S. Sinha

K. Chaudhuri, S. Sinha, K. Mukhopadhyay, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Pilot study indicate role of preferentially transmitted monoamine oxidase gene variants in behavioral problems of male ADHD probands

K. Mohanakumar, S. Maitra, A. Karmakar, 2017, BMC Medical Genetics.

Author ' s personal copy Sexual dimorphic effect in the genetic association of monoamine oxidase A ( MAOA ) markers with autism spectrum disorder

Saurabh Ghosh, K. Mohanakumar, A. Karmakar, 2014 .

Reelin gene polymorphisms in the Indian population: A possible paternal 5′UTR‐CGG‐repeat‐allele effect on autism

Saurabh Ghosh, S. Sinha, A. Chatterjee, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

SNaPshot Assay in Quantitative Detection of Allelic Nondisjunction in Down Syndrome.

K. Nandagopal, S. Sinha, A. Chatterjee, 2012, Genetic testing and molecular biomarkers.

No Evidence for Mutations that Deregulate GARS–AIRS–GART Protein Levels in Children with Down Syndrome

K. Nandagopal, S. Sinha, A. Chatterjee, 2012, Indian Journal of Clinical Biochemistry.

Exploratory Investigation on Functional Significance of ETS2 and SIM2 Genes in Down Syndrome

S. Sinha, K. Mukhopadhyay, A. Chatterjee, 2011, Disease markers.

Explorative Investigation on Thyroid Peroxidase and Sodium Iodide Symporter Gene Variants in Down Syndrome

S. Sinha, K. Mukhopadhyay, A. Maiti, 2016 .

No causal role for the G482T and G689T polymorphisms in translation regulation of serotonin transporter (SLC6A4) or association with attention-deficit-hyperactivity disorder (ADHD)

K. Nandagopal, S. Sinha, A. Chatterjee, 2009, Neuroscience Letters.

Cystathionine β-synthase T833C/844INS68 polymorphism: a family-based study on mentally retarded children

S. Sinha, K. Mukhopadhyay, J. Mukhopadhyay, 2005, Behavioral and Brain Functions.

Functional genetic polymorphisms in dopaminergic transporters: Association with ADHD traits in the Indian probands

S. Maitra, P. Ghosh, S. Sinha, 2017 .

A Pilot Study on the Contribution of Folate Gene Variants in the Cognitive Function of ADHD Probands

S. Sinha, K. Mukhopadhyay, T. Saha, 2014, Neurochemical Research.

Screening of rural children in West Bengal for fragile-X syndrome.

S. Sinha, K. Mukhopadhyay, M. Das, 2009, The Indian journal of medical research.

An Association Analysis of Reelin Gene (RELN) Polymorphisms with Childhood Epilepsy in Eastern Indian Population from West Bengal

Saurabh Ghosh, S. Sinha, A. Chatterjee, 2010, Cellular and Molecular Neurobiology.

Family‐based studies indicate association of Engrailed 2 gene with autism in an Indian population

S. Sinha, A. Chatterjee, R. Usha, 2010, Genes, brain, and behavior.

Analysis of serotonin receptor 2A gene (HTR2A): Association study with autism spectrum disorder in the Indian population and investigation of the gene expression in peripheral blood leukocytes

Saurabh Ghosh, S. Sinha, A. Chatterjee, 2009, Neurochemistry International.

Role of SNAP25 Explored in Eastern Indian Attention Deficit Hyperactivity Disorder Probands

Kanyakumarika Sarkar, P. Ghosh, S. Sinha, 2011, Neurochemical Research.

Potential contribution of SIM2 and ETS2 functional polymorphisms in Down syndrome associated malignancies

K. Chaudhuri, Avirup Dutta, A. Roy, 2013, BMC Medical Genetics.

Genetic variants of the folate metabolic system and mild hyperhomocysteinemia may affect ADHD associated behavioral problems

S. Sinha, K. Mukhopadhyay, Anirban Ray, 2018, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

Study on DBH Genetic Polymorphisms and Plasma Activity in Attention Deficit Hyperactivity Disorder Patients from Eastern India

Kanyakumarika Sarkar, S. Sinha, K. Mukhopadhyay, 2010, Cellular and Molecular Neurobiology.

SLC6A4 markers modulate platelet 5-HT level and specific behaviors of autism: A study from an Indian population

Saurabh Ghosh, M. Varghese, K. Mohanakumar, 2015, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

A Study of GluK1 Kainate Receptor Polymorphisms in Down Syndrome Reveals Allelic Non-Disjunction at 1173(C/T)

K. Nandagopal, S. Sinha, A. Chatterjee, 2009, Disease markers.

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

Saurabh Ghosh, S. Sinha, A. Chatterjee, 2006, Brain Research.

Glutamate Receptor 6 Gene (GluR6 or GRIK2) Polymorphisms in the Indian Population: A Genetic Association Study on Autism Spectrum Disorder

Saurabh Ghosh, S. Sinha, A. Chatterjee, 2007, Cellular and Molecular Neurobiology.

Analysis of neurotransmitters validates the importance of the dopaminergic system in autism spectrum disorder

S. Sinha, K. Mukhopadhyay, M. Chatterjee, 2023, World Journal of Pediatrics.

Significance of Dopaminergic Gene Variants in the Male Biasness of ADHD

Kanyakumarika Sarkar, P. Ghosh, S. Sinha, 2017, Journal of attention disorders.

Association of dopamine D4 receptor (DRD4) polymorphisms with attention deficit hyperactivity disorder in Indian population

K. Chaudhuri, S. Sinha, K. Mukhopadhyay, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Screening for methylenetetrahydrofolate reductase C677T and A1298C polymorphisms in Indian patients with idiopathic mental retardation

S. Sinha, K. Mukhopadhyay, S. Dutta, 2008, Nutritional neuroscience.

Folate System Gene Variant rs1801394 66A>G may have a Causal Role in Down Syndrome in the Eastern Indian Population

S. Maitra, S. Sinha, K. Mukhopadhyay, 2020, International journal of molecular and cellular medicine.

The Dopamine Receptor D5 May Influence Age of Onset

S. Maitra, Kanyakumarika Sarkar, S. Sinha, 2016, Journal of child neurology.

Cyclin-dependent Kinase 5: Novel role of gene variants identified in ADHD

S. Maitra, S. Sinha, K. Mukhopadhyay, 2017, Scientific Reports.

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)

K. Nandagopal, S. Sinha, A. Chatterjee, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Role of functional dopaminergic gene polymorphisms in the etiology of idiopathic intellectual disability

A. Saha, S. Chaudhury, S. Sinha, 2011, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

Role of SNAP25 Explored in Eastern Indian Attention Deficit Hyperactivity Disorder Probands

Kanyakumarika Sarkar, P. Ghosh, S. Sinha, 2012, Neurochemical Research.

Genetic analysis of reelin gene (RELN) SNPs: No association with autism spectrum disorder in the Indian population

Saurabh Ghosh, S. Sinha, A. Chatterjee, 2008, Neuroscience Letters.

Dimorphic association of dopaminergic transporter gene variants with treatment outcome: Pilot study in Indian ADHD probands

S. Maitra, P. Ghosh, A. Karmakar, 2017 .

Adhesion G protein-coupled receptor L3 gene variants: Statistically significant association observed in the male Indo-caucasoid Attention deficit hyperactivity disorder probands

S. Sinha, K. Mukhopadhyay, M. Chatterjee, 2021, Molecular Biology Reports.

A Pilot Study on the Contribution of Folate Gene Variants in the Cognitive Function of ADHD Probands

S. Sinha, K. Mukhopadhyay, S. Dutta, 2014, Neurochemical Research.

Gamma-Aminobutyric Acid Type A Receptor Variants are Associated with Autism Spectrum Disorders

S. Sinha, N. Banerjee, A. Bandyopadhyay, 2023, Journal of Molecular Neuroscience.

Monoamine oxidase B gene variants associated with attention deficit hyperactivity disorder in the Indo-Caucasoid population from West Bengal

K. Mohanakumar, S. Maitra, A. Karmakar, 2016, BMC Genetics.

Analysis of polymorphisms in the dopamine beta hydroxylase gene: association with attention deficit hyperactivity disorder in Indian children.

S. Sinha, K. Mukhopadhyay, N. Bhaduri, 2005, Indian pediatrics.

An Association Study of Gamma-Aminobutyric Acid Type A Receptor Variants and Susceptibility to Autism Spectrum Disorders

N. Banerjee, S. Sinha, Pallabi Adak, 2021, Journal of Autism and Developmental Disorders.

Glutamate receptor genetic variants affected peripheral glutamatergic transmission and treatment induced improvement of Indian ADHD probands

S. Sinha, K. Mukhopadhyay, M. Chatterjee, 2023, Scientific reports.

Importance of gene variants and co-factors of folate metabolic pathway in the etiology of idiopathic intellectual disability

Kanyakumarika Sarkar, S. Sinha, K. Mukhopadhyay, 2011, Nutritional neuroscience.

Indian ASD probands with 25(OH)D and vitamin D binding protein deficiency exhibited higher severity

S. Sinha, K. Mukhopadhyay, M. Chatterjee, 2024, Scientific reports.

Cystathionine β-synthase T833C/844INS68 polymorphism: a family-based study on mentally retarded children

S. Sinha, K. Mukhopadhyay, J. Mukhopadhyay, 2005, Behavioral and Brain Functions.