Ceren I. Tunca
Istanbul, 34010, Turkey
Last Updated: 09/26/2026
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Found 13 publications
Computational Short Tandem Repeat Genotyping Reveals Clinically Relevant Expansions in a Large Turkish Neurodegeneration Disease Cohort.
Journal: International journal of molecular sciences
Published: March 05, 2026
Sacsin levels in PBMCs: A diagnostic assay for SACS variants in peripheral blood cells - A PROSPAX study.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: May 17, 2024
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data.
Journal: Cell genomics
Published: April 01, 2024
A combined clinical and computational approach to understand the SOD1A4T-mediated pathogenesis of rapidly progressive familial amyotrophic lateral sclerosis.
Journal: Acta neurologica Belgica
Published: November 19, 2020
The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice.
The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: October 13, 2020
Phenotypic and genotypic features of patients diagnosed with ALS in the city of Sakarya, Turkey.
Journal: Acta neurologica Belgica
Published: April 25, 2020
Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database.
Journal: Human mutation
Published: December 12, 2019
A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification.
Journal: Brain : a journal of neurology
Published: January 17, 2019
Clinical and molecular characterization and response to acitretin in three families with Sjögren-Larsson syndrome.
Journal: International journal of dermatology
Published: February 14, 2018
ERLIN1 mutations cause teenage-onset slowly progressive ALS in a large Turkish pedigree.
Journal: European journal of human genetics : EJHG
Published: October 05, 2017
A new splice-site mutation in SLC12A6 causing Andermann syndrome with motor neuronopathy.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: September 27, 2017
Elevated Global DNA Methylation Is Not Exclusive to Amyotrophic Lateral Sclerosis and Is Also Observed in Spinocerebellar Ataxia Types 1 and 2.
Journal: Neuro-degenerative diseases
Published: July 07, 2017
Last Updated: 09/26/2026