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Dual burden of Zika and COVID-19 in India: challenges, opportunities and recommendations

Tropical medicine and health, 2021-10, Vol.49 (1), p.83-83, Article 83

2021

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Genetics and Genomics of Chronic Pancreatitis with a Focus on Disease Biology and Molecular Pathogenesis

Global medical genetics, 2023-12, Vol.10 (4), p.324-334

2023

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Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome

Journal of human genetics, 2021-08, Vol.66 (8), p.813-823

2021

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Tuberculosis amidst COVID-19 pandemic in India: unspoken challenges and the way forward

Tropical medicine and health, 2021-10, Vol.49 (1), p.84-84, Article 84

2021

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Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy

Scientific reports, 2023-09, Vol.13 (1), p.15095-15095, Article 15095

2023

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SARS-CoV-2 Vaccination in India: Considerations of Hesitancy and Bioethics in Global Health

Annals of global health, 2021, Vol.87 (1), p.124-124

2021

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Muscle ultrasonography in detecting fasciculations: A noninvasive diagnostic tool for amyotrophic lateral sclerosis

Journal of clinical ultrasound, 2022-02, Vol.50 (2), p.286-291

2022

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Correction: Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome

Journal of human genetics, 2021-08, Vol.66 (8), p.841-841

2021

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Self-medication prevalence and associated factors among adult population in Northern India: A community-based cross-sectional study

SAGE open medicine, 2024-01, Vol.12, p.20503121241240507-20503121241240507

2024

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Vaccine apartheid: the separation of the world’s poorest and most vulnerable and the birth of Omicron

Therapeutic advances in vaccines and immunotherapy, 2022, Vol.10, p.251513552211079

2022

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Classical Hirayama disease presenting as progressive spastic quadriparesis

Annals of the Indian Academy of Neurology, 2023-05, Vol.26 (3), p.308-310

2023

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Mutation spectrum of primary lipid storage myopathies

Annals of the Indian Academy of Neurology, 2022-01, Vol.25 (1), p.106-113

2022

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Identification of a Novel Intronic Mutation in VMA21 Associated with a Classical Form of X-Linked Myopathy with Autophagy

Global medical genetics, 2024-06, Vol.11 (2), p.167-174

2024

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Rise in cholera amid COVID-19: Spotlight on Pakistan and Bangladesh

The Lancet regional health. Southeast Asia, 2022-09, Vol.4, p.100041-100041, Article 100041

2022

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Exploring Health Care Disparities in Genetic Testing and Research for Hereditary Cardiomyopathy: Current State and Future Perspectives

Global medical genetics, 2024-01, Vol.11 (1), p.36-47

2024

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Lichtenstein-Knorr syndrome: A rare case of ataxia with sensorineural hearing loss

Annals of the Indian Academy of Neurology, 2022-09, Vol.25 (5), p.970-973

2022

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Animacy effects in fluency task performance in early Alzheimer's Disease-A case-control study

Annals of the Indian Academy of Neurology, 2022-09, Vol.25 (5), p.968-970

2022

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Qualitative and Quantitative Electrocardiogram Parameters in a Large Cohort of Children with Duchenne Muscle Dystrophy in Comparison with Age-Matched Healthy Subjects: A Study from South India

Annals of the Indian Academy of Neurology, 2024-01, Vol.27 (1), p.53-57

2024

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PET-MRI in idiopathic inflammatory myositis: a comparative study of clinical and immunological markers with imaging findings

Neurological research and practice, 2022-10, Vol.4 (1), p.49-49, Article 49

2022

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Expanding the Phenotypic Spectrum of ECEL1-Associated Distal Arthrogryposis

Children (Basel), 2021-10, Vol.8 (10), p.909

2021

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Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Mutations: The First Report from South Asia and Comprehensive Literature Review

Journal of Clinical Neurology, 2021, 17(3), , pp.409-418

2021

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Disease Progression and Mutation Pattern in a Large Cohort of LGMD R1/LGMD 2A Patients from India

Global medical genetics, 2022-03, Vol.9 (1), p.034-041

2022

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Genetic, Epigenetic, and Molecular Biology of Obesity: From Pathology to Therapeutics the Way Forward

Journal of the Association of Physicians of India, 2022-09, Vol.70 (9), p.76-82

2022

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Early intervention in psychosis: An analysis of the characteristics and service needs of patients over the age of 35

Early intervention in psychiatry, 2023-02, Vol.17 (2), p.177-182

2023

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Dual burden of Zika and COVID-19 in India: challenges, opportunities and recommendations

Genetics and Genomics of Chronic Pancreatitis with a Focus on Disease Biology and Molecular Pathogenesis

Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome

Tuberculosis amidst COVID-19 pandemic in India: unspoken challenges and the way forward

Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathy

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

SARS-CoV-2 Vaccination in India: Considerations of Hesitancy and Bioethics in Global Health

Muscle ultrasonography in detecting fasciculations: A noninvasive diagnostic tool for amyotrophic lateral sclerosis

Correction: Megaconial congenital muscular dystrophy secondary to novel CHKB mutations resemble atypical Rett syndrome

Self-medication prevalence and associated factors among adult population in Northern India: A community-based cross-sectional study

Vaccine apartheid: the separation of the world’s poorest and most vulnerable and the birth of Omicron

Classical Hirayama disease presenting as progressive spastic quadriparesis

Mutation spectrum of primary lipid storage myopathies

Identification of a Novel Intronic Mutation in VMA21 Associated with a Classical Form of X-Linked Myopathy with Autophagy

Rise in cholera amid COVID-19: Spotlight on Pakistan and Bangladesh

Exploring Health Care Disparities in Genetic Testing and Research for Hereditary Cardiomyopathy: Current State and Future Perspectives

Lichtenstein-Knorr syndrome: A rare case of ataxia with sensorineural hearing loss

Animacy effects in fluency task performance in early Alzheimer's Disease-A case-control study

Qualitative and Quantitative Electrocardiogram Parameters in a Large Cohort of Children with Duchenne Muscle Dystrophy in Comparison with Age-Matched Healthy Subjects: A Study from South India

PET-MRI in idiopathic inflammatory myositis: a comparative study of clinical and immunological markers with imaging findings

Expanding the Phenotypic Spectrum of ECEL1-Associated Distal Arthrogryposis

Nemaline Rod/Cap Myopathy Due to Novel Homozygous MYPN Mutations: The First Report from South Asia and Comprehensive Literature Review

Disease Progression and Mutation Pattern in a Large Cohort of LGMD R1/LGMD 2A Patients from India

Genetic, Epigenetic, and Molecular Biology of Obesity: From Pathology to Therapeutics the Way Forward

Early intervention in psychosis: An analysis of the characteristics and service needs of patients over the age of 35

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