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The European Journal of Neuroscience|March 9, 2026
Association of Bassoon (BSN) Gene Mutations With Gait and Motor Impairments in Parkinson's DiseasePrashanth Lingappa Kukkle, Ahamed Panikkaveettil Kaladiyil, Thenral S Geetha, et al.
Cell Reports|May 12, 2015
Differential connexin function enhances self-renewal in glioblastomaMasahiro Hitomi, Loic P Deleyrolle, Erin E Mulkearns-Hubert, et al.
American Journal of Human Genetics|December 3, 2013
Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinismJames A Poulter, Musallam Al-Araimi, Ivan Conte, et al.
Movement Disorders Clinical Practice|May 24, 2026
Progressive Supranuclear Palsy in India: Insights from a Large Multicenter Clinical Cohort (Project PAIR-PSP)Prashanth Lingappa Kukkle, Divyani Garg, Jacky Ganguly, et al.
Journal of Neurology|July 20, 2026
Systematic reanalysis of next-generation sequencing data in 101 neuromuscular disorder families enhances diagnostic yield, reveals intronic variants, and identifies a novel disease geneSivasankar Malaichamy, Kiran Polavarapu, Rachel Thompson, et al.
Advanced Biology|July 10, 2022
Genome-Wide Polygenic Score Predicts Large Number of High Risk Individuals in Monogenic Undiagnosed Young Onset Parkinson's Disease Patients from IndiaPrashanth Lingappa Kukkle, Thenral S Geetha, Ruchi Chaudhary, et al.
Journal of the American College of Cardiology|August 9, 2020
Validation of a Genome-Wide Polygenic Score for Coronary Artery Disease in South AsiansMinxian Wang, Ramesh Menon, Sanghamitra Mishra, et al.
Cancer Cell|November 20, 2018
Actionable Activating Oncogenic ERBB2/HER2 Transmembrane and Juxtamembrane Domain MutationsKanika Bajaj Pahuja, Thong T Nguyen, Bijay S Jaiswal, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 28, 2023
The Genetic Drivers of Juvenile, Young, and Early-Onset Parkinson's Disease in IndiaShan V Andrews, Prashanth L Kukkle, Ramesh Menon, et al.
Frontiers in Immunology|March 22, 2021
The Spectrum of Clinical, Immunological, and Molecular Findings in Familial Hemophagocytic Lymphohistiocytosis: Experience From IndiaSnehal Shabrish, Madhura Kelkar, Reetika Malik Yadav, et al.
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