Researchers

Results 161-180 of 395
Issue DateTitleAuthor(s)TypeМp-cat.
2018Genomic Variants in the FTO Gene are Associated with Sporadic Amyotrophic Lateral Sclerosis in Greek PatientsMitropoulos, Konstantinos; ...; Dobričić, Valerija S. ; Novaković, Ivana V.  ; Kostić, Vladimir S. ; ...; (broj koautora 30)Conference Paper
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2018The burden of rare genetic variants in genes involved in tumor necrosis factor (TNF) signalling pathway in multiple sclerosis (MS)Peterlin, Ana M.; Maver, Aleš; Hodžić, Alenka; Šega, Saša; Drulović, Jelena S.  ; Novaković, Ivana V.  ; Pekmezović, Tatjana D.  ; Ristić, Smiljana; Kapović, Miljenko; Peterlin, BorutConference Paper
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2018Analysis of pathogenic mtDNA mutations associated with Leber's hereditary optic neuropathy: our experienceDawod, Phepy Gamil Anwar; Rovčanin, Branislav  ; Branković, Marija  ; Marjanović, Ana  ; Janković, Milena  ; Novaković, Ivana  ; Motaleb, Fayda Ibrahim Abdel; Jančić, Jasna  ; Kostić, Vladimir Conference Paper
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2018Humana genetika : sveska za praktične radoveLuković, Ljiljana ; Novaković, Ivana  ; Bunjevački, Vera  ; Cvjetićanin, Suzana  ; Damnjanović, Tatjana  ; Jekić, Biljana  ; Perović, Vladimir  ; Bajčetić, Miloš  ; Ristanović, Momčilo  Text book
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2018Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortionHodžić, Alenka; Lavtar, Polona; Ristanović, Momčilo  ; Novaković, Ivana  ; Dotlić, Jelena  ; Peterlin, BorutArticle
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2018Identification of mutations in PARK2 gene in Serbian patients with Parkinson's diseaseJanković, Milena Z.  ; Dobričić, Valerija S. ; Kresojević, Nikola D. ; Marković, Vladana V.  ; Petrović, Igor N.  ; Svetel, Marina V. ; Pekmezović, Tatjana D.  ; Novaković, Ivana V.  ; Kostić, Vladimir K. Conference Paper
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2018NPC1 and NPC2 gene analysis in Serbian patients with Niemann-Pick disease type CBranković, Marija  ; Kresojević, Nikola D. ; Marjanović, Ana  ; Novaković, Ivana V.  ; Kostić, Vladimir K. Conference Paper
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2018Study of the polymorphisms in genes IL-17, IL-23, TGFb, RORgT and FOXP3 in Serbian patients with antiphospholipid syndromeNovaković, Ivana V.  ; Popović-Kuzmanović, Dragana; Stojanović, Ljudmila  ; Trajković, Vladimir S.  Conference Paper
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2018C9ORF72 genetic screening in Serbian patients with neurodegenerative disordersMarjanović, Ana  ; Dobričić, Valerija S. ; Marjanović, Ivan V.  ; Branković, Marija  ; Janković, Milena Z  ; Mandić, Gorana B.  ; Stević, Zorica D. ; Novaković, Ivana V.  ; Stefanova, Elka D. ; Kostić, Vladimir K. Conference Paper
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2017Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patientsMitropoulos, Konstantinos; ...; Dobričić, Valerija ; Novaković, Ivana V.  ; Kostić, Vladimir S. ; ...; (broj koautora 33)Article
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2017Genotype-phenotype correlation in Friedreich's ataxiaKovačević, G.; Todorović, S.; Novaković, Ivana  ; Pavićević-Savić, D.; Milić-Rašić, Vedrana ; Svetel, Marina ; Dobričić, Valerija Conference Paper
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2017FKBP5 Epigenetic Changes In Schizophrenia: Similarity To Stress-Related ConditionsMihaljević, Marina ; Franić, Dušanka ; Soldatović, Ivan  ; Andrić, Sanja  ; Mirjanić, Tijana; Novaković, Ivana  ; Adžić, Miroslav  ; Marić, Nađa  Conference Paper
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2017The analysis of ENOS 4a/4b polymorphism in surgical patients with secondary peritonitisMaksimović, Nela  ; Doklestić, Krstina  ; Grk, Milka  ; Damnjanović, Tatjana  ; Jekić, Biljana  ; Novaković, Ivana  Conference Paper
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2017The emerging role of the FKBP5 gene polymorphisms in vulnerability–stress model of schizophrenia: further evidence from a Serbian populationMihaljević, Marina ; Zeljić, Katarina  ; Soldatović, Ivan  ; Andrić, Sanja  ; Mirjanić, Tijana; Richards, Alexander; Mantripragada, Kiran; Pekmezović, Tatjana  ; Novaković, Ivana  ; Marić-Bojović, Nađa  Article
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2017Association of Fetuin Gene Polymorphisms with Coronary Artery Calcifications and Mortality in Renal Transplant and Chronic Kidney Disease PatientsJovičić-Pavlović, Svetlana; Simić-Ogrizović, Sanja P. ; Dopsaj, Violeta ; Novaković, Ivana V.  ; Bukumirić, Zoran M.  ; Naumović, Radomir T.  Conference Paper
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2017Next generation sequencing in dystonia - our experienceNovaković, Ivana  ; Branković, Marija  ; Marjanovic, Ana  ; Janković, Milena  ; Dobričić, Valerija ; Stojiljković, Maja  ; Petrović, Igor  ; Pavlović, Sonja  ; Svetel, Marina ; Kostić, Vladimir Conference Paper
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2017Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosisMaver, Ales; Lavtar, Polona; Ristić, Smiljana; Stopinšek, Sanja; Simčič, Saša; Hočevar, Keli; Sepčić, Juraj; Drulović, Jelena  ; Pekmezović, Tatjana  ; Novaković, Ivana  ;
Hodžić, Alenka; Rudolf, Gorazd; Šega, Saša; Starčević-Čizmarević, Nada; Palandačić, Anja; Zamolo, Gordana; Kapović, Miljenko; Likar, Tina; Peterlin, Borut;
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21aM21a
2017Study of ATXN2 repeath length in C9ORF72 expansion carriersMarjanović, Ana  ; Dobričić, Valerija ; Marjanović, Ivan  ; Branković, Marija  ; Janković, Milena  ; Mandić, Gordana; Stefanova, Elka ; Stević, Zorica ; Novaković, Ivana  ; Kostić, Vladimir Conference Paper
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2017SOD1, TDP-43, FUS/TLS and C9orf72 genes in Serbian ALS patients: long term surveyKeckarević, Dušan P.  ; Janković, Milena  ; Gagić, Milica; Keckarević-Marković, Milica P.  ; Kecmanović, Miljana M.  ; Marjanović, Ana S.  ; Marjanović, Ivan V.  ; Novaković, Ivana V.  ; Stević, Zorica D. Conference Paper
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2017A pilot study on predictors of brainstem raphe abnormality in patients with major depressive disorderKostić, Milutin  ; Jovanović, Ana; Pešić, Danilo; Peljto, Amir; Novaković, Ivana  ; Dobričić, Valerija ; Lečić Toševski, Dušica ; Mijajlović, Milija  Article
21M21