Mainak Bardhan, MBBS
Affiliations: | 2014-2020 | Pt Jawaharlal Nehru Memorial Medical College,Raipur,Chhattisgarh,India | |
| 2020-2021 | Neurology | National Institute of Mental Health and Neuro Sciences, Bangalore | |
| 2021-2023 | Clinical Medicine | Indian Council of Medical Research | |
| 2021-2023 | Molecular Microbiology | National Institute of Cholera and Enteric Diseases | |
| 2023- | Miami Cancer Institute | Baptist Health South Florida |
Area:
Neurology, Clinical Genetics, Oncology, Infectious Diseases, Public HealthWebsite:
https://scholar.google.com/citations?user=VCagZtIAAAAJGoogle:
"Mainak Bardhan"Bio:
Dr. Mainak Bardhan is a highly trained Physician Scientist specializing in the fields of Genetics, Genomics, Pathology, and Epidemiology of Neurological disorders,Neuromuscular and Rare Disorders as well as Infectious diseases. He has a strong focus on public health and is driven by his passion for biomedical research.
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Collaborators
Sign in to add collaborator| Atulya Khosla | collaborator | ||
| Ahmad Ozair | collaborator | ||
| Shreyas S. Bellur | collaborator | 2023- | Baptist Health South Florida |
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Publications
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| Nayak A, S B A, Bardhan M, et al. (2023) Evaluation of Cardiac, Autonomic Functions in Ambulant Patients with Duchenne Muscular Dystrophy. Sn Comprehensive Clinical Medicine. 5: 138 |
| Baskar D, Vengalil S, Nashi S, et al. (2023) MYH2-related Myopathy: Expanding the Clinical Spectrum of Chronic Progressive External Ophthalmoplegia (CPEO). Journal of Neuromuscular Diseases |
| Unnikrishnan G, Polavarapu K, Bardhan M, et al. (2023) Phenotype Genotype Characterization of FKRP-related Muscular Dystrophy among Indian Patients. Journal of Neuromuscular Diseases |
| Nishadham V, Rao S, Saravanan A, et al. (2023) Inflammatory myofibroblastic tumors: A short series with an emphasis on the diagnostic and therapeutic challenges. Clinical Neuropathology |
| Inbaraj G, Arjun K, Meghana A, et al. (2023) Neuro-Cardio-Autonomic Modulations in Children with Duchenne Muscular Dystrophy. Journal of Neuromuscular Diseases |
| Van Haute L, O'Connor E, Díaz-Maldonado H, et al. (2023) TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease. Nature Communications. 14: 1009 |
| Huang H, Mehta A, Kalmanovich J, et al. (2023) Immunological and inflammatory effects of infectious diseases in circadian rhythm disruption and future therapeutic directions. Molecular Biology Reports. 1-15 |
| Nashi S, Polavarapu K, Bardhan M, et al. (2022) Genotype-phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from India. Neurogenetics |
| Hesarur N, Bardhan M, Taallapalli A, et al. (2022) Lichtenstein-Knorr Syndrome: A Rare Case of Ataxia with Sensorineural Hearing Loss. Annals of Indian Academy of Neurology. 25: 970-973 |
| Pellerin D, Danzi MC, Wilke C, et al. (2022) Deep Intronic GAA Repeat Expansion in Late-Onset Cerebellar Ataxia. The New England Journal of Medicine |