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Browsing by Author Cuturilo, Goran
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| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2023 | 22q11.2 microdeletion is the most common genomic abnormality in Serbian newborns with critical congenital heart disease and could be rapidly detected by Multiplex ligation probe amplification analysis | Miletić, Aleksandra; Cuturilo, Goran; Ruml Stojanović, Jelena; Drakulić, Danijela   ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Stevanović, Milena | Conference Paper | Mp. category will be shown later |
| 2025 | 22Q11.2DS IPSCS AS MODEL SYSTEM FOR INVESTIGATION OF MOLECULAR MECHANISM AND NOVEL THERAPEUTIC TARGETS IN NDDS | Perić, Mina ; Simeunović, Ivana ; Ninković Stanisavljević, Danijela; Kovačević Grujičić, Nataša ; Kostić, Jovana ; Cuturilo, Goran; Petter, O.; Harwood, A.J.; Stevanović, Milena ; Drakulić, Danijela | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2013 | A case of a patient with multiple sSMC without phenotypic effect | Vesic, Marija; Jelisavcic, Marko; Niksic, Snezana B; Cuturilo, Goran; Ivanovic-Deretic, Vesna; Liehr, Thomas | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2018 | A novel CTNNB1 mutation in a patient with teratoma and multiple malformations - expansion of the phenotypic spectrum and possible new gene for Currarino phenotype | Mijovic, Marija; Miletic, Aleksandra; Ruml-Stojanovic, Jelena; Peterlin, Borut; Maver, Ales; Borlja, Nikola; Dimitrijevic, Brankica; Lukic, M; Cuturilo, Goran | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2023 | A novel splice-site FHOD3</i> founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study | Vodnjov, Nina; Toplisek, Janez; Maver, Ales; Cuturilo, Goran; Jaklic, Helena; Teran, Natasa; Visnjar, Tanja; Skrjanec, Pusenjak Marusa; Hodzic, Alenka; Miljanovic, Olivera;
Peterlin, Borut; Writzl, Karin; Mahdieh, Nejat;
| Научни чланак | 21M21 - Водећи међународни часопис категорије M21 |
| 2024 | A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans - a cohort study | Vodnjov, Nina; Toplisek, Janez; Maver, Ales; Cuturilo, Goran; Jaklic, Helena; Teran, Natasa; Visnjar, Tanja; Pusenjak, Marusa Skrjanec; Hodzic, Alenka; Miljanovic, Olivera;
Peterlin, Borut; Writzl, Karin;
| Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2008 | A rare association of interrupted aortic arch type C and microdeletion 22q11.2 | Cuturilo, Goran; Drakulić, Danijela ; Stevanović, Milena ; Jovanović, Ida; Đukić, Milan ; Miletić-Grković, Slobodanka ; Atanasković-Marković, Marina | Научни чланак | 22M22 - Међународни часопис категорије M22 |
| 2024 | An Overview of 22q11.2 Diagnostic and Research Facilities in the Countries of The Western Balkan Region | Cuturilo, Goran; Drakulić, Danijela ; Kovačević Grujičić, Nataša ; Perić, Mina ; Stevanović, Milena | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2023 | Analysis of cohort of patients with 22q11.2 deletion syndrome - a single-center experience from Serbia | Simeunović, Ivana ; Drakulić, Danijela ; Cuturilo, Goran; Kovačević-Grujičić, Nataša ; Kostić, Jovana ; Stevanović, Milena | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2008 | Aplastic anemia and Turner syndrome | Cuturilo, Goran; Škorić, Dejan ; Miletić-Grković, Slobodanka; Bojić, Vladislav; Rodić, Predrag ; Stefanović, Igor | Ostalo | Mp kategorija će biti prikazana naknadno. |
| 2023 | Application of principal component analysis (PCA) and analytical hierarchy process (AHP) in analysis of articulatory characteristics of phonemes of children with 22q11.2 Deletion Syndrome | Drakulić, Danijela ; Rakonjac, Marijana; Cuturilo, Goran; Kovačević-Grujičić, Nataša ; Kušić-Tišma, Jelena ; Morić, Ivana ; Zukić, Branka ; Stevanović, Milena | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2019 | Autistic traits and cognitive dysfunctions in children with patogenic copy number variants: a pilot study from Serbia | Mihaljević, Marina; Pejović-Milovancević, Milica ; Janeski, Hristina; Mandić-Maravić, Vanja; Grujicić, Roberto; Drakulić, Danijela ; Stevanović, Milena ; Cuturilo, Goran | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2025 | Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability | Kroll-Hermi, Ariane; ...; Cuturilo, Goran; ...; (broj, koautora 89) | Naučni članak | 21a+M21a+ - Vodeći međunarodni časopis kategorije M21a+ |
| 2024 | CHARACTERIZATION OF INDUCED PLURIPOTENT STEM CELLS FROM PATIENTS WITH 22Q11.2 DUPLICATION SYNDROME | Kostić, Jovana ; Cuturilo, Goran; Drakulić, Danijela ; Petter, Olena; Perić, Mina ; Simeunović, Ivana ; Stanisavljević Ninković, Danijela ; Harwood J., Adrian; Stevanović, Milena ; Kovačević-Grujicić, Nataša | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2024 | Clinical utility of diagnostic NGS for detection CNV variants in genes associated with skeletal dysplasia | Mijovic, Marija; Cuturilo, Goran; Ruml-Stojanovic, Jelena; Miletic, Aleksandra; Bosankic, Brankica; Petrovic, Hristina | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2023 | Constitutional mismatch repair deficiency syndrome (CMMRD): the significance of customized surveillance protocol for Lynch syndrome-related tumors in relatives at risk-a case report | Bosankic, Brankica; Cuturilo, Goran; Petrovic, Hristina; Mijovic, Marija; Ruml-Stojanovic, Jelena; Miletic, Aleksandra | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2023 | Detection rate of 22q11.2 microdeletion using strict diagnostic criteria | Drakulić, Danijela ; Cuturilo, Goran; Jovanović, Ida; Krstić, Aleksandar; Milivojević, Milena ; Stevanović, Milena | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2002 | Difference between asthma, rhinitis and eczema prevalence rate in children from rural and inner city areas | Raskovic, T; Zivkovic, Zorica M; Cuturilo, Goran; Kalaba, Zlatko | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 2025 | Disrupting integrator complex subunit INTS6 causes neurodevelopmental disorders and impairs neurogenesis and synapse development | Peng, Xiaoxia; ...; Cuturilo, Goran; ...; (broj, koautora 49) | Naučni članak | 21a+M21a+ - Vodeći međunarodni časopis kategorije M21a+ |
| 2024 | Dual molecular diagnosis in patients with skeletal dysplasia - data from tertiary genetic center | Mijovic, Marija; Cuturilo, Goran; Ruml-Stojanovic, Jelena; Miletic, Aleksandra; Bosankic, Brankica; Petrovic, Hristina; Vasic, Bojana; Vukasinovic, Nadja | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |