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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  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 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  Milosevski-Lomic Gordana  Gessner Michaela  Stajic Natasa  Patzer Ludwig  Emini Nora  Tasic Velibor  Hoefele Julia 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2022), vol. 30 br. SUPPL 1, Suppl. 1, str. 141-142
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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  
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