Publications by authors named "Moinak Banerjee"

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Pharmacoepigenomic effects of anti-hypertensive drugs on DNA methylation and its implication to drug response and side effects.
Samyukta Bhass, Moinak Banerjee

Epigenomics· November 2025

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Proinflammatory phenotype can be critical in defining and modulating the genetic risk of non-syndromic hearing loss.
K P Sindura, M Sebastian, P Davis, L Srinivas, S Sathyan, Moinak Banerjee

Hum Immunol· September 2025

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Whole Exome Sequencing Based Diagnostics in Complex Childhood Epilepsy Syndromes-A Cohort Study on Clinical Utility.
Alfiya Fasaludeen, Manna Jose, U Aswathi, Moinak Banerjee, Soumya Sundaram

Clin Genet· September 2025

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Impact of seasonal cycle on rheumatoid arthritis based on genetic and epigenetic mechanisms.
Krishna Priya E K, Shidhi P R, Sreedevi S, Moinak Banerjee

Front Immunol· September 2025

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Association of Gene Polymorphism of Matrix Metalloproteinase-9 With Chronic Periodontitis: A Cross-Sectional Survey in a South Indian Population.
Shahana C Mohamed, Raseena Beevi N, Moinak Banerjee, Sanish Sathyan, Bindu R Nayar

Cureus· September 2025

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Cross-Talk Between Hypoxia-Inducible Factors in Driving the Pathology of Oral Squamous Cell Carcinoma: An Immunohistochemical Analysis of the Role of Hypoxia-Inducible Factors and Cancer-Associated Fibroblasts.
Indu M, Beena Vt, Moinak Banerjee, Latha Mary Cherian, Aishwarya Menon P

Asian Pac J Cancer Prev· August 2025

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Integrated Pharmacoepigenomic Analysis Uncovers the Impact of Antiseizure Medications on Developmental Pathways and the Protective Effect of Folic Acid.
Neethu Mohan, Moinak Banerjee

Int J Mol Sci· August 2025

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Pharmacoepigenomic Impact of Antihypertensive Drugs on miRNome and Proteome and Its Potential Influence on Health and Side Effects.
Samyukta Bhass, Moinak Banerjee

Cells· August 2025

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A real-world comparison between the diagnostic yield of trio-whole exome sequencing and proband-only targeted exome sequencing in complex childhood epilepsy.
Alfiya Fasaludeen, Manna Jose, Aswathi U, Surabhi Prasannakumar, Moinak Banerjee

Seizure· July 2025

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Pro-inflammatory cytokine genetic variants show variable susceptibility to mild cognitive impairment, alzheimer's disease and frontotemporal dementia in South India.
Aswathy Peethambaran Mallika, Jairani Pushparajan Sulajamani, Mathuranath Pavagada Sivasankara, Ramshekhar N Menon, Moinak Banerjee

Neurogenetics· July 2025

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Neur-Ally: a deep learning model for regulatory variant prediction based on genomic and epigenomic features in brain and its validation in certain neurological disorders.
Anil Prakash, Moinak Banerjee

NAR Genom Bioinform· June 2025

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Whole Exome Sequencing Study of a Multizygotic Quadruplet Discordant for Autism Spectrum Disorder Reveals Novel Autism Candidate Genes.
Ayyappan Anitha, Moinak Banerjee, Ismail Thanseem, Nisha Melempatt, Anil Prakash

Neurol India· January 2025

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Rare Pathogenic Variants Identified in Whole Exome Sequencing of Monozygotic Twins With Autism Spectrum Disorder.
Ayyappan Anitha, Moinak Banerjee, Ismail Thanseem, Anil Prakash, Nisha Melempatt

Pediatr Neurol· September 2024

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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

Elife· September 2024

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Challenges in genetic testing for metabolic causes of developmental epileptic encephalopathy- relevance of genotype-phenotype correlations.
Manna Jose, Alfiya Fasaludeen, Harini Pavuluri, Pavan Kumar Rudrabhatla, Soumya V Chandrasekharan, Moinak Banerjee

Seizure· April 2024

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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

Epilepsy Res· March 2024

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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, Moinak Banerjee

Front Psychiatry· March 2024

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Comprehensive Genetic Study of a Monozygotic Triplet Discordant for Autism Spectrum Disorder.
Ismail Thanseem, Moinak Banerjee, Nisha Melempatt, Anil Prakash, Mary Iype

Neurol India· March 2024

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Metabolic causes of pediatric developmental & epileptic encephalopathies (DEE)- genetic variant analysis in a south Indian cohort.
Manna Jose, Alfiya Fasaludeen, Harini Pavuluri, Pavan Kumar Rudrabhatla, Soumya V Chandrasekharan, Moinak Banerjee

Seizure· February 2024

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Impact of variant subtype on electro-clinical phenotype of Dravet syndrome- a South Indian cohort study.
S Krishna, Alfiya Fasaludeen, Manna Jose, Moinak Banerjee, Soumya Sundaram

Seizure· February 2024

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Genetic Affinities and Adaptation of the South-West Coast Populations of India.
Lomous Kumar, Anuhya Chowdhari, Jaison J Sequeira, Mohammed S Mustak, Moinak Banerjee

Genome Biol Evol· December 2023

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Arginase deficiency-An unheralded cause of developmental epileptic encephalopathy.
Harini Pavuluri, Manna Jose, Alfiya Fasaludeen, Soumya Sundaram, Ashalatha Radhakrishnan, Moinak Banerjee

Epileptic Disord· August 2023

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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

Asian J Psychiatr· August 2023

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An interpretable block-attention network for identifying regulatory feature interactions.
Anil Prakash, Moinak Banerjee

Brief Bioinform· July 2023

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Visual-sensitive epilepsy in GLUT-1 deficiency syndrome: Expanding the phenotype.
Alfiya Fazal, Manna Jose, Pavan Kumar Rudrabhatla, Soumya V Chandrasekharan, Soumya Sundaram, Moinak Banerjee

Epileptic Disord· April 2023

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