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Nephrotic Syndrome in the First Year of Life: Two Thirds of Cases Are Caused by Mutations in 4 Genes (<i>NPHS1</i>, <i>NPHS2</i>, <i>WT1</i>, and <i>LAMB2</i>)Bernward Hinkes, Bettina E. Mucha, Christopher N. Vlangos et al.|PEDIATRICS|2007Cited by 440
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
Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disordersK Hasselbacher, Friedhelm Hildebrandt, Roger C. Wiggins et al.|Kidney International|2006Cited by 215
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