Истраживачи
Maksimović, Nela
Резултати 1-20 од 135
| Година | Наслов | Аутор(и) | Тип резултата | Мп-кат. |
|---|---|---|---|---|
| 2026 | Insight into Haploinsufficiency of the ERBB4 Gene: Expanding the Spectrum of Associated Phenotypes![]() | Mademont-Soler, Irene; ...; Perović, Dijana
(broj koautora 37);
| Научни чланак | 21M21 - Водећи међународни часопис категорије M21 |
| 2026 | Analysis of Copy Number and Sequence Variants Linked to Cardiac Development in Children with Syndromic Congenital Heart Defects![]() | Damnjanović, Tatjana | Article | 23M23 |
| 2025 | A Specific Haplotype of the MMP2 Gene Promoter May Increase the Risk of Developing Cerebral Palsy![]() | Đuranović-Uklein, Ana S. | Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 2025 | Association of NOS Gene Polymorphisms with Sepsis-Related Complications in Secondary Peritonitis![]() | Rašić, Milica | Article | 21M21 |
| 2025 | New evidence supporting female protective effect in patients with congenital anomalies and neurodevelopmental disorders![]() | Maksimović, Nela | Article | 21M21 |
| 2025 | The Association of ACSL1 and UCP2 3′ Utr Polymorphisms with the Clinicopathological Characteristics of Patients with Colorectal Cancer in Serbia![]() | Ajaj, E.; Cvetković, Dragana | Article | 23M23 |
| 2025 | A Novel 4.2 kb deletion of the 3'UTR of RUNX2 Gene Causes Cleidocranial Dysplasia: Further Delineation of the Role of yhe 3'UTR![]() | Mijović, Marija; Čuturilo, Goran | Article | 23M23 |
| 2025 | Analysis of the association between MMP-9 gene polymorphisms and the occurrence of hemorrhagic transformations in acute ischemic stroke patients treated with thrombolysis![]() | Dušanović-Pjević, Marija G. | Conference Paper | Mp. category will be shown later |
| 2025 | Prenatal diagnosis of chromothripsis causing complex chromosomal rearrangement involving chromosomes 5, 7 and 11 leading to TWIST1 deletion and Saethre-Chotzen syndrome![]() | Joksić, Ivana D.; Toljić, Mina | Article | 21M21 |
| 2025 | HIF-1A Gene Polymorphisms are Associated With Clinical and Biochemical Parameters in COVID-19 Patients in Serbian Population![]() | Ljujić, Biljana | Naučni članak | 22M22 - Međunarodni časopis kategorije M22 |
| 2025 | Chromosomal Microarray in Children Born Small for Gestational Age - Single Center Experience![]() | Perović, Dijana | Article | 23M23 |
| 2024 | Genetic and epigenetic mechanisms of aging![]() | Novaković, Ivana | Article | 52M52 |
| 2024 | Chromosomal microarray analysis in children with syndromic short stature![]() | Maksimović, Nela | Conference Paper | Mp. category will be shown later |
| 2024 | Diagnostic yield of chromosomal microarray analysis in patients with congenital heart disease![]() | Damnjanović, Tatjana | Conference Paper | Mp. category will be shown later |
| 2024 | Genetic polymorphisms and Methotrexate response in patients with rheumatoid arthritis![]() | Grk, Milka | Article | 23M23 |
| 2024 | Zbirka pitanja iz biologije - za pripremu prijemnog ispita![]() | Bunjevački, Vera | Text book | Mp. category will be shown later |
| 2024 | Galectin 3 Rs4644 Gene Polymorphism Is Associated with Metabolic Traits in Serbian Adolescent Population![]() | Vidović, Vanja; Novaković, Ivana | Article | 23M23 |
| 2024 | Association between IL10RA gene haplotypes and rheumatoid arthritis susceptibility![]() | Grk, Milka B. | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2024 | Association of LGALS3 gene polymorphisms with methotrexate treatment efficacy in patients with rheumatoid arthritis![]() | Maksimović, Nela | Conference Paper | Mp. category will be shown later |
| 2024 | Enrichment of pathogenic copy number variants on 17q chromosome in patients with skeletal findings![]() | Perović, Dijana | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
