Subhrangshu Guhathakurta
, et al.
·
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
·
35
PDF
Clinical profile of multiple sclerosis in Bengal.
1999
·
G Gangopadhyay
, S K Das
, et al.
·
PubMed
·
34
Pattern of motor neurone disease in eastern India
2009
·
S. P. Saha
, S. K. Das
, et al.
·
Acta Neurologica Scandinavica
·
32
PDF
Reduced NADH coenzyme Q dehydrogenase activity in platelets of Parkinson's disease, but not Parkinson plus patients, from an Indian population
2009
·
Merina Varghese
, Mritunjay Pandey
, et al.
·
Journal of the Neurological Sciences
·
27
Population-based association study and contrasting linkage disequilibrium pattern reveal genetic association of SLC6A4 with autism in the Indian population from West Bengal
2008
·
Subhrangshu Guhathakurta
, Swagata Sinha
, et al.
·
Brain Research
·
26
Short term mortality predictors in acute stroke
2012
·
Sukdeb Das
, Kartick Chandra Ghosh
, et al.
·
Annals of Neurosciences
·
24
Acute intranigral homocysteine administration produces stereotypic behavioral changes and striatal dopamine depletion in Sprague–Dawley rats
2006
·
Goutam Chandra
, Prasanta K. Gangopadhyay
, et al.
·
Brain Research
·
23
Parkinson's disease cybrids, differentiated or undifferentiated, maintain morphological and biochemical phenotypes different from those of control cybrids
2013
·
T.A. Appukuttan
, N. Ali
, et al.
·
Journal of Neuroscience Research
·
18
Subcortical white matter abnormalities related to drug resistance in Wilson disease
2006
·
D. Aikath
, A. Gupta
, et al.
·
Neurology
·
18
DNA linkage based diagnosis of Wilson disease in asymptomatic siblings.
2003
·
A Gupta
, R Neogi
, et al.
·
PubMed
·
16
Molecular aspects of Down syndrome.
2005
·
Samikshan Dutta
, Krishnadas Nandagopal
, et al.
·
PubMed
·
15
Analysis of polymorphisms in the dopamine beta hydroxylase gene: association with attention deficit hyperactivity disorder in Indian children.
2005
·
Nipa Bhaduri
, Swagata Sinha
, et al.
·
PubMed
·
15
Influence of Apolipoprotein E polymorphism on susceptibility of Wilson disease
2017
·
Shubhrajit Roy
, Kausik Ganguly
, et al.
·
Annals of Human Genetics
·
14
An Association Analysis of Reelin Gene (RELN) Polymorphisms with Childhood Epilepsy in Eastern Indian Population from West Bengal
2010
·
Shruti Dutta
, Prasanta K. Gangopadhyay
, et al.
·
Cellular and Molecular Neurobiology
·
14
Albuminuria and neuropathy in newly detected diabetics: profile and correlation.
2011
·
Rathindra Nath Karmakar
, M R Khandakar
, et al.
·
PubMed
·
13
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Works count:
45
Citation count:
985
H-index:
18
I10-index:
28
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