Friedhelm Hildebrandt

A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1

Friedhelm Hildebrandt, Edgar A. Otto, Hans Gerd Nothwang et al. · Nature Genetics · 1997 · 352 citations

Life Sciences, Genetics, Nephrology +6

Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes [published erratum appears in Hum Mol Genet 1997 Apr;6(4):650]

Lothar Károlyi, Martin Konrad, Arnold Köckerling et al. · Human Molecular Genetics · 1997 · 190 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Immunosuppression and Renal Outcome in Congenital and Pediatric Steroid-Resistant Nephrotic Syndrome

Anja Büscher, Birgitta Kranz, Rainer Büscher et al. · Clinical Journal of the American Society of Nephrology · 2010 · 184 citations · Full text

Medicine, Nephrology, Pediatrics +17

A Novel TRPC6 Mutation That Causes Childhood FSGS

Saskia F. Heeringa, Clemens Möller, Jianyang Du et al. · PLoS ONE · 2009 · 173 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome

Bernward Hinkes, Christopher N. Vlangos, Saskia F. Heeringa et al. · Journal of the American Society of Nephrology · 2008 · 156 citations · Full text

Medicine, Genetics, Molecular Genetics +15