▪ Ercoskun P, et al. Variant Spectrum of Renal Ciliopathies in Turkish Cohort and Genotype-Phenotype Association Specifically in Autosomal Dominant Polycystic Kidney Disease. Clin Genet. 2025

▪ Ercoskun P, et al. Delineating the Adult Phenotype of PGM2L1-Related Neurodevelopmental Disorder. Am J Med Genet A. Published online November 3, 2025.

▪ Ercoşkun P, et al.. HMGA2 associated ceRNA-HOTAIR pathway in breast cancer patients from clinicopathological perspective. Turk J Med Sci. 2025

▪ Ercoskun P, et al.. Genetic Characterization of Hereditary Cancer Syndromes Based on Targeted Next-Generation Sequencing. Mol Syndromol. 2022

▪ Ercoskun P, et al. Witteveen-Kolk syndrome: The first patient from Turkey. Am J Med Genet A. 2021

▪ Ercoskun P, et al. A new case of Turnpenny-Fry syndrome. Am J Med Genet A. 2022

▪ Şenol HKE, Ercoşkun P. The right to terminate pregnancy (abortion): reflections from Turkey. J Law Biosci. 2023

▪ Ercoskun P, et al. Novel Findings in Floating-Harbor Syndrome and a Mini-Review of the Literature. Mol Syndromol. 2021

▪ Kanjee M, Yuce Kahraman C, Ercoskun P, Tatar A, Kahraman M. A Novel nonsense variant in the CDH2 gene associated with ACOGS: A case report. Am J Med Genet A. 2022

▪ Yuce Kahraman C, Ercoskun P, Yakar O, Tatar A. A novel genomic variant in two siblings with very low-density lipoprotein receptor-associated cerebellar hypoplasia. Clin Dysmorphol. 2022

▪ Yuce Kahraman C, Kanjee M, Ercoskun P, Tatar A. Whole Exome Sequencing in Neurodevelopmental Disorders: A Single Center Study. BCN 2024

Spec. Peli̇n ERCOŞKUN, M.D.