Asha Kishore

Hong Kong University of Science and Technology — Hong Kong

Medicine · Health Sciences

31h-index3.1kcitations107works2.42yr avg
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Research Topics

Parkinson's Disease Mechanisms and Treatments(63), Neurological disorders and treatments(54), Transcranial Magnetic Stimulation Studies(27), Genetic Neurodegenerative Diseases(13), Botulinum Toxin and Related Neurological Disorders(12)

Publications104 total

TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations
npj Parkinson s Disease·2025· 2 citedOpen Access
Reply to: “Early Indian Age at Onset of Parkinson's: A Case for a Gene‐Environment Lens”
Movement Disorders·2025
Survival after Subthalamic Deep Brain Stimulation for Parkinson's Disease: 25‐Year Experience from a Single Center
Movement Disorders Clinical Practice·2025
Demographic and Clinical Profiles of Parkinson's Disease in India: Observations from a Nation‐Wide Multicenter Study
Movement Disorders·2025· 1 citedOpen Access
Unilateral Painless Legs and Moving Toes Syndrome with Bilateral Tarlov Cysts
Movement Disorders Clinical Practice·2025Open Access
The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population
npj Parkinson s Disease·2025· 3 citedOpen Access
Deciphering the Genetic Architecture of Parkinson’s Disease in India
2025· 9 citedOpen Access
Multimodality Brain Imaging Markers in <scp>Progressive Supranuclear Palsy</scp> Subtypes and Parkinson's Disease
Movement Disorders Clinical Practice·2025· 2 citedOpen Access
Treatable Hereditary Cerebellar Ataxias
Cambridge University Press eBooks·2025
Video-Oculography for Enhancing the Diagnostic Accuracy of Early Oculomotor Dysfunction in Progressive Supranuclear Palsy
Journal of Movement Disorders·2024· 3 citedOpen Access
Resequencing the complete SNCA locus in Indian patients with Parkinson’s disease
npj Parkinson s Disease·2024· 5 citedOpen Access
A Novel <scp><i>PINK1</i></scp> p.<scp>F385S</scp> Loss‐of‐Function Mutation in an Indian Family with Parkinson's Disease
Movement Disorders·2024· 3 citedOpen Access
Quantifying abnormal writing kinematics in writer’s cramp using a novel software platform
Acta Neurologica Belgica·2024· 1 cited
Novel <scp><i>PANK2</i></scp> Variant in Asian Indians with Atypical Pantothenate Kinase Associated Neurodegeneration
Movement Disorders·2024· 2 cited
ROLE OF CEREBELLUM BASAL GANGLIA DIRECT SUBCORTICAL NETWORK IN THE PATHOPHYSIOLOGY OF PARKINSON’S DISEASE
IBRO Neuroscience Reports·2023Open Access
Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)
npj Parkinson s Disease·2023· 1 citedOpen Access
Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
npj Parkinson s Disease·2023· 34 citedOpen Access
A Review on Implantable Neuroelectrodes
Critical Reviews in Biomedical Engineering·2023· 2 cited
Cerebellar and basal ganglia structural connections in humans: Effect of aging and relation with memory and learning
Frontiers in Aging Neuroscience·2023· 11 citedOpen Access
Automated analysis of pen-on-paper spirals for tremor detection, quantification, and differentiation
Annals of Movement Disorders·2023· 4 citedOpen Access
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Frequent Co-authors

Syam Krishnan(17), Traian Popa(12), Sabine Meunier(9), Roopa Rajan(8), P.S. Sarma(7), Raúl de la Fuente‐Fernández(7), Gangadhara Sarma(6), Donald B. Calne(6), S. Pradeep(5), Michael Schulzer(5), A. Jon Stoessl(4), Edwin Mak(4), K. P. Divya(4), Praveen James(4), Balu Velayudhan(3), Cécile Hubsch(3), Emmanuel Roze(3), A. Balachandran(3), B. J. Snow(3), Rupam Borgohain(3)