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Browsing by Author Novaković, Ivana
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| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2014 | 657del5 mutation of the NBS1 gene in myelodysplastic syndrome![]() | Bunjevački, Vera | Article | 22M22 |
| 2013 | A common polymorphism in the brain-derived neurotrophic factor gene in patients with adult-onset primary focal and segmental dystonia | Svetel, Marina | Article | 23M23 |
| 2011 | A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene | Papassotiropoulos, A; Stefanova, Elka | Article | 21a+M21a+ |
| 2009 | A genome-wide survey of human short-term memory | Papassotiropoulos, A; Henke, K; Stefanova, Elka | Article | 21a+M21a+ |
| 2024 | A Machine Learning Approach to Gene Expression in Hypertrophic Cardiomyopathy![]() | Pavić, Jelena | Article | 21aM21a |
| 2022 | A multicenter study of genetic testing for Parkinson’s disease in the clinical setting![]() | Kovanda, Anja; Rački, Valentino; Bergant, Gaber; Georgiev, Dejan; Flisar, Dušan; Papić, Eliša; Branković, Marija | Article | 21aM21a |
| 2012 | A NEW MISSENSE MUTATION WITHIN EXON - 3 OF NOTCH3 GENE IN A STROKE PATIENT | Kozić, Duško | Conference Paper | Mp. category will be shown later |
| 2014 | A novel AMELX mutation in a family with Amelogenesis imperfecta | Toljić, Boško M. | Conference Paper | Mp. category will be shown later |
| 2013 | A novel Notch3 Gly89Cys mutation in a Serbian CADASIL family | Pavlović, Aleksandra | Article | 23M23 |
| 2015 | A novel TOR1A mutation in a Serbian patient with cervical dystonia![]() | Dobričić, Valerija S. | Conference Paper | Mp. category will be shown later |
| 2017 | A pilot study on predictors of brainstem raphe abnormality in patients with major depressive disorder![]() | Kostić, Milutin | Article | 21M21 |
| 2025 | A Specific Haplotype of the MMP2 Gene Promoter May Increase the Risk of Developing Cerebral Palsy![]() | Đuranović-Uklein, Ana S. | Article | 21M21 |
| 2025 | ACE gene and male infertility: a South Slavic case-control study and multi-omics data integration![]() | Kunej, Tanja; Podgrajsek, Rebeka; Jaklic, Helena; Hodzic, Alenka; Stimpfel, Martin; Miljanovic, Olivera; Ristanović, Momčilo
Ostojic, Sasa; Buretic-Tomljanovic, Alena; Grskovic, Antun; Peterlin, Borut;
| Article | 22M22 |
| 2024 | Adrenal hypoplasia congenita and hypogonadotropic hypogonadism due to a novel NR0B1 (DAX1) gene mutation associated with common variable immunodeficiency and Hashimoto's thyroiditis![]() | Ćirić, Jasmina D. | Article | 22M22 |
| 2017 | Allele-Specific and Trauma-Related Epigenetic Changes in the FKBP5 Gene: Differences Between Psychotic Patients and Healthy Controls![]() | Mihaljević, Marina | Conference Paper | Mp. category will be shown later |
| 2009 | Alterations of c-Myc and c-erbB-2 genes in ovarian tumours | Pastor, Tibor; Popović, Branka | Article | 24M24 |
| 2014 | Altered basal ganglia echogenicity early in sporadic Creutzfeldt-Jakob disease![]() | Veselinović, Nikola | Article | 22M22 |
| 2012 | Amplification of cyclin A gene in Wilms tumor | Radojević-Škodrić, Sanja | Conference Paper | Mp. category will be shown later |
| 2019 | Analisys of the association of TNFα, IL1 β and IL6 promotor gene polymorphisms with the development of severe form of retinopathy of prematurity![]() | Ćućuz, Milica; Pantelić, Jelica; Varljen, Tatjana; Grk, Milka | Conference Paper | Mp. category will be shown later |
| 1998 | Analiza gena za distrofin kod bolesnika sa Becker-ovom mišićnom distrofijom![]() | Novaković, Ivana | Doctoral theses | 70M70 |
