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Milena Radmilovic · SciRah

Researcher profile · Semantic Scholar

Milena Radmilovic

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Milena Radmilovic — researcher profile on SciRah

h-index: 8
Works: 12
Citations: 341

Most-cited papers

Systematic documentation and analysis of human genetic variation using the microattribution approach
B. Giardine, Joseph J. Borg, D. Higgs, K. Peterson +47 more
2011Nature Genetics156 citations Open access
Semantic Scholar
Functional analysis of the role of the TPMT gene promoter VNTR polymorphism in TPMT gene transcription.
B. Zukic, Milena Radmilovic, M. Stojiljković, N. Tošić +7 more
2010Pharmacogenomics (London)45 citations
Semantic Scholar
Genomic variation in the MAP3K5 gene is associated with β-thalassemia disease severity and hydroxyurea treatment efficacy.
Christina Tafrali, Arsinoi Paizi, Joseph J. Borg, Milena Radmilovic +15 more
2013Pharmacogenomics (London)29 citations Open access
Semantic Scholar
Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin
Milena Radmilovic, B. Zukic, M. Petrovic, M. Bartsakoulia +6 more
2012Annals of Hematology29 citations
Semantic Scholar
6-mercaptopurine influences TPMT gene transcription in a TPMT gene promoter variable number of tandem repeats-dependent manner.
Nikola Kotur, B. Stanković, Katerina Kassela, Marianthi Georgitsi +14 more
2012Pharmacogenomics (London)22 citations Open access
Semantic Scholar
The influence of novel transcriptional regulatory element in intron 14 on the expression of Janus kinase 2 gene in myeloproliferative neoplasms
Vesna Spasovski, N. Tošić, G. Nikčević, M. Stojiljković +6 more
2012Journal of Applied Genetics20 citations
Semantic Scholar
Thalassemia Syndromes in Serbia: An update
Milena Radmilovic, B. Zukic, B. Stanković, T. Karan-Djurasevic +6 more
2010Hemoglobin13 citations
Semantic Scholar
Prognostic Impact of NPM1 Mutations in Serbian Adult Patients with Acute Myeloid Leukemia
M. Kuzmanovic, N. Tošić, N. Čolović, T. Karan-Djurasevic +9 more
2012Acta Haematologica12 citations
Semantic Scholar
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.
P. Kollia, A. Kalamaras, C. Chassanidis, M. Samara +5 more
2008Blood Cells, Molecules & Diseases8 citations
Semantic Scholar
Mutations in the PAH gene: A Tool for population genetics study
M. Stojiljković, A. Stevanovic, M. Djordjevic, B. Petrucev +5 more
20077 citations Open access
Semantic Scholar
Acknowledgements to referees
S. Sanabani, M. Conchon, M. Serpa, M. Novaes +56 more
2012Archives of Toxicology0 citations Open access
Semantic Scholar
Contents Vol. 128, 2012
S. Sanabani, M. Conchon, M. Serpa, M. Novaes +56 more
2012Acta Haematologica0 citations
Semantic Scholar

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