Autori: Stajic Natasa
Naslov | Genotype-Phenotype Correlation in a Cohort of Individuals with Disease-Causing Variants in COL4A3/COL4A4 Associated with Type-Iv-Collagen-Related Nephropathy (Alport Syndrome and Thin Basement Membrane Nephropathy) (Meeting Abstract) |
Autori | Simmendinger Hannes Riedhammer Korbinian Maria Tasic Velibor Putnik Jovana ![]() |
Info | PEDIATRIC NEPHROLOGY, (2022), vol. 37 br. 11, str. 2854-2854 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science Scopus |
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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 ![]() |
Info | FRONTIERS IN MEDICINE, (2022), vol. 9 br. , str. - |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | The first case of pediatric Cushing disease in Serbia (Meeting Abstract) |
Autori | Panic-Zaric Sanja Vukovic Rade M ![]() ![]() ![]() ![]() ![]() ![]() |
Info | HORMONE RESEARCH IN PAEDIATRICS, (2022), vol. 95 br. SUPPL 2, Suppl. 2, str. 444-444 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Delineation of the phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy - Alport syndrome and thin basement membrane nephropathy (Meeting Abstract) |
Autori | Riedhammer Korbinian Maria Braunisch Matthias C Comic Jasmina Lungu Adrian Putnik Jovana ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2022), vol. 30 br. SUPPL 1, Suppl. 1, str. 141-142 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Evaluation of carotid intima media thickness in children with idiopathic nephrotic syndrome (Article) |
Autori | Paripovic Aleksandra Stajic Natasa Putnik Jovana ![]() |
Info | NEPHROLOGIE & THERAPEUTIQUE, (2020), vol. 16 br. 7, str. 420-423 |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Exome Sequencing and Identification of Phenocopies in Patients With Clinically Presumed Hereditary Nephropathies (Article; Proceedings Paper) |
Autori | Riedhammer Korbinian Maria ... Putnik Jovana ![]() |
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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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