Eda T. Tahir-Turanlı
Istanbul, Turkey
Last Updated: 09/26/2026
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Found 24 publications
Human TBK1 deficiency: An expanded spectrum from autoinflammation to viral encephalitis.
Journal: Journal of human immunity
Published: November 17, 2025
Molecular Consequences of CCN6 Variants Encoding WISP3 in Progressive Pseudorheumatoid Dysplasia.
Journal: International journal of molecular sciences
Published: August 05, 2025
Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families.
Journal: Scientific reports
Published: November 30, 2024
Profiling of five urinary exosomal miRNAs for the differential diagnosis of patients with diabetic kidney disease and focal segmental glomerulosclerosis.
Journal: PloS one
Published: April 30, 2024
HLA-B gene methylation and expression in Behçet's syndrome: a potential role of epigenetics in the pathogenesis.
Journal: Clinical and experimental rheumatology
Published: August 02, 2023
A case with febrile attacks and vasculopathy associated with ADA2 and MEFV pathogenic variants.
Journal: Modern rheumatology case reports
Published: April 06, 2023
Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype.
Journal: Rheumatology (Oxford, England)
Published: October 22, 2022
Genome-wide analysis of schizophrenia and multiple sclerosis identifies shared genomic loci with mixed direction of effects.
Journal: Brain, behavior, and immunity
Published: March 10, 2022
Investigating the role of common and rare variants in multiplex multiple sclerosis families reveals an increased burden of common risk variation.
Journal: Scientific reports
Published: January 22, 2022
Translation of Cellular Senescence to Novel Therapeutics: Insights From Alternative Tools and Models.
Journal: Frontiers in aging
Published: December 02, 2021
Last Updated: 09/26/2026