| Association between FokI, ApaI and TaqI RFLP polymorphisms in VDR gene and Hashimoto's thyroiditis: preliminary data from female patients in Serbia J Djurovic, O Stojkovic, O Ozdemir, F Silan, C Akurut, J Todorovic, K Savic, ... International Journal of Immunogenetics 42 (3), 190-194, 2015 | 31 | 2015 |
| Genetics of suspected thrombophilia in Serbian females with infertility, including three cases, homozygous for FII 20210A or FV 1691A mutations J Djurovic, O Stojkovic, J Todorovic, A Brajic, S Stankovic, S Obradovic, ... Human Fertility 20 (2), 132-139, 2017 | 22 | 2017 |
| Polymorphisms and haplotypes in VDR gene are associated with female idiopathic infertility J Djurovic, G Stamenkovic, J Todorovic, N Aleksic, O Stojkovic Human Fertility 23 (2), 101-110, 2020 | 17 | 2020 |
| Cryptic Diversity of the European Blind Mole Rat Nannospalax leucodon Species Complex: Implications for Conservation V Bugarski-Stanojević, G Stamenković, V Jojić, N Ćosić, D Ćirović, ... Animals 12 (9), 1097, 2022 | 8 | 2022 |
| 16S rRNA gene polymorphism supports cryptic speciation within the lesser blind mole rat Nannospalax leucodon superspecies (Rodentia: Spalacidae) V Bugarski-Stanojević, G Stamenković, D Ćirović, D Ćirić, O Stojković, ... Mammalian Biology 100, 315-324, 2020 | 5 | 2020 |
| Prenatal diagnosis of aneuploidies and microdelation/duplication in amniotic fluid and fetal aborted material by QF-PCR and MLPA analysis E Ari, O Ozdemir, J Djurovic, F Silan Biomed Genet Genomics 3 (1), 2018 | 5 | 2018 |
| Blau Syndrome with a rare mutation in exon 9 of NOD2 gene J Velickovic, F Silan, FD Bir, C Silan, B Albuz, O Ozdemir Autoimmunity 52 (7-8), 256-263, 2019 | 3 | 2019 |
| Combinations of fibrinolytic gene polymorphisms (plasminogen activator inhibitor type 1 4G/5G, factor XIII Val34Leu and angiotensin-converting enzyme I/D) in women with … J Velickovic, M Jelicic, O Stojkovic Blood Coagulation & Fibrinolysis 32 (2), 103-107, 2021 | 2 | 2021 |
| Hemostasis-related gene polymorphisms and their epistatic relationship in women with idiopathic infertility J Velickovic, K Zeljic, J Todorovic, G Stamenkovic, O Stojkovic Blood Coagulation and Fibrinolysis 30 (6), 253-262, 2019 | 2 | 2019 |
| Should MTHFR 1298 A> C be tested together with MTHFR 677 C> T polymorphism in women with reproductive challenges? J Đurović, O Stojković, J Todorović, K Savić, G Stamenković Genetika 49 (2), 377-386, 2017 | 2 | 2017 |
| A New Case of Rare Microdeletion 10q22. 3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor … F Dincsoy Bir, F Silan, J Velickovic, M Berkay Akcan, O Ozdemir Molecular Syndromology 13 (3), 254-260, 2022 | | 2022 |
| Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale F Silan, J Djurovic, FD Bir, C Silan, Ö Özdemir Journal of Biotechnology 280, S65, 2018 | | 2018 |
