Jharna Ray

University of Calcutta — India

Medicine · Health Sciences

22h-index2.9kcitations111works0.02yr avg
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Research Topics

Parkinson's Disease Mechanisms and Treatments(21), Glaucoma and retinal disorders(16), Neurological disorders and treatments(11), Growth Hormone and Insulin-like Growth Factors(9), Lysosomal Storage Disorders Research(9)

Publications111 total

Green tea extract and its component EGCG enhance LTP while reducing LTD in the CA1 area of the hippocampus: A potential nootropic effect of EGCG
Pharmacological Research - Natural Products·2025
Identifying regulatory variants in Indian Wilson’s disease patients with missing heritability
Gene & Protein in Disease·2025Open Access
Outlier Detection in a Time Series Data
Lecture notes in networks and systems·2025
Parkinson’s disease-associated 18 bp promoter variant of DJ-1 alters REST binding and regulates its expression
Neuroscience Letters·2023· 2 cited
Missing heritability of Wilson disease: a search for the uncharacterized mutations
Mammalian Genome·2022· 6 cited
Genetic Polymorphisms in DRD4 and Risk for Parkinson's Disease Among Eastern Indians
Neurology India·2022· 10 citedOpen Access
Long-Term Efficacy of Pallidal Deep Brain Stimulation in a Patient with DYT-THAP1 (DYT-6) Dystonia from India
Annals of Indian Academy of Neurology·2022· 2 citedOpen Access
Parkinson's Disease Associated 18 bp Promoter Variant of <i>DJ-1</i> Alters Rest Binding and Regulates its Expression
SSRN Electronic Journal·2022Open Access
Identification of GBA mutations among neurodegenerative disease patients from eastern India
Neuroscience Letters·2021· 14 cited
Mitochondrial DNA Haplogroups and Three Independent Polymorphisms have no Association with the Risk of Parkinson's Disease in East Indian Population
Neurology India·2021· 5 cited
Analysis of Wilson disease mutations revealed that interactions between different ATP7B mutants modify their properties
Scientific Reports·2020· 37 citedOpen Access
Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in India
Journal of Molecular Neuroscience·2020· 2 cited
Role of LRRK2 variant p.Gly2019Ser in patients with Parkinsonism
The Indian Journal of Medical Research·2020· 2 citedOpen Access
Convolvulus pluricaulis extract can modulate synaptic plasticity in rat brain hippocampus
Neuroreport·2020· 12 cited
Association of APOE gene polymorphism with stroke patients from rural Eastern India
Annals of Indian Academy of Neurology·2019· 8 citedOpen Access
<i>Dopamine β hydroxylase</i> (<i>DBH</i>) polymorphisms do not contribute towards the clinical course of Wilson's disease in Indian patients
The Journal of Gene Medicine·2019· 3 cited
Role of Apolipoprotein E, Cathepsin D, and Brain-Derived Neurotrophic Factor in Parkinson’s Disease: A Study from Eastern India
NeuroMolecular Medicine·2019· 9 cited
Dopamine β Hydroxylase (DBH) is a potential modifier gene associated with Parkinson's disease in Eastern India
Neuroscience Letters·2019· 13 cited
A Compound Heterozygote for GCH1 Mutation Represents a Case of Atypical Dopa-Responsive Dystonia
Journal of Molecular Neuroscience·2019· 12 cited
Primary generalized dystonia due to TOR1A ΔGAG mutation in an Indian family with intrafamilial clinical heterogeneity
Neurology India·2019· 2 citedOpen Access
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Frequent Co-authors

Kunal Ray(22), Shyamal Kumar Das(11), Nancy E. Cooke(7), Arindam Biswas(7), Gautami Das(7), Tamal Sadhukhan(5), Gregory M. Acland(4), Stephen A. Liebhaber(4), Arijit Mukhopadhyay(4), Tufan Naiya(4), Shubhrajit Roy(4), Geoffrey K. Aguirre(3), Rajarshi Neogi(3), Somnath Datta(3), Marjory B. Brooks(3), Amar K. Misra(3), Mansi Vishal(3), Subhajit Giri(3), Tomás S. Alemán(2), Artur V. Cideciyan(2)