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The Protein Journal|November 1, 2024
Influence of Cataract Causing Mutations on αA-Crystallin: A Computational ApproachKajal Abrol, Jayarani Basumatari, Jupita Handique, et al.
Annals of Indian Academy of Neurology|October 16, 2025
Diagnostic Yield and Genetic Burden Analysis of Frequently Mutated Genes in Progressive AtaxiaPooja Sharma, Jupita Handique, Kriti Kashyap, et al.
Seizure|December 12, 2024
Drug-refractory epilepsy due to a novel CLN5 mutation: A report of three patients from an Indian familyShiny Joy, Ayush Agarwal, Jupita Handique, et al.
Movement Disorders Clinical Practice|October 4, 2025
MFSD8-Related CLN7 Disease with Adult-Onset Cerebellar Ataxia: A Five-Patient Case SeriesPooja Sharma, Ayush Agarwal, Tiyasha De, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 25, 2025
Deciphering ALS-linked genetic variants in indian patients using targeted and exome sequencing approachesShahrumi Reza, Jupita Handique, Pooja Sharma, et al.
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