P. Sneha - Concepedia

Author

P. Sneha

Vellore Institute of Technology University

Also Known As

P B Sneha, P Sneha, P. Sneha, P. U. Sneha, Panneerselvam Sneha, SNEHA P K, Safiq Hussain, Sneha P, Sneha P.

Publications

923

Citations

H-Index

Concepts

All Affiliations

Vellore Institute of Technology University Qatar University Sri Ramachandra Institute of Higher Education and Research

About

P. Sneha is an author at Vellore Institute of Technology University specializing in medicine, molecular biology, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	14	519
2	Natural Sciences	9	9	267
3	Engineering	2	2	97
4	Health Sciences	1	1	33
5	Public Health	1	1	61

P. Sneha

Publications

608

Citations

H-Index

Page 1

	Year	Citations
A profound computational study to prioritize the disease-causing mutations in PRPS1 gene Ashish Kumar Agrahari, P. Sneha, C. George Priya Doss, Metabolic Brain Disease Genetic AnalysisGeneticsComputational BiologyProfound Computational StudyMolecular Biology	2017	67
Genetic Epidemiology of Glucose-6-Phosphate Dehydrogenase Deficiency in the Arab World C. George Priya Doss, Dima R. Alasmar, Reem Ibrahim Bux, Scientific Reports Systematic SearchGeneticsGenetic EpidemiologyHuman PolymorphismPathology	2016	61
Determining the role of missense mutations in the POU domain of HNF1A that reduce the DNA-binding affinity: A computational approach P. Sneha, D. Thirumal Kumar, C. George Priya Doss, PLoS ONE Missense MutationsStructural BioinformaticsGeneticsYoung Type 3Genomic Mechanism	2017	55
Influence of V54M mutation in giant muscle protein titin: a computational screening and molecular dynamics approach D. Thirumal Kumar, C. George Priya Doss, P. Sneha, Journal of Biomolecular Structure and Dynamics Biophysical ModelingEngineeringStructural BioinformaticsBiomolecular Structure PredictionMolecular Biology	2016	50
Computational approach to unravel the impact of missense mutations of proteins (D2HGDH and IDH2) causing D-2-hydroxyglutaric aciduria 2 D. Thirumal Kumar, L. Jerushah Emerald, C. George Priya Doss, Metabolic Brain Disease Missense MutationsEngineeringSomatic VariantGenetic DisorderMedicine	2018	47
Molecular dynamics-based analyses of the structural instability and secondary structure of the fibrinogen gamma chain protein with the D356V mutation Shabana Kouser Ali, P. Sneha, J. Priyadharshini Christy, Journal of Biomolecular Structure and Dynamics Structural BioinformaticsProtein AssemblyBiomolecular Structure PredictionGeneticsMolecular Biology	2016	43
Implication of salt stress induces changes in pigment production, antioxidant enzyme activity, and qRT-PCR expression of genes involved in the biosynthetic pathway of Bixa orellana L. P. Sneha, C. George Priya Doss, J. Godwin Christopher, Functional & Integrative Genomics BiologyBiosynthesisOsmotic StressCarotenoidAbiotic Stress	2019	43
Structural Analysis of G1691S Variant in the Human <i>Filamin B</i> Gene Responsible for Larsen Syndrome: A Comparative Computational Approach P. Sneha, D. Thirumal Kumar, Himani Tanwar, Journal of Cellular Biochemistry	2017	41
Structural analysis of missense mutations in galactokinase 1 (GALK1) leading to galactosemia type‐2 P. Sneha, Elaheh Ebrahimi, Sara Ahmed Ghazala, Journal of Cellular Biochemistry Missense MutationsGeneticsGlycobiologyMolecular BiologyMolecular Genetics	2018	38
Effect of UV radiation and its implications on carotenoid pathway in Bixa orellana L. P. Sneha, C. George Priya Doss, Siva Ramamoorthy Journal of Photochemistry and Photobiology B Biology BiologyCarotenoidUv RadiationBotanyPhotochemistry	2017	33

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