Dr sc. Sanja Ćirković

Obrazovanje

• 2014: Specijalista biolog, Akademske specijalističke studije na Biološkom fakultetu Univerziteta u Beogradu, smer Genetika
• 2012: Doktor nauka – biološke nauke, Doktorske studije na Biološkom fakultetu Univerziteta u Beogradu, smer Genetika
• 2002: Diplomirani molekularni biolog i fiziolog, Biološki fakultet Univerziteta u Beogradu, studijska grupa Molekularna biologija i fiziologija, smer Primenjena genetika

Profesionalno iskustvo

Postnatalna i prenatalna citogenetička i molekularna dijagnostika naslednih bolesti u Laboratoriji za medicinsku genetiku IMD (2003 – )

Članstvo

• Društvo genetičara Srbije, sekcija Medicinska genetika (2008 – )
• Srpsko društvo za molekularnu biologiju (MolBioS) (2019 – )
• European Society of Human Genetics (ESHG) (2013 – )
• European Cytogeneticists Association (ECA) (2015 – )

Reference od značaja

1. 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.
2. Pešić M, Dragašević Mišković N, Marjanović A, Dobričić V, Maksimović N, Svetel M, Perović D, Novaković I, Ćirković S, Stanković I, Kostić V. Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism. Neurological Research 2021; 43(4): 321-6.
3. Sunjog K, Cirkovic S, Vukovic-Gacic B, Guc-Scekic M, Miskovic M, Vujic D, Skoric D. Comet assay and cytogenetic findings in differential diagnosis of Fanconi anemia. Genetika 2019; 51(3): 1113-26.
4. Dobric B, Radivojevic R, 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): 1009-19.
5. 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.
6. 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 Gyn Obst 2014; 124(2014): 55-8.
7. Vujić D, Petrović S, Lazić E, Kuzmanović M, Leskovac A, Joksić I, Mićić D, Jovanović A, Zečević Ž, Guć-Šćekić M, Ćirković S, Joksić G. Prevalence of FA-D2 Rare Complementation Group of Fanconi Anemia in Serbia. Ind J Pediatr 2014; 81(3): 260-5.
8. Liehr T, Cirkovic S, Lalic T, Guc-Scekic M, de Almeida C, Weimer J, Iourov I, Melaragno MI, Guilherme RS, Stefanou EG, Aktas D, Kreskowski K, Klein E, Ziegler M, Kosyakova N, Volleth M, Hamid AB. Complex small supernumerary marker chromosomes – an update. Mol Cytogenet 2013; 6(1): 46.
9. Ćirković S, Srdić-Rajić T, Guć-Šćekić M, Vujić D, Škorić D: Cell cycle analysis in patients with Fanconi anemia from Serbia . Genetika 2013; 45(1): 451-8.1.