Kanchan Mukhopadhyay

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 11

Top Topics

Circulating Tumor

Attention Deficit Hyperactivity Disorder

Top Venues

Molecular biology reports

World journal of pediatrics : WJP

Metabolic brain disease

This page only lists publications with an associated author ORCID identifier.

Publications

Sharmistha Saha, Mahasweta Chatterjee, Nilanjana Dutta, Swagata Sinha, Kanchan Mukhopadhyay
Analysis of neurotransmitters validates the importance of the dopaminergic system in autism spectrum disorder. World journal of pediatrics : WJP (2023)
Sharmistha Saha, Mahasweta Chatterjee, Nilanjana Dutta, Swagata Sinha, Kanchan Mukhopadhyay
GABA Receptor SNPs and Elevated Plasma GABA Levels Affect the Severity of the Indian ASD Probands. Journal of molecular neuroscience : MN 72 (6) (2022)
Mahasweta Chatterjee, Sharmistha Saha, Swagata Sinha, Kanchan Mukhopadhyay
A three-pronged analysis confirms the association of the serotoninergic system with attention deficit hyperactivity disorder. World journal of pediatrics : WJP 18 (12) (2022)
Mahasweta Chatterjee, Sharmistha Saha, Subhamita Maitra, Anirban Ray, Swagata Sinha, Kanchan Mukhopadhyay
Post-treatment symptomatic improvement of the eastern Indian ADHD probands is influenced by CYP2D6 genetic variations. Drug metabolism and personalized therapy (2022)
Subhamita Maitra, Mahasweta Chatterjee, Anirban Roychowdhury, Chinmay Kumar Panda, Swagata Sinha, Kanchan Mukhopadhyay
Specific dopaminergic genetic variants influence impulsivity, cognitive deficit, and disease severity of Indian ADHD probands. Molecular biology reports 49 (8) (2022)
Sharmistha Saha, Tanusree Saha, Usha Rajamma, Swagata Sinha, Kanchan Mukhopadhyay
Analysis of association between components of the folate metabolic pathway and autism spectrum disorder in eastern Indian subjects. Molecular biology reports (2021)
Mahasweta Chatterjee, Sharmistha Saha, Sayanti Shom, Swagata Sinha, Kanchan Mukhopadhyay
Adhesion G protein-coupled receptor L3 gene variants: Statistically significant association observed in the male Indo-caucasoid Attention deficit hyperactivity disorder probands. Molecular biology reports 48 (4) (2021)
Sharmistha Saha, Mahasweta Chatterjee, Sayanti Shom, Swagata Sinha, Kanchan Mukhopadhyay
Functional SLC6A3 polymorphisms differentially affect autism spectrum disorder severity: a study on Indian subjects. Metabolic brain disease (2021)
Subhamita Maitra, Kanchan Mukhopadhyay
Parental age and developmental milestones: pilot study indicated a role in understanding ADHD severity in Indian probands. BMC pediatrics 19 (1) (2019)
Arijit Karmakar, Rishov Goswami, Tanusree Saha, Subhamita Maitra, Anirban Roychowdhury, Chinmay Kumar Panda, Swagata Sinha, Anirban Ray, Kochupurackal P Mohanakumar, Usha Rajamma, Kanchan Mukhopadhyay
Pilot study indicate role of preferentially transmitted monoamine oxidase gene variants in behavioral problems of male ADHD probands. BMC medical genetics 18 (1) (2017)
Arijit Karmakar, Subhamita Maitra, Barnali Chakraborti, Deepak Verma, Swagata Sinha, Kochupurackal P Mohanakumar, Usha Rajamma, Kanchan Mukhopadhyay
Monoamine oxidase B gene variants associated with attention deficit hyperactivity disorder in the Indo-Caucasoid population from West Bengal. BMC genetics 17 (1) (2016)