Researchers



Results 21-30 of 30
Issue DateTitleAuthor(s)TypeМp-cat.
2023Functional characterization of novel variants in the dnai1 gene in a patient with primary ciliary dyskinesiaSkakić, Anita  ; Stevanović, Nina  ; Spasovski, Vesna  ; Parezanović, Marina  ; Ugrin, Milena  ; Komazec, Jovana  ; Klaassen, Kristel  ; Stanković, Sara  ; Pavlović, Sonja  ; Stojiljković, Maja  ;
Anđelković, Marina  ;
Conference Paper
Mp. category will be shown later
2023Improving the diagnostics of rare lung disorders using a uniquely designed pipeline for analysis of ngs dataAnđelković, Marina  ; Skakić, Anita  ; Stevanović, Nina  ; Parezanović, Marina  ; Komazec, Jovana  ; Klaassen, Kristel  ; Spasovski, Vesna  ; Stojiljković, Maja  ; Pavlović, Sonja  Conference Paper
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2023High-risk population screening for fabry disease in patients with chronic renal failure of unknown etiologyParezanović, Marina  ; Anđelković, Marina  ; Stevanović, Nina  ; Spasovski, Vesna  ; Ugrin, Milena  ; Komazec, Jovana  ; Klaassen, Kristel  ; Stanković, Sara  ; Pavlović, Sonja  ; Stojiljković, Maja  ;
Skakić, Anita  ;
Conference Paper
Mp. category will be shown later
2023The role of MIR-34 family members on the mucociliary process in the cellular respiratory model systemStevanović, Nina  ; Skakić, Anita  ; Parezanović, Marina  ; Spasovski, Vesna  ; Ugrin, Milena  ; Komazec, Jovana  ; Klaassen, Kristel  ; Stanković, Sara  ; Pavlović, Sonja  ; Stojiljković, Maja  ;
Anđelković, Marina  ;
Conference Paper
Mp. category will be shown later
2022Funkcionalna karatkerizacija novootkrivenih varijanti u genu DNAI1 kod pacijenta sa primarnom cilijarnom diskinezijomStevanović, Nina  ; Skakić, Anita  ; Spasovski, Vesna  ; Stojiljković, Maja  ; Parezanović, Marina  ; Ugrin, Milena  ; Pavlović, Sonja  ; Anđelković, Marina  Conference Paper
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2022Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifierKristel Klaassen  ; Đorđević, Maja; Skakić, Anita  ; Božica Kecman; Parezanović, Marina  ; Anđelković, Marina  ; Stevanović, Nina  ; Spasovski, Vesna  ; Ugrin, Milena  ; Drmanac, Radoje;
Pavlović, Sonja  ; Stojiljković, Maja  ;
Conference Paper
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2022Dizajniranje jedinstvenih smernica za standardizaciju analize NGS podataka kod pacijenata sa retkim plućnim bolestimaAnđelković, Marina  ; Skakić, Anita  ; Stevanović, Nina  ; Parezanović, Marina  ; Stojiljković, Maja  ; Spasovski, Vesna  ; Pavlović, Sonja  Conference Paper
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2022Retke bolesti u eri genomikeStojiljković, Maja  ; Klaassen, Kristel  ; Skakić, Anita  ; Anđelković, Marina  ; Spasovski, Vesna  ; Ugrin, Milena  ; Komazec, Jovana  ; Parezanović, Marina  ; Stevanović, Nina  ; Pavlović, Sonja  Conference Paper
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2022Molekularna dijagnostika Fabrijeve bolesti kod pacijenata sa hroničnom bubrežnom insuficijencijom nepoznate etiologijeParezanović, Marina  ; Stojiljković, Maja  ; Andjelkovic, Marina  ; Stevanovic, Nina  ; Vesna Spasovski  ; Milena Ugrin  ; Jovana Komazec  ; Tošic, Nataša  ; Pavlovic, Sonja  ; Celic, Dejan  ;
Vucenovic, Jelica; Skakic, Anita  ;
Conference Paper
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2021Identification and Classification of Novel Genetic Variants: En Route to the Diagnosis of Primary Ciliary DyskinesiaStevanović, Nina  ; Skakić, Anita  ; Minić, Predrag ; Sovtić, Aleksandar  ; Stojiljković, Maja  ; Pavlović, Sonja  ; Anđelković, Marina  Article
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