COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafnessSaskia F. Heeringa, Friedhelm Hildebrandt, Peter Mündel et al.|Journal of Clinical Investigation|2011Cited by 402
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signalingHeon Yung Gee, Friedhelm Hildebrandt, Pawaree Saisawat et al.|Journal of Clinical Investigation|2013Cited by 237
A Systematic Approach to Mapping Recessive Disease Genes in Individuals from Outbred PopulationsFriedhelm Hildebrandt, Edgar A. Otto, Saskia F. Heeringa et al.|PLoS Genetics|2009Cited by 164
Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 MutationsGil Chernin, Friedhelm Hildebrandt, Virginia Vega-Warner et al.|Clinical Journal of the American Society of Nephrology|2010Cited by 123
Exome Sequencing Reveals Cubilin Mutation as a Single-Gene Cause of ProteinuriaBuğsu Övünç, Friedhelm Hildebrandt, Edgar A. Otto et al.|Journal of the American Society of Nephrology|2011Cited by 112