Author

Esra Dirimtekin

Observed name: Dirimtekin E.

Institution: Marmara University

Observed institutions: Marmara University, University of Westminster

ORCID: 0009-0008-5811-4234

Observed ORCID: 0009-0008-5811-4234

OpenAlex ID: A5092492442

BRCA Mutations and MicroRNA Expression Patterns in the Peripheral Blood of Breast Cancer Patients

2024 · Ceren Alavanda, Esra Dirimtekin, et al. · ACS Omega · 8

miR-34a-FOXP1 Loop in Ovarian Cancer

2023 · Esra Dirimtekin, Maria Mortoglou, et al. · ACS Omega · 7

Perineural Invasion in Pancreatic Ductal Adenocarcinoma: Recapitulating Its Importance and Defining Future Directions

2025 · Martin Lovecek, Esra Dirimtekin, et al. · United European Gastroenterology Journal · 6

EBV BART microRNA Profiles and Host Gene Links in Gastric Cancer

2026 · Esra Dirimtekin, D. Alwyn Dart, et al. · Viruses · 3

A Family of LBR Biallelic Pathogenic Variants Resulting in Rhizomelic Skeletal Dysplasia with Pelger-Huët Anomaly

2025 · Esra Dirimtekin, Çekdar Kapazan, et al. · Molecular Syndromology · 2

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation

2026 · İrem Kalay, Tahir Atik, et al. · Balkan Medical Journal

Functional Impact of a Novel Intronic TG Variant in Congenital Goiter and Thyroid Dyshormonogenesis

2026 · Zehra Yavas Abalı, Esra Dirimtekin, et al. · Hormone Research in Paediatrics

Supplementary Material for: Functional impact of a novel intronic TG variant in congenital goiter and thyroid dyshormonogenesis

2026 · figshare admin karger, YavasAbalı Z., et al. · Figshare

Percc1-Associated Congenital Diarrhea and Enteropathy: Description of a Novel Variant

2026 · Bilge S. Akkelle, Emine Celik, et al. · Pediatric and Developmental Pathology

The First Turkish Spondylocarpotarsal Synostosis Syndrome Case with Ventricular Septal Defect and Pelvicaliectasia Caused by a Novel Homozygous Frameshift Variation in FLNB

2025 · Esra Dirimtekin, Esra Arslan Ateş, et al. · Journal of Pediatric Genetics

A novel biallelic intronic variant in the TG gene associated with thyroid dyshormonogenesis and fetal goiter

2025 · Abali Zehra Yavas, Esra Dirimtekin, et al. · Endocrine Abstracts

The Spondylocarpotarsal Synostosis Syndrome Case with Ventricular Septal Defect Caused by a Homozygous Frameshift Variation in FLNB

2024 · Esra Dirimtekin, Esra Arslan Ates, et al. · Journal of Pediatric Genetics

Works count: 12

Citation count: 26

H-index: 3

I10-index: