Büşra Özgüç Çalışkan (Busra Ozguc Caliskan)

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 7

Top Topics

Intellectual Disability

Dna Methylation

Optical Coherence Tomography

Top Venues

Ophthalmic genetics

Clinical genetics

American journal of medical genetics. Part A

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

Publications

Büşra Özgüç Çalışkan, Kubra Uslu, Neslihan Sinim Kahraman, Kuddusi Erkilic, Ayşe Öner, Munis Dündar
Beyond the phenotype: Exploring inherited retinal diseases with targeted next-generation sequencing in a Turkish cohort. Clinical 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 (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)
Büşra Özgüç Çalışkan, Kubra Uslu, Neslihan Sinim Kahraman, Kuddusi Erkilic, Ayşe Öner, Munis Dündar
Beyond the phenotype: Exploring inherited retinal diseases with targeted next-generation sequencing in a Turkish cohort. Clinical genetics 106 (3) (2024)
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)