Busranur Erozan Cavdarli

13PUBLICATIONS
67CO-AUTHORS
Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Metabolic medicineInfant and child healthOptical technology
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Publications (13)

|Jun 09, 2026
Clinical and Molecular Portraits of Pediatric RASopathies: A Study of 118 Genotype-Confirmed Cases.

|Mar 08, 2026
MLPA-Detected CFTR Exon Deletions in Children With Inconclusive CFTR Sequencing: A Single-Center Experience From Türkiye.

Sanem Eryılmaz Polat, Çelebi Yıldırım, Hande Yetişgin

|Feb 18, 2026
Expansion of the 3MC Syndrome Spectrum: Novel COLEC10 Variants and a MASP1 Exon-Level Deletion.

Duygu Çetinkaya, Büşranur Çavdarlı, Emre Kırat

|May 31, 2025
Thick Corpus Callosum: An Unusual Finding of TUBGCP2-Related Tubulinopathy.

Tuna Eren Esen, Didem Ardiçli, Avni Merter Keçelİ

|Oct 15, 2024
Cerebellar Hypoplasia and Treatment Course of a Two-Month-Old Infant With KCNQ2 Epileptic Encephalopathy Due to a De Novo Variant and Review of the Literature.

Dilek Cebeci, Busranur Cavdarli, Pinar Ozbudak

|Apr 02, 2024
Comparison of the optical coherence tomography-angiography (OCT-A) vascular measurements between molecularly confirmed MODY and age-matched healthy controls.

Cemal Çavdarlı, Gönül Büyükyılmaz, Büşranur Çavdarlı

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Frequent Collaborators

3 joint publications

Gönül Büyükyılmaz

2 joint publications

Esra Kılıç

2 joint publications

Gülsüm Özet

1 joint publications

Maha Sherif