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Michel Vidaud

Active 1986–2024

104
Papers
19,612
Citations
85
h-index
103
i10-index

Citations

Citations per year for Michel Vidaud1978: 1 citations1983: 1 citations1986: 1 citations1988: 4 citations1989: 10 citations1990: 11 citations1991: 12 citations1992: 27 citations1993: 13 citations1994: 16 citations1995: 25 citations1996: 21 citations1997: 33 citations1998: 43 citations1999: 52 citations2000: 90 citations2001: 135 citations2002: 174 citations2003: 209 citations2004: 235 citations2005: 175 citations2006: 187 citations2007: 171 citations2008: 160 citations2009: 163 citations2010: 239 citations2011: 242 citations2012: 200 citations2013: 177 citations2014: 177 citations2015: 173 citations2016: 173 citations2017: 129 citations2018: 104 citations2019: 356 citations2020: 334 citations2021: 328 citations2022: 200 citations2023: 146 citations2024: 224 citations2025: 94 citations2026: 2 citations1979–1982: no citations, so these years are not shown1984–1985: no citations, so these years are not shown1987: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 1,883 citing papers, 25.5% of this breakdownFrance: 809 citing papers, 11% of this breakdownChina: 488 citing papers, 6.6% of this breakdownUnited Kingdom: 474 citing papers, 6.4% of this breakdownGermany: 458 citing papers, 6.2% of this breakdownItaly: 392 citing papers, 5.3% of this breakdownCanada: 257 citing papers, 3.5% of this breakdownNetherlands: 241 citing papers, 3.3% of this breakdownSpain: 210 citing papers, 2.8% of this breakdownJapan: 209 citing papers, 2.8% of this breakdownAustralia: 204 citing papers, 2.8% of this breakdownSwitzerland: 145 citing papers, 2% of this breakdown
0%25.5%Other 21.8%

Institutions

Fields

  • Medicine54.6%
  • Biochemistry, Genetics and Molecular Biology34.2%
  • Immunology and Microbiology5.9%
  • Agricultural and Biological Sciences2%
  • Neuroscience1.6%
  • Environmental Science0.4%
  • Other1.3%

Topics

  • Liver Disease Diagnosis and Treatment5.2%
  • Hepatitis C virus research4.8%
  • Hepatitis B Virus Studies2.7%
  • Cancer-related molecular mechanisms research2.6%
  • RNA modifications and cancer2.5%
  • Neurofibromatosis and Schwannoma Cases1.9%
  • Other80.3%

Coauthors

All papers

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  1. Hematopoietic Stem Cell Gene Therapy with a Lentiviral Vector in X-Linked Adrenoleukodystrophy

    Authors: Nathalie Cartier, Salima Hacein‐Bey‐Abina, Cynthia C. Bartholomae, Gábor Veres, Manfred Schmidt, Ina Kutschera, Michel Vidaud, Ulrich Abel, Liliane Dal‐Cortivo, Laure Caccavelli, Nizar Mahlaoui, Véronique Kiermer, Denice Mittelstaedt, Céline Bellesme, Najiba Lahlou, François Lefrère, Stéphane Blanche, Muriel Audit, Emmanuel Payen, Philippe Leboulch, Bruno L’Homme, Pierre Bougnères, Christof von Kalle, Alain Fischer, Marina Cavazzana, Patrick Aubourg - Science 2009 cited by 1,515

  2. CYP46A1 inhibition, brain cholesterol accumulation and neurodegeneration pave the way for Alzheimer’s disease

    Authors: Fathia Djelti, Jérôme Braudeau, Eloïse Hudry, Marc Dhénain, Jennifer Varin, Ivan Bièche, Catherine Marquer, Farah Chali, Sophie Ayciriex, Nicolas Auzeil, Sandro Alves, Dominique Langui, Marie‐Claude Potier, Olivier Laprévôte, Michel Vidaud, Charles Duyckaerts, Richard Miles, Patrick Aubourg, Nathalie Cartier - Brain 2015 cited by 221

  3. PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapies

    Authors: Thomas De Raedt, Eline Beert, Éric Pasmant, Armelle Luscan, Hilde Brems, Nicolás Ortonne, Kristian Helin, Jason L. Hornick, Victor Mautner, Hildegard Kehrer‐Sawatzki, Wade Clapp, James E. Bradner, Michel Vidaud, Meena Upadhyaya, Eric Legius, Karen Cichowski - Nature 2014 cited by 469

  4. Prospective head-to-head comparison of non-invasive scores for diagnosis of fibrotic MASH in patients with type 2 diabetes

    Authors: Laurent Castéra, Philippe Garteiser, Cédric Laouenan, Tiphaine Vidal-Trécan, Anaïs Vallet‐Pichard, Pauline Manchon, Valérie Paradis, Sébastien Czernichow, Dominique Roulot, Étienne Larger, Stanislas Pol, Pierre Bédossa, Jean-Michel Corréas, Dominique Valla, Jean–François Gautier, Bernard E. Van Beers, Djamila Bellili, Ouarda Bessadi, Charlène Da Silveira, Fatima Zohra Djelouat, Benoît Girard, Vanessa Legrand, N. Neveux, Meriam Meziani, Ludovic Roy, Dahia Sekour, Manon Sens, Miassa Slimani, Ouassila Zatout, Delphine Bachelet, Krishna Bhavsar, Basma Basli-Baillet Jimmy Mullaert, Estelle Marcault, Nassima Si-Mohammed, Emmanuel Cosson, Miguel Albuquerque, Sabrina Doblas, Adel Hammoutène, Estefania Gonzalez Montpetit, Gwenaël Pagé, Béatrice Parfait, Catherine Postic, Agnès Lehuen, Amine Toubal, Camille Rousseau, Blandine Fruchet, Pauline Soulard, Zouriatou Gouda, Michel Vidaud, Franck Letourneur, Gilles Renault, Raphaël Scharfmann, Amel Ait-Boudaoud, Charles Barsamian, Claire Carette, Claire Rives‐Lange, R. Baida, Olivier Couture, Sofiane Decombas, Thomas Deffieux, Thu-Mai Nguyen, Mickaël Tanter, Tania Baltauss, Edwige-Ludiwyne Balzac, Pierre Barbier Saint Hilaire, Philippe Delerive, Valérie Duvivier, Arnaud Fillon, Julia Geronimi, Jessica Laplume, Erwan Werner, Laura Xuereb, Robin Liechti, Olivier Martin, Florence Mehl, Manuela Pruess, Jean-Marie Castille, Fabienne Drane, Olivier Deckmyn, Florence Castelli, B Cousin, François Fenaille, Laure Guilbaud, Allyre Lohier, Francois Chambellin, Lyddie Laaland, Catherine Clusel, Marie Hauduroy, Pierre Pautre - Journal of Hepatology 2024 cited by 45

  5. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

    Authors: Daniela Matuozzo, Estelle Talouarn, Astrid Marchal, Peng Zhang, Jérémy Manry, Yoann Seeleuthner, Yu Zhang, Alexandre Bolze, Matthieu Chaldebas, Baptiste Milisavljevic, Adrian Gervais, Paul Bastard, Takaki Asano, Lucy Bizien, Federica Barzaghi, Hassan Abolhassani, Ahmad Abou Tayoun, Alessandro Aiuti, Ilad Alavi Darazam, Luis M. Allende, Rebeca Alonso‐Arias, Andrés A. Arias, Gökhan Aytekіn, Peter Bergman, Simone Bondesan, Yenan T. Bryceson, Ingrid G. Bustos, Óscar Cabrera-Marante, Sheila Cárcel, Paola Carrera, Giorgio Casari, Khalil Chaïbi, Roger Colobrán, Antônio Condino‐Neto, Laura Covill, Ottavia M. Delmonte, Loubna El Zein, Carlos Flores, Peter K. Gregersen, Marta Gut, Filomeen Haerynck, Rabih Halwani, Selda Hançerli, Lennart Hammarström, Nevin Hatipoğlu, Adem Karbuz, Sevgi Keleş, Christèle Kyheng, Rafael León‐López, José Luis Franco, Davood Mansouri, Javier Martínez‐Picado, Özge Metin Akcan, Isabelle Migeotte, Pierre‐Emmanuel Morange, Guillaume Morelle, Andrea Martín-Nalda, Giuseppe Novelli, Antonio Novelli, Tayfun Özçelık, Figen Palabıyık, Qiang Pan‐Hammarström, Rebeca Pérez de Diego, Laura Planas‐Serra, Daniel E. Pleguezuelo, Carolina Prando, Aurora Pujol, Luis Felipe Reyes, Jacques G. Rivière, Carlos Rodríguez‐Gallego, Julián Rojas, Patrizia Rovere–Querini, Agatha Schlüter, Mohammad Shahrooei, Ali Sobh, Pere Soler‐Palacín, Yacine Tandjaoui-Lambiotte, Imran Tipu, Cristina Tresoldi, Jesús Troya, Diederik van de Beek, Mayana Zatz, Paweł Zawadzki, Saleh Zaid Al-Muhsen, Mohammed F. Alosaimi, Fahad Alsohime, Hagit Baris Feldman, Manish J. Butte, Stefan N. Constantinescu, Megan A. Cooper, Clifton L. Dalgard, Jacques Fellay, James R. Heath, YL Lau, Richard P. Lifton, Tom Maniatis, Trine H. Mogensen, Horst von Bernuth, Alban Lermine, Michel Vidaud and 1,410 more - Genome Medicine 2023 cited by 77

  6. OTX008, a selective small-molecule inhibitor of galectin-1, downregulates cancer cell proliferation, invasion and tumour angiogenesis

    Authors: Lucile Astorgues‐Xerri, María E. Riveiro, Annemilaï Tijeras‐Raballand, Maria Serova, Gabriel A. Rabinovich, Ivan Bièche, Michel Vidaud, Armand de Gramont, Mathieu Martinet, Esteban Cvitkovic, Sandrine Faivre, Éric Raymond - European Journal of Cancer 2014 cited by 137

  7. High glucose and hyperinsulinemia stimulate connective tissue growth factor expression: A potential mechanism involved in progression to fibrosis in nonalcoholic steatohepatitis

    Authors: Valérie Paradis, Gabriel Perlemuter, Franck Bonvoust, Delphine Dargère, Béatrice Parfait, Michel Vidaud, Marc Conti, Stéphane Huet, Nathalie Bâ, Catherine Buffet, Pierre Bédossa - Hepatology 2001 cited by 542

  8. Characterization of a Germ-Line Deletion, Including the Entire INK4/ARF Locus, in a Melanoma-Neural System Tumor Family: Identification of ANRIL , an Antisense Noncoding RNA Whose Expression Coclusters with ARF

    Authors: Éric Pasmant, Ingrid Laurendeau, Delphine Héron, Michel Vidaud, Dominique Vidaud, Ivan Bièche - Cancer Research 2007 cited by 614

  9. Direct Involvement of HERV-W Env Glycoprotein in Human Trophoblast Cell Fusion and Differentiation

    Authors: Jean‐Louis Frendo, Delphine Olivier, Valérie Cheynet, Jean-Luc Blond, Olivier Bouton, Michel Vidaud, M Rabreau, Danièle Evain‐Brion, François Mallet - Molecular and Cellular Biology 2003 cited by 429

  10. NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype

    Authors: Éric Pasmant, Audrey Sabbagh, Gill Spurlock, Ingrid Laurendeau, Elisa Grillo, Marie-José Hamel, Ludovic Martin, S. Barbarot, Bruno Leheup, Diana Rodriguez, Didier Lacombe, Hélène Dollfus, Laurent Pasquier, Bertrand Isidor, S. Ferkal, Jean Soulier, Marc Sanson, Anne Dieux‐Coëslier, Ivan Bièche, Béatrice Parfait, Michel Vidaud, P. Wolkenstein, Meena Upadhyaya, Dominique Vidaud - Human Mutation 2010 cited by 241

  11. NF1 Molecular Characterization and Neurofibromatosis Type I Genotype-Phenotype Correlation: The French Experience

    Authors: Audrey Sabbagh, Éric Pasmant, Apolline Imbard, Armelle Luscan, Magali Soares, Hélène Blanché, Ingrid Laurendeau, S. Ferkal, Michel Vidaud, S. Pinson, Christine Bellanné‐Chantelot, Dominique Vidaud, the members of the NF France Network, Béatrice Parfait, P. Wolkenstein - Human Mutation 2013 cited by 175

  12. Insulin Resistance in Chronic Hepatitis C: Association With Genotypes 1 and 4, Serum HCV RNA Level, and Liver Fibrosis

    Authors: Rami Moucari, Tarik Asselah, Dominique Cazals‐Hatem, Hélène Voitot, Nathalie Boyer, Marie–Pierre Ripault, Rodolphe Sobesky, Michèle Martinot‐Peignoux, Sarah Maylin, Marie–Hélène Nicolas–Chanoine, Valérie Paradis, Michel Vidaud, Dominique Valla, Pierre Bédossa, Patrick Marcellin - Gastroenterology 2007 cited by 543

  13. Mutations in SETD2 cause a novel overgrowth condition

    Authors: Armelle Luscan, Ingrid Laurendeau, Valérie Malan, Christine Francannet, Sylvie Odent, Fabienne Giuliano, Didier Lacombe, Renaud Touraine, Michel Vidaud, Éric Pasmant, Valérie Cormier‐Daire - Journal of Medical Genetics 2014 cited by 145

  14. EZH1/2 function mostly within canonical PRC2 and exhibit proliferation-dependent redundancy that shapes mutational signatures in cancer

    Authors: Michel Wassef, Armelle Luscan, Setareh Aflaki, Dina Zielinski, Pascal W.T.C. Jansen, H. Irem Baymaz, Aude Battistella, Carole Kersouani, Nicolas Servant, Margaret R. Wallace, P. Romero, Olivier Kosmider, Pierre‐Alexandre Just, Mikaël Hivelin, Sébastien Jacques, Anne Vincent‐Salomon, Michiel Vermeulen, Michel Vidaud, Éric Pasmant, Raphaël Margueron - National Academy of Sciences, Proceedings of the National Academy of Sciences 2019 cited by 68

  15. Severe Phenotype in Patients with Large Deletions of NF1

    Authors: Laurence Pacot, Dominique Vidaud, Audrey Sabbagh, Ingrid Laurendeau, Audrey Briand‐Suleau, Audrey Coustier, Théodora Maillard, Cécile Barbance, Fanny Morice‐Picard, Sabine Sigaudy, Olga O. Glazunova, Léna Damaj, Valérie Layet, Chloé Quēlin, Brigitte Gilbert‐Dussardier, Frédérique Audic, Hélène Dollfus, Anne‐Marie Guerrot, James Lespinasse, Sophie Julia, Marie‐Christine Vantyghem, Magali Drouard, Marilyn Lackmy, Bruno Leheup, Yves Alembik, Alexia Lemaire, Patrick Nitschké, Florence Petit, Anne Dieux Coeslier, Eugénie Mutez, Alain Taı̈eb, Mélanie Fradin, Yline Capri, Hala Nasser, Lyse Ruaud, Benjamin Dauriat, Sylvie Bourthoumieu, David Geneviève, Séverine Audebert‐Bellanger, Mathilde Nizon, Radka Stoeva, G. Hickman, Gaël Nicolas, J. Mazereeuw‐Hautier, A. Jannic, S. Ferkal, Béatrice Parfait, Michel Vidaud, members of the NF France Network, P. Wolkenstein, Éric Pasmant - Cancers 2021 cited by 39

  16. Characterization of Human Villous and Extravillous Trophoblasts Isolated from First Trimester Placenta

    Authors: Anne Couturier‐Tarrade, René Lai Kuen, André Malassiné, Viviane Tricottet, P. L. Blain, Michel Vidaud, Danièle Evain‐Brion - Laboratory Investigation 2001 cited by 255

  17. Neurofibromatosis type 1: from genotype to phenotype

    Authors: Éric Pasmant, Michel Vidaud, Dominique Vidaud, P. Wolkenstein - Journal of Medical Genetics 2012 cited by 163

  18. Interleukin-25: a cytokine linking eosinophils and adaptive immunity in Churg-Strauss syndrome

    Authors: Benjamin Terrier, Ivan Bièche, Thierry Maisonobe, Ingrid Laurendeau, Michèlle Rosenzwajg, Jean‐Emmanuel Kahn, Marie‐Claude Diemert, Lucile Musset, Michel Vidaud, D. Sène, N. Costedoat‐Chalumeau, Du Le Thi-Huong, Zahir Amoura, David Klatzmann, P. Cacoub, David Saadoun - Blood 2010 cited by 146

  19. PPARγ/RXRα Heterodimers Are Involved in Human CGβ Synthesis and Human Trophoblast Differentiation

    Authors: Anne Couturier‐Tarrade, Kristina Schoonjans, Jean Guibourdenche, Jean Michel Bidart, Michel Vidaud, Johan Auwerx, Cécile Rochette‐Egly, Danièle Evain‐Brion - Endocrinology 2001 cited by 146

  20. PAR-1 Activation on Human Late Endothelial Progenitor Cells Enhances Angiogenesis In Vitro With Upregulation of the SDF-1/CXCR4 System

    Authors: David M. Smadja, Ivan Bièche, Georges Uzan, Heidi Bompais, Laurent Muller, Catherine Boisson‐Vidal, Michel Vidaud, Martine Aiach, Pascale Gaussem - Arteriosclerosis Thrombosis and Vascular Biology 2005 cited by 128

  21. In vivo hepatic endoplasmic reticulum stress in patients with chronic hepatitis C

    Authors: Tarik Asselah, Ivan Bièche, Abdellah Mansouri, Ingrid Laurendeau, Dominique Cazals‐Hatem, Gérard Feldmann, Pierre Bédossa, Valérie Paradis, Michelle Martinot‐Peignoux, Didier Lebrec, Cécile Guichard, Éric Ogier‐Denis, Michel Vidaud, Z. Tellier, Vassili Soumelis, Patrick Marcellin, Richard Moreau - The Journal of Pathology 2010 cited by 124

  22. Loss of SMARCE1 expression is a specific diagnostic marker of clear cell meningioma: a comprehensive immunophenotypical and molecular analysis

    Authors: Arnault Tauziède‐Espariat, Béatrice Parfait, Aurore Besnard, Joëlle Lacombe, Johan Pallud, Sanaa Tazi, Stéphanie Puget, Guillaume Lot, Benoît Terris, Joëlle Cohen, Michel Vidaud, Dominique Figarella‐Branger, Franck Monnien, Marc Polivka, Homa Adle‐Biassette, Pascale Varlet - Brain Pathology 2017 cited by 78

  23. Neurofibromatosis type 1 molecular diagnosis: what can NGS do for you when you have a large gene with loss of function mutations?

    Authors: Éric Pasmant, Béatrice Parfait, Armelle Luscan, P. Goussard, Audrey Briand‐Suleau, Ingrid Laurendeau, Corinne Fouveaut, Chrystel Leroy, Annelore Montadert, P. Wolkenstein, Michel Vidaud, Dominique Vidaud - European Journal of Human Genetics 2014 cited by 121

  24. Bone Morphogenetic Proteins 2 and 4 Are Selectively Expressed by Late Outgrowth Endothelial Progenitor Cells and Promote Neoangiogenesis

    Authors: David M. Smadja, Ivan Bièche, Jean‐Sébastien Silvestre, Stéphane Germain, Adeline Cornet, Ingrid Laurendeau, Jean-Paul Duong-Van-Huyen, Joseph Emmerich, Michel Vidaud, Martine Aiach, Pascale Gaussem - Arteriosclerosis Thrombosis and Vascular Biology 2008 cited by 113