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Patrick Niaudet

Active 1984–2023

89
Papers
18,086
Citations
80
h-index
88
i10-index

Citations

Citations per year for Patrick Niaudet1966: 1 citations1971: 1 citations1986: 2 citations1987: 2 citations1988: 2 citations1989: 1 citations1990: 5 citations1991: 5 citations1992: 2 citations1993: 17 citations1994: 13 citations1995: 12 citations1996: 12 citations1997: 13 citations1998: 35 citations1999: 60 citations2000: 63 citations2001: 90 citations2002: 96 citations2003: 112 citations2004: 99 citations2005: 122 citations2006: 126 citations2007: 116 citations2008: 121 citations2009: 143 citations2010: 166 citations2011: 147 citations2012: 156 citations2013: 204 citations2014: 152 citations2015: 142 citations2016: 158 citations2017: 101 citations2018: 109 citations2019: 358 citations2020: 333 citations2021: 274 citations2022: 236 citations2023: 154 citations2024: 225 citations2025: 90 citations2026: 2 citations1967–1970: no citations, so these years are not shown1972–1985: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 1,464 citing papers, 23.1% of this breakdownFrance: 568 citing papers, 8.9% of this breakdownUnited Kingdom: 531 citing papers, 8.4% of this breakdownGermany: 509 citing papers, 8% of this breakdownItaly: 388 citing papers, 6.1% of this breakdownNetherlands: 289 citing papers, 4.6% of this breakdownCanada: 233 citing papers, 3.7% of this breakdownChina: 189 citing papers, 3% of this breakdownJapan: 188 citing papers, 3% of this breakdownSpain: 168 citing papers, 2.6% of this breakdownSwitzerland: 159 citing papers, 2.5% of this breakdownBelgium: 140 citing papers, 2.2% of this breakdown
0%23.1%Other 23.9%

Institutions

Fields

  • Medicine52.7%
  • Biochemistry, Genetics and Molecular Biology28.9%
  • Immunology and Microbiology16.3%
  • Neuroscience0.6%
  • Nursing0.4%
  • Agricultural and Biological Sciences0.3%
  • Other0.8%

Topics

  • Renal Diseases and Glomerulopathies12.3%
  • Complement system in diseases6.4%
  • Renal and related cancers4.8%
  • Chronic Kidney Disease and Diabetes3.8%
  • Genetic and Kidney Cyst Diseases3.7%
  • Ion Transport and Channel Regulation2.5%
  • Other66.5%

Coauthors

All papers

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  1. Genetics and Outcome of Atypical Hemolytic Uremic Syndrome

    Authors: 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 - Clinical Journal of the American Society of Nephrology 2013 cited by 713

  2. Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies

    Authors: Aude Servais, Laure‐Hélène Noël, Lubka T. Roumenina, Moglie Le Quintrec, Stéphanie Ngo, Marie‐Agnès Dragon‐Durey, Marie-Alice Macher, Julien Zuber, Alexandre Karras, François Provôt, Bruno Moulin, Jean‐Pierre Grünfeld, Patrick Niaudet, Philippe Lesavre, Véronique Frémeaux‐Bacchi - Kidney International 2012 cited by 567

  3. Strict Blood-Pressure Control and Progression of Renal Failure in Children

    Authors: The ESCAPE Trial Group, Antonella Trivelli, Stefano Picca, Mieczyslaw Litwin, Amira Peco-Antic, Aleksandra Zurowska, Sara Testa, Augustina Jankauskiene, Sevinc Emre, Alberto Caldas-Afonso, Ali Anarat, Patrick Niaudet, Sevgi Mir, Aysin Bakkaloglu, Barbara Enke, Giovanni Montini, Ann-Margret Wingen, Peter Sallay, Nikola Jeck, Ulla Berg, Salim Caliskan, Simone Wygoda, Katharina Hohbach-Hohenfellner, Jiri Dusek, Tomasz Urasinski, Klaus Arbeiter, Thomas Neuhaus, Jutta Gellermann, Dorota Drozdz, Michel Fischbach, Kristina Möller, Marianne Wigger, Licia Peruzzi, Otto Mehls, Franz Schaefer - New England Journal of Medicine 2009 cited by 951

  4. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

    Authors: Nicolas Boute, Olivier Gribouval, Séverine Roselli, France Benessy, Hyunjoo Lee, Arno Fuchshuber, Karin Dahan, Marie-Claire Gübler, Patrick Niaudet, Corinne Antignac - Nature Genetics 2000 cited by 1,449

  5. Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy

    Authors: 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 - Kidney International 2011 cited by 363

  6. Clinical Features of Anti-Factor H Autoantibody–Associated Hemolytic Uremic Syndrome

    Authors: Marie‐Agnès Dragon‐Durey, Sidharth Kumar Sethi, Arvind Bagga, Caroline Blanc, Jacques Blouin, Bruno Ranchin, Jean-Luc André, Nobuaki Takagi, Hae Il Cheong, Pankaj Hari, Moglie Le Quintrec, Patrick Niaudet, Chantal Loirat, Wolf H. Fridman, Véronique Frémeaux‐Bacchi - Journal of the American Society of Nephrology 2010 cited by 295

  7. A randomised Phase I/II trial to evaluate the efficacy and safety of orally administered Oxalobacter formigenes to treat primary hyperoxaluria

    Authors: Bernd Höppe, Patrick Niaudet, Rémi Salomon, Jérôme Harambat, Sally‐Anne Hulton, William van’t Hoff, Shabbir H. Moochhala, Georges Deschênes, Elisabeth Lindner, Anna Sjögren, Pierre Cochat - Pediatric Nephrology 2016 cited by 84

  8. Donor splice-site mutations in WT1 are responsible for Frasier syndrome

    Authors: Sandrine Barbaux, Patrick Niaudet, Marie-Claire Gübler, Jean‐Pierre Grünfeld, Francis Jaubert, Frédérique Kuttenn, C Fekete, Nicole Souleyreau-Therville, E Thibaud, Marc Fellous, Ken McElreavey - Nature Genetics 1997 cited by 748

  9. Timing and Outcome of Renal Replacement Therapy in Patients with Congenital Malformations of the Kidney and Urinary Tract

    Authors: Elke Wühl, Karlijn J. van Stralen, Enrico Verrina, Anna Bjerre, Christoph Wanner, James Heaf, Óscar Zurriaga, Andries J. Hoitsma, Patrick Niaudet, Runólfur Pálsson, Pietro Ravani, Kitty J. Jager, Franz Schaefer - Clinical Journal of the American Society of Nephrology 2012 cited by 234

  10. The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies

    Authors: Friederike Petzold, Katy Billot, Xiaoyi Chen, C. Henry, Emilie Filhol, Yoann Martin, Marina Avramescu, Maxime Douillet, Vincent Morinière, Pauline Krug, Marc Jeanpierre, Kálmán Tory, Olivia Boyer, Anita Burgun, Aude Servais, Rémi Salomon, Alexandre Benmerah, Laurence Heidet, Nicolas Garcelon, Corinne Antignac, Mohamad Zaidan, Sophie Saunier, Tania Attié‐Bitach, Valerie Comier-Daire, Jean‐Michel Rozet, Yaacov Frishberg, Brigitte Llanas, M. Broyer, Nabil Mohsin, Marie‐Alice Macher, Nicole Philip, Véronique Baudouin, D. Brackman, Chantal Loirat, Marina Charbit, Maud Dehennault, C. Guyot, Pierre Bataille, Mariet Elting, Georges Deschênes, Andrea Gropman, Geneviève Guest, Marie‐France Gagnadoux, Philippe Nicoud, Pierre Cochat, Bruno Ranchin, A Bensman, Anne‐Marie Guerrot, Bertrand Knebelmann, İlmay Bilge, Danièle Bruno, Stéphane Burtey, Caroline Rousset Rouvière, Valérie Caudwell, Denis Morin, Hélène Dollfus, Anne Maisin, Christian Hamel, Éric Bieth, Sophie Gié, Judith Goodship, G. Roussey, Hermine La Selve, Hubert Nivet, Lucie Bessenay, Mathilde Caillez, Jean Bernard Palcoux, Stéphane L. Benoit, Philippe Dubot, Marc Fila, Fabienne Giuliano, Daouya Iftene, M. Kessler, Thérèsa Kwon, A. Lahoche, Audrey Laurent, Anne-Laure Leclerc, David V. Milford, Thomas J. Neuhaus, Sylvie Odent, Philippe Eckart, Dominique Chauveau, Patrick Niaudet, Horacio A. Repetto, Sophie Taque, Alexandra Bruel, Alexandra Noel-Botte, Emma Allain Launay, Lisa Allard, Dany Anlicheau, Anne-Laure Adra, Arnaud Garnier, Arvind Nagra, Remy Baatard, Justine Bacchetta, Banu Sadıkoğlu, Christine Barnérias, Anne Barthélémy, Lina Basel, Nader Bassilios and 229 more - Kidney International 2023 cited by 50

  11. Differential Impact of Complement Mutations on Clinical Characteristics in Atypical Hemolytic Uremic Syndrome

    Authors: Anne‐Laure Sellier‐Leclerc, Véronique Frémeaux‐Bacchi, Marie‐Agnès Dragon‐Durey, Marie-Alice Macher, Patrick Niaudet, Geneviève Guest, B. Boudailliez, F Bouissou, Georges Deschênes, Sophie Gié, Michel Tsimaratos, Michel Fischbach, Denis Morin, Hubert Nivet, Corinne Alberti, Chantal Loirat - Journal of the American Society of Nephrology 2007 cited by 429

  12. A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure

    Authors: Pascale de Lonlay, Isabelle Valnot, Antoni Barrientos, Marina S. Gorbatyuk, Alexander Tzagoloff, Jan‐Willem Taanman, Emmanuel Benayoun, Dominique Chrétien, Noman Kadhom, Anne Lombès, Hélène Ogier de Baulny, Patrick Niaudet, Arnold Münnich, Pierre Rustin, Agnès Rötig - Nature Genetics 2001 cited by 318

  13. Initial presentation of childhood-onset systemic lupus erythematosus: A French multicenter study

    Authors: Brigitte Bader‐Meunier, Jean-Baptiste Armengaud, Élie Haddad, Rémi Salomon, Georges Deschênes, Isabelle Koné‐Paut, Thierry Leblanc, Chantal Loirat, Patrick Niaudet, J.C. Piette - The Journal of Pediatrics 2005 cited by 258

  14. Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectruma

    Authors: Verena Matejas, Bernward Hinkes, Faisal Alkandari, Lihadh Al‐Gazali, E. Annexstad, Mehmet Baha Aytaç, Margaret Barrow, Květa Bláhová, Detlef Böckenhauer, Hae Il Cheong, Iwona Maruniak‐Chudek, Pierre Cochat, Jörg Dötsch, Priya Gajjar, Raoul C. M. Hennekam, Françoise Janssen, Mikhail Kagan, Ariana Kariminejad, Markus J. Kemper, Jens Koenig, Jillene Kogan, Hester Y. Kroes, Eberhard Kuwertz-Bröking, Amy Feldman Lewanda, Ana Medeira, Jutta Muscheites, Patrick Niaudet, Michel Pierson, Anand Saggar, Laurie H. Seaver, Mohnish Suri, А.Н. Цыгин, Elke Wühl, Aleksandra Żurowska, Steffen Uebe, Friedhelm Hildebrandt, Corinne Antignac, Martin Zenker - Human Mutation 2010 cited by 205

  15. Acute kidney injury complicating nephrotic syndrome of minimal change disease

    Authors: A Meyrier, Patrick Niaudet - Kidney International 2018 cited by 107

  16. Overall Neutralization of Complement Factor H by Autoantibodies in the Acute Phase of the Autoimmune Form of Atypical Hemolytic Uremic Syndrome

    Authors: Caroline Blanc, Lubka T. Roumenina, Yahya Ashraf, Satu Hyvärinen, Sidharth Kumar Sethi, Bruno Ranchin, Patrick Niaudet, Chantal Loirat, Ashima Gulati, Arvind Bagga, Wolf H. Fridman, Catherine Sautès‐Fridman, T. Sakari Jokiranta, Véronique Frémeaux‐Bacchi, Marie‐Agnès Dragon‐Durey - The Journal of Immunology 2012 cited by 103

  17. Mutation Update of theCLCN5Gene Responsible for Dent Disease 1

    Authors: Lamisse Mansour‐Hendili, Anne Blanchard, Nelly Le Pottier, Isabelle Roncelin, Stéphane Lourdel, Cyrielle Tréard, Wendy González, Ariela Vergara‐Jaque, Gilles Morin, Estelle Colin, Muriel Holder‐Espinasse, Justine Bacchetta, Véronique Baudouin, Stéphane L. Benoit, E. Bérard, Guylhène Bourdat-Michel, Karim Bouchireb, Stéphane Burtey, Mathilde Cailliez, Gérard Cardon, C. Cartery, Gérard Champion, Dominique Chauveau, Pierre Cochat, Karin Dahan, Renaud de la Faille, François-Guillaume Debray, Laurenne Dehoux, Georges Deschênes, Éstelle Desport, Olivier Devuyst, Stella M. Dieguez, Francesco Emma, Michel Fischbach, Denis Fouque, Jacques Fourcade, Hélène François, Brigitte Gilbert‐Dussardier, Thierry Hannedouche, Pascal Houillier, Hassan Izzedine, Marco Janner, Alexandre Karras, Bertrand Knebelmann, Marie‐Pierre Lavocat, Sandrine Lemoine, Valériane Leroy, Chantal Loirat, Marie-Alice Macher, Dominique Martin‐Coignard, Denis Morin, Patrick Niaudet, Hubert Nivet, François Nobili, Robert Novo, Laurence Faivre, Claire Rigothier, Gwenaëlle Roussey‐Kesler, Rémi Salomon, Andreas Schleich, A.L. Sellier-Leclerc, Kenza Soulami, A. Tiple, Tim Ulinski, Philippe Vanhille, Nicole Van Regemorter, Xavier Jeunemaı̂tre, Rosa Vargas‐Poussou - Human Mutation 2015 cited by 91

  18. An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis

    Authors: Francesco Emma, William van’t Hoff, Katharina Hohenfellner, Rezan Topaloğlu, Marcella Greco, Gema Ariceta, Chiara Bettini, Detlef Böckenhauer, Koenraad Veys, Lars Pape, Sally A. Hulton, Suzanne Collin, Fatih Özaltın, Aude Servais, Georges Deschênes, Robert Novo, Aurélia Bertholet‐Thomas, Jun Oh, Elisabeth A. M. Cornelissen, Mirian C. H. Janssen, Dieter Haffner, Lucilla Ravà, Corinne Antignac, Olivier Devuyst, Patrick Niaudet, Elena Levtchenko - Kidney International 2021 cited by 71

  19. NPHS2 mutation analysis shows genetic heterogeneityof steroid-resistant nephrotic syndrome and lowpost-transplant recurrence

    Authors: Stefanie Weber, Olivier Gribouval, Ernie Esquivel, Vincent Morinière, Marie-Josèphe Tête, Christophe Legendre, Patrick Niaudet, Corinne Antignac - Kidney International 2004 cited by 373

  20. KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron

    Authors: Hélène Louis-Dit-Picard, Julien Barc, Daniel Trujillano, Stéphanie Miserey‐Lenkei, Nabila Bouatia‐Naji, Olena Pylypenko, Geneviève Beaurain, Amélie Bonnefond, Olivier Sand, Christophe Simian, Emmanuelle Vidal‐Petiot, Christelle Soukaseum, Chantal Mandet, Françoise Broux, Olivier Chabre, Michel Delahousse, Vincent Esnault, B. Fiquet, Pascal Houillier, Corinne Isnard Bagnis, Jens Koenig, Martin Konrad, Paul Landais, Chebel Mourani, Patrick Niaudet, Vincent Probst, Christel Thauvin, Robert J. Unwin, Steven D. Soroka, Georg Ehret, Stephan Ossowski, Mark J. Caulfield, Patrick Bruneval, Xavier Estivill, Philippe Froguel, Juliette Hadchouel, Jean‐Jacques Schott, Xavier Jeunemaı̂tre - Nature Genetics 2012 cited by 337

  21. Methylprednisolone pulse therapy in the treatment of severe forms of Schönlein-Henoch purpura nephritis

    Authors: Patrick Niaudet, Renée Habib - Pediatric Nephrology 1998 cited by 301

  22. Eculizumab for Atypical Hemolytic Uremic Syndrome Recurrence in Renal Transplantation

    Authors: Julien Zuber, Moglie Le Quintrec, Saoussen Krid, Caroline Bertoye, Victor Gueutin, A. Lahoche, Nils Heyne, Gianluigi Ardissino, Valérie Châtelet, Laure‐Hélène Noël, Maryvonne Hourmant, Patrick Niaudet, Véronique Frémeaux‐Bacchi, Éric Rondeau, Christophe Legendre, Chantal Loirat - American Journal of Transplantation 2012 cited by 259

  23. Cysteamine therapy delays the progression of nephropathic cystinosis in late adolescents and adults

    Authors: Albane Brodin-Sartorius, Marie-Josèphe Tête, Patrick Niaudet, Corinne Antignac, Geneviève Guest, Chris Ottolenghi, Marina Charbit, Dominique Moyse, Christophe Legendre, Philippe Lesavre, Pierre Cochat, Aude Servais - Kidney International 2011 cited by 239

  24. Nephronophthisis

    Authors: Rémi Salomon, Sophie Saunier, Patrick Niaudet - Pediatric Nephrology 2008 cited by 166