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 (2024) Exome Sequencing in a Cohort of Individuals with Microscopic Hematuria and Clinical Suspicion of Type-IV-Collagen-Related-Nephropathy, PEDIATRIC NEPHROLOGY, vol. 39, br. 1, str. S260-S260 (Meeting Abstract) 

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 (2024) Phenotypic and genotypic spectrum of familial cases with congenital anomalies of the kidney and urinary tract (CAKUT), PEDIATRIC NEPHROLOGY, vol. 39, br. 1, str. S11-S12 (Meeting Abstract) 

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 (2024) Is there a dominant-negative effect in individuals with heterozygous disease-causing variants in <i>COL4A3/COL4A4</i>?, CLINICAL GENETICS, vol. 105, br. 4, str. 406-414 (Article) 

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 (2023) Phenotypic Variability of Individuals with Cakut, PEDIATRIC NEPHROLOGY, vol. 38, br. , str. S54-S55 (Meeting Abstract) 

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 (2023) Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 31, br. 6, str. 674-680 (Article) 

Comic Jasmina,Riedhammer Korbinian Maria,Tasic Velibor,Putnik Jovana,Abazi-Emini Nora,Paripovic Aleksandra,Stajic Natasa,Nushi-Stavileci Valbona,Braunisch Matthias C,Hoefele Julia (2022) Exome Sequencing in Individuals with Congenital Anomalies of the Kidney and Urinary Tract (Cakut): a Single-Center Experience, PEDIATRIC NEPHROLOGY, vol. 37, br. 11, str. 2889-2889 (Meeting Abstract) 

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 (2022) 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), PEDIATRIC NEPHROLOGY, vol. 37, br. 11, str. 2854-2854 (Meeting Abstract) 

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 (2022) Delineation of the phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy - Alport syndrome and thin basement membrane nephropathy, EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 30, br. SUPPL 1, str. 141-142 (Meeting Abstract) 

Riedhammer Korbinian Maria,...,Putnik Jovana,Stajic Natasa,...,(broj koautora 20) (2020) Exome Sequencing and Identification of Phenocopies in Patients With Clinically Presumed Hereditary Nephropathies, AMERICAN JOURNAL OF KIDNEY DISEASES, vol. 76, br. 4, str. 460-470 (Article; Proceedings Paper)