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Naslov Exome Sequencing in a Cohort of Individuals with Microscopic Hematuria and Clinical Suspicion of Type-IV-Collagen-Related-Nephropathy (Meeting Abstract)
Autori Bittmann Marina  Riedhammer Korbinian Maria  Stajic Natasa  Lungu Adrian  Tasic Velibor  Abazi Emini Nora  Braunisch Matthias C  Nushi Stavileci Valbona  Paripovic Aleksandra  Putnik Jovana  Comic Jasmina  Hoefele Julia 
Info PEDIATRIC NEPHROLOGY, (2024), vol. 39 br. 1, Suppl. S, str. S260-S260
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Phenotypic and genotypic spectrum of familial cases with congenital anomalies of the kidney and urinary tract (CAKUT) (Meeting Abstract)
Autori Schniedermeier Timo  Goldammer Stephanie  Tasic Velibor  Vollhardt Anne  Abazi Emini Nora  Gessner Michaela  Putnik Jovana  Stavileci Valbona  Mueller Dominik  Specht Sabine  Stajic Natasa  Braunisch Matthias C  Riedhammer Korbinian Maria  Weber Stefanie  Hoefele Julia 
Info PEDIATRIC NEPHROLOGY, (2024), vol. 39 br. 1, Suppl. S, str. S11-S12
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Is there a dominant-negative effect in individuals with heterozygous disease-causing variants in COL4A3/COL4A4? (Article)
Autori Riedhammer Korbinian Maria  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. 105 br. 4, str. 406-414
Projekat Deutsche Forschungsgemeinschaft; German Research Foundation (DFG); Technical University of Munich (TUM)
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Phenotypic Variability of Individuals with Cakut (Meeting Abstract)
Autori Kraljevic Bernard  Riedhammer Korbinian Maria  Tasic Velibor  Abazi-Emini Nora  Gessner Michaela  Lange-Sperandio Baerbel  Stavileci Valbona  Putnik Jovana  Paripovic Aleksandra  Stajic Natasa  Comic Jasmina  Hoefele Julia 
Info PEDIATRIC NEPHROLOGY, (2023), vol. 38 br. , Suppl. 2, str. S54-S55
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience (Article)
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. 31 br. 6, str. 674-680
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 Exome Sequencing in Individuals with Congenital Anomalies of the Kidney and Urinary Tract (Cakut): a Single-Center Experience (Meeting Abstract)
Autori Comic Jasmina  Riedhammer Korbinian Maria  Tasic Velibor  Putnik Jovana  Abazi-Emini Nora  Paripovic Aleksandra  Stajic Natasa  Nushi-Stavileci Valbona  Braunisch Matthias C  Hoefele Julia 
Info PEDIATRIC NEPHROLOGY, (2022), vol. 37 br. 11, str. 2889-2889
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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  Abazi-Emini Nora  Stajic Natasa  Weidenbusch Marc  Patzer Ludwig  Lungu Adrian  Milosevski-Lomic Gordana  Braunisch Matthias C  Guenthner Roman  Comic Jasmina  Hoefele Julia 
Info PEDIATRIC NEPHROLOGY, (2022), vol. 37 br. 11, str. 2854-2854
Ispravka ISI/Web of Science   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 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  
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