Yusuf Ozkul (Yusuf Özkul)

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 9

Top Topics

Intellectual Disability

Optical Coherence Tomography

Epstein Barr Virus

Top Venues

Ophthalmic genetics

Turkish journal of medical sciences

American journal of medical genetics. Part A

Turkish journal of ophthalmology

This page only lists publications with an associated author ORCID identifier.

Publications

Neslihan Sinim Kahraman, Büşra Özgüç Çalışkan, Nefise Kandemir, Ayşe Öner, Munis Dündar, Yusuf Ozkul
ABCA4 variant screening in a Turkish cohort with Stargardt disease. Ophthalmic genetics (2024)
Neslihan Sinim Kahraman, Büşra Özgüç Çalışkan, Nefise Kandemir, Ayşe Öner, Munis Dündar, Yusuf Ozkul
ABCA4 variant screening in a Turkish cohort with Stargardt disease. Ophthalmic genetics 45 (2) (2024)
Neslihan Sinim Kahraman, Büşra Özgüç Çalışkan, Nefise Kandemir, Ayşe Öner, Munis Dündar, Yusuf Ozkul
ABCA4 variant screening in a Turkish cohort with Stargardt disease. Ophthalmic genetics 45 (2) (2024)
Neslihan Sinim Kahraman, Büşra Özgüç Çalışkan, Nefise Kandemir, Ayşe Öner, Munis Dündar, Yusuf Ozkul
ABCA4 variant screening in a Turkish cohort with Stargardt disease. Ophthalmic genetics 45 (2) (2024)
İzem Olcay Şahin, Emine Karataş, Mikail Demir, Büşra Tan, Huseyin Per, Yusuf Ozkul, Munis Dündar
A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort. Turkish journal of medical sciences 54 (1) (2023)
Firat Ozcelik, Sezai Arslan, Büşra Özgüç Çalışkan, Fatih Kardas, Yusuf Ozkul, Munis Dündar
PPM1K defects cause mild maple syrup urine disease: The second case in the literature. American journal of medical genetics. Part A (2023)
İzem Olcay Şahin, Emine Karataş, Mikail Demir, Büşra Tan, Huseyin Per, Yusuf Ozkul, Munis Dündar
A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort. Turkish journal of medical sciences 54 (1) (2023)
Firat Ozcelik, Kubra Aslan, Veysel Gok, Mucahit Bilgehan Ari, Alper Ozcan, Ahmet Eken, Ekrem Ünal, Yusuf Ozkul, Munis Dündar
A case of autoimmune lymphoproliferative syndrome with a novel de novo FAS variant. Pediatric hematology and oncology (2023)
Neslihan Sinim Kahraman, Ayşe Öner, Yusuf Ozkul, Munis Dündar
Frequency of RPE65 Gene Mutation in Patients with Hereditary Retinal Dystrophy. Turkish journal of ophthalmology 52 (4) (2022)