Fulya Yaylacıoğlu Tuncay

8PUBLICATIONS
15CO-AUTHORS
NeurogeneticsOptical technologyOther education not elsewhere classifiedOphthalmologyMolecular targets
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Publications (8)

|Apr 20, 2026
Bietti crystalline dystrophy in Türkiye: A genetic crossroads between Asia and Europe.

|Nov 14, 2025
Contribution of genetic test results to patient management in ophthalmology: results from a Turkish Stargardt disease cohort.

Fulya Yaylacioğlu Tuncay, Şengül Özdek, Burak Acar

|Aug 29, 2024
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Fulya Yaylacıoğlu Tuncay, Kübra Serbest Ceylanoğlu, Sezen Güntekin Ergün

|Jun 04, 2024
Current clinical practice and needs assessment in inherited eye diseases from the perspective of ophthalmologists.

Fulya Yaylacioglu Tuncay, Eda Karaismailoglu, Şengül Özdek

|Apr 22, 2024
The Role of FOXP3 Polymorphisms in Graves' Disease with or without Ophthalmopathy in a Turkish Population.

Fulya Yaylacıoğlu Tuncay, Kübra Serbest Ceylanoğlu, Sezen Güntekin Ergün

|Jan 02, 2024
Mimicking TGFBI Hot-Spot Mutation Did Not Result in Any Deposit Formation in the Zebrafish Cornea.

Fulya Yaylacıoğlu Tuncay, Beril Talim, Pervin Rukiye Dinçer

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