Researchers

Results 21-40 of 394
Issue DateTitleAuthor(s)TypeМp-cat.
2025A Specific Haplotype of the MMP2 Gene Promoter May Increase the Risk of Developing Cerebral PalsyĐuranović-Uklein, Ana S.  ; Cerovac, Nataša  ; Perović, Dijana  ; Maksimović, Nela S.  ; Jekić, Biljana B.  ; Grk, Milka B.  ; Dušanović-Pjević, Marija G.  ; Rašić, Milica  ; Stojanovski, Nataša  ; Pešić, Milica  ;
Novaković, Ivana V.  ; Damnjanović, Tatjana M.  ;
Article
21M21
2025Clinical application of whole exome sequencing in the diagnosis of men with severely impaired spermatogenesisPodgrajsek, Rebeka; Hodzic, Alenka; Maver, Aleš; Stimpfel, Martin; Andjelic, Aleksander; Miljanovic, Olivera; Ristanović, Momčilo  ; Novaković, Ivana V.  ; Plaseska-Karanfilska, Dijana; Noveski, Predrag;
Ostojic, Sasa; Buretic-Tomljanovic, Alena; Peterlin, Borut;
Conference Paper
Mp. category will be shown later
2025Is GBA1 mutation status a game-changer for impulse control behaviour in Parkinson's disease?Kresojević, Nikola ; Marković, Vladana  ; Geratović, Cveta; Ječmenica-Lukić, Milica  ; Tomić, Aleksandra  ; Dobričić, Valerija ; Stanković, Iva D. ; Stojkovic, Tanja  ; Dragašević, Nataša  ; Šarčević, Maksim;
Jankovic, Milena  ; Marjanovic, Ana ; Novaković, Ivana  ; Kostić, Vladimir ; Svetel, Marina ; Petrović, Igor  ;
Article
22M22
2025Chromosomal Microarray in Children Born Small for Gestational Age - Single Center ExperiencePerović, Dijana  ; Barzegar, P.; Damnjanović, Tatjana M.  ; Jekić, Biljana B.  ; Grk, Milka B.  ; Dušanović-Pjević, Marija G.  ; Cvetković, Dragana  ; Đuranović-Uklein, Ana  ; Stojanovski, Nataša  ; Rašić, Milica  ;
Novaković, Ivana V.  ; Elhayani, B.; Maksimović, Nela S.  ;
Article
23M23
2024Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory CenterStefanova, Elka D. ; Marjanović, Ana ; Dobričić, Valerija S. ; Mandić-Stojmenović, Gorana B.  ; Stojković, Tanja  ; Branković, Marija  ; Šarčević, Maksim; Novaković, Ivana V.  ; Kostić, Vladimir S. Article
22M22
2024Influence of polymorphisms in genes for interleukin-6 and interleukin-10 on dialysis patients survivalJovičić-Pavlović, Svetlana M.; Simić-Ogrizović, Sanja P. ; Pavlović, Natalija; Bukumirić, Zoran M.  ; Novaković, Ivana V.  Conference Paper
Mp. category will be shown later
2024Analysis of clinical exome panel in rare movement and cognitive disordersBranković, Marija  ; Dragašević, Nataša  ; Svetel, Marina ; Stefanova, Elka ; Mandić, Gorana  ; Stojković, Tanja  ; Milovanović, Andona ; Marković, Vladana  ; Janković, Milena ; Marjanović, Ana ;
Dobričić, Valerija ; Novaković, Ivana  ; Kostić, Vladimir ;
Conference Paper
Mp. category will be shown later
2024APOE genotype, ATXN1 and ATXN2 repeats size in C9orf72 expansion carriersMarjanović, Ana ; Mandić-Stojmenović, Gorana  ; Virić, Vanja  ; Branković, Marija  ; Janković, Milena ; Stojković, Tanja  ; Novaković, Ivana  ; Stević, Zorica ; Stefanova, Elka Conference Paper
Mp. category will be shown later
2024Galectin 3 Rs4644 Gene Polymorphism Is Associated with Metabolic Traits in Serbian Adolescent PopulationVidović, Vanja; Novaković, Ivana  ; Damnjanović, Tatjana  ; Radić-Savić, Zana; Vidović, Stojko; Krbić, Ranko; Maksimović, Nela  Article
23M23
2024Whole exome sequencing in Serbian patients with hereditary spastic paraplegiaBranković, Marija  ; Ivanović, Vukan ; Basta, Ivana  ; Khang, Rin; Lee, Eugene; Stević, Zorica ; Ralić, Branislav; Tubić, Radoje  ; Seo, GoHun; Marković, Vladana  ;
Božović, Ivo ; Svetel, Marina ; Marjanović, Ana ; Veselinović, Nikola; Mesaroš, Šarlota  ; Janković, Milena ; Savić-Pavićević, Dušanka  ; Jovin, Zita; Novaković, Ivana  ; Lee, Hane; Perić, Stojan  ;
Article
22M22
2024Genetic and epigenetic mechanisms of agingNovaković, Ivana  ; Filipović, Tamara  ; Maksimović, Nela  ; Nikolić, Dejan  Article
52M52
2024Adrenal hypoplasia congenita and hypogonadotropic hypogonadism due to a novel NR0B1 (DAX1) gene mutation associated with common variable immunodeficiency and Hashimoto's thyroiditisĆirić, Jasmina D. ; Novaković, Ivana  ; Perić-Popadić, Aleksandra Z.  ; Žarković, Miloš P.  ; Beleslin-Nedeljković, Biljana Z.  ; Bonači-Nikolić, Branka M.  Article
22M22
2024ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case SeriesMilovanović, Andona ; Westenberger, Ana; Stanković, Iva D. ; Tamaš, Olivera S.; Branković, Marija  ; Marjanović, Ana ; ...; Branković, Vesna; Novaković, Ivana V.  ; Petrović, Igor N.  ;
Svetel, Marina V. ; Klein, Christine; Kostić, Vladimir S. ; Dragašević-Mišković, Nataša T.  ; (broj koautora 18);
Article
21a+M21a+
2024Етички аспекти генетског тестирањаНоваковић, Ивана  Conference Paper
Mp. category will be shown later
2024Challenges in rare diseases: The example of mitochondrial diseasesNovaković, Ivana  ; Janković, Milena ; Marjanović, Ana ; Branković, Marija  ; Svetel, Marina ; Jančić, Jasna  Conference Paper
Mp. category will be shown later
2024C9orf72 genetic screening in patients with ALS/FTD phenotype from SerbiaMarjanović, Ana ; Mandić-Stojmenović, Gorana  ; Milićević, Ognjen  ; Stojković, Tanja  ; Virić, Vanja  ; Janković, Milena ; Branković, Marija  ; Palibrk, Aleksa  ; Ivanović, Vukan ; Dobričić, Valerija ;
Perić, Stojan  ; Novaković, Ivana  ; Stević, Zorica ; Stefanova, Elka ;
Conference Paper
Mp. category will be shown later
2024Wilson’s diseaseSvetel, Marina ; Kresojević, Nikola ; Tomić, Aleksandra  ; Ječmenica-Lukić, Milica  ; Marković, Vladana  ; Stanković, Iva ; Petrović, Igor  ; Pekmezović, Tatjana  ; Novaković, Ivana  ; Božić, Marija  ;
Svetel, Marko ; Vitković, Jelena; Dragašević, Nataša  ;
Article
23M23
2024Exclusive breastfeeding may be a protective factor in individuals with familial multiple sclerosis. A population registry-based case-control studyJovanović, Aleksa Lj. ; Pekmezović, Tatjana D.  ; Mesaroš, Šarlota T.  ; Novaković, Ivana V.  ; Peterlin, Borut; Veselinović, Nikola D.  ; Tamaš, Olivera S.; Ivanović, Jovana B. ; Marić, Gorica D.  ; Andabaka, Marko M. ;
Momčilović, Nikola; Drulović, Jelena S. ;
Article
21M21
2024Earlier age of symptom onset in younger generation of familial cases of multiple sclerosisJovanović, Aleksa Lj. ; Pekmezović, Tatjana D.  ; Mesaroš, Šarlota T.  ; Novaković, Ivana V.  ; Peterlin, Borut; Veselinović, Nikola D.  ; Tamaš, Olivera S.; Ivanović, Jovana B. ; Marić, Gorica D.  ; Andabaka, Marko M. ;
Momčilović, Nikola; Drulović, Jelena S. ;
Article
22M22
2024Sleep problems in female carriers of premutation in the FMR1 genePešić, Milica  ; Stevanović, Milena; Andrejić, Nikola; Pešović, Jovan  ; Ćirković, Sanja; Dimitrijević, Sanja S.; Baščarević, Danijela; Dragašević-Mišković, Nataša  ; Novaković, Ivana V.  ; Protić, Dragana  Conference Paper
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