Irmak Şahbaz
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Neurological diseases and metabolism, Amyotrophic Lateral Sclerosis Research, DNA Repair Mechanisms
Most-Cited Works
- → Elevated Global DNA Methylation Is Not Exclusive to Amyotrophic Lateral Sclerosis and Is Also Observed in Spinocerebellar Ataxia Types 1 and 2(2018)34 cited
- → Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease(2024)26 cited
- → The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice(2021)16 cited
- → Coexistence of autosomal recessive spastic ataxia of Charlevoix Saguenay and spondyloepiphyseal dysplasia in a Turkish patient(2015)5 cited
- → Phenotypic and Genotypic Analysis of Hereditary Ataxia Patients in Sakarya City, Turkey(2017)3 cited
- → Computational Short Tandem Repeat Genotyping Reveals Clinically Relevant Expansions in a large Turkish Neurodegeneration Cohort(2026)
- → Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS): a family with five affected sibs from Turkey(2024)
- → Supplementary Material for: Elevated Global DNA Methylation Is Not Exclusive to Amyotrophic Lateral Sclerosis and Is Also Observed in Spinocerebellar Ataxia Types 1 and 2(2018)