Patrick Niaudet
1984–2023 年に発表
- 89
- 論文数
- 18,086
- 被引用数
- 80
- h 指数
- 88
- i10 指数
被引用数
引用元
国・地域
機関
分野
- Medicine52.7%
- Biochemistry, Genetics and Molecular Biology28.9%
- Immunology and Microbiology16.3%
- Neuroscience0.6%
- Nursing0.4%
- Agricultural and Biological Sciences0.3%
- その他0.8%
トピック
- 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%
- その他66.5%
共著者
- Chantal Loirat19
- Georges Deschênes15
- Marie-Claire Gübler15
- Rémi Salomon13
- Corinne Antignac12
- Pierre Cochat11
- M. Broyer9
- Véronique Frémeaux‐Bacchi9
- Marina Charbit8
- A Bensman7
- Aude Servais7
- Marie-Alice Macher6
- Marie‐Agnès Dragon‐Durey6
- Olivier Gribouval6
- Geneviève Guest5
- Jean‐Pierre Grünfeld5
- Marie‐France Gagnadoux5
- Olivia Boyer5
- Arnold Münnich4
- Brigitte Llanas4
- Elisabeth A. M. Cornelissen4
- Hubert Nivet4
- Julien Zuber4
- Marie-Josèphe Tête4
全論文
- Genetics and Outcome of Atypical Hemolytic Uremic Syndrome
著者: 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 被引用: 713
- Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies
著者: 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 被引用: 567
- Strict Blood-Pressure Control and Progression of Renal Failure in Children
著者: 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 被引用: 951
- NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
著者: Nicolas Boute, Olivier Gribouval, Séverine Roselli, France Benessy, Hyunjoo Lee, Arno Fuchshuber, Karin Dahan, Marie-Claire Gübler, Patrick Niaudet, Corinne Antignac - Nature Genetics 2000 被引用: 1,449
- Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy
著者: 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 被引用: 363
- Clinical Features of Anti-Factor H Autoantibody–Associated Hemolytic Uremic Syndrome
著者: 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 被引用: 295
- A randomised Phase I/II trial to evaluate the efficacy and safety of orally administered Oxalobacter formigenes to treat primary hyperoxaluria
著者: 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 被引用: 84
- Donor splice-site mutations in WT1 are responsible for Frasier syndrome
著者: 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 被引用: 748
- Timing and Outcome of Renal Replacement Therapy in Patients with Congenital Malformations of the Kidney and Urinary Tract
著者: 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 被引用: 234
- The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies
著者: 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 ほか 229 名 - Kidney International 2023 被引用: 50
- Differential Impact of Complement Mutations on Clinical Characteristics in Atypical Hemolytic Uremic Syndrome
著者: 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 被引用: 429
- A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure
著者: 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 被引用: 318
- Initial presentation of childhood-onset systemic lupus erythematosus: A French multicenter study
著者: 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 被引用: 258
- Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectruma
著者: 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 被引用: 205
- Acute kidney injury complicating nephrotic syndrome of minimal change disease
著者: A Meyrier, Patrick Niaudet - Kidney International 2018 被引用: 107
- Overall Neutralization of Complement Factor H by Autoantibodies in the Acute Phase of the Autoimmune Form of Atypical Hemolytic Uremic Syndrome
著者: 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 被引用: 103
- Mutation Update of theCLCN5Gene Responsible for Dent Disease 1
著者: 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 被引用: 91
- An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis
著者: 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 被引用: 71
- NPHS2 mutation analysis shows genetic heterogeneityof steroid-resistant nephrotic syndrome and lowpost-transplant recurrence
著者: Stefanie Weber, Olivier Gribouval, Ernie Esquivel, Vincent Morinière, Marie-Josèphe Tête, Christophe Legendre, Patrick Niaudet, Corinne Antignac - Kidney International 2004 被引用: 373
- KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron
著者: 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 被引用: 337
- Methylprednisolone pulse therapy in the treatment of severe forms of Schönlein-Henoch purpura nephritis
著者: Patrick Niaudet, Renée Habib - Pediatric Nephrology 1998 被引用: 301
- Eculizumab for Atypical Hemolytic Uremic Syndrome Recurrence in Renal Transplantation
著者: 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 被引用: 259
- Cysteamine therapy delays the progression of nephropathic cystinosis in late adolescents and adults
著者: 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 被引用: 239
- Nephronophthisis
著者: Rémi Salomon, Sophie Saunier, Patrick Niaudet - Pediatric Nephrology 2008 被引用: 166
