Patrick Niaudet
Santé Publique France(FR)
Publications by Year
Research Areas
Renal Diseases and Glomerulopathies, Biomedical Research and Pathophysiology, Renal Transplantation Outcomes and Treatments, Neonatal Health and Biochemistry, Renal and related cancers
Most-Cited Works
- → NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome(2000)1,439 cited
- → Donor splice-site mutations in WT1 are responsible for Frasier syndrome(1997)744 cited
- → Genetics and Outcome of Atypical Hemolytic Uremic Syndrome(2013)703 cited
- → Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies(2012)558 cited
- → The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome(2007)489 cited
- → Differential Impact of Complement Mutations on Clinical Characteristics in Atypical Hemolytic Uremic Syndrome(2007)428 cited