Parental age and developmental milestones: pilot study indicated a role in understanding ADHD severity in Indian probands

Por Maitra, Subhamita, Mukhopadhyay, Kanchan
Publicado no BMC Pediatr (2019)

Risk of Down syndrome conferred by MTHFR C677T polymorphism: Ethnic variations

Por Dutta, Samikshan, Das, Aneek Bhowmik, Mukhopadhyay, Kanchan
Publicado em 2007

Chromosomal abnormalities associated with mental retardation in female subjects

Por Dutta, Samikshan, Shaw, Jyothi, Sinha, Swagata, Mukhopadhyay, Kanchan
Publicado em 2009

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

Por Chatterjee, Arpita, Dutta, Samikshan, Sinha, Swagata, Mukhopadhyay, Kanchan
Publicado em 2011

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

Por Maitra, Subhamita, Chatterjee, Mahasweta, Sinha, Swagata, Mukhopadhyay, Kanchan
Publicado no Sci Rep (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 no Sci Rep (2021)

Dopamine receptor D4 exon 3 variable number of tandem repeat polymorphism: Distribution in eastern Indian population

Por Bhaduri, Nipa, Das, Manali, Das, Aneek Bhowmik, Mukhopadhyay, Kanchan
Publicado em 2007

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 no Int J Mol Cell Med (2020)

Congenital Pouch Colon with Unilateral Renal Agenesis and Monorchism

Por Chaudhury, Subhramoy, Chatterjee, Indranil, Dutta, Samikshan, Vaid, LalitKumar, Mukhopadhyay, Kanchan
Publicado em 2010

Use of RNA Arbitrarily Primed-PCR Fingerprinting To Identify Vibrio cholerae Genes Differentially Expressed in the Host following Infection

Por Chakrabortty, Amit, Das, Soumita, Majumdar, Sabita, Mukhopadhyay, Kanchan, Roychoudhury, Susanta, Chaudhuri, Keya
Publicado em 2000

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 em 2013

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

Por Mukhopadhyay Jotideb, Gangopadhyay Prasanta, Chattopadhyay Anindita, Sinha Swagata, Dutta Samikshan, Singh Manoranjan, Mukhopadhyay Kanchan
Publicado em 2005-12-01

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 em 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 em 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 no BMC Genet (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 no BBA Clin (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 no Front Neurosci (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 em 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 no BMC Med Genet (2017)