Akhilesh K. Sonakar

Mathura Road
Delhi, DL 110025, India

Last Updated: 09/26/2026

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Found 10 publications

MFSD8-Related CLN7 Disease with Adult-Onset Cerebellar Ataxia: A Five-Patient Case Series.

MFSD8-Related CLN7 Disease with Adult-Onset Cerebellar Ataxia: A Five-Patient Case Series.

Journal: Movement disorders clinical practice

Published: July 09, 2025

Mitochondrial DNA Haplogroups and Age at Onset of Spinocerebellar Ataxia Type 2: A Study in Indian Patients.

Mitochondrial DNA Haplogroups and Age at Onset of Spinocerebellar Ataxia Type 2: A Study in Indian Patients.

Journal: Annals of Indian Academy of Neurology

Published: May 06, 2025

Diagnostic Yield and Genetic Burden Analysis of Frequently Mutated Genes in Progressive Ataxia.

Diagnostic Yield and Genetic Burden Analysis of Frequently Mutated Genes in Progressive Ataxia.

Journal: Annals of Indian Academy of Neurology

Published: March 28, 2025

Founder SPG11 Mutation in the Baniya Community of India.

Founder SPG11 Mutation in the Baniya Community of India.

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

Published: May 08, 2024

Spinocerebellar ataxia type 27B (SCA27B) in India: insights from a large cohort study suggest ancient origin.

Spinocerebellar ataxia type 27B (SCA27B) in India: insights from a large cohort study suggest ancient origin.

Journal: Neurogenetics

Published: March 07, 2024

Investigation of RFC1 tandem nucleotide repeat locus in diverse neurodegenerative outcomes in an Indian cohort.

Investigation of RFC1 tandem nucleotide repeat locus in diverse neurodegenerative outcomes in an Indian cohort.

Journal: Neurogenetics

Published: June 02, 2023

Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening Tool.

Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening Tool.

Journal: Advanced genetics (Hoboken, N.J.)

Published: December 22, 2021

A Novel Co-existence of Spinocerebellar Ataxia 1 and Spinocerebellar Ataxia 2 Mutations in Indian Patients.

A Novel Co-existence of Spinocerebellar Ataxia 1 and Spinocerebellar Ataxia 2 Mutations in Indian Patients.

Journal: Movement disorders clinical practice

Published: November 19, 2021

SCA2 in the Indian population: Unified haplotype and variable phenotypic patterns in a large case series.

SCA2 in the Indian population: Unified haplotype and variable phenotypic patterns in a large case series.

Journal: Parkinsonism & related disorders

Published: April 17, 2021

Pharmacogenetic landscape of DPYD variants in south Asian populations by integration of genome-scale data.

Pharmacogenetic landscape of DPYD variants in south Asian populations by integration of genome-scale data.

Journal: Pharmacogenomics

Published: December 15, 2017

Showing 1-10 of 10

Last Updated: 09/26/2026