Researchers
Novaković, Ivana
Results 1-20 of 391
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2025 | Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis | Turk, Aleksander; Maver, Aleš; Juvan, Peter; Drulović, Jelena S.  ; Mesaroš, Šarlota T.  ; Novaković, Ivana V. ; Starčević-Čizmarević, Nada; Ristič, Smiljana; Stanković-Matić, Ivana; Peterlin, Borut | Article | 21M21 |
| 2025 | Genetic and Clinical Insights into ALS/FTD: Profiling a Rare Cohort to Explore Spectrum Heterogeneity | Marjanović, Ana ; Stefanova, Elka ; Virić, Vanja ; Palibrk, Aleksa; Mandić-Stojmenović, Gorana ; Stojković, Tanja ; Stojadinović, Lenka ; Basta, Ivana ; Novaković, Ivana ; Stević, Zorica ;
Janković, Milena
; | 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 ; Novaković, Ivana V. ; Plaseska-Karanfilska, Dijana; Noveski, Predrag;
Ostojic, Sasa; Buretic-Tomljanovic, Alena; Grskovic, Antun; Peterlin, Borut;
| Article | 22M22 |
| 2025 | HIF-1A Gene Polymorphisms are Associated With Clinical and Biochemical Parameters in COVID-19 Patients in Serbian Population | Ljujić, Biljana ; Maksimović, Nela ; Damnjanović, Tatjana M. ; Novaković, Ivana ; Grk, Milka B. ; Gulić, Milica ; Dušanović-Pjević, Marija G. ; Popovska-Jovičić, Biljana D. ; Rakovic, Ivana R ; Gazdic-Jankovic, Marina ;
Miletić-Kovačević, Marina
; Jekić, Biljana B. ; | Article | 22M22 |
| 2025 | APOE, ATXN1 and ATXN2 genetic analysis in ALS/FTD patients | Marjanović, Ana ; Virić, Vanja ; Mandić, Gorana ; Stojković, Tanja ; Perić, Stojan ; Basta, Ivana ; Janković, Milena ; Stojadinović, Lenka ; Jovanović, Emilija; Branković, Marija ;
Novaković, Ivana
; Stević, Zorica ; Stefanova, Elka ; | Conference Paper | Mp. category will be shown later |
| 2025 | The role of DNA mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility: a systematic review and cohort study | Podgrajšek, Rebeka; Hodžić, Alenka; Maver, Aleš; Stimpfel, Martin; Anđelić, Aleksander; Miljanović, Olivera; Ristanović, Momčilo ; Novaković, Ivana ; Plašeska-Karanfilska, Dijana; Noveski, Predrag;
Ostojić, Saša; Buretić-Tomljanović, Alena; Peterlin, Borut;
| Reviews | 21aM21a |
| 2025 | A Specific Haplotype of the MMP2 Gene Promoter May Increase the Risk of Developing Cerebral Palsy | Đuranović-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 |
| 2025 | Clinical exome sequencing identifies pathogenic SQSTM1 variant in a patient with chorea and gaze palsy | Stojadinović, Lenka ; Petrović, Igor ; Dragašević-Mišković, Nataša ; Jovanović, Emilija; Marković, Vladana ; Janković, Milena ; Novaković, Ivana ; Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2025 | Genetic Testing for Monogenic Forms of Male Infertility Contributes to the Clinical Diagnosis of Men with Severe Idiopathic Male Infertility | Podgrajsek, Rebeka; Hodzic, Alenka; Maver, Ales; Stimpfel, Martin; Andjelic, Aleksander; Miljanovic, Olivera; Ristanović, Momčilo ; Novaković, Ivana ; Plaseska-Karanfilska, Dijana; Noveski, Predrag;
Ostojic, Sasa; Grskovic, Antun; Buretic-Tomljanovic, Alena; Peterlin, Borut;
| Article | 21aM21a |
| 2025 | Increased burden of rare variants in GWAS associated genes in familial multiple sclerosis | Turk, Aleksander; Maver, Aleš; Juvan, Peter; Drulović, Jelena S. ; Mesaroš, Šarlota ; Novaković, Ivana ; Čizmarević, Nada S.; Ristić, Smiljana; Matić, Ivana S.; Peterlin, Borut | Conference Paper | Mp. category will be shown later |
| 2025 | Biallelic RFC1 expansions as a rare cause of familial and early onset Parkinson's disease in the Slavic population | Kovanda, Anja; Šušmelj, Lara; Lukežič, Tadeja; Maver, Aleš; Rački, Valentino; Vuletić, Vladimira; Svetel, Marina V. ; Novaković, Ivana ; Peterlin, Borut | Conference Paper | Mp. category will be shown later |
| 2025 | New evidence supporting female protective effect in patients with congenital anomalies and neurodevelopmental disorders | Maksimović, Nela ; Damnjanović, Tatjana ; Jekić, Biljana ; Novaković, Ivana ; Đurić-Zdravković, Aleksandra ; Dušanović-Pjević, Marija ; Grk, Milka ; Pešić, Milica ; Đuranović-Uklein, Ana ; Rašić, Milica ;
Stojanovski, Nataša
; Perović, Dijana ; | Article | 21M21 |
| 2025 | Frequency of TREM2 and APOE rare variants in patients with Alzheimer’s disease in Serbia | Stojadinović, Lenka ; Marjanović, Ana ; Branković, Marija ; Mandić, Gorana ; Stojković, Tanja ; Jovanović, Emilija; Novaković, Ivana ; Stefanova, Elka ; Janković, Milena | Conference Paper | Mp. category will be shown later |
| 2025 | Association of NOS Gene Polymorphisms with Sepsis-Related Complications in Secondary Peritonitis | Rašić, Milica ; Maksimović, Nela S. ; Grk, Milka B. ; Dušanović-Pjević, Marija G. ; Rašić, Petar; Svirčev, Miloš ; Damnjanović, Tatjana M. ; Perović, Dijana ; Đuranović-Uklein, Ana S. ; Stojanovski, Nataša ;
Pešić, Milica
; Novaković, Ivana V. ; Doklestić-Vasiljev, Krstina S. ; | Article | 21M21 |
| 2025 | Chromosomal Microarray in Children Born Small for Gestational Age - Single Center Experience | Perović, 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 |
| 2025 | Is 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 |
| 2025 | Clinical application of whole exome sequencing in the diagnosis of men with severely impaired spermatogenesis | Podgrajsek, 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 |
| 2025 | Whole-exome sequencing in pediatric patients with glomerulonephritis | Perić, Marina; Branković, Marija ; Stajić, Nataša; Putnik, Jovana; Paripović, Aleksandra; Janković, Milena ; Nikolić, Dejan ; Milanović, Filip; Novaković, Ivana ; Vukomanović, Vladislav | Article | 22M22 |
| 2025 | Multi-Center National Study of Genotype-Phenotype Correlation and Clinical Characteristics in Children and Young Adults with Friedreich's Ataxia from Serbia | Kovačević, Gordana ; Todorović, Slobodanka ; Novaković, Ivana ; Dobričić, Valerija ; Savić-Pavićević, Dušanka ; Milić-Rašić, Vedrana ; Svetel, Marina ; Brkušanin, Miloš ; Vukomanović, Vladislav ; Vučinić, Dragana;
Ostojić, Slavica; Putnik, Jovana; Kosać, Ana
; | Article | 21M21 |
| 2025 | Genetic Susceptibility to Glomerulonephritis in Children: Analysis of Structural Kidney Genes and Immune System Genes | Perić, Marina; Aničin, Aleksandra ; Branković, Marija ; Stajić, Nataša; Putnik, Jovana; Paripović, Aleksandra; Janković, Milena ; Božović, Ivo ; Perović, Vladimir S. ; Novaković, Ivana ;
Vukomanović, Vladislav A.
; Milošević, Emina ; | Article | 21M21 |