Uday B. Muthane

No 58, C/12, Kudlu Village, Hosur Main Road
Bengaluru, KA 560068, India

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 20 publications

The Genetic Drivers of Juvenile, Young, and Early-Onset Parkinson's Disease in India.

The Genetic Drivers of Juvenile, Young, and Early-Onset Parkinson's Disease in India.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: July 13, 2023

Genome-Wide Polygenic Score Predicts Large Number of High Risk Individuals in Monogenic Undiagnosed Young Onset Parkinson's Disease Patients from India.

Genome-Wide Polygenic Score Predicts Large Number of High Risk Individuals in Monogenic Undiagnosed Young Onset Parkinson's Disease Patients from India.

Journal: Advanced biology

Published: December 26, 2021

South Asian medical cohorts reveal strong founder effects and high rates of homozygosity.

South Asian medical cohorts reveal strong founder effects and high rates of homozygosity.

Journal: Nature communications

Published: September 08, 2021

Clinical Study of 668 Indian Subjects with Juvenile, Young, and Early Onset Parkinson's Disease.

Clinical Study of 668 Indian Subjects with Juvenile, Young, and Early Onset Parkinson's Disease.

Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

Published: March 09, 2021

The Spectrum of Movement Disorders in Tertiary Care Centers in India: A Tale of Three Cities.

The Spectrum of Movement Disorders in Tertiary Care Centers in India: A Tale of Three Cities.

Journal: Annals of Indian Academy of Neurology

Published: December 12, 2020

Compound heterozygous variants in Wiskott-Aldrich syndrome like (WASL) gene segregating in a family with early onset Parkinson's disease.

Compound heterozygous variants in Wiskott-Aldrich syndrome like (WASL) gene segregating in a family with early onset Parkinson's disease.

Journal: Parkinsonism & related disorders

Published: September 29, 2020

Novel and reported variants in Parkinson's disease genes confer high disease burden among Indians.

Novel and reported variants in Parkinson's disease genes confer high disease burden among Indians.

Journal: Parkinsonism & related disorders

Published: January 31, 2020

Exome Sequencing Identifies a Novel Homozygous Missense ATP13A2 Mutation.

Exome Sequencing Identifies a Novel Homozygous Missense ATP13A2 Mutation.

Journal: Movement disorders clinical practice

Published: February 06, 2016

Early Onset Parkinson's disease due to DJ1 mutations: An Indian study.

Early Onset Parkinson's disease due to DJ1 mutations: An Indian study.

Journal: Parkinsonism & related disorders

Published: December 09, 2015

Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes.

Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes.

Journal: Journal of medical genetics

Published: November 03, 2015

Discovery of a frameshift mutation in podocalyxin-like (PODXL) gene, coding for a neural adhesion molecule, as causal for autosomal-recessive juvenile Parkinsonism.

Discovery of a frameshift mutation in podocalyxin-like (PODXL) gene, coding for a neural adhesion molecule, as causal for autosomal-recessive juvenile Parkinsonism.

Journal: Journal of medical genetics

Published: August 15, 2015

Secondary parkinsonism with Mumps infection.

Secondary parkinsonism with Mumps infection.

Journal: Parkinsonism & related disorders

Published: July 06, 2015

Showing 1-12 of 20

Last Updated: 09/26/2026