Edukacija
- 2006: Doktor nauka – biološke nauke, Poslediplomske doktorske studije na Biološkom fakultetu Univerziteta u Beogradu, smer Genetika
- 1999: Magistar bioloških nauka, Poslediplomske studije – magisterijum na Biološkom fakultetu Univerziteta u Beogradu, smer Genetika
- 1995: Diplomirani molekularni biolog i fiziolog, Biološki fakultet Univerziteta u Beogradu, studijska grupa Molekularna biologija i fiziologija, smer Eksperimentalna biomedicina
Izbor u naučno-istraživačka zvanja
- 2022: Naučni saradnik na Biološkom fakultetu Univerziteta u Beogradu, oblast Biologija, ponovni izbor
- 2014: Naučni saradnik na Biološkom fakultetu Univerziteta u Beogradu, oblast Biologija, ponovni izbor
- 2007: Naučni saradnik na Biološkom fakultetu Univerziteta u Beogradu, oblast Biologija
- 1999: Istraživač saradnik na Biološkom fakultetu Univerziteta u Beogradu, oblast Biologija
Članstvo
- Društvo genetičara Srbije, sekcija Medicinska genetika
- Srpsko društvo za molekularnu biologiju (MolBioS)
- European Society of Human Genetics (ESHG)
- European Cytogeneticists Association (ECA)
- EQA ocenjivač-saradnik udruženja European Molecular Genetics Quality Network (EMQN)
- Saradnik na međunarodnom projektu CFTR2
Reference od značaja
- Ilic N, Maric N, Maver A, Armengol L, Kravljanac R, Cirkovic J, Krstic J, Radivojevic D, Cirkovic S, Ostojic S, Krasic S, Paripovic A, Vukomanovic V, Peterlin B, Maric G, Sarajlija A. Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability – An Exception or a Necessity? Genes 2024; 15(6): 789.
- Kosac A, Pesovic J, Radenkovic L, Brkusanin M, Radovanovic N, Djurisic M, Radivojevic D, Mladenovic J, Ostojic S. Kovacevic G , Kravljanac R, Savic Pavicevic D, Milic Rasic V. LTBP4, SPP1, and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian Patients. Genes (Basel) 2022; 13(8): 1385.
- Dobrić B, Radivojević D, Ječmenica J, Fanis P, Neocleous V, Phylactou LA, Đurišić M. Prevalence of variants in DFNB1 locus in Serbian patients with autosomal recessive non-syndromic hearing loss. Genetika 2022;54(1):447-56.
- Dobric B, Radivojevic D, Jecmenica J., Neocleous V., Fanis P., Phylactou L.A., Djurisic M. Audiological features in Serbian patients with hearing impairment identified with c.35delG in the GJB2 gene. Srp Arh Celok Lek 2021; 149(11-12):685-690.
- Sosic GM, Sretenovic S, Radivojevic D, Jovic N, Varjacic M. Impact of gene variants FV Leiden, FII G20210A, MTHFR C667T and PAI-1 4G/5G on pregnancy loss in women from Central Serbia. Ser J Exp Clin Res (Experimental and Applied Biomedical Research (EABR)) 2020; 21(1): 19-25.
- Dobric B, Radivojevic D, Lalic T, Miskovic M, Cirkovic S, Djordjevic M, Djurisic M. Incidence of genetic causes of idiopathic male infertility in Serbia – ten years’ experience of single centre. Genetika 2019; 51(3): 1009-1019.
- Aguilera CA, Vinas-Jornet M, Baena N, Gaban E, Fernandez C, Capdevila N, Cirkovic S, Sarajlija A, Miskovic M, Radivojevic D, Ruiz A, Guitart M. Novel intragenic deletions within UBE3A gene in two unrelated patients with Angelman Syndrome: Case report and review of the literature. BMC Med Genet 2017; 18(1):137.
- Miskovic M, Lalic T, Radivojevic D, Cirkovic S, Ostojic S, Guc-Scekic M. Ten years of experience in molecular prenatal diagnosis and carrier testing for spinal muscular atrophy among families from Serbia. Int J Gynaecol Obstet. 2014 Jan;124(1):55-8.
- Radivojevic D, Sovtic A, Minic P, Grkovic S, Guc-Scekic M, Lalic T, Miskovic M. Newborn screening for CF. Pediatr Int 2013; 55(2): 181-4.