Selected Publications

Ethnic and region-specific genetic risk variants of stroke and its comorbid conditions can define the variations in the burden of stroke and its phenotypic traits

Rashmi Sukumaran , Achuthsankar S. Nair Moinak Banerjee (2024)

eLife https://doi.org/10.7554/eLife.94088.2

Methylome-wide and meQTL analysis helps to distinguish treatment response from non-response and pathogenesis markers in schizophrenia

Binithamol K. Polakkattil, Neetha N. Vellichirammal, Indu V. Nair, Chandrasekharan M. Nair and Moinak Banerjee (2024)

Frontiers in Psychiatry doi: 10.1093/bib/bbad250

Genetic variant interpretation for the neurologist - A pragmatic approach in the next-generation sequencing era in childhood epilepsy.

Alfiya Fasaludeen, Amy McTague, Manna Jose, Moinak Banerjee, Soumya Sundaram, U.K. Madhusoodanan, Ashalatha Radhakrishnan, Ramshekhar N. Menon. (2024)

Epilepsy Research doi: 10.1016/j.eplepsyres.2024.107341

An interpretable block-attention network for identifying regulatory feature interactions

Anil Prakash, Moinak Banerjee (2023)

Briefings in Bioinformatics https://doi.org/10.1093/bib/bbad250

Effects of a six-month yoga intervention on the immune-inflammatory pathway in antipsychotic-stabilized schizophrenia patients: A randomized controlled trial

Thrinath Mullapudi, Monojit Debnath, Ramajayam Govindaraj, Praveen Raj, Moinak Banerjee, Shivarama Varambally (2023)

Asian Journal of Psychiatry https://doi.org/10.1016/j.ajp.2023.103636

Contribution from MHC-Mediated Risk in Schizophrenia Can Reflect a More Ethnic-Specific Genetic and Comorbid Background

Lekshmy Srinivas,Neetha N. Vellichirammal,Indu V. Nair,Chandrasekharan M. Nair and Moinak Banerjee (2022)

Cells https://doi.org/10.3390/cells11172695

Understanding Pharmaco-Epigenomic Response of Antipsychotic Drugs Using Genome-Wide MicroRNA Expression Profile in Liver Cell Line.

Swathy Babu and Moinak Banerjee (2022)

Frontiers in Molecular Neuroscience doi.org/10.3389/fnmol.2022.786632

Pharmacoepigenomics: a key determinant in resolving epigenomic parameters in pathogenesis and treatment response in complex diseases

Moinak Banerjee (2022)

Pharmacogenomics doi.org/10.2217/pgs-2021-0140
VOL. 23, NO. 2 | EDITORIAL

Genomic selection signatures in autism spectrum disorder identifies cognitive genomic tradeoff and its relevance in paradoxical phenotypes of deficits versus potentialities.

Anil Prakash & Moinak Banerjee (2021)

Scientific Reports https://rdcu.be/ckx51

Methylation map genes can be critical in determining the methylome of intracranial aneurysm patients.

Shafeeque CM, Sathyan S, Saradalekshmi KR, Premkumar S, Allapatt JP, Banerjee M(2020)

Epigenomics doi:10.2217/epi-2019-0280.

Genetic gateways to COVID?19 infection: Implications for risk, severity, and outcomes.and genes involved in neurotransmission in neuronal cells.

Debnath M,Banerjee M, Berk M(2020).

The FASEB Journal doi.org/10.1096/fj.202001115R

Vessel wall thickening and enhancement in high resolution intracranial vessel wall imaging: A predictor of future ischemic events in Moya moya disease.

Kathuveetil A, Sylaja PN, Senthilvelan S, Kesavadas C, Banerjee M, Jayanand Sudhir B(2020)

American Journal of Neuroradiology 41(1):100-105.

Chapters in Book / Text

Swathy Babu, Binithamol K Polakkattil, Moinak Banerjee. Chapter 25 Pharmacoepigenetics of antipsychotic drugs. Book Titled "Pharmacoepigenetics", Volume 10 in Translational Epigenetics. Ed. Ramón Cacabelos and Oscar Teijido. Academic Press. 733-739, June 2019. ISBN 978-0-12-813939-4. doi.org/10.1016/C2017-0-00603-

Submissions

Gene Bank
1. AY310165 Homo sapiens truncated proliferating cell nuclear antigen (PCNA) gene, complete cds.
2. AY310164 Homo sapiens PCNA gene, exon 1 and partial cds.
3. AY310163 Homo sapiens PCNA gene, exon 1 and partial cds.
4. AY310162 Homo sapiens PCNA gene, exon 1 and partial cds.
5. Y490254 Homo sapiens P-glycoprotein (MDR1) gene, partial cds.
6. NM_000015 Homo sapiens N-acetyltransferase 2 (arylamine N-acetyltransferase)
7. AY847950 Cytochrome b gene, partial sequence; mitochondrial of H. puera
8. AY847951 NADH dehydrogenase subunit-4(ND4) gene, partial sequence; mitochondrial of H. puera C.
9. AY847952 Cytochrome b gene, partial sequence; mitochondrial of H. puera C. (Coimbatore)
10. AY847953 Cytochrome oxidase subunit I (COI) gene, partial sequence; mitochondrial of H. puera C.
11. AY847954 NADH dehydrogenase subunit 1 (ND1) gene, partial sequence; mitochondrial of H. puera C.
12. AY571148 Cytochrome oxidase I subunit of H. puera C.
13. AY572232 16S rRNA gene of H. puera C.
14. AY572235 Cytochrome oxidase gene of H. puera C.
15. AY575214 12SrRNA gene of H. puera C.
16. AY572233 28S ribosomal RNA gene of H. puera C.
17. AY572234 Beta-tubulin intron gene of H. puera C.
18. AY572236 18s ribosomal RNA gene of H. puera C.
19. AY572237 Elongation factor I alpha introns of H. puera C.
20. AY572238 Wingless gene of H. puera C.
21. AY575215 Elongation factor I alpha gene of H. puera C.
22. AY847957 Tabanus atratus calo protein-like mRNA, partial cds
23. AY847955 Moricin I mRNA, partial cds of H. puera C.
24. AY847956 Moricin II mRNA, partial cds of H. puera C.

Software

1. Developed Allele Typer a Windows based Allele typing software used for mutation studies.
2. Developed Genome Profile Analysis (GPA) a windows based software used for mutation analysis on genes of Pharmacogenomic and Immunogenetic interests.
3. Developed GENOPACK a Linux based software for Allele sequence matching, Sequence Alignment, Complementary and reverse complementary strand generation, Protein translation, Position Matching, Motif matching, Restriction Mapping, Consensus sequence generation, Searching for open reading frames and the corresponding patterns and supports Format conversion.
4. Developed software, Psychiatric Patient Management System (PPMS) is a PHP PERL based patient data management software based on DSM IV criteria. All the commonly used psychiatric rating scales and side effects rating scales are integrated into the software. It automatically scores the patients positive, negative, cognitive and overall symptoms profile at initial presentation and subsequent followups. It is useful to clinicians, researchers, public health professionals and health inspectors.

Abstracts / Presentations / Invited Lectures

Conference Presentations

Priya, Krishna, Sasikala, Kesavarao, Banerjee, Moinak, Sreenivas, Lakshmi, Sathyan, Sanish, & Nil, Rajesh. (2015). ASSOCIATION OF IL-1 beta Polymorphisms with Rheumatoid Arthritis is Independent on autoantibody status in South Indian population. Tissue Antigens 85 (5), 394.
Srinivas, L., Neetha, N., Nair, C., Allencherry, P. M. & Banerjee, M. (2014). Association of pro-inflammatory cytokine gene polymorphisms with schizophrenia in South Indian population. Molecular Cytogenetics, 7, P41.
Sebastian M, Davis P, Ramdas P, Banerjee M (2014) A novel mutation in 3'UTR of GJB2 gene in autosomal recessive nonsyndromic sensorineural hearing loss in South Indian population. Molecular Cytogenetics 7: P113
Priya EK, Banerjee M, Rajesh S, Sasikala K (2014) IL 10 gene-1082 G/A shows an associatoin with rheumatoid arthritis patients of South Indian Population. Molecular Cytogenetics 7: P114.
Nair FK, Suresh P, Banerjee M (2014) Genetic variation of ITGB3 is associated with Autism Spectrum Disorders (ASD) in South Indian children. Molecular Cytogenetics 7: P109.
Alex AM, Suresh P, Banerjee M (2014) Association of clock gene variants with Autism Spectrum Disorder in South Indian population. Molecular Cytogenetics 7: P117.
Balan, S., Sumitha, P., Bharadwaj, T., Lekshmi, S., Sathyan, S., Radhakrishnan, K., and Banerjee, M. (2012). Role of ABCB1 Variants on Postoperative Seizure Recurrence in Patients with AED-Resistant Temporal Lobe Epilepsy. Neurology 78. P05.079.
Sathyan, S., Balan, S., Koshy, L, Easwer HV, Premkumar S, Alapatt J P, Nair S, Bhattacharya RN , Banerjee M. (2011). The role of Versican and collagen type I alpha2polymorphisms in intracranial aneurysms in a south Indian population. HUGO Journal 5, P127. (Conference proceeding in Journal; Human Genome Organisation-Human Genome Meeting 2011)
Balan, S., Sumitha, P., Bharadwaj, T., Lekshmi, S., Sathyan, S., Radhakrishnan, K., and Banerjee, M. (2011). An inquiry into the role of ABCB1 genetic variants in predisposition to epilepsy and pharmaco resistance. HUGO Journal 5, P83.
Das, A., Mathew, A., Vijayan, N., Radhakrishnan, K., and Banerjee, M. (2009). A Novel Association of ATP-Binding Cassette Family Gene (ABCB1) among South Indian Patients with Epilepsy. Neurology 72, A7.
Neetha N V, Linda Koshy Vaidyan, Chandrasekhar N, Mathew Anila, Chandrashekharan Nair, Allencherry Priya, Moinak Banerjee. (2008) Association studies of neurotransmitter receptor and transporter genes in the theranostics of schizophrenia in a South Indian population. Genomic Med; 2:389�400.
Vijayan, N., L. Srinivas, L. V. Koshy, C. Natarajan, P. M. Allencherry, C. M. Nair, and M. Banerjee. (2008) "274-Understanding treatment response and association of genotype phenotype correlates in schizophrenia from a population genetics viewpoint." Schizophrenia Research 98: 146-146.
Anna Alkelai, James Crowley , Tania Das Banerjee, Sophia Docherty, Elizabeth Hare, Michael J Galsworthy, Deepak Grover, Dylan Grubb, Robert Karlsson, Jonathan Mill, Srigan Sen, Marlon P. Quinones, Eric Vallender, RanjanaVerma, Neetha.N.Vijayan, Sandra Villafuerte, Aristotle N. Voineskos, Heather Volk, Lan Yu, Petra Zimmerman, Coordinated by: Lynn E. DeLisi. (2008) The XVth World Congress of Psychiatric Genetics, October 7-11, 2007; Rapporteur summaries of oral presentations; American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 147B, 2, 233-277.
Neetha N V, Sujatha Bhaskar, Linda Koshy Vaidyan, Chandrasekhar N, Chandrashekharan Nair, Moinak Banerjee. (2005). Association of dopamine receptor polymorphisms in schizophrenia. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics 131B, 1, 110.
Neetha, N. V., C. Nair, and M. Banjeree. (2004) "Association of SER311CYS DRD2 polymorphism in patients with schizophrenia from South India." American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, vol. 130B, 1, 144.

Moinak Banerjee, PhD

Scientist G