ScholarIQanswers from OpenAlex & ORCID
Patrick Niaudet
ResearcherPublications, citations & collaboration network
Patrick Niaudet is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Patrick Niaudet have?
ScholarIQindexed works
Patrick Niaudet has 477 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Patrick Niaudet have?
ScholarIQcitation count
Patrick Niaudet has 23,764 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Patrick Niaudet?
ScholarIQh-index
Patrick Niaudet has an h-index of 80 in OpenAlex.
What is the i10-index of Patrick Niaudet?
ScholarIQi10-index
Patrick Niaudet has an i10-index of 237 in OpenAlex.
What is the OpenAlex record for Patrick Niaudet?
ScholarIQopenalex
The OpenAlex for Patrick Niaudet is on the source record.
What are the most-cited papers on Patrick Niaudet?
ScholarIQmost cited works
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
Nicolas Boute, Olivier Gribouval, Séverine Roselli, France Benessy, Hyunjoo Lee, Arno Fuchshuber, Karin Dahan, Marie-Claire Gübler, Patrick Niaudet, Corinne Antignac
Genetics and Outcome of Atypical Hemolytic Uremic Syndrome
Véronique Frémeaux‐Bacchi, Fádi Fakhouri, Arnaud Garnier, Frank Bienaimé, Marie‐Agnès Dragon‐Durey, Stéphanie Ngo, Bruno Moulin, Aude Servais, François Provôt, Lionel Rostaing, Stéphane Burtey, Patrick Niaudet, Georges Deschênes, Yvon Lebranchu, Julien Zuber, Chantal Loirat
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome
Marion Delous, Lekbir Baala, Rémi Salomon, Christine Laclef, Jeanette Vierkotten, Kálmán Tory, Christelle Golzio, Tiphanie Lacoste, Laurianne Besse, Catherine Ozilou, Imane Moutkine, Nathan E. Hellman, Isabelle Anselme, Flora Silbermann, Christine Vesque, Christoph Gerhardt, Eleanor Rattenberry, Matthias T. F. Wolf, Marie-Claire Gübler, Jéléna Martinovic, Férechté Encha‐Razavi, Nathalie Boddaert, Marie Gonzalès, Marie Alice Macher, Hubert Nivet, Gérard Champion, Jean Pierre Berthélémé, Patrick Niaudet, Fiona McDonald, Friedhelm Hildebrandt, Colin A. Johnson, Michel Vekemans, Corinne Antignac, Ulrich Rüther, Sylvie Schneider‐Maunoury, Tania Attié‐Bitach, Sophie Saunier
Structure of the Gene for Congenital Nephrotic Syndrome of the Finnish Type (NPHS1) and Characterization of Mutations
Ulla Lenkkeri, Minna Männikkö, Paula McCready, Jane E. Lamerdin, Olivier Gribouval, Patrick Niaudet, Corinne Antignac, Clifford E. Kashtan, Christer Holmberg, Anne S. Olsen, Marjo Kestilä, Karl Tryggvason
Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy
Oliver Groß, Christoph Licht, Hans‐Joachim Anders, Bernd Höppe, Bodo B. Beck, Burkhard Tönshoff, Britta Höcker, Simone Wygoda, J. H. H. Ehrich, Lars Pape, Martin Konrad, Wolfgang Rascher, Jörg Dötsch, Dirk E. Müller‐Wiefel, Peter F. Hoyer, Bertrand Knebelmann, Yves Pirson, Jean‐Pierre Grünfeld, Patrick Niaudet, Pierre Cochat, Laurence Heidet, Saïd Lebbah, Roser Torrá, Tim Friede, Katharina Lange, Gerhard A. Müller, Manfred Weber