Hamide Betul Gerik-Celebi

7PUBLICATIONS
23CO-AUTHORS
Ophthalmology and optometry not elsewhere classifiedEpigenetics (incl. genome methylation and epigenomics)Gene mappingNeurogeneticsCell and nuclear division
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Journal

Publications (7)

|Jul 15, 2026
Hereditary Hyperferritinemia Cataract Syndrome Mimicking Iron Overload in a Pediatric Patient With Coexisting HFE H63D Homozygosity.

|Apr 28, 2026
The Impact of 8p23 Copy Number Variations on Neurodevelopmental Aetiology: A Focus on Rare Deletions.

|Mar 26, 2026
A novel compound heterozygous YY1AP1 variant in Grange syndrome: importance of early signs in preventing life-threatening vascular complications.

Gul Unsel-Bolat, Neslihan Tezcan, Dilan Genç-Akdağ

|Feb 18, 2026
Keipert syndrome beyond classical features: novel GPC4 variant associated with epilepsy but preserved cognition.

Hilmi Bolat, Hilal Aydın, Dilan Genç-Akdağ

|Oct 22, 2024
Utility of Optical Genome Mapping in Repeat Disorders.

Mehmet Burak Mutlu, Taner Karakaya, Hamide Betül Gerik Çelebi

|Dec 11, 2023
A novel CACNA1A mutation in a neonate with severe encephalopathy at birth.

Mine Ozdil, Arzu Eroglu, Hamide Betul Gerik-Celebi

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Frequent Collaborators

1 joint publications

Melike Batum

1 joint publications

Ayşın Kısabay Ak

1 joint publications

Güldeniz Çetin

1 joint publications

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