Naučni saradnik
Laboratorija za molekularnu biomedicinu

Institut za molekularnu genetiku i genetičko inženjerstvo (IMGGI),
Univerzitet u Beogradu,

V. Stepe 444a, 11010 Beograd, Srbija
Mob:   +381 65 3976445
Tel:     +381 11 3976445
Fax:    +381 11 3975808
E-mail: milena.radmilovic@imgge.bg.ac.rs

OBRAZOVANJE

2011 - Doktor bioloških nauka, Biološki fakultet (BF), Univerzitet u Beogradu (UB),
(Doktorska teza: "Varijante u genima-modifikatorima β-talasemijskih sindroma kao regulatori genske ekspresije
i populaciono-genetički markeri.")
2005 - Diplomirani molekularni biolog i fiziolog, BF, UB                     

ISTRAŽIVAČKO ISKUSTVO

2012 - naučni saradnik, IMGGI, UB
2011 – 2012 - istraživač saradnik, IMGGI, UB
2010 – 2011 - istraživač pripravnik, IMGGI, UB

RADNO ISKUSTVO

2010 – Laboratorija za molekularnu biomedicinu

OSTALE AKTIVNOSTI           

2009 - 2012 - učesnik u projektu “Mala škola DNKlogije” (MNTRS)
2011 - učesnik u projektu Noć istraživača, “RENIFEVER” (EU, CSA-SA, FP7-PEOPLE-2011-NIGHT-287432, 2011.)
2012 - rukovodilac podprojekta u okviru projekta Noć istraživača,  “SCIMFONICOM” (EU, CSA-SA, FP7-PEOPLE-2012-NIGHT-316471, 2012.)
2013 - zamenik rukovodioca projekta “SCIMFONICOM 2.013” (EU, CSA-SA, FP7-PEOPLE-2012-NIGHT-609724, 2013)
2014 - 2015 - učesnik u projektu Noć istraživača “SCIMFONICOM 2014-2015” (EU, CSA-SA, FP7-PEOPLE-2012-NIGHT-633376, 2014-2015)

OBLAST NAUČNOG INTERESOVANJA

Talasemijski sindromi, geni-modifikatori beta talasemijskih sindroma, uticaj genetičkih varijanti na expresiju gena-modifikatora i na kliničku sliku talasemijskih sindroma.

ODABRANI NAUČNI RADOVI

Radmilovic M, Zukic B, Stojiljkovic Petrovic M, Bartsakoulia M, Stankovic B, Kotur N, Dokmanovic L, Georgitsi M, Patrinos GP, Pavlovic S. Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin. Ann Hematol. 2013;92(1):53-8.

Kotur N, Stankovic B, Kassela K, Georgitsi M, Vicha A, Dokmanovic L, Janic D, Krstovski N, Klaassen K, Radmilovic M, Stojiljkovic M, Nikcevic G, Simeonidis A, Sivolapenko G, Pavlovic S, Patrinos GP, Zukic B. Six-mercaptopurine influences TPMT gene transcription in a TPMT gene promoter variable number of tandem repeats-dependent manner. Pharmacogenomics. 2012; 13(3): 283-295.

Giardine B, Borg J, Higgs D, Peterson K, Philipsen S, Maglott D, Singleton B, Anstee D, Basak AN, Clark B, Costa F, Faustino P, Fedosyuk H, Felice A, Francina A, Galanello R, Gallivan M, Georgitsi M, Gibbons R, Giordano P, Harteveld C, Hoyer J, Jarvis M, Joly P, Kanavakis E, Kollia P, Menzel S, Miller W, Moradkhani K, Old J, Papachatzopoulou A, Papadakis M, Papadopoulos P, Pavlovic S, Perseu L, Radmilovic M, Riemer C, Satta S, Schrijver I, Stojiljkovic M, Thein SL, Traeger-Synodinos J, Tully R, Wada T, Waye J, Wiemann C, Zukic B, Chui D, Wajcman H, Hardison R, Patrinos P. Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach. Nat Genet. 2011; 43(4):295-301.

Zukic B, Radmilovic M, Stojiljkovic M, Tosic N, Pourfarzad F, Dokmanovic L, Janic D, Colovic N, Philipsen S, Patrinos G, Pavlovic S. Functional analysis of the role of the TPMT gene promoter VNTR polymorphism in gene transcription. Pharmacogenomics. 2010; 11(4):547-557.

Radmilovic M, Zukic B, Stankovic B, Karan-Djurasevic T, Stojiljkovic M, Spasovski V, Tosic N, Dokmanovic L, Janic D, Pavlovic S. Thalassemia Syndromes in Serbia: An update.  Hemoglobin. 2010; 34(5):477-485.

Kollia P, Kalamaras A, Chassanidis C, Samara M, Vamvakopoulos NK, Radmilovic M, Pavlovic S, Papadakis MN, Patrinos GP., Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and beta-thalassemia or Hb Sabine confirms the functional role of the Agamma -158 C>T mutation in gamma-globin gene transcription, Blood Cells Mol Dis. 2008; 41(3):263-264.