Busranur Erozan Cavdarli

14PUBLICATIONS
70CO-AUTHORS
NeurogeneticsNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Metabolic medicineInfant and child health
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Publications (14)

|Oct 12, 2026
Phenotypic spectrum of 1q21.1 copy number variants in 42 children: genotype-phenotype correlations and clinical implications.

|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

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Frequent Collaborators

3 joint publications

Esra Kılıç

3 joint publications

Gönül Büyükyılmaz

2 joint publications

Ahmet Cevdet Ceylan

2 joint publications

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