Vykuntaraju K. Gowda

Statistics

Publications

Citations

143

H-Index

Active since

2020

Affiliations

Indira Gandhi Institute of Child Health(Current)

University College London

National Hospital for Neurology and Neurosurgery

Mashhad University of Medical Sciences

St George's, University of London

Vykuntaraju K. Gowda is an author at Indira Gandhi Institute of Child Health specializing in life sciences, neurodevelopmental disorders, and neurogenetic disorders.

ORCID

Publications per year

2020–2024

Publications

Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals

Ken Saida, Reza Maroofian, Toru Sengoku et al. · Genetics in Medicine · 2022 · 39 citations · Full text

Life Sciences, Neurology, Neuroscience +16

Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia

Heba Morsy, Mehdi Benkirane, Elisa Calì et al. · Genetics in Medicine · 2022 · 28 citations · Full text

Medicine, Neurology, Neuroscience +12

Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature

Jessica Priestley, Lisa M. Pace, Kuntal Sen et al. · Molecular Genetics and Metabolism Reports · 2022 · 21 citations · Full text

Medicine, Neurology, Pediatrics +12

Comprehensive immunoprofiling of neurodevelopmental disorders suggests three distinct classes based on increased neurogenesis, Th-1 polarization or IL-1 signaling

Nikhitha Sreenivas, Michaël Maes, Hansashree Padmanabha et al. · Brain Behavior and Immunity · 2023 · 19 citations · Full text

Life Sciences, Immunology, Neuroscience +15

Brown−Vialetto−Van Laere and Fazio−Londe syndromes: <i>SLC52A3</i> mutations with puzzling phenotypes and inheritance

Santhalingam Gayathri, Vykuntaraju K. Gowda, Tamilarasan Udhayabanu et al. · European Journal of Neurology · 2020 · 13 citations

Life Sciences, Genetics, Molecular Genetics +16

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