Duygu Duman
Ankara, Turkey
Last Updated: 09/26/2026
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Found 45 publications
CDK4 and CDK6 variants in patients with primary microcephaly lead to cell cycle defects and mitochondria-induced apoptosis.
Journal: Journal of medical genetics
Published: September 25, 2025
Two Siblings with LRPPRC Mutation: Mitochondrial Complex IV Deficiency: Case Report.
Journal: Molecular syndromology
Published: August 13, 2025
Distal enhancer-insulator module of GDF6 is essential for cochlear formation.
Journal: JCI insight
Published: May 09, 2025
Carboxypeptidase D deficiency causes hearing loss amenable to treatment.
Journal: The Journal of clinical investigation
Published: February 07, 2025
Identifying DNA Variants in a Turkish Cohort with Inner Ear Anomalies.
Journal: Ear, nose, & throat journal
Published: October 26, 2024
Siblings with a Homozygous Variant in the NHP2 Gene: A Case Report and Review of Literature.
Journal: Molecular syndromology
Published: October 05, 2024
Human Organoids for Rapid Validation of Gene Variants Linked to Cochlear Malformations.
Journal: Research square
Published: July 01, 2024
Human organoids for rapid validation of gene variants linked to cochlear malformations.
Journal: Human genetics
Published: May 24, 2024
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss.
Journal: American journal of medical genetics. Part A
Published: November 14, 2023
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2.
Journal: European journal of human genetics : EJHG
Published: May 25, 2023
Novel GPR156 variants confirm its role in moderate sensorineural hearing loss.
Journal: Scientific reports
Published: May 19, 2023
Dispersed DNA variants underlie hearing loss in South Florida's minority population.
Journal: Human genomics
Published: April 13, 2023
Last Updated: 09/26/2026