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Browsing by Author Bosankić, Brankica

Showing results 1 to 10 of 10
Issue DateTitleAuthor(s)TypeМp-cat.
202322q11.2 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 analysisMiletić, Aleksandra; Cuturilo, Goran; Ruml Stojanović, Jelena; Drakulić, Danijela  ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Stevanović, Milena  Conference Paper
Mp. category will be shown later
2025A Novel 4.2 kb deletion of the 3'UTR of RUNX2 Gene Causes Cleidocranial Dysplasia: Further Delineation of the Role of yhe 3'UTRMijović, Marija; Čuturilo, Goran  ; Ruml-Stojanović, Jelena ; Branković, Marija  ; Miletić, Aleksandra; Bosankić, Brankica; Dedović, Maja; Perović, Dijana  ; Maksimović, Nela  ; Damnjanović, Tatjana M.  Article
23M23
2026Analysis of Copy Number and Sequence Variants Linked to Cardiac Development in Children with Syndromic Congenital Heart DefectsDamnjanović, Tatjana  ; Maksimović, Nela  ; Đuranović-Uklein, Ana  ; Bosankić, Brankica; Jekić, Biljana  ; Grk, Milka  ; Dušanovic-Pjević, Marija  ; Rašić, Milica  ; Stojanovski, Nataša  ; Pešić, Milica  ;
Novaković, Ivana  ; Čuturilo, Goran  ; Perović, Dijana  ;
Article
23M23
2025Diabetes triggered by renal transplantation in patients with HNF1B variants - Single center experienceCvetković, Mirjana; Petrović, Ana; Pavlović, Sonja  ; Paripović, Dušan  ; Miloševski-Lomić, Gordana; Gojković, Ivana; Matijas, Kristina; Zdravković, Vera  ; Radović, Tijana; Pavićević, Polina  ;
Čuturilo, Goran  ; Bosankić, Brankica; Spasojević, Brankica  ;
Konferencijski rad
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2025Diagnostic challenges in skeletal dysplasia: a clinical overview based on a 10-year retrospective study of single genetic departmentMijović, Marija; Čuturilo, Goran  ; Ruml-Stojanović, Jelena ; Mileticć Aleksandra; Bosankić, Brankica; Dedović, Maja; Branković, Marija  Konferencijski rad
Mp kategorija će biti prikazana naknadno.
2023EP06.016 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 analysisMiletić, Aleksandra; Cuturilo, Goran; Ruml Stojanović, Jelena; Drakulić, Danijela  ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Stevanović, Milena  Conference Paper
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2021Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unitMiletić, Aleksandra; Ruml-Stojanović, Jelena ; Parezanović, Vojislav  ; Rsovac, Snežana; Drakulić, Danijela  ; Soldatović, Ivan  ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Borlja, Nikola;
Milivojević, Milena  ; Marjanović, Ana  ; Branković, Marija  ; Čuturilo, Goran  ;
Научни чланак
21aM21a - Водећи међународни часопис категорије M21a
2026Implementation and clinical utility of the GATK gCNV pipeline for rare disease diagnostics using whole exome sequencingPavlović, Đorđe  ; Skakić, Anita  ; Klaassen, Kristel  ; Marjanović, Irena  ; Parezanović, Marina  ; Stevanović, Nina  ; Čuturilo, Goran; Branković, Marija; Bosankić, Brankica; Ruml Stojanovic, Jelena;
Ristivojević, Bojan  ; Zukić, Branka  ; Stojiljković, Maja  ; Anđelković, Marina  ;
Conference Paper
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2026Insight into Haploinsufficiency of the ERBB4 Gene: Expanding the Spectrum of Associated PhenotypesMademont-Soler, Irene; ...; Perović, Dijana  ; ...; Kravljanac, Ružica M.  ; ...; Bosankić, Brankica; ...; Maksimović, Nela S.  ; ...;
(broj koautora 37);
Article
21M21
2025The coexistence of APC and FH germline variants: a case report of cooccurrence of two hereditary cancer predisposition syndromes in a single patientBosankić, Brankica; Čuturilo, Goran  ; Mijović, Marija; Ruml-Stojanović, Jelena ; Miletić, Aleksandra; Dedović, Maja; Branković, Marija  Conference Paper
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Showing results 1 to 10 of 10