Mahmut Cerkez Ergoren

33PUBLICATIONS
79CO-AUTHORS
NeonatologyCancer diagnosisCardiology (incl. cardiovascular diseases)GenomicsNeurology and neuromuscular diseases
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Publications (33)

|Sep 28, 2026
FOXG1 syndrome: genetic background revealed by trio WES in case of a critically ill neonate.

|Aug 27, 2026
Expression Profiling and Transcriptional Coordination of Canonical Wnt Signaling Pathway Genes (FZD2, DVL2, and AXIN1) in Chronic Venous Insufficiency.

|Aug 04, 2026
Low Prevalence of the HBB c.20A > T (HbS) Allele in a Turkish Cypriot Cohort: A Molecular Screening Study.

|May 26, 2026
Compound Heterozygous SLC12A3 Variants in Gitelman Syndrome Presenting With Ventricular Fibrillation and Cardiac Arrest.

|Nov 14, 2025
Determination of the Frequency of HBB (c.20 A > T) Gene Mutation in the Nigerian and Zimbabwean Populations in Northern Cyprus.

Havva Çobanoğulları, Dabbah Maima Gbassay, Mardea F Zaway

|Oct 01, 2025
Carrier frequency of SMA by quantitative analysis of the SMN1 deletion in the Northern-Cyprus population.

Sara Abbasigharaei, Aysegul Bostanci, Kiana Tabari

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Frequent Collaborators

7 joint publications

Sehime Gulsun Temel

4 joint publications

Gulten Tuncel

4 joint publications

Aya Badeea Ismail

3 joint publications

Gamze Mocan