@ARTICLE{
author={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},
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},
}