Concepedia

Author

B. Sunitha

National Institute of Mental Health and Neurosciences

Also Known As

B. Sunitha, Balaraju Sunitha, S. Balaraju, Sunitha Balaraju

20

Publications

290

Citations

10

H-Index

37

Concepts

All Affiliations

National Institute of Mental Health and NeurosciencesNewcastle UniversityUniversity of CambridgeInstitute of BioinformaticsUniversity of Freiburg
BS

About

B. Sunitha is an author at National Institute of Mental Health and Neurosciences specializing in medicine, neuromuscular pathology, and pathology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

5

5

137

2

Natural Sciences

2

2

55

3

Biochemistry

2

2

55

4

Health Sciences

1

1

36

5

Public Health

1

1

16

B. Sunitha

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10

Publications

285

Citations

10

H-Index

YearCitations

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

Renjini Ramadasan-Nair, Narayanappa Gayathri, Sudha Mishra,

Journal of Biological Chemistry

2013

67

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

Niya Gowthami, B. Sunitha, Manish Kumar,

Journal of Chemical Neuroanatomy

2018

43

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

B. Sunitha, Narayanappa Gayathri, Manish Kumar,

Journal of Neurochemistry

2016

36

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

B. Sunitha, Ana Töpf, Grace McMacken,

European Journal of Human Genetics

2019

33

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

Amirtharaj Francis, B. Sunitha, Kandavalli Vinodh,

PLoS ONE

2014

30

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

Atchayaram Nalini, Kiran Polavarapu, B. Sunitha,

Neurology India

2015

18

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

Serdal Güngör, Yavuz Oktay, Álvaro Aranguren‐Ibáñez,

iScience

2020

16

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

Kiran Polavarapu, B. Sunitha, Ana Töpf,

Brain

2023

16

Severe neurodevelopmental disease caused by a homozygous TLK2 variant

Ana Töpf, Yavuz Oktay, B. Sunitha,

European Journal of Human Genetics

2019

14

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

B. Sunitha, Manish Kumar, Niya Gowthami,

Journal of Proteomics

2019

12

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