Autori: Stajic Natasa
| Naslov | Outcomes of steroid-resistant nephrotic syndrome in children not treated with intensified immunosuppression (Article) |
| Autori | Trautmann Agnes ... Stajic Natasa ... (broj koautora 28) |
| Info | PEDIATRIC NEPHROLOGY, (2023), vol. 38 br. 5, str. 1499-1511 |
| 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 |
| Naslov | Evaluation of carotid intima media thickness in children with idiopathic nephrotic syndrome (Article) |
| Autori | Paripovic Aleksandra Stajic Natasa Putnik Jovana Gazikalovic Ana Bogdanovic Radovan M Vukomanovic Vladislav A |
| Info | NEPHROLOGIE & THERAPEUTIQUE, (2020), vol. 16 br. 7, str. 420-423 |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Exome Sequencing and Identification of Phenocopies in Patients With Clinically Presumed Hereditary Nephropathies (Article; Proceedings Paper) |
| Autori | Riedhammer Korbinian Maria ... Putnik Jovana Stajic Natasa ... (broj koautora 20) |
| Info | AMERICAN JOURNAL OF KIDNEY DISEASES, (2020), vol. 76 br. 4, str. 460-470 |
| Projekat | German Research Foundation (Deutsche Forschungsgemeinschaft, DFG)German Research Foundation (DFG) [HO 2583/8-3]; Baxter, USA |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans (Article) |
| Autori | Kitzler Thomas M ... Bogdanovic Radovan M Stajic Natasa ... (broj koautora 22) |
| Info | HUMAN GENETICS, (2019), vol. 138 br. 10, str. 1105-1115 |
| Projekat | National Institutes of Health (NIH) - USANIH National Human Genome Research Institute (NHGRI) [UM1 HG008900, U54 HG006504]; National Institutes of HealthUnited Stat |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract (Article) |
| Autori | van der Ven Amelie T ... Bogdanovic Radovan M Stajic Natasa ... (broj koautora 64) |
| Info | JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, (2018), vol. 29 br. 9, str. 2348-2361 |
| Projekat | German Research Foundation (DFG) [VE969-7]; Health Research Board, Ireland grant [HPF-206-674]; International Pediatric Research Foundation Early Investigators' Exchange Program; Amgen Irish Nephrology Society Specialist Registrar Bursary; National Instit |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment (Article) |
| Autori | Ashraf Shazia ... Bogdanovic Radovan M Stajic Natasa ... (broj koautora 65) |
| Info | NATURE COMMUNICATIONS, (2018), vol. 9 br. , str. - |
| Projekat | National Institutes of Health [DK076683]; Howard Hughes Medical Institute; German National Academy of Sciences Leopoldina [LPDS-2015-07]; ASN Foundation for Kidney Research; DFG-fellowship [HE 7456/1-1, VE 196/1-1]; Deutsche Forschungsgemeinschaft [Jo 132 |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
