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Naslov Severe neurological complications in a child with multisystem inflammatory syndrome in children after asymptomatic COVID-19 (Article)
Autori Kravljanac Ruzica M  Stajic Natasa  Vukomanovic Vladislav A  Petrovic Gordana  Kuzmanovic Milos B 
Info SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, (2024), vol. 152 br. 3-4, str. 182-185
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Is there a dominant-negative effect in individuals with heterozygous disease-causing variants in COL4A3/COL4A4? (Article; Early Access)
Autori Riedhammer Korbinian M  Simmendinger Hannes  Tasic Velibor  Putnik Jovana  Abazi-Emini Nora  Stajic Natasa  Berutti Riccardo  Weidenbusch Marc  Patzer Ludwig  Lungu Adrian  Milosevski-Lomic Gordana  Guenthner Roman  Braunisch Matthias C  Comic Jasmina  Hoefele Julia 
Info CLINICAL GENETICS, (2024), vol. br. , str. -
Projekat Deutsche Forschungsgemeinschaft; German Research Foundation (DFG); Technical University of Munich (TUM)
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21 (Article)
Autori Paripovic Aleksandra  Maver Ales  Stajic Natasa  Putnik Jovana  Ostojic Slavica  Alimpic Biljana  Ilic Nina  Sarajlija Adrijan 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 2, str. 59-64
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Moyamoya syndrome in Schimke immuno-osseous dysplasia (Article)
Autori Vujic Ana J  Obradovic Slobodan  Igrutinovic Zoran R  Protrka Zoran M  Jankovic Marijana  Radovanovic Marija D  Stajic Natasa  Medovic Rasa H  Jankovic Sveta 
Info VOJNOSANITETSKI PREGLED, (2023), vol. 80 br. 3, str. 270-274
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience (Article; Early Access)
Autori Riedhammer Korbinian Maria  Comic Jasmina  Tasic Velibor  Putnik Jovana  Abazi-Emini Nora  Paripovic Aleksandra  Stajic Natasa  Meitinger Thomas  Nushi-Stavileci Valbona  Berutti Riccardo  Braunisch Matthias C  Hoefele Julia 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. br. , str. -
Projekat CAKUT/UTI/Bladder Dysfunction of the European Society for Paediatric Nephrology (ESPN); German Research Foundation (DFG); Technical University of Munich (TUM)
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Outcomes of steroid-resistant nephrotic syndrome in children not treated with intensified immunosuppression (Article; Early Access)
Autori Trautmann Agnes  ...  Stajic Natasa  ...  (broj koautora 28) 
Info PEDIATRIC NEPHROLOGY, (2022), vol. br. , str. -
Projekat Projekt DEAL; ERKNet, the European Rare Kidney Disease Reference Network; European Union
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract (Article)
Autori Wu Chen-Han Wilfred  ...  Stajic Natasa  ...  (broj koautora 36) 
Info EUROPEAN UROLOGY OPEN SCIENCE, (2022), vol. 44 br. , str. 106-112
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy-A human genetics department experience (Article)
Autori Comic Jasmina  ...  Nushi-Stavileci Valbona  Putnik Jovana  Stajic Natasa  ...  (broj koautora 20) 
Info FRONTIERS IN MEDICINE, (2022), vol. 9 br. , str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract (Article)
Autori Zheng Bixia  ...  Stajic Natasa  ...  (broj koautora 17) 
Info NEPHROLOGY DIALYSIS TRANSPLANTATION, (2022), vol. 37 br. 10, str. 1833-1843
Projekat Begg Family Foundation; program of China Scholarships Council [201908320472]; Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [442070894]; Health Research Board, Ireland [HPF-206-674]; International Pediatric Research Foundation Early Investigators' Exchange Program; Irish Nephrology Society Specialist Registrar Bursary - Eugen Drewlo Chair for Kidney Research and Innovation at the Schulich School of Medicine & Dentistry at Western University, London, Ontario, Canada; American College of Medical Genetics and Genomics Foundation; National Institutes of Health [T32-DK007726, U54HG006504]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov FHR-5 Serum Levels and CFHR5 Genetic Variations in Patients With Immune Complex-Mediated Membranoproliferative Glomerulonephritis and C3-Glomerulopathy (Article)
Autori Garam Nora  ...  Stajic Natasa  ...  (broj koautora 68) 
Info FRONTIERS IN IMMUNOLOGY, (2021), vol. 12 br. , str. -
Projekat Premium Postdoctoral Fellowship Program of the Hungarian Academy of Sciences [PPD2018-016/2018]; Higher Education Institutional Excellence Program of the Ministry of Human Capacities in Hungary within the framework of the molecular biology thematic progra
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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