ARHIV PUBLIKACIJ / PUBLICATIONS ARCHIVE

Pubmed

SICRIS

ČLANKI / RESEARCH PAPERS 2018

JENKO, Barbara, TOMŠIČ, Matija, JEKIĆ, Biljana, MILIĆ, Vera, DOLŽAN, Vita, PRAPROTNIK, Sonja. Clinical pharmacogenetic models of treatment response to methotrexate monotherapy in Slovenian and Serbian rheumatoid arthritis patients : differences in patient's management may preclude generalization of the models. Frontiers in pharmacology, 2018, vol. 9, 1-8, doi: 10.3389/fphar.2018.00020. [COBISS.SI-ID 33649113]

ŠENK, Barbara, GORIČAR, Katja, KRAVOS, Nika Aleksandra, JENSTERLE SEVER, Mojca, JANEŽ, Andrej, DOLŽAN, Vita. SLC6A4 5HTTLPR polymorphism affects insulin secretion in patients with polycystic ovary syndrome. International Journal of Endocrinology (Online), 2018, doi: 10.1155/2018/6130487. [COBISS.SI-ID 33842649]

GUTIERREZ-CAMINO, Angela, DOLŽAN, Vita, JAZBEC, Janez, CARBONE-BAÑERES, Ana, ANDOIN, Nagore Garcia, SASTRE, Ana, ASTIGARRAGA, Itziar, NAVAJAS, Aurora, GARCIA-ORAD, Africa. Involvement of SNPs in miR-3117 and miR-3689d2 in childhood acute lymphoblastic leukemia risk. Oncotarget, 2018, vol. 9, no. 22907-22914, doi: 10.18632/oncotarget.25144. [COBISS.SI-ID 33834969]

FERDIN, Jana, GORIČAR, Katja, DOLŽAN, Vita, PLEMENITAŠ, Ana, MARTIN, Jeffrey, PETERLIN, Matija Boris, DEEKS, Steven G, LENASSI, Metka. Viral protein Nef is detected in plasma of half of HIV-infected adults with undetectable plasma HIV RNA. PloS one, 2018, vol. 13, 1-10, doi: 10.1371/journal.pone.0191613. [COBISS.SI-ID 33608665]

FRANKO, Alenka, KOTNIK, Nika, GORIČAR, Katja, KOVAČ, Viljem, DODIČ-FIKFAK, Metoda, DOLŽAN, Vita. The influence of genetic variability on the risk of developing malignant mesothelioma. Radiology and oncology, 2018, vol. 52, 105-111, doi: 10.1515/raon-2018-0004. [COBISS.SI-ID 2854779]

ŠTRBAC, Danijela, GORIČAR, Katja, DOLŽAN, Vita, KOVAČ, Viljem. Matrix metalloproteinases polymorphisms as baseline risk predictors in malignant pleural mesothelioma. Radiology and oncology, 2018, vol. 52, 160-166, doi: 10.1515/raon-2018-0005. [COBISS.SI-ID 2840955]

GASIC, Vladimir, ZUKIC, Branka, STANKOVIĆ, Biljana, JANIĆ, Dragana, DOKMANOVIC, Lidija, LAZIC, Jelena, KRSTOVSKI, Nada, DOLŽAN, Vita, JAZBEC, Janez, PAVLOVIČ, Sonja, KOTUR, Nikola. Pharmacogenomic markers of glucorticoid responses in the initial phase of remission induction therapy in childhood acute lymphoblastic leukemia. Radiology and oncology, 2018, vol. 52, 296-306, doi: 10.2478/raon-2018-0034. [COBISS.SI-ID 5314476]

LÓPEZ-RODRÍGUEZ, Rosario, FERREIRO-IGLESIAS, Aida, LIMA, Aurea, BERNARDES, Miguel, PAWLIK, Andrzej, PARADOWSKA- GORYCKA, Agnieszka, ŚWIERKOT, Jerzy, SLEZAK, Ryszard, DOLŽAN, Vita, GONZÁLEZ-ÁLVARO, Isidoro, et al. Replication study of polymorphisms associated with response to methotrexate in patients with rheumatoid arthritis. Scientific reports, 2018, vol. 8, 1-8. [COBISS.SI-ID 33834713]

MARTIN-GUERRERO, Idoia, BILBAO-ALDAITURRIAGA, Nerea, GUTIERREZ-CAMINO, Angela, SANTOS-ZORROZUA, Borja, DOLŽAN, Vita, PATIÑO-GARCIA, Ana, GARCIA-ORAD, Africa. Variants in the 14q32 miRNA cluster are associated with osteosarcoma risk in the Spanish population. Scientific reports, 2018, vol. 8, 1-8. doi: 10.1038/s41598-018-33712-4. [COBISS.SI-ID 34009817]

REDENŠEK, Sara, DOLŽAN, Vita, KUNEJ, Tanja. From genomics to omics landscapes of Parkinsonʼs disease : revealing the molecular mechanisms. Omics : a journal of integrative biology, 2018, vol. 22, 1-16, doi: 10.1089/omi.2017.0181. [COBISS.SI-ID 4035720]

ČLANKI / RESEARCH PAPERS 2017

GORIČAR, Katja, KOVAČ, Viljem, DOLŽAN, Vita. Clinical-pharmacogenetic models for personalized cancer treatment : application to malignant mesothelioma. Scientific reports, 2017, vol. 7, 1-9, doi: 10.1038/srep46537. [COBISS.SI-ID 2641275]

ESIH, Katarina, GORIČAR, Katja, DOLŽAN, Vita, RENER-PRIMEC, Zvonka. Antioxidant polymorphisms do not influence the risk of epilepsy or its drug resistance after neonatal hypoxic-ischemic brain injury. Seizure, 2017, vol. 46, 38-42, doi: 10.1016/j.seizure.2017.01.005. [COBISS.SI-ID 33101273]

WOUDEN, Cathelijne H., CAMBON-THOMSEN, Anne, CECCHIN, Erika, CHEUNG, Ka-Chun, DÁVILA-FAJARDO, Cristina Lucía, DENEER, Vera H., DOLŽAN, Vita, INGELMAN-SUNDBERG, Magnus, JÖNSSON, Siv, KARLSSON, Mats O., KLEN, Jasna, MLINŠEK, Gregor, POPLAS-SUSIČ, Tonka, et al, Ubiquitous Pharmacogenomics Consortium. Implementing pharmacogenomics in Europe : design and implementation Strategy of the Ubiquitous Pharmacogenomics Consortium. Clinical pharmacology and therapeutics, 2017, vol. 101, 341-358, doi: 10.1002/cpt.602. [COBISS.SI-ID 33082329]

REDENŠEK, Sara, TROŠT, Maja, DOLŽAN, Vita. Genetic determinants of Parkinson's disease : can they help to stratify the patients based on the underlying molecular defect?. Frontiers in aging neuroscience, 2017, vol. 9, 1-17, doi: 10.3389/fnagi.2017.00020. [COBISS.SI-ID 33093849]

HLADNIK, Anžej, FERDIN, Jana, GORIČAR, Katja, DEEKS, Steven G, PETERLIN, Matija Boris, PLEMENITAŠ, Ana, DOLŽAN, Vita, LENASSI, Metka. Trans-activation response element RNA is detectable in the plasma of a subset of aviremic HIV-1-infected patients. Acta chimica slovenica, 2017, vol. 64, 530-536, doi: 10.17344/acsi.2016.2863. [COBISS.SI-ID 33286873]

MLINŠEK, Gregor, DOLŽAN, Vita, GORIČAR, Katja, BUTUROVIĆ-PONIKVAR, Jadranka, ARNOL, Miha. The role of single nucleotide polymorphisms of CYP3A and ABCB1 on tacrolimus predose concentration in kidney transplant recipients. Clinical nephrology, 2017, vol. 88, suppl. 1, S115-S118, doi: 10.5414/CNP88FX25. [COBISS.SI-ID 3993772]

ŠTRBAC, Danijela, GORIČAR, Katja, DOLŽAN, Vita, KOVAČ, Viljem. Matrix metalloproteinases polymorphisms as prognostic biomarkers in malignant pleural mesothelioma. Disease markers, 2017, vol. 2017, 1-8, doi: 10.1155/2017/8069529. [COBISS.SI-ID 2743675]

BERTOK, Sara, DOLŽAN, Vita, GORIČAR, Katja, TREBUŠAK PODKRAJŠEK, Katarina, BATTELINO, Tadej, RENER-PRIMEC, Zvonka. The association of SCN1A p.Thr1067Ala polymorphism with epilepsy risk and the response to antiepileptic drugs in Slovenian children and adolescents with epilepsy. Seizure, 2017, vol. 51, 9-13, doi: 10.1016/j.seizure.2017.07.007. [COBISS.SI-ID 33339353]

JENKO, Barbara, LUSA, Lara, TOMŠIČ, Matija, PRAPROTNIK, Sonja, DOLŽAN, Vita. Clinical-pharmacogenetic predictive models for MTX discontinuation due to adverse events in rheumatoid arthritis. Pharmacogenomics journal, 2017, vol. 17, iss. 5, 412-418, doi: 10.1038/tpj.2016.36. [COBISS.SI-ID 32687833]

ZAJC AVRAMOVIČ, Mojca, DOLŽAN, Vita, TOPLAK, Nataša, ACCETTO, Meta, LUSA, Lara, AVČIN, Tadej. Relationship between polymorphisms in methotrexate pathway genes and outcome of methotrexate treatment in a cohort of 119 patients with juvenile idiopathic arthritis. The journal of rheumatology, 2017, vol. 44, iss. 8, 1216-1223, doi: 10.3899/jrheum.160950. [COBISS.SI-ID 4404396]

FAGANEL, Barbara, JAZBEC, Janez, BOHANEC GRABAR, Petra, RODRIGUEZ-ANTONA, Christina, DOLŽAN, Vita. Association between SLC19A1 gene polymorphism and high dose methotrexate toxicity in childhood acute lymphoblastic leukaemia and non Hodgkin malignant lymphoma : introducing a haplotype based approach. Radiology and oncology, 2017, vol. 51, 455-462, doi: 10.1515/raon-2017-0040. [COBISS.SI-ID 4563628]

ČLANKI / RESEARCH PAPERS 2016

GROŠELJ, Urh, ŽERJAV-TANŠEK, Mojca, TREBUŠAK PODKRAJŠEK, Katarina, HOVNIK, Tinka, BATTELINO, Tadej, DOLŽAN, Vita. Clinical role of CYP2C19 polymorphisms in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Acta chimica slovenica, 2016, vol. 63, no. 1, 33-37, doi: 10.17344/acsi.2015.1797. [COBISS.SI-ID 32544473]

MILOSHESKA, Daniela, LORBER, Bogdan, VOVK, Tomaž, KASTELIC, Matej, DOLŽAN, Vita, GRABNAR, Iztok. Pharmacokinetics of lamotrigine and its metabolite N-2-glucuronide : influence of polymorphism of UDP-glucuronosyltransferases and drug transporters. British journal of clinical pharmacology, 2016, vol. 82, no. 2, 399-411, doi: 10.1111/bcp.12984. [COBISS.SI-ID 4065137]

ESIH, Katarina, GORIČAR, Katja, DOLŽAN, Vita, RENER-PRIMEC, Zvonka. The association between antioxidant enzyme polymorphisms and cerebral palsy after perinatal hypoxic-ischaemic encephalopathy. European journal of paediatric neurology, 2016, vol. 20, iss. 5, 704-708, doi: 10.1016/j.ejpn.2016.05.018. [COBISS.SI-ID 32688345]

HROVAT, Ana, KRAVOS, Nika Aleksandra, GORIČAR, Katja, JENSTERLE SEVER, Mojca, JANEŽ, Andrej, DOLŽAN, Vita. SORCS1 polymorphism and insulin secretion in obese women with polycystic ovary syndrome. Gynecological endocrinology, 2016, vol. 32, iss. 5, 395-398, doi: 10.3109/09513590.2015.1126818. [COBISS.SI-ID 32436697]

PETRIČ, Rok, GAZIĆ, Barbara, GORIČAR, Katja, DOLŽAN, Vita, DZODIĆ, Radan, BEŠIĆ, Nikola. Expression of miRNA and occurrence of distant metastases in patients with Hürthle cell carcinoma. International Journal of Endocrinology, 2016, 1-6, doi: 10.1155/2016/8945247. [COBISS.SI-ID 2406011]

JENKO, Barbara, PRAPROTNIK, Sonja, TOMŠIČ, Matija, DOLŽAN, Vita. NLRP3 and CARD8 polymorphisms influence higher disease activity in rheumatoid arthritis = Polimorfizmi NLRP3 I CARD8 utiču na pojačanu aktivnost bolesti u reumatoidnom artritisu. Journal of Medical Biochemistry, 2016, vol. 35, no. 3, 319-323, doi: 10.1515/jomb-2016-0008. [COBISS.SI-ID 32604121]

TURČIN, Arijana, DOLŽAN, Vita, PORCELLI, Stefano, SERRETTI, Alessandro, KORES-PLESNIČAR, Blanka. Adenosine hypothesis of antipsychotic drugs revisited : pharmacogenomics variation in nonacute schizophrenia. Omics., 2016, vol. 20, no. 5, 283-289, doi: 10.1089/omi.2016.0003. [COBISS.SI-ID 32742105]

KUMUTHINI, Judit, MBIYAVANGA, Mamana, CHIMUSA, Emile, PATHAK, Jyotishman, SOMERVUO, Panu, SCHAIK, Ron H. N. van, DOLŽAN, Vita, MIZZI, Clint, KALIDEEN, Kusha, RAMESAR, Raj S, MAČEK, Milan, PATRINOS, George P., SQUASSINA, Alessio. Minimum information required for a DMET experiment reporting. Pharmacogenomics, 2016, doi: 10.2217/pgs-2016-0015. [COBISS.SI-ID 32807129]

JENKO, Barbara, PRAPROTNIK, Sonja, ČUČNIK, Saša, ROTAR, Žiga, TOMŠIČ, Matija, DOLŽAN, Vita. Survivin polymorphism is associated with disease activity in rheumatoid arthritis patients. Pharmacogenomics, 2016, vol. 17, no. 1, 37-45, doi: 10.2217/pgs.15.147. [COBISS.SI-ID 32477145]

MIZZI, Clint, DALABIRA, Eleni, KUMUTHINI, Judit, DZIMIRI, Nduna, BALOGH, István, BAŞAK, Nazli, BÖHM, Ruwen, BORG, John Joseph, BORGIANI, Paola, DOLŽAN, Vita, et al. A European spectrum of pharmacogenomic biomarkers : implications for clinical pharmacogenomics. PloS one, 2016, vol. 11, iss. 9, 1-19, doi: 10.1371/journal.pone.0162866. [COBISS.SI-ID 32828377]

TERZIČ, Tea, KASTELIC, Matej, DOLŽAN, Vita, KORES-PLESNIČAR, Blanka. Genetic polymorphisms in dopaminergic system and treatment-resistant schizophrenia. Psychiatria Danubina, 2016, vol. 28, no. 2, 127-131, http://www.hdbp.org/psychiatria_danubina/pdf/dnb_vol28_no2/dnb_vol28_no2_127.pdf. [COBISS.SI-ID 32741593]

VODUŠEK, Ana Lina, GORIČAR, Katja, GAZIĆ, Barbara, DOLŽAN, Vita, JAZBEC, Janez. Antioxidant defence-related genetic variants are not associated with higher risk of secondary thyroid cancer after treatment of malignancy in childhood or adolescence. Radiology and oncology, 2016, vol. 50, no. 1, 80-86, VI, doi: 10.1515/raon-2015-0026. [COBISS.SI-ID 32155865]

KRHIN, Blaž, GORIČAR, Katja, GAZIĆ, Barbara, DOLŽAN, Vita, BEŠIĆ, Nikola. Functional polymorphisms in antioxidant genes in Hurthle cell thyroid neoplasm - an association of GPX1 polymorphism and recurrent Hurthle cell thyroid carcinoma. Radiology and oncology, 2016, vol. 50, iss. 3, 289-296, doi: 10.1515/raon-2016-0031. [COBISS.SI-ID 2365307]

VOZIKIS, Athanassios, COOPER, David N., MITROPOULOU, Christina, KAMBOURIS, Manousos E., BRAND, Angela, DOLŽAN, Vita, FORTINA, Paolo, INNOCENTI, Federico, LEE, Ming Ta Michael, LEYENS, Lada, MAČEK, Milan, AL-MULLA, Fahd, PRAINSACK, Barbara, SQUASSINA, Alessio, TARUSCIO, Domenica, VAN SCHAIK, Ron H., VAYENA, Effy, WILLIAMS, Marc S., PATRINOS, George P. Test pricing and reimbursement in genomic medicine: towards a general strategy. Public Health Genomics, 2016, doi: 10.1159/000449152. [COBISS.SI-ID 32853721]

BILBAO-ALDAITURRIAGA, Nerea, ASKAITURRIETA, Ziortza, GRANADO-TAJADA, Itsasne, GORIČAR, Katja, DOLŽAN, Vita, Slovenian Osteosarcoma Study Group (KOVAČ, Viljem, JAZBEC, Janez, LAMOVEC, Janez), GARCIA-MIGUEL, Purificación, GARCIA DE ANDOIN, Nagore, MARTIN-GUERRERO, Idoia, GARCIA-ORAD, Africa. A systematic review and meta-analysis of MDM2 polymorphisms in osteosarcoma susceptibility. Pediatric research, 2016, doi: 10.1038/pr.2016.120. [COBISS.SI-ID 32780249]

ČLANKI / RESEARCH PAPERS 2015

PLEMENITAŠ, Anja, KASTELIC, Matej, PORCELLI, Stefano, SERRETTI, Alessandro, RUS-MAKOVEC, Maja, KORES-PLESNIČAR, Blanka, DOLŽAN, Vita. Genetic variability in CYP2E1 and catalase gene among currently and formerly alcohol-dependent male subjects. Alcohol and alcoholism, 2015, vol. 50, iss. 2, 140-145. doi: 10.1093/alcalc/agu088. [COBISS.SI-ID 31770841]

GORIČAR, Katja, KOVAČ, Viljem, JAZBEC, Janez, ZAKOTNIK, Branko, LAMOVEC, Janez, DOLŽAN, Vita. Genetic variability of DNA repair mechanisms and glutathione-S-transferase genes influences treatment outcome in osteosarcoma. Cancer epidemiology, 2015, vol. 39, no. 2, 182-188, doi: 10.1016/j.canep.2014.12.009. [COBISS.SI-ID 31771353]

GORIČAR, Katja, KOVAČ, Viljem, FRANKO, Alenka, DODIČ-FIKFAK, Metoda, DOLŽAN, Vita. Serum survivin levels and outcome of chemotherapy in patients with malignant mesothelioma. Disease markers, 2015, vol. 2015, 1-8. doi: 10.1155/2015/316739. [COBISS.SI-ID 32176857]

JENSTERLE SEVER, Mojca, PIRŠ, Boštjan, GORIČAR, Katja, DOLŽAN, Vita, JANEŽ, Andrej. Genetic variability in GLP-1 receptor is associated with inter-individual differences in weight lowering potential of liraglutide in obese women with PCOS : a pilot study. European Journal of Clinical Pharmacology, 2015, vol. 71, iss. 7, 817-824. doi: 10.1007/s00228-015-1868-1. [COBISS.SI-ID 2318252]

TERZIČ, Tea, DOLŽAN, Vita, KORES-PLESNIČAR, Blanka. CYP3A4 rs35599367 ne vpliva na zdravljenje z antipsihotiki pri slovenskih bolnikih s shizofrenijo = CYP3A4 rs35599367 does not influence antipsychotic treatment in Slovenian patients with schizophrenia. Farmacevtski vestnik, 2015, letn. 66, št. 5, 402-406. http://www.sfd.si/uploads/datoteke/terzi.pdf. [COBISS.SI-ID 29122343]

GORIČAR, Katja, ERČULJ, Nina, FAGANEL, Barbara, DEBELJAK, Maruša, HOVNIK, Tinka, JAZBEC, Janez, DOLŽAN, Vita. The association of folate pathway and DNA repair polymorphisms with susceptibility to childhood acute lymphoblastic leukemia. Gene, 2015, vol. 562, no. 2, 203-209. doi: 10.1016/j.gene.2015.02.077. [COBISS.SI-ID 31882201]

KLEN, Jasna, GORIČAR, Katja, JANEŽ, Andrej, DOLŽAN, Vita. NLRP3 inflammasome polymorphism and macrovascular complications in type 2 diabetes patients. Journal of diabetes research, 2015, vol. 2015. http://www.hindawi.com/journals/jdr/aa/616747/. [COBISS.SI-ID 32035801]

GORIČAR, Katja, KOVAČ, Viljem, JAZBEC, Janez, LAMOVEC, Janez, DOLŽAN, Vita. Homologous recombination repair polymorphisms and the risk for osteosarcoma = Polimorfizam gena odgovornih za reparaciju DNK homolognom rekombinacijom i rizik za pojavu osteosarkoma. Journal of Medical Biochemistry, 2015, vol. 34, no. 2, 200-206, doi: 10.2478/jomb-2014-0031. [COBISS.SI-ID 31398361]

TERZIČ, Tea, KASTELIC, Matej, DOLŽAN, Vita, KORES-PLESNIČAR, Blanka. Genetic variability testing of neurodevelopmental genes in schizophrenic patients. Journal of molecular neuroscience, 2015, vol. 56, iss. 1, 205-211. doi: 10.1007/s12031-014-0482-5. [COBISS.SI-ID 31770585]

TERZIČ, Tea, KASTELIC, Matej, DOLŽAN, Vita, KORES-PLESNIČAR, Blanka. Influence of 5-HT1A and 5-HTTLPR genetic variants on the schizophrenia symptoms and occurrence of treatment-resistant schizophrenia. Neuropsychiatric Disease and Treatment, 2015, vol. 11, vol. 11, 453-459. doi: 10.2147/NDT.S76494. [COBISS.SI-ID 31881689]

PLEMENITAŠ, Anja, KASTELIC, Matej, PORCELLI, Stefano, SERRETTI, Alessandro, DOLŽAN, Vita, KORES-PLESNIČAR, Blanka. Alcohol dependence and genetic variability in the serotonin pathway among currently and formerly alcohol-dependent males. Neuropsychobiology, 2015, vol. 72, no. 1, 57-64, doi: 10.1159/000437432. [COBISS.SI-ID 5518911]

PLEMENITAŠ, Anja, KORES-PLESNIČAR, Blanka, KASTELIC, Matej, PORCELLI, Stefano, SERRETTI, Alessandro, DOLŽAN, Vita. Genetic variability in tryptophan hydroxylase 2 gene in alcohol dependence and alcohol-related psychopathological symptoms. Neuroscience letters, 2015, vol. 604, 86-90. doi: 10.1016/j.neulet.2015.07.037. [COBISS.SI-ID 5518655]

GORIČAR, Katja, KOVAČ, Viljem, JAZBEC, Janez, ZAKOTNIK, Branko, LAMOVEC, Janez, DOLŽAN, Vita. Translesion polymerase genes polymorphisms and haplotypes influence survival of osteosarcoma patients. Omics., 2015, vol. 19, no. 3, 180-185. [COBISS.SI-ID 31881945]

KLEN, Jasna, GORIČAR, Katja, JANEŽ, Andrej, DOLŽAN, Vita. Common polymorphisms in antioxidant genes are associated with diabetic nephropathy in Type 2 diabetes patients. Personalized medicine, 2015, vol. 12, iss. 3, 187-200. doi: 10.2217/PME.14.86. [COBISS.SI-ID 2316460]

GORIČAR, Katja, DOLŽAN, Vita. Homologous recombination repair polymorphisms, cancer susceptibility and treatment outcome. In: CHEN, Clark C. (eds.). Advances in DNA repair. Rijeka: InTech, 2015, 291-313, doi: 10.5772/59729. [COBISS.SI-ID 32336345]

DOKTORSKE NALOGE / PhD THESES

2018

ZAJC AVRAMOVIČ, Mojca. Genetski dejavniki učinkovitosti in varnosti zdravljenja juvenilnega idiopatskega artritisa z metotreksatom in zaviralci tumor nekrotizirajočega faktorja alfa / Genetic determinants of juvenile idiopathic arthritis treatment with methotrexate and tumor necrosis factor alpha blockers. Mentor: Tadej Avčin, somentor / comentor: Vita Dolžan. [COBISS.SI-ID 3914516]

2017

TURČIN, Arijana. Vpliv polimorfizmov gena za adenozinske receptorje (ADORA) na simptomatiko shizofrenije in pojavnost ekstrapiramidnih neželenih učinkov antipsihotičnih zdravil. Mentor: Blanka Kores Plesničar, somentor / comentor: Vita Dolžan. [COBISS.SI-ID 288920064]

2016

JENKO, Barbara. Klinično farmakogenetski modeli za bolniku prilagojeno zdravljenje revmatoidnega artritisa / Clinical pharmacogenetic models for personalized rheumatoid arthritis treatment. Mentor: Vita Dolžan, somentor / comentor: Sonja Praprotnik. [COBISS.SI-ID 285932032]

KRHIN, Blaž. Genetski označevalci raka Huerthlejevih celic ščitnice / Genetic Markers of Huerthle Cell Carcinoma. Mentor: Nikola Bešić, somentor / comentor: Vita Dolžan. [COBISS.SI-ID 2507899]

2015

VODUŠEK, Ana Lina. Genetski polimorfizmi antioksidativnih encimov in mehanizmov popravljanja DNA pri sekundarnem raku ščitnice / Genetic polymorphisms of oxidative stress defence and DNA repair in secondary thyroid cancer. 2015. Mentor: Janez Jazbec, somentor / comentor: Vita Dolžan. [COBISS.SI-ID 282793728]

TERZIČ, Tea. Genska variabilnost nevrotransmiterskih poti centralnega živčnega sistema ter presnove antipsihotikov pri terapevtsko rezistentni shizofreniji / Genetic variability in neurotransmiter pathways of central nervous system and antipsychotic disposition in treatment refractory schizophrenia. 2015. Mentor: Blanka Kores-Plesničar, somentor / comentor: Vita Dolžan. [COBISS.SI-ID 282753024]

KLEN, Jasna. Vpliv genetskih polimorfizmov v presnovi sulfonilsečnin in metformina na urejenost sladkorne bolezni tipa 2 / The influence of genetic polymorphisms in the metabolism of sulfonylureas and metformin on glycemic control in type 2 diabetic patients. 2015. Mentor: Andrej Janež, somentor / comentor: Vita Dolžan. [COBISS.SI-ID 278563072]

PLEMENITAŠ, Anja. Vpliv genske variabilnosti presnove etanola in serotoninskega sistema na abstinenco in izražanje psiholoških komponent pri odvisnosti od alkohola / Genetic influences in metabolism of ethanol and serotonergic system on abstinence and expression of psychological traits. 2015. Mentor: Blanka Kores-Plesničar, somentor / comentor: Vita Dolžan. [COBISS.SI-ID 282737152]

MAGISTRSKE, DIPLOMSKE IN RAZISKOVALNE NALOGE / STUDENT THESES

2018

HERMAN, Rok. Vpliv genetske variabilnosti v signalnih poteh oksidativnega stresa na metabolične značilnosti bolnic s sindromom policističnih ovarijev in na njihov odgovor na zdravljenje. 2018. Mentor: Vita Dolžan, somentor / comentor: Mojca Jensterle. [COBISS.SI-ID 5198508]. Prešernovo priznanje Medicinske fakultete 2018.

KUKEC, Eva. Vpliv polimorfizmov HIF1A na tveganje za nastanek epilepsije ter cerebralne paralize po neonatalni hipoksično-ishemični možganski okvari. 2018. Mentor: Zvonka Rener-Primec. [COBISS.SI-ID 3943700]. Prešernovo priznanje Medicinske fakultete 2018.

LEVPUŠČEK, Kristina. Genetska variabilnost mehanizmov popravljanja DNA in tveganja za nastanek malignega mezotelioma. Mentor: Alenka Franko. [COBISS.SI-ID 5525676]. Prešernova nagrada Medicinske fakultete 2018.

HROVATIN, Karin. Genetska variabilnost v uravnavanju genov serotoninske poti pri bolnikih s shizofrenijo. 2018. Mentor: Tanja Kunej, somentor / comentor: Vita Dolžan. [COBISS.SI-ID 9006713]

2017

MESARIČ, Vita Andreja. Vpliv genetske variabilnosti v inkretinslem sistemu na metabolične značilnosti bolnic s sindromom policističnih ovarijev in na njihov odgovor na zdravljenje z inhibitorjem dipeptidil peptidaze 4. 2017. Mentor: Vita Dolžan, somentor / comentor: Mojca Jensterle. [COBISS.SI-ID 4201644]. Prešernova nagrada Medicinske fakultete 2017.

2016

PETELIN, Kristina. Vpliv polimorfizmov folatne poti na simptomatiko shizofrenije in odgovor na zdravljenje z antipsihotičnimi zdravili. 2016. Mentor: Vita Dolžan, somentor / comentor: Blanka Kores Plesničar. [COBISS.SI-ID 3865364]. Prešernova nagrada Medicinske fakultete 2016.

ŽAGAR, Tina. Polimorfizmi izbranih genov serotoninske poti pri žrtvah samomora v Sloveniji / Polymorphic genes of serotonergic system in suicide victims in Slovenia. 2016. Mentor: Vita Dolžan. [COBISS.SI-ID 3852308]

2015

PIRŠ, Boštjan. Genetski označevalci odgovora na zdravljenje z liraglutidom pri bolnicah s sindromom policističnih ovarijev. 2015. Mentor: Andrej Janež. [COBISS.SI-ID 3795732]. Prešernova nagrada Univerze v Ljubljani 2015.

BATAGELJ, Nevenka. Genetska variabilnost dopaminergičnega sistema in izločanje inzulina ter metabolični odgovor na zdravljenje pri bolnicah s sindromom policističnih ovarijev. 2015. Mentor: Vita Dolžan, somentor / comentor: Mojca Jensterle Sever. [COBISS.SI-ID 3798804]. Prešernova nagrada Medicinske fakultete 2015.

BOŽIČ, Tim. Analiza genetske variabilnosti gena DEPTOR in vpliva na kazalce debelosti pri bolnicah s sindromom policističnih ovarijev. 2015. Mentor: Simon Horvat. [COBISS.SI-ID 1536486083]

ŠENK, Barbara. Genetska variabilnost serotoninskega sistema in izločanje inzulina ter vedenjski vzorci prehranjevanja pri bolnicah s sindromom policističnih ovarijev / Genetic variability of serotoninergic system and insulin secretion and eating behaviour in patients with polycystic ovary syndrome. 2015. Mentor: Vita Dolžan, somentor / comentor: Mojca Jensterle Sever. [COBISS.SI-ID 2716844]