Ruken Yıldırım

21PUBLICATIONS
118CO-AUTHORS
Obstetrics and gynaecologyGene expression (incl. microarray and other genome-wide approaches)Infant and child healthEpigenetics (incl. genome methylation and epigenomics)Cancer therapy (excl. chemotherapy and radiation therapy)
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Publications (21)

|Apr 25, 2026
Final Height in Patients with Turner Syndrome Treated With Growth Hormone Therapy.

|Apr 18, 2026
A Novel YY1AP1 Variant in Grange Syndrome: Clinical and Molecular Findings in Eight Individuals With a Dual Molecular Diagnosis Involving CLMP in One Patient.

|Nov 27, 2025
A Comprehensive Perspective on Febrile Seizures in Children: A Prospective Cohort Study with Evaluation of Clinical, Laboratory, and Genetic Features.

Gülşen Yalçın, Ruken Yıldırım, Edip Unal

|Jul 08, 2025
Genetic Diseases Mimicking Rheumatic Disorders: Insights From Southeastern Turkey.

Akçahan Akalın, Hatice Dilara Karakaş, Canan Çelebi

|Dec 23, 2024
Central Adrenal Insufficiency: Etiology and Diagnostic Approach

Melek Yıldız, Ruken Yıldırım, Firdevs Baş

|Dec 06, 2024
Clinical and molecular spectrum along with genotype-phenotype correlation of 25 patients diagnosed with 3 M syndrome: a study from Turkey.

Akçahan Akalın, Şervan Özalkak, Ruken Yıldırım

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Frequent Collaborators

13 joint publications

Edip Unal

9 joint publications

Şervan Özalkak

6 joint publications

Funda Feryal Taş

6 joint publications

Mehmet Nuri Özbek