@ARTICLE{
author={Tasic Velibor,...,Stojanovic Vesna D,...,(broj koautora 53)},
year={2024},
title={Diversity of kidney care referral pathways in national child health systems of 48 European countries},
journal={FRONTIERS IN PEDIATRICS},
volume={12},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={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},
year={2024},
title={Is there a dominant-negative effect in individuals with heterozygous disease-causing variants in <i>COL4A3/COL4A4</i>?},
journal={CLINICAL GENETICS},
volume={105},
number={4},
pages={406-414},
document_type={Article},
} 

@ARTICLE{
author={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},
year={2023},
title={Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={6},
pages={674-680},
document_type={Article},
} 

@ARTICLE{
author={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},
year={2014},
title={Mild Recessive Mutations in Six Fraser Syndrome-Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract},
journal={JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY},
volume={25},
number={9},
pages={1917-1922},
document_type={Article},
} 

@ARTICLE{
author={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},
year={2014},
title={Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract},
journal={KIDNEY INTERNATIONAL},
volume={85},
number={6},
pages={1429-1433},
document_type={Article},
} 

@ARTICLE{
author={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},
year={2014},
title={Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association},
journal={KIDNEY INTERNATIONAL},
volume={85},
number={6},
pages={1310-1317},
document_type={Article},
} 

@ARTICLE{
author={Popovska-Jankovic Katerina,Tasic Velibor,Bogdanovic Radovan M,Miljkovic Predrag,Golubovic Emilija,Soylu A,Saraga Marjan,Pavicevic Snezana,Baskin E,Akil I,Gregoric Alojz,Lilova Marusia,Topaloglu R,Sukarova-Stefanovska Emilija,Plaseska-Karanfilska D},
year={2013},
title={Molecular characterization of cystinuria in south-eastern European countries},
journal={UROLITHIASIS},
volume={41},
number={1},
pages={21-30},
document_type={Article},
} 

@ARTICLE{
author={Gucev Zoran,Tasic Velibor,Saranac Ljiljana,Stobbe Heike,Kratzsch Juergen,Klammt Juergen,Pfaeffle Roland},
year={2012},
title={A Novel GH1 Mutation in a Family with Isolated Growth Hormone Deficiency Type II},
journal={HORMONE RESEARCH IN PAEDIATRICS},
volume={77},
number={3},
pages={1-5},
document_type={Article},
} 

@ARTICLE{
author={Popovska-Jankovic Katerina,Tasic Velibor,Bogdanovic Radovan M,Miljkovic Predrag,Baskin E,Efremov G,Plaseska-Karanfilska Dijana},
year={2009},
title={Five Novel Mutations In Cystinuria Genes Slc3a1 And Slc7a9},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={12},
number={1},
pages={15-20},
document_type={Article},
} 

@ARTICLE{
author={Konrad Martin,Hou Jianghui,Weber Stefanie,Doetsch Joerg,Kari Jameela A,Seeman Tomas,Kuwertz-Broeking Eberhard,Peco-Antic Amira E,Tasic Velibor,Dittrich Katalin,Alshaya Hammad O,von Vigier Rodo O,Gallati Sabina,Goodenough Daniel A,Schaller Andre},
year={2008},
title={CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis},
journal={JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY},
volume={19},
number={1},
pages={171-181},
document_type={Article},
} 

@ARTICLE{
author={Schonfelder EM,Knuppel T,Tasic Velibor,Miljkovic Predrag,Konrad Martin,Wuhl E,Antignac C,Bakkaloglu A,Schaefer F,Weber Stefanie},
year={2006},
title={Mutations in uroplakin IIIA are a rare cause of renal hypodysplasia in humans},
journal={AMERICAN JOURNAL OF KIDNEY DISEASES},
volume={47},
number={6},
pages={1004-1012},
document_type={Article},
}