| Year |
Citation |
Score |
| 2023 |
Nayak A, S B A, Bardhan M, Rashmi R, Arunachal G, Prathyusha PV, Nalini A, Sathyaprabha TN, Udupa K. Evaluation of Cardiac, Autonomic Functions in Ambulant Patients with Duchenne Muscular Dystrophy. Sn Comprehensive Clinical Medicine. 5: 138. PMID 37193318 DOI: 10.1007/s42399-023-01473-5 |
0.262 |
|
| 2023 |
Baskar D, Vengalil S, Nashi S, Bardhan M, Srivatsava K, Sanka SB, Polavarapu K, Menon D, Preethish-Kumar V, Padmanabha H, Arunachal G, Nalini A. MYH2-related Myopathy: Expanding the Clinical Spectrum of Chronic Progressive External Ophthalmoplegia (CPEO). Journal of Neuromuscular Diseases. PMID 37154181 DOI: 10.3233/JND-230017 |
0.262 |
|
| 2023 |
Unnikrishnan G, Polavarapu K, Bardhan M, Nashi S, Vengalil S, Preethish-Kumar V, Valasani RK, Huddar A, Nishadham V, Nandeesh BN, Nalini A. Phenotype Genotype Characterization of FKRP-related Muscular Dystrophy among Indian Patients. Journal of Neuromuscular Diseases. PMID 37154180 DOI: 10.3233/JND-221618 |
0.262 |
|
| 2023 |
Nishadham V, Rao S, Saravanan A, Kulanthaivelu K, Vengalil S, Venkatappa HA, Valasani RK, Bardhan M, Pruti N, Nalini A, Mahadevan A. Inflammatory myofibroblastic tumors: A short series with an emphasis on the diagnostic and therapeutic challenges. Clinical Neuropathology. PMID 37051870 DOI: 10.5414/NP301540 |
0.262 |
|
| 2023 |
Inbaraj G, Arjun K, Meghana A, Preethish-Kumar V, John AP, Polavarapu K, Nashi S, Sekar D, Udupa K, Prathuysha PV, Prasad K, Bardhan M, Raju TR, Kramer BW, Nalini A, et al. Neuro-Cardio-Autonomic Modulations in Children with Duchenne Muscular Dystrophy. Journal of Neuromuscular Diseases. PMID 36847014 DOI: 10.3233/JND-221621 |
0.236 |
|
| 2023 |
Van Haute L, O'Connor E, Díaz-Maldonado H, Munro B, Polavarapu K, Hock DH, Arunachal G, Athanasiou-Fragkouli A, Bardhan M, Barth M, Bonneau D, Brunetti-Pierri N, Cappuccio G, Caruana NJ, Dominik N, et al. TEFM variants impair mitochondrial transcription causing childhood-onset neurological disease. Nature Communications. 14: 1009. PMID 36823193 DOI: 10.1038/s41467-023-36277-7 |
0.227 |
|
| 2023 |
Huang H, Mehta A, Kalmanovich J, Anand A, Bejarano MC, Garg T, Khan N, Tonpouwo GK, Shkodina AD, Bardhan M. Immunological and inflammatory effects of infectious diseases in circadian rhythm disruption and future therapeutic directions. Molecular Biology Reports. 1-15. PMID 36656437 DOI: 10.1007/s11033-023-08276-w |
0.224 |
|
| 2022 |
Nashi S, Polavarapu K, Bardhan M, Anjanappa RM, Preethish-Kumar V, Vengalil S, Padmanabha H, Geetha TS, Prathyusha PV, Ramprasad V, Joshi A, Chawla T, Unnikrishnan G, Sharma P, Huddar A, et al. Genotype-phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from India. Neurogenetics. PMID 36580222 DOI: 10.1007/s10048-022-00707-3 |
0.257 |
|
| 2022 |
Hesarur N, Bardhan M, Taallapalli A, Nashi S, Udupi GA, Kulkarni GB. Lichtenstein-Knorr Syndrome: A Rare Case of Ataxia with Sensorineural Hearing Loss. Annals of Indian Academy of Neurology. 25: 970-973. PMID 36561016 DOI: 10.4103/aian.aian_288_22 |
0.227 |
|
| 2022 |
Pellerin D, Danzi MC, Wilke C, Renaud M, Fazal S, Dicaire MJ, Scriba CK, Ashton C, Yanick C, Beijer D, Rebelo A, Rocca C, Jaunmuktane Z, Sonnen JA, Larivière R, ... ... Bardhan M, et al. Deep Intronic GAA Repeat Expansion in Late-Onset Cerebellar Ataxia. The New England Journal of Medicine. PMID 36516086 DOI: 10.1056/NEJMoa2207406 |
0.231 |
|
| 2022 |
Asri S, Bardhan M, Juneja K. Ukraine-Russia Crisis and COVID-19 Pandemic: Impending Danger over Public Health. Disaster Medicine and Public Health Preparedness. 17: e307. PMID 36510820 DOI: 10.1017/dmp.2022.273 |
0.262 |
|
| 2022 |
Girija MS, Tiwari R, Vengalil S, Nashi S, Preethish-Kumar V, Polavarapu K, Kulanthaivelu K, Arbind A, Bardhan M, Huddar A, Unnikrishnan G, Kiran VR, Chawla T, Nandeesh B, Nagaraj C, et al. PET-MRI in idiopathic inflammatory myositis: a comparative study of clinical and immunological markers with imaging findings. Neurological Research and Practice. 4: 49. PMID 36210472 DOI: 10.1186/s42466-022-00213-9 |
0.262 |
|
| 2022 |
Banik S, Bardhan M, Basak S. Genetic, Epigenetic, and Molecular Biology of Obesity: From Pathology to Therapeutics the Way Forward. The Journal of the Association of Physicians of India. 70: 11-12. PMID 36082890 DOI: 10.5005/japi-11001-0080 |
0.262 |
|
| 2022 |
Sindhu DM, Huddar A, Saini J, Vengalil S, Nashi S, Bardhan M, Unnikrishnan G, Rajula RR, Kandavel T, Bathala L, Visser LH, Nalini A. Cross-Sectional Area Reference Values of Nerves in the Upper and Lower Extremities using Ultrasonography in the Indian Population. Annals of Indian Academy of Neurology. 25: 449-456. PMID 35936619 DOI: 10.4103/aian.aian_727_21 |
0.262 |
|
| 2022 |
Prasad S, Shahid A, Co ELF, Khatri G, Cheema HA, Rocha ICN, Bardhan M, Hasan MM. Vaccine apartheid: the separation of the world's poorest and most vulnerable and the birth of Omicron. Therapeutic Advances in Vaccines and Immunotherapy. 10: 25151355221107975. PMID 35832726 DOI: 10.1177/25151355221107975 |
0.399 |
|
| 2022 |
Ahmed SH, Shaikh TG, Waseem S, Hasan MM, Bardhan M, Mukerjee N. Rise in Cholera amid COVID-19: Spotlight on Pakistan and Bangladesh. The Lancet Regional Health. Southeast Asia. 100041. PMID 35822107 DOI: 10.1016/j.lansea.2022.100041 |
0.256 |
|
| 2022 |
Adeyemo AO, Aborode AT, Bello MA, Obianuju AF, Hasan MM, Kehinde DO, Hossain MS, Bardhan M, Imisioluwa JO, Akintola AA. Malaria vaccine: The lasting solution to malaria burden in Africa. Annals of Medicine and Surgery (2012). 104031. PMID 35761818 DOI: 10.1016/j.amsu.2022.104031 |
0.397 |
|
| 2022 |
Thakrar V, Bardhan M, Chakraborty N. Early intervention in psychosis: An analysis of the characteristics and service needs of patients over the age of 35. Early Intervention in Psychiatry. PMID 35739609 DOI: 10.1111/eip.13318 |
0.262 |
|
| 2022 |
Boiko DI, Shkodina AD, Hasan MM, Bardhan M, Kazmi SK, Chopra H, Bhutra P, Baig AA, Skrypnikov AM. Melatonergic Receptors (Mt1/Mt2) as a Potential Additional Target of Novel Drugs for Depression. Neurochemical Research. PMID 35689787 DOI: 10.1007/s11064-022-03646-5 |
0.228 |
|
| 2022 |
Ray I, Bardhan M, Hasan MM, Sahito AM, Khan E, Patel S, Jani I, Bhatt PK, Sp R, Swed S. Over the counter drugs and self-medication: A worldwide paranoia and a troublesome situation in India during the COVID-19 pandemic. Annals of Medicine and Surgery (2012). 103797. PMID 35637885 DOI: 10.1016/j.amsu.2022.103797 |
0.224 |
|
| 2022 |
Ray I, Hasan MM, Shah PA, Sahito AM, Sarkar A, Ghosh D, Bardhan M, Mukerjee N, Essar MY. HIV epidemic amidst COVID-19 pandemic in India: a conundrum for the country's healthcare system. Epidemiology and Infection. 1-11. PMID 35615920 DOI: 10.1017/S095026882200098X |
0.236 |
|
| 2022 |
Khan E, Jani I, Bardhan M, Hasan MM. Anti-depressants and COVID-19: A New Ray of Hope. Psychiatria Danubina. 34: 171-173. PMID 35467635 DOI: 10.24869/psyd.2022.171 |
0.251 |
|
| 2022 |
Nishadham V, Bardhan M, Polavarapu K, Vengalil S, Nashi S, Menon D, Ganaraja VH, Preethish-Kumar V, Valasani RK, Huddar A, Unnikrishnan GK, Thomas A, Saravanan A, Kulanthaivelu K, Nalini A, et al. Thymic Lesions in Myasthenia Gravis: A Clinicopathological Study from India. Journal of Neuromuscular Diseases. PMID 35431258 DOI: 10.3233/JND-210785 |
0.262 |
|
| 2022 |
Bardhan M, Anjanappa RM, Polavarapu K, Preethish-Kumar V, Vengalil S, Nashi S, Sanga S, Padmanabh H, Valasani RK, Nishadham V, Keerthipriya M, Geetha TS, Ramprasad V, Arunachal G, Thomas PT, et al. Clinical, genetic profile and disease progression of sarcoglycanopathies in a large cohort from India: high prevalence of SGCB c.544A > C. Neurogenetics. PMID 35416532 DOI: 10.1007/s10048-022-00690-9 |
0.262 |
|
| 2022 |
Vengalil S, Polavarapu K, Preethish-Kumar V, Nashi S, Arunachal G, Chawla T, Bardhan M, Mohan D, Christopher R, Bevinahalli N, Kulanthaivelu K, Nishino I, Faruq M, Nalini A. Mutation Spectrum of Primary Lipid Storage Myopathies. Annals of Indian Academy of Neurology. 25: 106-113. PMID 35342266 DOI: 10.4103/aian.aian_333_21 |
0.262 |
|
| 2022 |
Ghosh D, Chowdhury G, Samanta P, Shaw S, Deb AK, Bardhan M, Manna A, Miyoshi SI, Ramamurthy T, Dutta S, Mukhopadhyay AK. Characterization of diarrhoeagenic Escherichia coli with special reference to antimicrobial resistance isolated from hospitalized diarrhoeal patients in Kolkata (2012-2019), India. Journal of Applied Microbiology. PMID 35338762 DOI: 10.1111/jam.15548 |
0.224 |
|
| 2022 |
Beijer D, Polavarapu K, Preethish-Kumar V, Bardhan M, Dohrn MF, Rebelo A, Züchner S, Nalini A. Homozygous N-terminal missense variant in PLEKHG5 associated with intermediate CMT: A case report. Journal of Neuromuscular Diseases. 9: 347-351. PMID 34897098 DOI: 10.3233/JND-210716 |
0.247 |
|
| 2022 |
Chawla T, Preethish-Kumar V, Polavarapu K, Vengalil S, Bardhan M, Puri R, Verma J, Christopher R, Supriya M, Nashi S, Prasad C, Nadeesh B, Nalini A. Late Onset Pompe Disease with Novel Mutations and Atypical Phenotypes. Journal of Neuromuscular Diseases. 9: 261-273. PMID 34864681 DOI: 10.3233/JND-210728 |
0.262 |
|
| 2021 |
Ganaraja VH, Polavarapu K, Bardhan M, Preethish-Kumar V, Leena S, Anjanappa RM, Vengalil S, Nashi S, Arunachal G, Gunasekaran S, Mohan D, Raju S, Unnikrishnan G, Huddar A, Ravi-Kiran V, et al. Disease Progression and Mutation Pattern in a Large Cohort of LGMD R1/LGMD 2A Patients from India. Global Medical Genetics. 9: 34-41. PMID 35169782 DOI: 10.1055/s-0041-1736567 |
0.262 |
|
| 2021 |
Sarkar MA, Ozair A, Singh KK, Subash NR, Bardhan M, Khulbe Y. SARS-CoV-2 Vaccination in India: Considerations of Hesitancy and Bioethics in Global Health. Annals of Global Health. 87: 124. PMID 34963880 DOI: 10.5334/aogh.3530 |
0.578 |
|
| 2021 |
Huddar A, Polavarapu K, Preethish-Kumar V, Bardhan M, Unnikrishnan G, Nashi S, Vengalil S, Priyadarshini P, Kulanthaivelu K, Arunachal G, Lochmüller H, Nalini A. Expanding the Phenotypic Spectrum of -Associated Distal Arthrogryposis. Children (Basel, Switzerland). 8. PMID 34682174 DOI: 10.3390/children8100909 |
0.262 |
|
| 2021 |
Bardhan M, Hasan MM, Ray I, Sarkar A, Chahal P, Rackimuthu S, Essar MY. Tuberculosis amidst COVID-19 pandemic in India: unspoken challenges and the way forward. Tropical Medicine and Health. 49: 84. PMID 34674772 DOI: 10.1186/s41182-021-00377-1 |
0.247 |
|
| 2021 |
Bardhan M, Pramanik D, Riyaz R, Hasan MM, Essar MY. Dual burden of Zika and COVID-19 in India: challenges, opportunities and recommendations. Tropical Medicine and Health. 49: 83. PMID 34657633 DOI: 10.1186/s41182-021-00378-0 |
0.277 |
|
| 2021 |
Rajula RR, Saini J, Unnikrishnan G, Vengalil S, Nashi S, Bardhan M, Huddar A, Chawla T, Sindhu DM, Ganaraja VH, Polavarapu K, Preethish-Kumar V, Kandavel T, Nalini A. Muscle ultrasonography in detecting fasciculations: A noninvasive diagnostic tool for amyotrophic lateral sclerosis. Journal of Clinical Ultrasound : Jcu. 50: 286-291. PMID 34653263 DOI: 10.1002/jcu.23084 |
0.262 |
|
| 2021 |
Siddiqui S, Polavarapu K, Bardhan M, Preethish-Kumar V, Joshi A, Nashi S, Vengalil S, Raju S, Chawla T, Leena S, Mathur A, Nayak S, Mohan D, Shamim U, Prasad C, et al. Distinct and Recognisable Muscle MRI Pattern in a Series of Adults Harbouring an Identical GMPPB Gene Mutation. Journal of Neuromuscular Diseases. PMID 34633329 DOI: 10.3233/JND-200628 |
0.255 |
|
| 2021 |
Rajula RR, Saini J, Unnikrishnan G, Vengalil S, Nashi S, Bardhan M, Huddar A, Chawla T, Sindhu DM, Ganaraja VH, Polavarapu K, Preethish-Kumar V, Kandavel T, Sathyaprabha TN, Nalini A. Diaphragmatic ultrasound: Prospects as a tool to assess respiratory muscle involvement in amyotrophic lateral sclerosis. Journal of Clinical Ultrasound : Jcu. 50: 131-135. PMID 34609007 DOI: 10.1002/jcu.23069 |
0.262 |
|
| 2021 |
Rackimuthu S, Hasan MM, Bardhan M, Essar MY. COVID-19 vaccination strategies and policies in India: The need for further re-evaluation is a pressing priority. The International Journal of Health Planning and Management. PMID 34510541 DOI: 10.1002/hpm.3321 |
0.412 |
|
| 2021 |
Polavarapu K, Mathur A, Joshi A, Nashi S, Preethish-Kumar V, Bardhan M, Sharma P, Parveen S, Seth M, Vengalil S, Chawla T, Shingavi L, Shamim U, Nayak S, Vivekanand A, et al. A founder mutation in the GMPPB gene [c.1000G > A (p.Asp334Asn)] causes a mild form of limb-girdle muscular dystrophy/congenital myasthenic syndrome (LGMD/CMS) in South Indian patients. Neurogenetics. PMID 34333724 DOI: 10.1007/s10048-021-00658-1 |
0.27 |
|
| 2021 |
Polavarapu K, Bardhan M, Anjanappa RM, Vengalil S, Preethish-Kumar V, Shingavi L, Chawla T, Nashi S, Mohan D, Arunachal G, Geetha TS, Ramprasad V, Nalini A. Nemaline Rod/Cap Myopathy Due to Novel Homozygous Mutations: The First Report from South Asia and Comprehensive Literature Review. Journal of Clinical Neurology (Seoul, Korea). 17: 409-418. PMID 34184449 DOI: 10.3988/jcn.2021.17.3.409 |
0.262 |
|
| 2021 |
Nagabushana D, Polavarapu K, Bardhan M, Arunachal G, Gunasekaran S, Preethish-Kumar V, Anjanappa RM, Thomas P, Sadasivan A, Vengalil S, Nashi S, Chawla T, Warrier M, Keerthipriya M, Raju S, et al. Comparison of The Carrier Frequency of Pathogenic Variants of DMD Gene in an Indian Cohort. Journal of Neuromuscular Diseases. PMID 33843695 DOI: 10.3233/JND-210658 |
0.237 |
|
| 2021 |
Bardhan M, Polavarapu K, Bevinahalli NN, Preethish-Kumar V, Anjanappa RM, Arunachal G, Shingavi L, Vengalil S, Nashi S, Chawla T, Nagabushana D, Mohan D, Horvath R, Nishino I, Nalini A. Correction: Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome. Journal of Human Genetics. PMID 33767318 DOI: 10.1038/s10038-021-00920-2 |
0.262 |
|
| 2021 |
Bardhan M, Polavarapu K, Bevinahalli NN, Veeramani PK, Anjanappa RM, Arunachal G, Shingavi L, Vengalil S, Nashi S, Chawla T, Nagabushana D, Mohan D, Horvath R, Nishino I, Atchayaram N. Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome. Journal of Human Genetics. PMID 33712684 DOI: 10.1038/s10038-021-00913-1 |
0.262 |
|
| 2021 |
Polavarapu K, Vengalil S, Preethish-Kumar V, Arunachal G, Nashi S, Mohan D, Chawla T, Bardhan M, Nandeesh B, Gupta P, Gowda VK, Lochmüller H, Nalini A. Recessive VAMP1 mutations associated with severe congenital myasthenic syndromes - A recognizable clinical phenotype. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 31: 54-60. PMID 33631708 DOI: 10.1016/j.ejpn.2021.02.005 |
0.268 |
|
| 2020 |
Sanga S, Ghosh A, Kumar K, Polavarapu K, Kumar VP, Vengalil S, Nashi S, Bardhan M, Arunachal G, Raju S, Gayathri N, Biswas NK, Chakrabarti S, Nalini A, Roy S, et al. Whole Exome Analyses of Congenital Muscular Dystrophy and Congenital Myopathy Patients from India Reveal a Wide Spectrum of Known and Novel Mutations. European Journal of Neurology. PMID 33124102 DOI: 10.1111/ene.14616 |
0.269 |
|
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