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Autori: Tasic Velibor

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Naslov Diversity of kidney care referral pathways in national child health systems of 48 European countries (Article)
Autori Tasic Velibor ... Stojanovic Vesna D  ... (broj koautora 53) 
Info FRONTIERS IN PEDIATRICS, (2024), vol. 12 br. , str. -
Ispravka Web of Science   Članak   Elečas   Rang časopisa  
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Naslov Is there a dominant-negative effect in individuals with heterozygous disease-causing variants in COL4A3/COL4A4? (Article)
Autori Riedhammer Korbinian M 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 Web of Science   Članak   Elečas   Rang časopisa   Citati:
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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 Web of Science   Elečas   Rang časopisa  
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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)
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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 Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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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 Web of Science   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  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 Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Mild Recessive Mutations in Six Fraser Syndrome-Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract (Article)
Autori Kohl Stefan Hwang Daw-Yang Dworschak Gabriel C Hilger Alina C Saisawat Pawaree Vivante Asaf Stajic Natasa Bogdanovic Radovan M Reutter Heiko M Kehinde Elijah O Tasic Velibor Hildebrandt Friedhelm 
Info JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, (2014), vol. 25 br. 9, str. 1917-1922
Projekat National Institutes of Health [R01-DK045345, R01-DK088767]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract (Article)
Autori Hwang Daw-Yang Dworschak Gabriel C Kohl Stefan Saisawat Pawaree Vivante Asaf Hilger Alina C Reutter Heiko M Soliman Neveen A Bogdanovic Radovan M Kehinde Elijah O Tasic Velibor Hildebrandt Friedhelm 
Info KIDNEY INTERNATIONAL, (2014), vol. 85 br. 6, str. 1429-1433
Projekat National Institutes of Health [R01-DK088767]; March of Dimes Foundation [6FY11-241]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association (Article)
Autori Saisawat Pawaree Kohl Stefan Hilger Alina C Hwang Daw-Yang Gee Heon Yung Dworschak Gabriel C Tasic Velibor Pennimpede Tracie Natarajan Sivakumar Sperry Ethan Matassa Danilo S Stajic Natasa Bogdanovic Radovan M de Blaauw Ivo Marcelis Carlo LM Wijers Charlotte HW Bartels Enrika Schmiedeke Eberhard Schmidt Dominik Maerzheuser Stefanie Grasshoff-Derr Sabine Holland-Cunz Stefan Ludwig Michael Noethen Markus M Draaken Markus Brosens Erwin Heij Hugo Tibboel Dick Herrmann Bernhard G Solomon Benjamin D de Klein Annelies van Rooij Iris ALM Esposito Franca Reutter Heiko M Hildebrandt Friedhelm 
Info KIDNEY INTERNATIONAL, (2014), vol. 85 br. 6, str. 1310-1317
Projekat National Institutes of Health [R01-DK045345, R01-DK088767]; March of Dimes Foundation [6FY11-241]; Division of Intramural Research; National Human Genome Research Institute (NHGRI); National Institutes of Health and Human services; Bundesministerium fur B
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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