Author

Balaraju Sunitha

Observed names: B. Sunitha, Sunitha Balaraju

Institutions: Centre for Human Genetics, University of Oxford

Observed institutions: Centre for Human Genetics, University of Cambridge, University of Oxford, National Institute of Mental Health and Neurosciences, Newcastle University

ORCID: 0000-0003-0273-1918

Observed ORCID: 0000-0003-0273-1918

OpenAlex ID: A5033005656

Mitochondrial Alterations and Oxidative Stress in an Acute Transient Mouse Model of Muscle Degeneration

2013 · Renjini Ramadasan-Nair, Narayanappa Gayathri, et al. · Journal of Biological Chemistry · 68

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Muscle biopsies from human muscle diseases with myopathic pathology reveal common alterations in mitochondrial function

2016 · Balaraju Sunitha, Narayanappa Gayathri, et al. · Journal of Neurochemistry · 40

Congenital myasthenic syndrome with mild intellectual disability caused by a recurrent SLC25A1 variant

2019 · Sunitha Balaraju, Ana Töpf, et al. · European Journal of Human Genetics · 35

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Novel TCAP Mutation c.32C>A Causing Limb Girdle Muscular Dystrophy 2G

2014 · Amirtharaj Francis, Balaraju Sunitha, et al. · PLoS ONE · 34

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Mapping the protein phosphorylation sites in human mitochondrial complex I (NADH: Ubiquinone oxidoreductase): A bioinformatics study with implications for brain aging and neurodegeneration

2018 · Niya Gowthami, B. Sunitha, et al. · Journal of Chemical Neuroanatomy · 32

Clinical and genetic characterisation of a large Indian congenital myasthenic syndrome cohort

2023 · Kiran Polavarapu, Balaraju Sunitha, et al. · Brain · 24

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A prospective study on the immunophenotypic characterization of limb girdle muscular dystrophies 2 in India

2015 · Atchayaram Nalini, Kiran Polavarapu, et al. · Neurology India · 18

Regulatory T cells attenuate chronic inflammation and cardiac fibrosis in hypertrophic cardiomyopathy

2025 · Ying-Jie Wang, Kamayani Singh, et al. · Science Translational Medicine · 17

Autosomal recessive variants in TUBGCP2 alter the γ-tubulin ring complex leading to neurodevelopmental disease

2020 · Serdal Gungor, Yavuz Oktay, et al. · iScience · 16

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Human muscle pathology is associated with altered phosphoprotein profile of mitochondrial proteins in the skeletal muscle

2019 · B. Sunitha, Manish Kumar, et al. · Journal of Proteomics · 12

Severe neurodevelopmental disease caused by a homozygous TLK2 variant

2019 · Ana Töpf, Yavuz Oktay, et al. · European Journal of Human Genetics · 12

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Unique genotypic pattern in Indian DPAGT1 congenital myasthenic syndrome patients with two likely founder mutations

2023 · Kiran Polavarapu, Balaraju Sunitha, et al. · Journal of the Neurological Sciences

New Insights Into Cellular or Muscle Function

2021 · B. Sunitha, M. Kumar, et al. · Neuromuscular Disorders

Muscle magnetic resonance imaging (MRI) in patients with LGMD 2I confirmed by immunohistochemistry and/or immunoblotting

2013 · A. Ramakrishna, A. Nalini, et al. · Journal of the Neurological Sciences

Detection of limb girdle muscular dystrophy 2A (calpainopathy) by autocatalytic activity of calpain and by quantification of calpain bands by densitometry

2013 · S. Modi, A. Nalini, et al. · Journal of the Neurological Sciences

Magnetic resonance imaging findings in immunohistochemically confirmed sarcoglycanopathies

2013 · A. Ramakrishna, A. Nalini, et al. · Journal of the Neurological Sciences

LGMD2I: Immunohistochemical and immunoblot technique assisted identification of 51 cases with both duchenne and becker phenotype

2013 · S. Modi, A. Nalini, et al. · Journal of the Neurological Sciences

Works count: 17

Citation count: 308

H-index: 11

I10-index: 11