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Corinne Antignac
ResearcherPublications, citations & collaboration network
Corinne Antignac is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 427 works, 31,170 citations, an h-index of 106 and an i10-index of 254.
427
Works
31,170
Citations
106
h-index
254
i10-index
How has Corinne Antignac's publication output changed over time?
ScholarIQpublication output · 1994–2013
Output grew0% over the shown period — from 1 works in 1994 to 1 in 2013.
1
1
1
2
1
3
1
1
1
199419981999200020012003200720122013
What are the most-cited papers on Corinne Antignac?
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
S137905309. 20001,456 Citations
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
Edgar A. Otto, Bernhard Schermer, Tomoko Obara, John F. O’Toole, Karl S. Hiller, Adelheid M. Mueller, Rainer Ruf, Julia Hoefele, Frank Beekmann, Daniel Landau, John W. Foreman, Judith A. Goodship, Tom Strachan, Andreas Kispert, Matthias T. F. Wolf, M. F. Gagnadoux, Hubert Nivet, Corinne Antignac, Gerd Walz, Iain A. Drummond, Thomas Benzing, Friedhelm Hildebrandt
S137905309. 2003651 CitationsOPEN ACCESS
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis
Margaret Town, G Jean, Stéphanie Cherqui, Marlene Attard, Lionel Forestier, S.A. Whitmore, David F. Callen, Olivier Gribouval, M. Broyer, Gillian P. Bates, William van’t Hoff, Corinne Antignac
S137905309. 1998644 Citations
X-linked Alport Syndrome
Jean Philippe Jaïs, Bertrand Knebelmann, Iannis Giatras, Mario Marchi, Gianfranco Rizzoni, Alessandra Renieri, Manfred Weber, Oliver Groß, Kai‐Olaf Netzer, Frances Flinter, Yves Pirson, Christine Verellen, Jörgen Wieslander, Ulf Persson, Karl Tryggvason, Paula Martin, Jens Michael Hertz, Cornelis H. Schröder, Marek Sanak, S Krejcová, Maria Fernanda Carvalho de Camargo, Juan Saus, Corinne Antignac, Hubert J.M. Smeets, Marie-Claire Gübler
Journal of the American Society of Nephrology. 2000598 Citations
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
Ralf Birkenhäger, Edgar A. Otto, Maria J. Schürmann, Martin Vollmer, Eva-Maria Ruf, Irina Maier-Lutz, Frank Beekmann, Andrea Fekete, Heymut Omran, Delphine Feldmann, David V. Milford, Nicola Jeck, Martin Konrad, Daniel Landau, Nine V.A.M. Knoers, Corinne Antignac, Ralf Sudbrak, Andreas Kispert, Friedhelm Hildebrandt
S137905309. 2001538 Citations
Related on ScholarIQ
Inserm
Institution
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
Paper
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
Paper
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis
Paper
X-linked Alport Syndrome
Paper
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
Paper