Chromosomal abnormalities associated with mental retardation in female subjects

por Dutta, Samikshan, Shaw, Jyothi, Sinha, Swagata, Mukhopadhyay, Kanchan
Publicado 2009

Discerning non-disjunction in Down syndrome patients by means of GluK1-(AGAT)(n) and D21S2055-(GATA)(n) microsatellites on chromosome 21

por Ghosh, Debarati, Sinha, Swagata, Chatterjee, Anindita, Nandagopal, Krishnadas
Publicado 2012

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

por Chatterjee, Arpita, Dutta, Samikshan, Sinha, Swagata, Mukhopadhyay, Kanchan
Publicado 2011

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

por Ghosh, Debarati, Sinha, Swagata, Chatterjee, Anindita, Nandagopal, Krishnadas
Publicado 2009

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

por Maitra, Subhamita, Chatterjee, Mahasweta, Sinha, Swagata, Mukhopadhyay, Kanchan
Publicado 2017

A pioneering study indicate role of GABRQ rs3810651 in ASD severity of Indo-Caucasoid female probands

por Saha, Sharmistha, Chatterjee, Mahasweta, Sinha, Swagata, Mukhopadhyay, Kanchan
Publicado 2021

A STUDY OF PSYCHIATRIC DISORDERS OTHER PSYCHOSIS IN THE REFERRED CASES WITH SOMATIC COMPLAINTS

por Banerjee, Gautam, Sinha, Swagata, Mukerjee, D.G., Sen, G.
Publicado 1987

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

por Chatterjee, Mahasweta, Saha, Tanusree, Maitra, Subhamita, Sinha, Swagata, Mukhopadhyay, Kanchan
Publicado 2020

Kainate receptor subunit 1 (GRIK1) risk variants and GRIK1 deficiency were detected in the Indian ADHD probands

por Chatterjee, Mahasweta, Saha, Sharmistha, Dutta, Nilanjana, Sinha, Swagata, Mukhopadhyay, Kanchan
Publicado 2022

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

por Chatterjee, Mahasweta, Saha, Sharmistha, Shom, Sayanti, Dutta, Nilanjana, Sinha, Swagata, Mukhopadhyay, Kanchan
Publicado 2023

Down Syndrome Related Muscle Hypotonia: Association with COL6A3 Functional SNP rs2270669

por Dey, Arpita, Bhowmik, Krishnendu, Chatterjee, Arpita, Chakrabarty, Pit Baran, Sinha, Swagata, Mukhopadhyay, Kanchan
Publicado 2013

Catecholaminergic Gene Variants: Contribution in ADHD and Associated Comorbid Attributes in the Eastern Indian Probands

por Ghosh, Paramita, Sarkar, Kanyakumarika, Bhaduri, Nipa, Ray, Anirban, Sarkar, Keka, Sinha, Swagata, Mukhopadhyay, Kanchan
Publicado 2013

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

por Dutta, Samikshan, Sinha, Swagata, Chattopadhyay, Anindita, Gangopadhyay, Prasanta Kumar, Mukhopadhyay, Jotideb, Singh, Manoranjan, Mukhopadhyay, Kanchan
Publicado 2005

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

por Karmakar, Arijit, Maitra, Subhamita, Chakraborti, Barnali, Verma, Deepak, Sinha, Swagata, Mohanakumar, Kochupurackal P., Rajamma, Usha, Mukhopadhyay, Kanchan
Publicado 2016

Attention deficit-hyperactivity disorder suffers from mitochondrial dysfunction

por Verma, Poonam, Singh, Alpana, Nthenge-Ngumbau, Dominic Ngima, Rajamma, Usha, Sinha, Swagata, Mukhopadhyay, Kanchan, Mohanakumar, Kochupurackal P
Publicado 2016

Gender-Specific Effect of 5-HT and 5-HIAA on Threshold Level of Behavioral Symptoms and Sex-Bias in Prevalence of Autism Spectrum Disorder

por Chakraborti, Barnali, Verma, Deepak, Guhathakurta, Subhrangshu, Jaiswal, Preeti, Singh, Asem Surindro, Sinha, Swagata, Ghosh, Saurabh, Mukhopadhyay, Kanchan, Mohanakumar, Kochupurackal P., Rajamma, Usha
Publicado 2020

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

por Chatterjee, Arpita, Dutta, Samikshan, Mukherjee, Sanjit, Mukherjee, Nupur, Dutta, Avirup, Mukherjee, Ashis, Sinha, Swagata, Panda, Chinmay Kumar, Chaudhuri, Keya, Roy, Ananda L, Mukhopadhyay, Kanchan
Publicado 2013

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

por Karmakar, Arijit, Goswami, Rishov, Saha, Tanusree, Maitra, Subhamita, Roychowdhury, Anirban, Panda, Chinmay Kumar, Sinha, Swagata, Ray, Anirban, Mohanakumar, Kochupurackal P., Rajamma, Usha, Mukhopadhyay, Kanchan
Publicado 2017