Researchers
Novaković, Ivana
Results 21-40 of 391
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 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
Ostojic, Sasa; Buretic-Tomljanovic, Alena; Peterlin, Borut;
| Conference Paper | Mp. category will be shown later |
| 2024 | A Machine Learning Approach to Gene Expression in Hypertrophic Cardiomyopathy![]() | Pavić, Jelena | Article | 21aM21a |
| 2024 | Genetic testing for monogenic forms of male infertility contributes to the clinical diagnosis of men with idiopathic severe male infertility![]() | Podgrajšek, Rebeka; Hodžić, Alenka; Maver, Aleš; Štimpfel, Martin; Anđelić, Aleksander; Miljanović, Olivera; Ristanović, Momčilo
Ostojić, Saša; Gršković, Antun; Buretić-Tomljanović, Alena; Peterlin, Borut;
| Conference Paper | Mp. category will be shown later |
| 2024 | R47H TREM2 variant among Serbian Alzheimer's disease patients![]() | Andrejić, Nikola | Conference Paper | Mp. category will be shown later |
| 2024 | Association of AQP-4 polymorphisms with the clinical and paraclinical characteristics of patients with NMOSD![]() | Andabaka, Marko M. | Conference Paper | Mp. category will be shown later |
| 2024 | Earlier age of symptom onset in younger generation of familial cases of multiple sclerosis![]() | Jovanović, Aleksa Lj. | Article | 22M22 |
| 2024 | NOTCH3 genetic analysis in patients with cerebral small vessel disease![]() | Jovanović, Marija; Vojvodić, Ljubica; Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2024 | Continuous glucose monitoring in pregnancy![]() | Novaković, Ivana | Article | 23M23 |
| 2024 | Galectin 3 Rs4644 Gene Polymorphism Is Associated with Metabolic Traits in Serbian Adolescent Population![]() | Vidović, Vanja; Novaković, Ivana | Article | 23M23 |
| 2024 | APOE genotype, ATXN1 and ATXN2 repeats size in C9orf72 expansion carriers![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2024 | Genetic polymorphisms and Methotrexate response in patients with rheumatoid arthritis![]() | Grk, Milka | Article | 23M23 |
| 2024 | Sleep problems in female carriers of premutation in the FMR1 gene![]() | Pešić, Milica | Conference Paper | Mp. category will be shown later |
| 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 |
| 2024 | Етички аспекти генетског тестирања![]() | Новаковић, Ивана | Conference Paper | Mp. category will be shown later |
| 2024 | ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series![]() | Milovanović, Andona | Article | 21a+M21a+ |
| 2024 | Challenges in rare diseases: The example of mitochondrial diseases![]() | Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2024 | Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory Center![]() | Stefanova, Elka D. | Article | 22M22 |
| 2024 | Whole exome sequencing in Serbian patients with hereditary spastic paraplegia![]() | Branković, Marija | Article | 22M22 |
| 2024 | Analysis of clinical exome panel in rare movement and cognitive disorders![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2024 | Influence of polymorphisms in genes for interleukin-6 and interleukin-10 on dialysis patients survival![]() | Jovičić-Pavlović, Svetlana M.; Simić-Ogrizović, Sanja P. | Conference Paper | Mp. category will be shown later |
