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

Yazar: Maitra, Subhamita, Mukhopadhyay, Kanchan
Yayımlandı BMC Pediatr (2019)

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

Yazar: Dutta, Samikshan, Das, Aneek Bhowmik, Mukhopadhyay, Kanchan
Baskı/Yayın Bilgisi 2007

Chromosomal abnormalities associated with mental retardation in female subjects

Yazar: Dutta, Samikshan, Shaw, Jyothi, Sinha, Swagata, Mukhopadhyay, Kanchan
Baskı/Yayın Bilgisi 2009

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

Yazar: Chatterjee, Arpita, Dutta, Samikshan, Sinha, Swagata, Mukhopadhyay, Kanchan
Baskı/Yayın Bilgisi 2011

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

Yazar: Maitra, Subhamita, Chatterjee, Mahasweta, Sinha, Swagata, Mukhopadhyay, Kanchan
Yayımlandı Sci Rep (2017)

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

Yazar: Saha, Sharmistha, Chatterjee, Mahasweta, Sinha, Swagata, Mukhopadhyay, Kanchan
Yayımlandı Sci Rep (2021)

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

Yazar: Bhaduri, Nipa, Das, Manali, Das, Aneek Bhowmik, Mukhopadhyay, Kanchan
Baskı/Yayın Bilgisi 2007

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

Yazar: Chatterjee, Mahasweta, Saha, Tanusree, Maitra, Subhamita, Sinha, Swagata, Mukhopadhyay, Kanchan
Yayımlandı Int J Mol Cell Med (2020)

Congenital Pouch Colon with Unilateral Renal Agenesis and Monorchism

Yazar: Chaudhury, Subhramoy, Chatterjee, Indranil, Dutta, Samikshan, Vaid, LalitKumar, Mukhopadhyay, Kanchan
Baskı/Yayın Bilgisi 2010

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

Yazar: Chakrabortty, Amit, Das, Soumita, Majumdar, Sabita, Mukhopadhyay, Kanchan, Roychoudhury, Susanta, Chaudhuri, Keya
Baskı/Yayın Bilgisi 2000

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

Yazar: Dey, Arpita, Bhowmik, Krishnendu, Chatterjee, Arpita, Chakrabarty, Pit Baran, Sinha, Swagata, Mukhopadhyay, Kanchan
Baskı/Yayın Bilgisi 2013

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

Yazar: Mukhopadhyay Jotideb, Gangopadhyay Prasanta, Chattopadhyay Anindita, Sinha Swagata, Dutta Samikshan, Singh Manoranjan, Mukhopadhyay Kanchan
Baskı/Yayın Bilgisi 2005-12-01

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

Yazar: Ghosh, Paramita, Sarkar, Kanyakumarika, Bhaduri, Nipa, Ray, Anirban, Sarkar, Keka, Sinha, Swagata, Mukhopadhyay, Kanchan
Baskı/Yayın Bilgisi 2013

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

Yazar: Dutta, Samikshan, Sinha, Swagata, Chattopadhyay, Anindita, Gangopadhyay, Prasanta Kumar, Mukhopadhyay, Jotideb, Singh, Manoranjan, Mukhopadhyay, Kanchan
Baskı/Yayın Bilgisi 2005

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

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

Attention deficit-hyperactivity disorder suffers from mitochondrial dysfunction

Yazar: Verma, Poonam, Singh, Alpana, Nthenge-Ngumbau, Dominic Ngima, Rajamma, Usha, Sinha, Swagata, Mukhopadhyay, Kanchan, Mohanakumar, Kochupurackal P
Yayımlandı 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

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

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

Yazar: Chatterjee, Arpita, Dutta, Samikshan, Mukherjee, Sanjit, Mukherjee, Nupur, Dutta, Avirup, Mukherjee, Ashis, Sinha, Swagata, Panda, Chinmay Kumar, Chaudhuri, Keya, Roy, Ananda L, Mukhopadhyay, Kanchan
Baskı/Yayın Bilgisi 2013

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

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