Concepedia

Author

Shwetha Chiplunkar

National Institute of Mental Health and Neurosciences

Also Known As

Chiplunkar Shwetha, Shwetha Chiplunkar

22

Publications

265

Citations

11

H-Index

37

Concepts

All Affiliations

National Institute of Mental Health and NeurosciencesCentre for Cellular and Molecular BiologyChildren's Hospital at WestmeadCentre for DNA Fingerprinting and Diagnostics
SC

About

Shwetha Chiplunkar is an author at National Institute of Mental Health and Neurosciences specializing in medicine, mitochondrial function, and pathology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

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2

Health Sciences

1

1

22

3

Public Health

1

1

17

4

Cell Biology

1

1

17

5

Metabolism

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24

Shwetha Chiplunkar

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11

Publications

235

Citations

10

H-Index

YearCitations

Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children?

Parayil Sankaran Bindu, Kothari Sonam, Shwetha Chiplunkar,

Multiple Sclerosis and Related Disorders

2018

42

Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south India

Parayil Sankaran Bindu, Hanumanthapura R. Arvinda, Arun B. Taly,

Mitochondrion

2015

31

Huppke-Brendel syndrome in a seven months old boy with a novel 2-bp deletion in SLC33A1

Shwetha Chiplunkar, Bindu Parayil Sankaran, Madhu Nagappa,

Metabolic Brain Disease

2016

25

Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India

Kothari Sonam, Parayil Sankaran Bindu, MM Srinivas Bharath,

Mitochondrion

2016

24

Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations

Parayil Sankaran Bindu, Kothari Sonam, Periyasamy Govindaraj,

Clinical Neurology and Neurosurgery

2017

22

Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome

V.P. Vandana, Bindu Parayil Sankaran, Kothari Sonam,

Clinical Neurology and Neurosurgery

2016

19

Leukodystrophies and Genetic Leukoencephalopathies in Children Specified by Exome Sequencing in an Expanded Gene Panel

Bindu Parayil Sankaran, Madhu Nagappa, Shwetha Chiplunkar,

Journal of Child Neurology

2020

17

Serum fibroblast growth factor 21 and growth differentiation factor 15: Two sensitive biomarkers in the diagnosis of mitochondrial disorders

Akshata Huddar, Periyasamy Govindaraj, Shwetha Chiplunkar,

Mitochondrion

2021

17

Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in 4-aminobutyrate aminotransferase (ABAT) gene

Madhu Nagappa, Parayil Sankaran Bindu, Shwetha Chiplunkar,

Brain and Development

2016

15

Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India

Parayil Sankaran Bindu, C. Govindaraju, Kothari Sonam,

Mitochondrion

2016

13

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