| Issue Date | Title | Author(s) |
| 2015 | Ankaferd Blood Stopper induces apoptosis and regulates PAR1 and EPCR expression in human leukemia cells | Mumcuoğlu M.; Akın, D. F.; Ezer, U.; Akar, Mehmet Nejat |
| 2019 | Asymptomatic hemochromatosis case with HFE c.1007−47G>A, c.340+4T>C heterozygous mutations and alpha globin −3.7 kb deletion | Çelik, Vesile Deniz; Kılıç, Betül Orhan; Ardıçoğlu Akışın, Nazife Yasemin ; Akar, Nejat |
| 2016 | Detection of TET2, KRAS and CBL variants by Next Generation Sequencing and analysis of their correlation with JAK2 and FLT3 in childhood AML | Akın, D. F.; Öner D. A.; Mumcuoğlu M.; Ezer, U.; Bahce M.; Kurekci E.; Akar, Mehmet Nejat |
| Jan-2020 | Further observation of Hemoglobin Fontainebleau (a21(B2) Ala-Pro) in a Turkish family | Akar, Nejat; Ceylaner, Serdar; Ardıçoğlu Akışın, Nazife Yasemin ; Taştan, Gökçe Su |
| Jul-2018 | A novel MYH9 mutation in a beta thalassemia major patient with thrombocytopenia. | Özkan, Didem Torun; Akar, Mehmet Nejat |
| 2015 | Radioactive fallout and neural tube defects | Akar, Nejat |
| 2017 | Screening of polymorphisms in the folate pathway in Turkish pediatric Acute Lymphoblastic Leukemia patients | Akın, D. F.; Öner D. A.; Sipahi K.; Mumcuoğlu M.; Kurekci E.; Ezer, U.; Akar, Mehmet Nejat |
| 2022 | A Turkish case of incontinentia pigmenti with a deletion mutation at Inhibitor of kappa B kinase gamma gene | Ergin, Filiz Basak Cengiz; Tekin, Mustafa; Gunes, Meltem; Gunes, Begum; Baysun, Şahika; Akar, Nejat |
