Ugur Ozbek

13PUBLICATIONS
106CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Cancer therapy (excl. chemotherapy and radiation therapy)Epigenetics (incl. genome methylation and epigenomics)Predictive and prognostic markersCardiovascular medicine and haematology not elsewhere classified
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Publications (13)

|Jul 09, 2026
Integrative and systematic genomic approaches to improve diagnosis in rare and undiagnosed diseases: results from the RareBoost project.

|Apr 06, 2026
Grange-Like Phenotype Associated With an RNF213 Pathogenic Variant: Expanding the Vasculopathy Spectrum.

Serife Ozturk Yilmaz, Ayca Yigit, Sevcan Hatipoglu

|Mar 24, 2026
Evolving Concepts and Contemporary Management of Early-Stage Breast Cancer: An Evidence-Based Approach to Grey Zones from a Comprehensive Breast Unit Part 1: Locoregional Therapy, Pathology, Radiology.

Elif Şenocak Taşçı, Halil Kara, Emir Çapkınoğlu

|Feb 03, 2025
Genomics of rare diseases in the Greater Middle East.

Ikram Chekroun, Shruti Shenbagam, Mohamed A Almarri

|Jan 09, 2025
Status of IKZF1 Deletions in Diagnose and Relapsed Pediatric B-ALL Patients.

Yücel Erbilgin, Sinem Firtina, Elif Kirat

|Oct 21, 2024
Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon.

Angelica Maria Delgado-Vega, Helene Cederroth, Fulya Taylan

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Frequent Collaborators

5 joint publications

Ozden Hatirnaz Ng

4 joint publications

Muge Sayitoglu

3 joint publications

Yucel Erbilgin

2 joint publications

Zeynep Karakas