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Christine Petit

1986–2024 年に発表

137
論文数
27,029
被引用数
101
h 指数
135
i10 指数

被引用数

Christine Petit の年別被引用数1986 年: 被引用 2 件1987 年: 被引用 8 件1988 年: 被引用 6 件1989 年: 被引用 4 件1990 年: 被引用 12 件1991 年: 被引用 17 件1992 年: 被引用 16 件1993 年: 被引用 27 件1994 年: 被引用 23 件1995 年: 被引用 37 件1996 年: 被引用 58 件1997 年: 被引用 114 件1998 年: 被引用 135 件1999 年: 被引用 166 件2000 年: 被引用 207 件2001 年: 被引用 244 件2002 年: 被引用 249 件2003 年: 被引用 254 件2004 年: 被引用 270 件2005 年: 被引用 243 件2006 年: 被引用 310 件2007 年: 被引用 258 件2008 年: 被引用 288 件2009 年: 被引用 278 件2010 年: 被引用 318 件2011 年: 被引用 299 件2012 年: 被引用 218 件2013 年: 被引用 176 件2014 年: 被引用 168 件2015 年: 被引用 165 件2016 年: 被引用 98 件2017 年: 被引用 165 件2018 年: 被引用 135 件2019 年: 被引用 500 件2020 年: 被引用 624 件2021 年: 被引用 559 件2022 年: 被引用 379 件2023 年: 被引用 298 件2024 年: 被引用 434 件2025 年: 被引用 155 件2026 年: 被引用 1 件

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 2,159 件、この内訳の 32.4%イギリス: 引用元論文 580 件、この内訳の 8.7%ドイツ: 引用元論文 505 件、この内訳の 7.6%フランス: 引用元論文 483 件、この内訳の 7.3%中国: 引用元論文 413 件、この内訳の 6.2%イタリア: 引用元論文 237 件、この内訳の 3.6%日本: 引用元論文 227 件、この内訳の 3.4%カナダ: 引用元論文 166 件、この内訳の 2.5%スペイン: 引用元論文 158 件、この内訳の 2.4%オランダ: 引用元論文 156 件、この内訳の 2.3%オーストラリア: 引用元論文 129 件、この内訳の 1.9%スイス: 引用元論文 120 件、この内訳の 1.8%
0%32.4%その他 19.9%

機関

分野

  • Biochemistry, Genetics and Molecular Biology43.5%
  • Neuroscience36.4%
  • Medicine15.8%
  • Immunology and Microbiology1.5%
  • Agricultural and Biological Sciences0.8%
  • Environmental Science0.5%
  • その他1.5%

トピック

  • Hearing, Cochlea, Tinnitus, Genetics12.6%
  • Vestibular and auditory disorders3.7%
  • Connexins and lens biology3.4%
  • Ion channel regulation and function3.2%
  • Hearing Loss and Rehabilitation3.2%
  • Retinal Development and Disorders2.2%
  • その他71.7%

共著者

全論文

検索で開く
  1. Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model

    著者: Omar Akil, Frank M. Dyka, Charlotte Calvet, Alice Emptoz, Ghizlène Lahlou, Sylvie Nouaille, Jacques Boutet de Monvel, Jean‐Pierre Hardelin, William W. Hauswirth, Paul Avan, Christine Petit, Saaïd Safieddine, Lawrence R. Lustig - National Academy of Sciences, Proceedings of the National Academy of Sciences 2019 被引用: 294

  2. Otoferlin, Defective in a Human Deafness Form, Is Essential for Exocytosis at the Auditory Ribbon Synapse

    著者: Isabelle Roux, Saaïd Safieddine, Régis Nouvian, M’hamed Grati, Marie‐Christine Simmler, Amel Bahloul, Isabelle Perfettini, Morgane Le Gall, Philippe Rostaing, Ghislaine Hamard, Antoine Triller, Paul Avan, Tobias Moser, Christine Petit - Cell 2006 被引用: 750

  3. Deafness: from genetic architecture to gene therapy

    著者: Christine Petit, Crystel Bonnet, Saaïd Safieddine - Nature Reviews Genetics 2023 被引用: 139

  4. Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies

    著者: Philippe Jean, Fabienne Wong Jun Tai, Amrit Singh‐Estivalet, Andrea Lelli, Cyril Scandola, Sébastien Megharba, Sandrine Schmutz, Solène Roux, Sabrina Méchaussier, Muriel Sudres, Enguerran Mouly, A.-C. Heritier, Crystel Bonnet, Adeline Mallet, Sophie Novault, Valentina Libri, Christine Petit, Nicolas Michalski - National Academy of Sciences, Proceedings of the National Academy of Sciences 2023 被引用: 88

  5. Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

    著者: Sedigheh Delmaghani, Francisco Castillo, Vincent Michel, Michel Leibovici, Asadollah Aghaie, Uri Ron, Lut Van Laer, Nir Ben‐Tal, Guy Van Camp, Dominique Weil, Francina Langa, Mark Lathrop, Paul Avan, Christine Petit - Nature Genetics 2006 被引用: 330

  6. Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes

    著者: Sedigheh Delmaghani, Jean Defourny, Asadollah Aghaie, Maryline Beurg, Didier Dulon, Nicolas Thelen, Isabelle Perfettini, Tibor Zelles, Máté Aller, Anaïs Meyer, Alice Emptoz, Fabrice Giraudet, Michel Leibovici, Sylvie Dartevelle, Guillaume Soubigou, Marc Thiry, E. Sylvester Vizi, Saaïd Safieddine, Jean-Pierre Hardelin, Paul Avan, Christine Petit - Cell 2015 被引用: 219

  7. Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome

    著者: Didier Dulon, Samantha Papal, Pranav Patni, Matteo Cortese, Philippe Vincent, Margot Tertrais, Alice Emptoz, Abdelaziz Tlili, Yohan Bouleau, Vincent Michel, Sedigheh Delmaghani, Alain Aghaie, Elise Pepermans, Olinda Alegria-Prévot, Omar Akil, Lawrence R. Lustig, Paul Avan, Saaïd Safieddine, Christine Petit, A. Amraoui - Journal of Clinical Investigation 2018 被引用: 138

  8. A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

    著者: Shin’ichiro Yasunaga, M’hamed Grati, Martine Cohen‐Salmon, A. Amraoui, Mirna Mustapha, Nabiha Salem, Elie El‐Zir, Jacques Loiselet, Christine Petit - Nature Genetics 1999 被引用: 585

  9. Pejvakin-mediated pexophagy protects auditory hair cells against noise-induced damage

    著者: Jean Defourny, Alain Aghaie, Isabelle Perfettini, Paul Avan, Sedigheh Delmaghani, Christine Petit - National Academy of Sciences, Proceedings of the National Academy of Sciences 2019 被引用: 116

  10. Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia

    著者: Elisa Caberlotto, Vincent Michel, Isabelle Foucher, Amel Bahloul, Richard J. Goodyear, Elise Pepermans, Nicolas Michalski, Isabelle Perfettini, Olinda Alegria-Prévot, Sébastien Chardenoux, Marcio Do Cruzeiro, Jean‐Pierre Hardelin, Guy P. Richardson, Paul Avan, Dominique Weil, Christine Petit - National Academy of Sciences, Proceedings of the National Academy of Sciences 2011 被引用: 154

  11. Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G

    著者: Alice Emptoz, Vincent Michel, Andrea Lelli, Omar Akil, Jacques Boutet de Monvel, Ghizlène Lahlou, Anaïs Meyer, Typhaine Dupont, Sylvie Nouaille, Elody Ey, Filipa França de Barros, Mathieu Beraneck, Didier Dulon, Jean‐Pierre Hardelin, Lawrence R. Lustig, Paul Avan, Christine Petit, Saaïd Safieddine - National Academy of Sciences, Proceedings of the National Academy of Sciences 2017 被引用: 138

  12. KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness

    著者: Christian Kubisch, Björn C. Schroeder, Thomas Friedrich, Björn Lütjohann, A. Amraoui, Sandrine Marlin, Christine Petit, Thomas J. Jentsch - Cell 1999 被引用: 874

  13. SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1–SIX1–DNA complexes

    著者: Rainer Ruf, Pin‐Xian Xu, Derek Silvius, Edgar A. Otto, Frank Beekmann, Ulla Muerb, Shrawan Kumar, Thomas J. Neuhaus, Markus J. Kemper, Richard M. Raymond, Patrick D. Brophy, Jennifer Berkman, Michael Gattas, V.J. Hyland, Eva-Maria Ruf, Charles E. Schwartz, Eugene H. Chang, Richard J. Smith, Constantine A. Stratakis, Dominique Weil, Christine Petit, Friedhelm Hildebrandt - National Academy of Sciences, Proceedings of the National Academy of Sciences 2004 被引用: 419

  14. Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice

    著者: Iman Sahly, Éric Dufour, Cataldo Schietroma, Vincent Michel, Amel Bahloul, Isabelle Perfettini, Elise Pepermans, Amrit Singh‐Estivalet, Diane Carette, Asadollah Aghaie, Inga Ebermann, Andrea Lelli, María Iribarne, Jean‐Pierre Hardelin, Dominique Weil, José‐Alain Sahel, A. Amraoui, Christine Petit - The Journal of Cell Biology 2012 被引用: 191

  15. Defective myosin VIIA gene responsible for Usher syndrome type IB

    著者: Dominique Well, Stéphane Blanchard, Josseline Kaplan, Parry Guilford, F A Gibson, James Walsh, Philomena Mburu, Anabel Varela, Jacqueline Levilliers, Michael D. Weston, Phillip M. Kelley, William J. Kimberling, Mariette Wagenaar, Fabienne Lévi-Acobas, Dominique Larget‐Piet, Arnold Münnich, Karen P. Steel, Steve D. M. Brown, Christine Petit - Nature 1995 被引用: 1,074

  16. Mechanotransduction is required for establishing and maintaining mature inner hair cells and regulating efferent innervation

    著者: Laura F. Corns, Stuart L. Johnson, Terri Roberts, Kishani M. Ranatunga, Aenea Hendry, Federico Ceriani, Saaïd Safieddine, Karen P. Steel, Andrew Forge, Christine Petit, David N. Furness, Corné J. Kros, Walter Marcotti - Nature Communications 2018 被引用: 90

  17. A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

    著者: Sonia Abdelhak, Vasiliki Kalatzis, Roland Heilig, Sylvie Compain, Delphine Samson, C. Vincent, Dominique Weil, Corinne Cruaud, Iman Sahly, Michel Leibovici, Maria Bitner‐Glindzicz, Mary C. Francis, Didier Lacombe, Jacqueline Vigneron, R Charachon, Katia Boven, P Bedbeder, Nicole Van Regemorter, Jean Weissenbach, Christine Petit - Nature Genetics 1997 被引用: 679

  18. Ciliary proteins link basal body polarization to planar cell polarity regulation

    著者: Chonnettia Jones, Venus C. Roper, Isabelle Foucher, Dong Qian, Boglárka Banizs, Christine Petit, Bradley K. Yoder, Ping Chen - Nature Genetics 2007 被引用: 335

  19. Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane

    著者: Elisabeth Verpy, Michel Leibovici, Nicolas Michalski, Richard J. Goodyear, Carine Houdon, Dominique Weil, Guy P. Richardson, Christine Petit - The Journal of Comparative Neurology 2010 被引用: 142

  20. Hearing Is Normal without Connexin30

    著者: Anne Boulay, Francisco Castillo, Fabrice Giraudet, Ghislaine Hamard, Christian Giaume, Christine Petit, Paul Avan, Martine Cohen‐Salmon - Journal of Neuroscience 2013 被引用: 87

  21. Cost-effectiveness of influenza vaccination with a high dose quadrivalent vaccine of the elderly population in Belgium, Finland, and Portugal

    著者: Fabián P. Alvarez, Pierre Chevalier, Matthias Borms, Hélène Bricout, Cátia Marques, Anu Soininen, T. Sainio, Christine Petit, Caroline de Courville - Journal of Medical Economics 2023 被引用: 28

  22. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

    著者: Nathalie Neyroud, Frédérique Tesson, Isabelle Denjoy, Michel Leibovici, Claire Donger, Jacques Barhanin, Sabine Fauré, Françoise Gary, P Coumel, Christine Petit, Ketty Schwartz, Pascale Guicheney - Nature Genetics 1997 被引用: 883

  23. Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

    著者: Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont, Anne De Paepe, Nathalie Le Dû, Nadia Soussi‐Yanicostas, Roney S. Coimbra, Sedigheh Delmaghani, Sylvie Compain-Nouaille, Françoise Baverel, Christophe Pécheux, Dominique Le Tessier, Corinne Cruaud, Marc Delpech, Frank Speleman, Stefan Vermeulen, Andrea Amalfitano, Y. Bachelot, Philippe Bouchard, Sylvie Cabrol, Jean‐Claude Carel, Henriette Delemarre-van de Waal, B. Goulet-Salmon, Marie‐Laure Kottler, Odile Richard, Franco Sánchez‐Franco, Robert Saura, Jacques Young, Christine Petit, Jean‐Pierre Hardelin - Nature Genetics 2003 被引用: 830

  24. Targeted Ablation of Connexin26 in the Inner Ear Epithelial Gap Junction Network Causes Hearing Impairment and Cell Death

    著者: Martine Cohen‐Salmon, Thomas Ott, Vincent Michel, Jean-Pierre Hardelin, Isabelle Perfettini, Michel Eybalin, Tao Wu, Daniel C. Marcus, Philine Wangemann, Klaus Willecke, Christine Petit - Current Biology 2002 被引用: 447