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Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and Their Genotype-phenotype Correlation.
Özen S, Gökşen D, Evin F, Işık E, Onay H, Akgün B, Ata A, Atik T, Düzcan F, Özkınay F, Darcan Ş, Çoğulu Ö. Özen S, et al. Among authors: isik e. J Clin Res Pediatr Endocrinol. 2024 Jun 3. doi: 10.4274/jcrpe.galenos.2024.2022-12-8. Online ahead of print. J Clin Res Pediatr Endocrinol. 2024. PMID: 38828893 Free article.
Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis.
Isik E, Aydinok Y, Albayrak C, Durmus B, Karakas Z, Orhan MF, Sarper N, Aydın S, Unal S, Oymak Y, Karadas N, Turedi A, Albayrak D, Tayfun F, Tugcu D, Karaman S, Tobu M, Unal E, Ozcan A, Unal S, Aksu T, Unuvar A, Bilici M, Azik F, Ay Y, Gelen SA, Zengin E, Albudak E, Eker I, Karakaya T, Cogulu O, Ozkinay F, Atik T. Isik E, et al. Eur J Haematol. 2024 Jul;113(1):82-89. doi: 10.1111/ejh.14194. Epub 2024 Mar 31. Eur J Haematol. 2024. PMID: 38556258
Pandemics, Income Inequality, and Refugees: The Case of COVID-19.
Büyükakın F, Özyılmaz A, Işık E, Bayraktar Y, Olgun MF, Toprak M. Büyükakın F, et al. Among authors: isik e. Soc Work Public Health. 2024 Jan 2;39(1):78-92. doi: 10.1080/19371918.2024.2318372. Epub 2024 Feb 19. Soc Work Public Health. 2024. PMID: 38372287
332 results