Browsing eNauka

Browsing by Author Novaković, Ivana

Showing results 1 to 20 of 443  next >
Issue DateTitleAuthor(s)TypeМp-cat.
2014657del5 mutation of the NBS1 gene in myelodysplastic syndromeBunjevački, Vera  ; Maksimović, Nela  ; Damnjanović, Tatjana  ; Cvjetićanin, Suzana  ; Novaković, Ivana  ; Luković, Ljiljana ; Ristanović, Momčilo  ; Bogdanović, Andrija  ; Jekić, Biljana  Article
22M22
2013A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystoniaSvetel, Marina ; Djuric, Gordana; Novaković, Ivana  ; Dobricic, Valerija; Stefanova, Elka ; Kresojevic, Nikola ; Tomić, Aleksandra  ; Jankovic, Milena ; Petrović, Igor  ; Pekmezović, Tatjana  ;
Kostić, Vladimir ;
Article
23M23
2011A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related genePapassotiropoulos, A; Stefanova, Elka ; Vogler, C; Gschwind, L; Ackermann, S; Spalek, K; Rasch, B; Heck, A; Aerni, A; Hanser, E;
Demougin, P; Huynh, K-D; Luechinger, R; Klarhöfer, M; Novaković, Ivana  ; Kostić, Vladimir ; Boesiger, P; Scheffler, K; de, Quervain D J-F;
Article
21a+M21a+
2009A genome-wide survey of human short-term memoryPapassotiropoulos, A; Henke, K; Stefanova, Elka ; Aerni, A; Müller, A; Demougin, P; Vogler, C; Sigmund, J C; Gschwind, L; Huynh, K-D;
Coluccia, D; Mondadori, C R; Hänggi, J; Buchmann, A; Kostić, Vladimir ; Novakovic, I  ; van, den Bussche H; Kaduszkiewicz, H; Weyerer, S; Bickel, H; Riedel-Heller, S; Pentzek, M; Wiese, B; Dichgans, M; Wagner, M; Jessen, F; Maier, W; de, Quervain D J-F;
Article
21a+M21a+
2024A Machine Learning Approach to Gene Expression in Hypertrophic CardiomyopathyPavić, Jelena  ; Živanović, Marko  ; Tanasković, Irena  ; Pavić, Ognjen  ; Stanković, Vesna  ; Virijević, Katarina  ; Mladenović, Tamara  ; Košarić, Jelena  ; Milićević, Bogdan  ; Qamar, Safi Ur Rehman  ;
Velicki, Lazar  ; Novaković, Ivana  ; Preveden, Andrej  ; Popović, Dejana  ; Tesić, Milorad  ; Seman, Stefan; Filipović, Nenad  ;
Article
21aM21a
2022A multicenter study of genetic testing for Parkinson’s disease in the clinical settingKovanda, Anja; Rački, Valentino; Bergant, Gaber; Georgiev, Dejan; Flisar, Dušan; Papić, Eliša; Branković, Marija  ; Janković, Milena ; Svetel, Marina ; Teran, Nataša;
Maver, Aleš; Kostić, Vladimir S. ; Novaković, Ivana  ; Pirtošek, Zvezdan; Rakuša, Martin; Vuletić, Vladimira; Peterlin, Borut;
Article
21aM21a
2012A NEW MISSENSE MUTATION WITHIN EXON - 3 OF NOTCH3 GENE IN A STROKE PATIENTKozić, Duško  ; Novaković, Ivana  ; Pavlović, Aleksandra  ; Nadežda Čovičković-Šternić; Tamara ŠvabićConference Paper
Mp. category will be shown later
2014A novel AMELX mutation in a family with Amelogenesis imperfectaToljić, Boško M.  ; K. Aleksić Babić; V. Dobričić; Novaković, Ivana V.  ; Milašin, Jelena M.  Conference Paper
Mp. category will be shown later
2013A novel Notch3 Gly89Cys mutation in a Serbian CADASIL familyPavlović, Aleksandra  ; Dobricic, V.; Semnic, R.; Lackovic, V.; Novaković, Ivana  ; Bajčetić, Miloš  ; Sternic, N.Article
23M23
2015A novel TOR1A mutation in a Serbian patient with cervical dystoniaDobričić, Valerija S. ; Kresojević, Nikola D. ; Žarković, Milena; Tomić, Aleksandra D.  ; Svetel, Marina V. ; Novaković, Ivana V.  ; Kostić, Vladimir S. Conference Paper
Mp. category will be shown later
2017A pilot study on predictors of brainstem raphe abnormality in patients with major depressive disorderKostić, Milutin  ; Jovanović, Ana; Pešić, Danilo; Peljto, Amir; Novaković, Ivana  ; Dobričić, Valerija ; Lečić Toševski, Dušica ; Mijajlović, Milija  Article
21M21
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
2025ACE gene and male infertility: a South Slavic case-control study and multi-omics data integrationKunej, Tanja; Podgrajsek, Rebeka; Jaklic, Helena; Hodzic, Alenka; Stimpfel, Martin; Miljanovic, Olivera; Ristanović, Momčilo  ; Novaković, Ivana V.  ; Plaseska-Karanfilska, Dijana; Noveski, Predrag;
Ostojic, Sasa; Buretic-Tomljanovic, Alena; Grskovic, Antun; Peterlin, Borut;
Article
22M22
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
2017Allele-Specific and Trauma-Related Epigenetic Changes in the FKBP5 Gene: Differences Between Psychotic Patients and Healthy ControlsMihaljević, Marina ; Franić, Dušica ; Soldatović, Ivan  ; Andrić, Sanja  ; Mirjanić, Tijana; Novaković, Ivana  ; Adžić, Miroslav  ; Marić Bojović, Nađa  Conference Paper
Mp. category will be shown later
2009Alterations of c-Myc and c-erbB-2 genes in ovarian tumoursPastor, Tibor; Popović, Branka  ; Gvozdenović, Ana; Boro, Aleksandar; Petrović, Bojana ; Novaković, Ivana  ; Puzović, Dragana  ; Luković, Ljiljana; Milašin, Jelena  Article
24M24
2014Altered basal ganglia echogenicity early in sporadic Creutzfeldt-Jakob diseaseVeselinović, Nikola  ; Pavlović, Aleksandra M.  ; Petrović, Boris; Ristić, Aleksandar  ; Novaković, Ivana  ; Švabić-Međedović, Tamara ; Pavlović, Dragan ; Šternić, Nadežda Article
22M22
2012Amplification of cyclin A gene in Wilms tumorRadojević-Škodrić, Sanja  ; Brašanac, Dimitrije  ; Novaković, Ivana  ; Bogdanović, Ljiljana  ; Krstić, Zoran ; Basta-Jovanović, Gordana Conference Paper
Mp. category will be shown later
2019Analisys of the association of TNFα, IL1 β and IL6 promotor gene polymorphisms with the development of severe form of retinopathy of prematurityĆućuz, Milica; Pantelić, Jelica; Varljen, Tatjana; Grk, Milka  ; Novaković, Ivana  ; Damnjanović, Tatjana  Conference Paper
Mp. category will be shown later
1998Analiza gena za distrofin kod bolesnika sa Becker-ovom mišićnom distrofijomNovaković, Ivana  Doctoral theses
70M70