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

nork Maitra, Subhamita, Mukhopadhyay, Kanchan
Argitaratua izan da BMC Pediatr (2019)

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

nork Dutta, Samikshan, Das, Aneek Bhowmik, Mukhopadhyay, Kanchan
Argitaratua 2007

Chromosomal abnormalities associated with mental retardation in female subjects

nork Dutta, Samikshan, Shaw, Jyothi, Sinha, Swagata, Mukhopadhyay, Kanchan
Argitaratua 2009

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

nork Chatterjee, Arpita, Dutta, Samikshan, Sinha, Swagata, Mukhopadhyay, Kanchan
Argitaratua 2011

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

nork Maitra, Subhamita, Chatterjee, Mahasweta, Sinha, Swagata, Mukhopadhyay, Kanchan
Argitaratua izan da Sci Rep (2017)

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

nork Saha, Sharmistha, Chatterjee, Mahasweta, Sinha, Swagata, Mukhopadhyay, Kanchan
Argitaratua izan da Sci Rep (2021)

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

nork Bhaduri, Nipa, Das, Manali, Das, Aneek Bhowmik, Mukhopadhyay, Kanchan
Argitaratua 2007

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

nork Chatterjee, Mahasweta, Saha, Tanusree, Maitra, Subhamita, Sinha, Swagata, Mukhopadhyay, Kanchan
Argitaratua izan da Int J Mol Cell Med (2020)

Congenital Pouch Colon with Unilateral Renal Agenesis and Monorchism

nork Chaudhury, Subhramoy, Chatterjee, Indranil, Dutta, Samikshan, Vaid, LalitKumar, Mukhopadhyay, Kanchan
Argitaratua 2010

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

nork Chakrabortty, Amit, Das, Soumita, Majumdar, Sabita, Mukhopadhyay, Kanchan, Roychoudhury, Susanta, Chaudhuri, Keya
Argitaratua 2000

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

nork Dey, Arpita, Bhowmik, Krishnendu, Chatterjee, Arpita, Chakrabarty, Pit Baran, Sinha, Swagata, Mukhopadhyay, Kanchan
Argitaratua 2013

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

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

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

nork Ghosh, Paramita, Sarkar, Kanyakumarika, Bhaduri, Nipa, Ray, Anirban, Sarkar, Keka, Sinha, Swagata, Mukhopadhyay, Kanchan
Argitaratua 2013

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

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

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

nork Karmakar, Arijit, Maitra, Subhamita, Chakraborti, Barnali, Verma, Deepak, Sinha, Swagata, Mohanakumar, Kochupurackal P., Rajamma, Usha, Mukhopadhyay, Kanchan
Argitaratua izan da BMC Genet (2016)

Attention deficit-hyperactivity disorder suffers from mitochondrial dysfunction

nork Verma, Poonam, Singh, Alpana, Nthenge-Ngumbau, Dominic Ngima, Rajamma, Usha, Sinha, Swagata, Mukhopadhyay, Kanchan, Mohanakumar, Kochupurackal P
Argitaratua izan da 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

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

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

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

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

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