Filiz Hazan

8PUBLICATIONS
34CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Immunogenetics (incl. genetic immunology)Craniofacial biologyMedical molecular engineering of nucleic acids and proteins
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Publications (8)

|Aug 20, 2026
Retrovesical Hybrid Benign Peripheral Nerve Sheath Tumor with a Heterozygous Germline NF2 Deletion in a 12-Year-Old Boy: A Case Report.

|May 11, 2026
Genetic evaluation of a group of patients with transient congenital hypothyroidism by targeted exome sequencing.

|Nov 12, 2025
Expanding the clinical spectrum of Cernunnos/XLF deficiency: a literature review of a rare cause of severe combined immunodeficiency including a novel case.

Gizem Kabadayı, Özge Atay, Damla Baysal Bakır

|Sep 19, 2024
A rare case of skeletal dysplasia: biallelic variant in ACAN gene.

Gülçin Arslan, Filiz Hazan, Gülin Tabanlı

|Jun 19, 2023
A rare cause of intellectual disability: Novel mutations of NFIX gene in two patients with clinical features of Marshall-Smith syndrome and Malan syndrome.

Ceren Yılmaz Uzman, Semra Gürsoy, Filiz Hazan

|May 06, 2022
A Neonatal Case of Infantile Malignant Osteopetrosis Presenting with Thrombocytopenia and Hypotonicity: A Novel Mutation in Chloride Voltage-Gated Channel 7 Gene.

Isik Odaman Al, Yesim Oymak, Filiz Hazan

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Frequent Collaborators

5 joint publications

Semra Gürsoy

4 joint publications

Behzat Özkan

3 joint publications

Özlem Nalbantoğlu

2 joint publications

Gülçin Arslan