Author

Kanchan Mukhopadhyay

Manovikas Kendra, Kolkata - Cited by 1,159 - Cell Biology - Molecular genetics

Biography

Kanchan Mukhopadhyay is a Professor at the Diagnosis department, Biomedical Research and Diagnostic Centre, Manovikas Kendra, Kolkata, India. He has published over 05 refereed articles in a wide range of highly recognised international journals. He has a keen interest in ?yroid function. He is currently working in the project ‘’ Molecular aspects of Down syndrome’’. His research focuses on Down syndrome.
Title
Cited by
Year
Sexual dimorphic effect in the genetic association of monoamine oxidase A (MAOA) markers with autism spectrum disorder
D Verma, B Chakraborti, A Karmakar, T Bandyopadhyay, AS Singh, ...Progress in Neuro-Psychopharmacology and Biological Psychiatry 50, 11-20, 2014201
47
2014
Attention deficit-hyperactivity disorder suffers from mitochondrial dysfunction
P Verma, A Singh, DN Nthenge-Ngumbau, U Rajamma, S Sinha, ...BBA clinical 6, 153-158, 2016201
43
2016
Genetic variants of the folate metabolic system and mild hyperhomocysteinemia may affect ADHD associated behavioral problems
T Saha, M Chatterjee, D Verma, A Ray, S Sinha, U Rajamma, ...Progress in Neuro-Psychopharmacology and Biological Psychiatry 84, 1-10, 2018201
22
2018
Components of the folate metabolic pathway and ADHD core traits: an exploration in eastern Indian probands
T Saha, M Chatterjee, S Sinha, U Rajamma, K MukhopadhyayJournal of human genetics 62 (7), 687-695, 2017201
21
2017
Potential contribution of dopaminergic gene variants in ADHD core traits and co-morbidity: a study on eastern Indian probands
S Maitra, K Sarkar, P Ghosh, A Karmakar, A Bhattacharjee, S Sinha, ...Cellular and molecular neurobiology 34 (4), 549-564, 2014201
18
2014
Potential contribution of SIM2 and ETS2 functional polymorphisms in Down syndrome associated malignancies
A Chatterjee, S Dutta, S Mukherjee, N Mukherjee, A Dutta, A Mukherjee, ...BMC Medical Genetics 14 (1), 1-17, 2013201
16
2013
Significance of dopaminergic gene variants in the male biasness of ADHD
A Das Bhowmik, K Sarkar, P Ghosh, M Das, N Bhaduri, K Sarkar, A Ray, ...Journal of Attention Disorders 21 (3), 200-208, 2017201
15
2017
Potential contribution of monoamine oxidase a gene variants in ADHD and behavioral co-morbidities: scenario in eastern Indian probands
A Karmakar, S Maitra, D Verma, B Chakraborti, R Goswami, P Ghosh, ...Neurochemical research 39, 843-852, 202
14
2014
Gender-specific effect of 5-HT and 5-HIAA on threshold level of behavioral symptoms and sex-bias in prevalence of autism spectrum disorder
B Chakraborti, D Verma, S Guhathakurta, P Jaiswal, AS Singh, S Sinha, ...Frontiers in Neuroscience 13, 1375, 2020202
14
2020
Cyclin-dependent Kinase 5: Novel role of gene variants identified in ADHD
S Maitra, M Chatterjee, S Sinha, K MukhopadhyayScientific reports 7 (1), 6828, 2017201
13
2017
A pilot study on the contribution of folate gene variants in the cognitive function of ADHD probands
T Saha, S Dutta, U Rajamma, S Sinha, K MukhopadhyayNeurochemical research 39 (11), 2058-2067, 2014201
13
2014
Pilot study indicate role of preferentially transmitted monoamine oxidase gene variants in behavioral problems of male ADHD probands
A Karmakar, R Goswami, T Saha, S Maitra, A Roychowdhury, CK Panda, ...BMC medical genetics 18 (1), 1-12, 2017201
11
2017
The dopamine receptor D5 may influence age of onset: an exploratory study on indo-Caucasoid ADHD subjects
S Maitra, K Sarkar, S Sinha, K MukhopadhyayJournal of Child Neurology 31 (), 1250-1256, 2016201
10
2016
Catecholaminergic gene variants: contribution in ADHD and associated comorbid attributes in the eastern Indian probands
P Ghosh, K Sarkar, N Bhaduri, A Ray, K Sarkar, S Sinha, ...BioMed Research International 2013, 2013201
10
2013
Autistic traits and components of the folate metabolic system: an explorative analysis in the eastern Indian ASD subjects
S Saha, T Saha, S Sinha, U Rajamma, K MukhopadhyayNutritional Neuroscience 23 (11), 60-67, 2020202
8
2020
Monoamine oxidase B gene variants associated with attention deficit hyperactivity disorder in the Indo-Caucasoid population from West Bengal
A Karmakar, S Maitra, B Chakraborti, D Verma, S Sinha, ...BMC genetics 17 (1), 1-15, 2016201
8
2016
Dimorphic association of dopaminergic transporter gene variants with treatment outcome: pilot study in Indian ADHD probands
A Ray, S Maitra, M Chatterjee, P Ghosh, A Karmakar, S Sinha, ...Meta Gene 11, 4-9, 2017201
6
2017
Folate System Gene Variant rs1801394 66A> G may have a Causal Role in Down Syndrome in the Eastern Indian Population
Folate System Gene Variant rs180139 66A> G may have a Causal Role in Down Syndrome in the Eastern Indian PopulationM Chatterjee, T Saha, S Maitra, S Sinha, K MukhopadhyayInternational Journal of Molecular and Cellular Medicine 9 (3), 215, 2020202
4
2020
Functional SLC6A3 polymorphisms differentially affect autism spectrum disorder severity: a study on Indian subjects
S Saha, M Chatterjee, S Shom, S Sinha, K MukhopadhyayMetabolic Brain Disease 37 (2), 397-10, 2022202
4
2022
Parental age and developmental milestones: pilot study indicated a role in understanding ADHD severity in Indian probands
S Maitra, K MukhopadhyayBMC pediatrics 19 (1), 1-8, 2019201
3
2019

Referred From: https://scholar.google.com/citations?hl=en&user=fLL6iV4AAAAJ

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