Sunil Shakya
New Delhi, DL, India
Last Updated: 09/26/2026
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Found 10 publications
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
Impact of SARS-CoV-2 Infection in Spinocerebellar Ataxia 12 Patients.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: August 16, 2021
RET gene mutation analysis and long-term clinical outcomes of medullary thyroid cancer patients.
Journal: Nuclear medicine communications
Published: August 16, 2020
BRAF V600E and TERT promoter mutations in paediatric and young adult papillary thyroid cancer and clinicopathological correlation.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: April 05, 2020
Long-term Clinicopathological Features of a Family with Multiple Endocrine Neoplasia Type 2A Caused by C634R RET Gene Mutation.
Journal: Indian journal of nuclear medicine : IJNM : the official journal of the Society of Nuclear Medicine, India
Published: September 09, 2019
Transforming growth factor-β1 (C509T, G800A, and T869C) gene polymorphisms and risk of ischemic stroke in North Indian population: A hospital-based case-control study.
Journal: Annals of Indian Academy of Neurology
Published: March 17, 2017
Single-step blood direct PCR: A robust and rapid method to diagnose triplet repeat disorders.
Journal: Journal of the neurological sciences
Published: March 08, 2017
Iron related hemochromatosis (HFE) gene mutations in Friedreich Ataxia patients.
Journal: Parkinsonism & related disorders
Published: April 12, 2016
Spinocerebellar Ataxia 2 and 12 Mutations in an Indian Family with Cerebellar Ataxia and Slow Saccades.
Journal: Movement disorders clinical practice
Published: March 18, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026