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

由 Maitra, Subhamita, Mukhopadhyay, Kanchan
發表在 BMC Pediatr (2019)

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

由 Dutta, Samikshan, Das, Aneek Bhowmik, Mukhopadhyay, Kanchan
出版 2007

Chromosomal abnormalities associated with mental retardation in female subjects

由 Dutta, Samikshan, Shaw, Jyothi, Sinha, Swagata, Mukhopadhyay, Kanchan
出版 2009

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

由 Chatterjee, Arpita, Dutta, Samikshan, Sinha, Swagata, Mukhopadhyay, Kanchan
出版 2011

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

由 Maitra, Subhamita, Chatterjee, Mahasweta, Sinha, Swagata, Mukhopadhyay, Kanchan
發表在 Sci Rep (2017)

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

由 Saha, Sharmistha, Chatterjee, Mahasweta, Sinha, Swagata, Mukhopadhyay, Kanchan
發表在 Sci Rep (2021)

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

由 Bhaduri, Nipa, Das, Manali, Das, Aneek Bhowmik, Mukhopadhyay, Kanchan
出版 2007

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

由 Chatterjee, Mahasweta, Saha, Tanusree, Maitra, Subhamita, Sinha, Swagata, Mukhopadhyay, Kanchan
發表在 Int J Mol Cell Med (2020)

Congenital Pouch Colon with Unilateral Renal Agenesis and Monorchism

由 Chaudhury, Subhramoy, Chatterjee, Indranil, Dutta, Samikshan, Vaid, LalitKumar, Mukhopadhyay, Kanchan
出版 2010

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

由 Chakrabortty, Amit, Das, Soumita, Majumdar, Sabita, Mukhopadhyay, Kanchan, Roychoudhury, Susanta, Chaudhuri, Keya
出版 2000

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

由 Dey, Arpita, Bhowmik, Krishnendu, Chatterjee, Arpita, Chakrabarty, Pit Baran, Sinha, Swagata, Mukhopadhyay, Kanchan
出版 2013

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

由 Mukhopadhyay Jotideb, Gangopadhyay Prasanta, Chattopadhyay Anindita, Sinha Swagata, Dutta Samikshan, Singh Manoranjan, Mukhopadhyay Kanchan
出版 2005-12-01

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

由 Ghosh, Paramita, Sarkar, Kanyakumarika, Bhaduri, Nipa, Ray, Anirban, Sarkar, Keka, Sinha, Swagata, Mukhopadhyay, Kanchan
出版 2013

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

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

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

由 Karmakar, Arijit, Maitra, Subhamita, Chakraborti, Barnali, Verma, Deepak, Sinha, Swagata, Mohanakumar, Kochupurackal P., Rajamma, Usha, Mukhopadhyay, Kanchan
發表在 BMC Genet (2016)

Attention deficit-hyperactivity disorder suffers from mitochondrial dysfunction

由 Verma, Poonam, Singh, Alpana, Nthenge-Ngumbau, Dominic Ngima, Rajamma, Usha, Sinha, Swagata, Mukhopadhyay, Kanchan, Mohanakumar, Kochupurackal P
發表在 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

由 Chakraborti, Barnali, Verma, Deepak, Guhathakurta, Subhrangshu, Jaiswal, Preeti, Singh, Asem Surindro, Sinha, Swagata, Ghosh, Saurabh, Mukhopadhyay, Kanchan, Mohanakumar, Kochupurackal P., Rajamma, Usha
發表在 Front Neurosci (2020)

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

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

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

由 Karmakar, Arijit, Goswami, Rishov, Saha, Tanusree, Maitra, Subhamita, Roychowdhury, Anirban, Panda, Chinmay Kumar, Sinha, Swagata, Ray, Anirban, Mohanakumar, Kochupurackal P., Rajamma, Usha, Mukhopadhyay, Kanchan
發表在 BMC Med Genet (2017)