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| Issue Date | Title | Author(s) |
| 2014 | Assessment of HbF QTLs Affecting Disease Severity and Genetic Analysis in Patients Homozygous for Codon 8 (-AA) beta(0)-Thalassemia Mutation | Jiang, Zhihua; Huang, Shengwen; Luo, Hong Yuan; Akar, Nejat; Başak, A. Nazlı; Al-Allawi, Nasir; Chui, David H. K. |
| 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 | Behcet's: A Disease or a Syndrome? Answer from an Expression Profiling Study | Oğuz, Ali Kemal; Yılmaz, Seda Tasir; Oygur, Çağdaş Sahap; Candar, Tuba; Sayın, Irmak; Kılıçoğlu, Sibel Serin; Akar, Nejat |
| 2022 | Beta-lactam antibiotic-induced thrombocytopenia: MYH9 & TUBB1 genes | Ozkan, Didem; Akisin, Yasemin Ardicoglu; Bali, Dilara Fatma Akin; Akar, Nejat |
| 2015 | Cerebral Sinovenous Thrombosis in Children and Neonates: Clinical Experience, Laboratory, Treatment, and Outcome | Bektaş, Ömer; Teber, Serap; Akar, Nejat; Uysal, Leyla Zümrüt; Arsan, Saadet; Ataşay, Begüm; Deda, Gülhis |
| 2012 | Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis based proteomic analysis in hereditary elliptocytosis and spherocytosis | Demiralp, Duygu Özel; Peker, Selen; Turgut, Burhan; Akar, Nejat |
| 2018 | Determination of CEBPA mutations by next generation sequencing in pediatric acute leukemia | Akın, DF; Öner, DA; Kürekci, E; Akar, Nejat |
| 2019 | Diamond-Gardner Syndrome: Autoerythrocyte Sensitization Syndrome | Akar, Nejat; Karagöz, Zeynep Nur; Ardıçoğlu Akışın, Nazife Yasemin |
| 2012 | Does FVL have an effect on longevity? | Akın, Dilara Fatma; Eğin, Yonca; Akar, Nejat |
| 2019 | Effects of Ankaferd Hemostat on Helicobacter pylori strains and antibiotic resistance | Çiftçiler, R.; Koluman, A.; Haznedaroğlu, İbrahim Celalettin; Akar, Nejat |
| Sep-2016 | Endothelial Cells, Ankaferd Hemostat, And Estradiol | Ardıçoğlu Akışın, Nazife Yasemin ; Akar, Nejat; Haznedaroğlu, İbrahim |
| 2012 | A further note on filicide with suicide in Turkey | Akar, Nejat |
| 2016 | A Further Note on the Thalassemia Screening Program in the Mugla Region of Turkey | Akar, 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 |
| 2014 | gamma A gene repeats polymorphism for the analysis of haplotypes of abnormal hemoglobins | Akar, Nejat; Sipahi, Kadir; Akar, Ece; Yılmaz, Erkan |
| Dec-2020 | Genetic Analysis of Afibrinogenemia and Hypofibrinogenemia: Novel Mutations in the FGB Gene in the Turkish Population | Özkan, Didem Torun; Sarper, Nazan; Akar, Nejat |
| 2022 | Genetic Profiling of Pediatric Patients with B-Cell Precursor Acute Lymphoblastic Leukemia | Akin-Bali, Dilara Fatma; Erdogan, Beyza Doganay; Oner, Deniz Aslar; Mahmud, Akkan; Tasdelen, Serpil; Kurekci, Emin; Akar, Nejat |
| 2021 | Glucose-6-phosphate dehydrogenase gene Ala365Thr mutation in an Iraqi family with confusing clinical differences | Ardıçoğlu Akışın, N. Yasemin; Arslan, Zafer ; Ceylaner, Serdar; Akar, Nejat |
| 2016 | Grandmother's Effect On Child Weight In Turkish Community | Akar, Nejat |
| 2016 | Hemoglobin H Disease in Turkey: Experience from Eight Centers | Ünal, Selma; Oktay, Gönül; Acıpayam, Can; İlhan, Gül; Gali, Edip; Celkan, Tiraje; Toptaş, Tayfur; Akar, Nejat |
