Researchers



Results 1-15 of 15
Issue DateTitleAuthor(s)TypeМp-cat.
2016Tryptophan Hydroxylase 1 Variant rs1800532 is Associated with Suicide Attempt in Serbian Psychiatric Patients but does not Moderate the Effect of Recent Stressful Life EventsKaranović, Jelena  ; Ivković, Maja  ; Jovanović, Vladimir  ; Pantović, Maja; Pavlović-Janković, Nataša; Damjanović, Aleksandar ; Brajušković, Goran  ; Romac, Stanka ; Savić-Pavićević, Dušanka  Article
21aM21a
2015Varijantni ponovci kao mogući genetički modifikatori DM1Pešović, Jovan  ; Rakočević-Stojanović, Vidosava ; Perić, Stojan  ; Brkušanin, Miloš  ; Brajušković, Goran  ; Romac, Stanka ; Savić-Pavićević, Dušanka  Conference Paper
Mp. category will be shown later
2015Joint effect of ADARB1 gene, HTR2C gene and stressful life events on suicide attempt risk in patients with major psychiatric disordersKaranović, Jelena  ; Šviković, Saša; Pantović, Maja; Durica, Svetlana; Brajušković, Goran  ; Damjanović, Aleksandar ; Jovanović, Vladimir  ; Ivković, Maja  ; Romac, Stanka ; Savić-Pavićević, Dušanka  Article
21aM21a
2015Variant repeats as genetic modifiers of DM1 – a case reportPešović, Jovan  ; Stojanović, Vidosava ; Perić, Stojan  ; Brajušković, Goran  ; Romac, Stanka ; Savić-Pavićević, Dušanka  Conference Paper
Mp. category will be shown later
2015Variant repeats in DM1 patients might be associated with milder clinical presentationPešović, Jovan  ; Stojanović, Vidosava ; Perić, Stojan  ; Brkušanin, Miloš  ; Brajušković, Goran  ; Romac, Stanka ; Savić-Pavićević, Dušanka  Conference Paper
Mp. category will be shown later
2015Pacijenti sa miotoničnom distrofijom tip 2 iz Srbije nose evropske osnivačke haplotipoveKovčić, Vlado; Stojanović, Vidosava ; Perić, Stojan  ; Pešović, Jovan  ; Brkušanin, Miloš  ; Ranum, Laura; Brajušković, Goran  ; Romac, Stanka ; Savić-Pavićević, Dušanka  Conference Paper
Mp. category will be shown later
2015TPH2 variant rs7305115 and its interaction with acute stressful life events in etiology of suicide attempt in Serbian psychiatric patientsKaranović, Jelena  ; Ivković, Maja  ; Pantović, Maja; Brajušković, Goran  ; Romac, Stanka ; Savić-Pavićević, Dušanka  Article
Mp. category will be shown later
2015Intellectual ability in the Duchenne muscular dystrophy and dystrophin gene mutation locationMilić-Rašić, Vedrana ; Vojinović, Dina ; Pešović, Jovan  ; Mijalković, Gordana; Lukić, Vera; Mladenović, Jelena; Kosać, Ana ; Novaković, Ivana  ; Maksimović, Nela  ; Romac, Stanka ;
Todorović, Slobodanka ; Savić-Pavićević, Dušanka  ;
Article
23M23
2014A shared haplotype indicates a founder event in Unverricht-Lundborg disease patients from SerbiaKecmanović, Miljana  ; Ristić, Aleksandar  ; Ercegovac, Marko  ; Keckarević-Marković, Milica  ; Keckarević, Dušan  ; Sokić, Dragoslav  ; Romac, Stanka Article
23M23
2009Coexistence of Unverricht-Lundborg disease and congenital deafness - molecular resolution of a complex comorbidityKecmanović, Miljana  ; Ristić, Aleksandar J.  ; Sokić, Dragoslav  ; Keckarević-Marković, Milica  ; Vojvodić, Nikola  ; Ercegovac, Marko  ; Janković, Slavko; Keckarević, Dušan  ; Savić-Pavićević, Dušanka  ; Romac, Stanka Article
21aM21a
2009Congenital cataracts facial dysmorphism neuropathy in Serbian Romani patientsKeckarević-Marković, Milica  ; Milić-Rašić, Vedrana M. ; Kecmanović, Miljana  ; Keckarević, Dušan P.  ; Romac, Stanka Conference Paper
Mp. category will be shown later
2009Mutational analysis of GJB1, MPZ, PMP22, EGR2, and LITAF/SIMPLE in Serbian Charcot-Marie-Tooth patientsKeckarević-Marković, Milica  ; Milić-Rašić, Vedrana ; Mladenović, Jelena; Dacković, Jelena; Kecmanović, Miljana  ; Keckarević, Dušan  ; Savić-Pavićević, Dušanka  ; Romac, Stanka Article
21M21
2008A novel 9-bp duplication in the connexin 32 gene causing X-linked Charcot-Marie-Tooth diseaseKeckarević-Marković, Milica  ; Milić-Rašić, Vedrana M. ; Kecmanović, Miljana  ; Keckarević, Dušan P.  ; Todorović, Slobodanka; Romac, Stanka Conference Paper
Mp. category will be shown later
2007Frequency of the hemochromatosis gene mutations in patients with hereditary hemochromatosis and in control subjects from serbia and montenegroŠarić, M.; Zamurović, Lj.; Kečkarević-Marković, M.  ; Kečkarević, Dušan  ; Kecmanović, Miljana  ; Savić-Pavićević, Dušanka  ; Jović, J.; Romac, Stanka Conference Paper
Mp. category will be shown later
2007MECP2 mutations in Serbian Rett syndrome patientsĐarmati, Ana; Dobričić, Valerija ; Kecmanović, Miljana  ; Marsh, P.; Jančić, Jasna  ; Klein, Christine; Đurić, Milena; Romac, Stanka Article
22M22