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Issue DateTitleAuthor(s)Rank
1-Jun-2015Joint effect of ADARB1 gene, HTR2C gene and stressful life events on suicide attempt risk in patients with major psychiatric disordersKaranović, Jelena ; Šviković, Saša; Pantović, Maja; Durica, Svetlana; Brajušković, Goran ; Damjanović, Aleksandar; Jovanović, Vladimir; Ivković, Maja; Romac, Stanka; Savić Pavićević, Dušanka 
1-Nov-2015Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patientsBrkušanin, Miloš ; Kosać, Ana; Jovanović, Vladimir; Pešović, Jovan ; Brajušković, Goran ; Dimitrijević, Nikola; Todorović, Slobodanka; Romac, Stanka; Milić Rašić, Vedrana; Savić Pavićević, Dušanka 
Sep-2017Joint effects of variants in RNA editing and serotonergic system genes and stressful life events in predisposition for suicide attempt in psychiatric patientsKaranović, Jelena ; Ivković Maja; Pantović Maja; Damjanović Aleksandar; Jovanović Vladimir; Brajušković, Goran ; Savić-Pavićević, Dušanka M64
Apr-2005JP-3 gene polymorphism in a healthy population of Serbia and MontenegroKeckarević, M. ; Savić, D. ; Romac, S.
2022Lokus CTLA4 je asociran sa rizikom za razvoj rane forme miastenije gravis u populaciji SrbijeGarai, Nemanja; Dejanović Ivana; Perić Stojan; Brkušanin, Miloš ; Karanović, Jelena ; Pešović, Jovan ; Apostolski Slobodan; Lavrnić Dragana; Savić-Pavićević, Dušanka M64
2024Longitudinal analysis of CTG repeat somatic instability in myotonic dystrophy type 1 patientsRadovanović, Nemanja ; Pešović, J.; Perić, S.; Radenković, L. ; Brajušković, Goran ; Rakočević Stojanović, V.; Savić-Pavićević, Dušanka M34
4-Aug-2022 LTBP4, SPP1, and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian PatientsKosac Ana; Pešović, Jovan ; Radenković, Lana ; Brkušanin, Miloš ; Radovanović, Nemanja ; Đurišić, Marina; Radivojević, Danijela; Mladenović, Jelena; Ostojić, Slavica; Kovačević, Gordana; Kravljanac, Ružica; Savić-Pavićević, Dušanka ; Milić Rašić, VedranaM22
1-Sep-2017Magnetic resonance imaging of leg muscles in patients with myotonic dystrophiesPeric, Stojan; Maksimovic, Ruzica; Banko, Bojan; Durdic, Milica; Bjelica, Bogdan; Bozovic, Ivo; Balcik, Yunus; Pešović, Jovan ; Savić Pavićević, Dušanka ; Rakocevic-Stojanovic, Vidosava
1-Jan-2018Metabolic impairments in patients with myotonic dystrophy type 2Vujnic, Milorad; Peric, Stojan; Calic, Zeljka; Benovic, Natasa; Nisic, Tanja; Pešović, Jovan ; Savić Pavićević, Dušanka ; Rakocevic-Stojanovic, Vidosava
9-Dec-2022MiR-375 and miR-21 as Potential Biomarkers of Prostate Cancer: Comparison of Matching Samples of Plasma and ExosomesMatijašević, Suzana ; Dobrijević, Zorana; Kotarac, Nevena ; Filipović, Lidija; Popović, Milica; Korać, Aleksandra ; Vuković, Ivan; Savić-Pavićević, Dušanka ; Brajušković, Goran M22
29-Dec-2021Molecular and Clinical Implications of Variant Repeats in Myotonic Dystrophy Type 1Perić, Stojan; Pešović, Jovan ; Rakočević Stojanović, Vidosava; Savić-Pavićević, Dušanka ; Meola, GiovanniM21
1-Dec-2017Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansionsPešović, Jovan ; Perić, S.; Brkušanin, Miloš ; Brajušković, Goran ; Rakočević-Stojanović, V.; Savić Pavićević, Dušanka 
29-Apr-2013Molecular genetics and genetic testing in myotonic dystrophy type 1Savić Pavićević, Dušanka ; Karanović, Jelena ; Brkušanin, Miloš ; Šviković, Saša; Djurica, Svetlana; Brajušković, Goran ; Romac, StankaM23
Sep-2011Molecular genetics of diseases with unstable expansion of repeatsSavić-Pavićević, Dušanka ; Mladenović, Jelena; Rakočević Stojanović, Vidosava; Pekmezović, T; Karanović, Jelena ; Brajušković, Goran ; Apostolski, Slobodan; Todorović, Slobodanka; Romac, StankaM62
May-2023Mutation rates of 22 autosomal STR loci in a European population from central Balkan, Republic of SerbiaGarai Nemanja; Pešović, Jovan ; Dobrijević Zorana; Brkušanin, Miloš ; Matijašević, Suzana ; Radenković, Lana ; Radovanović, Nemanja ; Karanović, Jelena ; Brajušković, Goran ; Savić-Pavićević, Dušanka M34
Jun-2009Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patientsKeckarević Marković, Milica ; Milic-Rasic, Vedrana; Mladenovic, Jelena; Dackovic, Jelena; Kecmanović, Miljana ; Keckarević, Dušan ; Savić Pavićević, Dušanka ; Romac, Stanka
1-Jan-2018Myotonic Dystrophy Type 2 - Data from the Serbian RegistryBozovic, Ivo; Peric, Stojan; Pešović, Jovan ; Bjelica, Bogdan; Brkušanin, Miloš ; Basta, Ivana; Bozic, Marija; Sencanic, Ivan; Marjanovic, Ana; Brankovic, Marija; Savić Pavićević, Dušanka ; Rakocevic-Stojanovic, Vidosava
Jul-2022Myotonic Dystrophy Type 2 and Autoimmune DiseasesPerić, S.; Zlatar J,; Pešović, Jovan ; Nikolić, L.; Božović, I.; Ivanović, V.; Palibrk, A.; Basta, I.; Savić-Pavićević, Dušanka ; Rakocevic-Stojanovic VidosavaM34
Sep-2022Neonatal screening (NBS) for spinal muscular atrophy (SMA) in Serbia – first resultsNikolić, Dimitrije; Jovanović, K; Brkušanin, Miloš ; Karanović, Jelena ; Savić-Pavićević, Dušanka ; Garai, Nemanja; Šljivančanin Jakovljević, TamaraM32
6-Oct-2023Neurofilament as a biomarker of response to genetically designed therapies for spinal muscular atrophyBrkušanin, Miloš ; Milić-Rašić, V.; Branković, V.; Stević, Z.; Nikolić, D.; Kosać, A.; Jovanović, K.; Karanović, Jelena ; Pešović, Jovan ; Brajušković, Goran ; Savić-Pavićević, Dušanka M62