Marina Svetel

1. MAVER, Aleš, KOVANDA, Anja, BERGANT, Gaber, TERAN, Nataša, VREČAR, Irena, BRANKOVIĆ, Marija, JANKOVIĆ, Milena, SVETEL, Marina, KOSTIĆ, Vladimir S., NOVAKOVIĆ, Ivana, PETERLIN, Borut, et al. Diagnostic yield of whole exome sequencing in early-onset and familial Parkinson's disease in the Balkans : invited lecture at the ESHG 2021-virtual conference, August 28-31, 2021. [COBISS.SI-ID 77479683]

2. KOVANDA, 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. A multicenter study of genetic testing for Parkinson's disease in the clinical setting. NPJ Parkinson's disease. 2022, [vol.] 8, str. [1]-4. ISSN 2373-8057. https://www.nature.com/articles/s41531-022-00408-6, https://doi.org/10.1038/s41531-022-00408-6, DOI: 10.1038/s41531-022-00408-6. [COBISS.SI-ID 128202755]
project: IP-2019-04-7276; funder: Croatian Science Foundation
project: 18-1981353; funder: University of Rijeka
project: 175090 to V.S.K.; funder: Ministry of Education, Science and Technological Development of the Republic of Serbia
project: J3-9280 Identifikacija novih genetskih dejavnikov in mehanizmov za nevrodegenerativne bolezni s pristopi sekvenciranja nove generacije; funder: ARRS
project: V3-1911 Slovenski genomski projekt; funder: ARRS

3. KOVANDA, Anja, ŠUŠMELJ, Lara, LUKEŽIČ, Tadeja, MAVER, Aleš, RAČKI, Valentino, VULETIĆ, Vladimira, SVETEL, Marina, NOVAKOVIĆ, Ivana, PETERLIN, Borut. Biallelic RFC1 expansions as a rare cause of familial and early onset Parkinson’s disease in the Slavic population. In: ESHG 2025 : May 24–27, 2025, Milan, Italy. Vienna: European Society of Human Genetics. 2025, 1 spletni vir. https://cattendee.abstractsonline.com/meeting/21105/presentation/2777. [COBISS.SI-ID 240929795]

4. STOJSAVLJEVIĆ, Aleksandar, KOZLICA, Katarina, ŠARAC, Ivana, LAZIĆ, Una, VITKOVIĆ, Jelena, RADIŠIĆ, Vanja, POLOVIĆ, Natalija Đ., SVETEL, Marina, ŠČANČAR, Janez. Copper speciation and total essential trace element levels in Wilson’s disease. Journal of pharmaceutical and biomedical analysis. [Print ed.]. 2025, vol. 265, art. 117029, str. 1-8. ISSN 0731-7085. DOI: 10.1016/j.jpba.2025.117029. [COBISS.SI-ID 239655427]

5. BERGANT, Gaber, VAN MIDDEN, Vesna M., TSYGANKOVA, Polina, LASLO, Dorian, RAČKI, Valentino, GEORGIEV, Dejan, PAPIĆ, Eliša, BRANKOVIĆ, Marija, JANKOVIĆ, Milena, SVETEL, Marina, TERAN, Nataša, DRAGASEVIĆ MISKOVIĆ, Natasa, PETROVIĆ, Igor N., MAVER, Aleš, NOVAKOVIĆ, Ivana, PIRTOŠEK, Zvezdan, RAKUŠA, Martin, VULETIĆ, Vladimira, PETERLIN, Borut. Enrichment of rare variants in nuclear-encoded mitochondrial metabolism genes in patients with early-onset or familial parkinson’s disease. Genes. 2026, vol. 17, issue 4, str. [1]-8. ISSN 2073-4425. https://www.mdpi.com/2073-4425/17/4/472, https://doi.org/10.3390/genes17040472, DiRROS - Digital repository of Slovenian research organizations, Repository of the University of Ljubljana – RUL , DOI: 10.3390/genes17040472. [COBISS.SI-ID 276781571]