@ARTICLE{
author={Schniedermeier Timo|,Goldammer Stephanie|,Tasic Velibor|,Vollhardt Anne|,Abazi Emini Nora|,Gessner Michaela|,Putnik Jovana|0000-0002-2085-4834,Stavileci Valbona|,Mueller Dominik|,Specht Sabine|,Stajic Natasa|,Braunisch Matthias C|,Riedhammer Korbinian Maria|,Weber Stefanie|,Hoefele Julia|},
year={2024},
title={Phenotypic and genotypic spectrum of familial cases with congenital anomalies of the kidney and urinary tract (CAKUT)},
journal={PEDIATRIC NEPHROLOGY},
volume={39},
number={1},
pages={S11-S12},
document_type={Meeting Abstract},
} 

@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={Weber Stefanie|,Moriniere V|,Knuppel T|,Charbit M|,Dusek J|,Ghiggeri GM|,Jankauskiene A|,Mir S|,Montini G|,Peco-Antic Amira E|,Wuhl E|,Zurowska AM|,Mehls O|,Antignac C|,Schaefer F|,Salomon R|},
year={2006},
title={Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: Results of the ESCAPE study},
journal={JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY},
volume={17},
number={10},
pages={2864-2870},
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},
}