M
Milena Ugrin
Researcher at University of Belgrade
Publications - 21
Citations - 145
Milena Ugrin is an academic researcher from University of Belgrade. The author has contributed to research in topics: Gene & Population. The author has an hindex of 6, co-authored 17 publications receiving 108 citations.
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Book ChapterDOI
Molecular Genetics and Genotype-Based Estimation of BH4-Responsiveness in Serbian PKU Patients: Spotlight on Phenotypic Implications of p.L48S
Maja Djordjevic,Kristel Klaassen,Adrijan Sarajlija,Natasa Tosic,Branka Zukic,Bozica Kecman,Milena Ugrin,Vesna Spasovski,Sonja Pavlovic,Maja Stojiljkovic +9 more
TL;DR: It is concluded that BH4-supplementation therapy could bring benefit to Serbian PKU patients and phenotypic inconsistency found in homozygotes suggested that interallelic complementation and/or additional factors play a role in genotype-phenotype correlation.
Journal ArticleDOI
Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants.
Anita Skakic,Maja Djordjevic,Adrijan Sarajlija,Kristel Klaassen,Natasa Tosic,Bozica Kecman,Milena Ugrin,Vesna Spasovski,Sonja Pavlovic,Maja Stojiljkovic +9 more
TL;DR: In the cohort, hepatomegaly, hypoglycemia and failure to thrive were the most frequent presenting signs of GSD Ia, while hepatomeGaly and recurrent bacterial infections were clinical hallmarks of G SD Ib.
Journal ArticleDOI
Use of Wilms Tumor 1 Gene Expression as a Reliable Marker for Prognosis and Minimal Residual Disease Monitoring in Acute Myeloid Leukemia With Normal Karyotype Patients.
Irena Marjanovic,Teodora Karan-Djurasevic,Milena Ugrin,Marijana Virijevic,Ana Vidovic,Dragica Tomin,Nada Suvajdzic Vukovic,Sonja Pavlovic,Natasa Tosic +8 more
TL;DR: It was found that overexpression of the WT1 gene (WT1high status), present in 25.5% of patients, was an independent unfavorable factor for achieving complete remission and was also associated with resistance to therapy and shorter disease‐free survival and overall survival.
Journal ArticleDOI
Molecular genetic study of congenital adrenal hyperplasia in Serbia: novel p.Leu129Pro and p.Ser165Pro CYP21A2 gene mutations
I. Milacic,M. Barac,Tatjana Milenkovic,Milena Ugrin,Kristel Klaassen,Anita Skakic,Maja Jesic,I. Joksic,Katarina Mitrovic,Sladjana Todorovic,Svetlana Vujovic,Sonja Pavlovic,Maja Stojiljkovic +12 more
TL;DR: The first comprehensive molecular genetic study of Serbian CAH patients revealed two novel CYP21A2 mutations, both of them novel, which will enable genetic counseling in the population and contribute to better understanding of molecular landscape of CAH in Europe.
Journal ArticleDOI
Expression of TLR7 , TLR9 , JAK2 , and STAT3 genes in peripheral blood mononuclear cells from patients with systemic sclerosis
Misa Vreca,Ana Zekovic,Nemanja Damjanov,Marina Andjelkovic,Milena Ugrin,Sonja Pavlovic,Vesna Spasovski +6 more
TL;DR: The results show that TLR7, TLR9, and JAK2 genes are potential biomarkers for SSc, and could contribute to better classification, monitoring, and outcome prediction of patients with SSc based on genetics.