M
Matthieu Bouaziz
Researcher at University of Paris
Publications - 17
Citations - 558
Matthieu Bouaziz is an academic researcher from University of Paris. The author has contributed to research in topics: Population stratification & Sample size determination. The author has an hindex of 6, co-authored 17 publications receiving 361 citations. Previous affiliations of Matthieu Bouaziz include French Institute of Health and Medical Research & Paris Descartes University.
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Journal ArticleDOI
Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant
Stéphanie Boisson-Dupuis,Stéphanie Boisson-Dupuis,Stéphanie Boisson-Dupuis,Noé Ramírez-Alejo,Zhi Li,Zhi Li,Etienne Patin,Etienne Patin,Geetha Rao,Gaspard Kerner,Gaspard Kerner,Che Kang Lim,Che Kang Lim,Dimitry N. Krementsov,Nicholas Hernandez,Cindy S. Ma,Cindy S. Ma,Qian Zhang,Qian Zhang,Janet Markle,Rubén Martínez-Barricarte,Kathryn Payne,Robert Fisch,Caroline Deswarte,Caroline Deswarte,Joshua Halpern,Matthieu Bouaziz,Matthieu Bouaziz,Jeanette Mulwa,Durga Sivanesan,Durga Sivanesan,Tomi Lazarov,Rodrigo Naves,Patricia García,Yuval Itan,Yuval Itan,Bertrand Boisson,Bertrand Boisson,Bertrand Boisson,Alix Checchi,Alix Checchi,Fabienne Jabot-Hanin,Fabienne Jabot-Hanin,Aurélie Cobat,Aurélie Cobat,Andrea Guennoun,Carolyn C. Jackson,Carolyn C. Jackson,Sevgi Pekcan,Zafer Caliskaner,Jaime Inostroza,Beatriz Tavares Costa-Carvalho,Jose Antonio Tavares de Albuquerque,Humberto García-Ortiz,Lorena Orozco,Tayfun Ozcelik,Ahmed Abid,Ismail Abderahmani Rhorfi,Hicham Souhi,Hicham Naji Amrani,Adil Zegmout,Frederic Geissmann,Stephen W. Michnick,Ingrid Müller-Fleckenstein,Bernhard Fleckenstein,Anne Puel,Anne Puel,Anne Puel,Michael J. Ciancanelli,Nico Marr,Hassan Abolhassani,Hassan Abolhassani,María Elvira Balcells,Antonio Condino-Neto,Alexis Strickler,Katia Abarca,Cory Teuscher,Hans D. Ochs,Ismail Reisli,Esra Hazar Sayar,Jamila El-Baghdadi,Jacinta Bustamante,Lennart Hammarström,Lennart Hammarström,Lennart Hammarström,Stuart G. Tangye,Stuart G. Tangye,Sandra Pellegrini,Sandra Pellegrini,Lluis Quintana-Murci,Lluis Quintana-Murci,Laurent Abel,Laurent Abel,Laurent Abel,Jean-Laurent Casanova +94 more
TL;DR: Homozygosity for the catalytically inactive P1104A missense variant of the TYK2 Janus kinase selectively disrupts the induction of IFN-γ by IL-23 and is a common monogenic etiology of tuberculosis.
Journal ArticleDOI
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity
Vivien Béziat,Vivien Béziat,Juan Li,Jian-Xin Lin,Cindy S. Ma,Cindy S. Ma,Peng Li,Aziz Bousfiha,Isabelle Pellier,Samaneh Zoghi,Samaneh Zoghi,Safa Baris,Sevgi Keles,Paul Gray,Paul Gray,Ning Du,Yi Wang,Yi Wang,Yoann Zerbib,Yoann Zerbib,Romain Lévy,Romain Lévy,Thibaut Leclercq,Thibaut Leclercq,Frédégonde About,Frédégonde About,Ai Ing Lim,Ai Ing Lim,Geetha Rao,Kathryn Payne,Simon J. Pelham,Simon J. Pelham,Danielle T. Avery,Elissa K. Deenick,Elissa K. Deenick,Bethany Pillay,Bethany Pillay,Janet Chou,Janet Chou,Romain Guery,Romain Guery,Aziz Belkadi,Aziz Belkadi,Antoine Guérin,Antoine Guérin,Mélanie Migaud,Mélanie Migaud,Vimel Rattina,Vimel Rattina,Fatima Ailal,Ibtihal Benhsaien,Matthieu Bouaziz,Matthieu Bouaziz,Tanwir Habib,Damien Chaussabel,Nico Marr,Jamel El-Benna,Bodo Grimbacher,Orli Wargon,Jacinta Bustamante,Bertrand Boisson,Bertrand Boisson,Bertrand Boisson,Ingrid Müller-Fleckenstein,Bernhard Fleckenstein,Marie-Olivia Chandesris,Matthias Titeux,Matthias Titeux,Sylvie Fraitag,Marie-Alexandra Alyanakian,Marianne Leruez-Ville,Capucine Picard,Isabelle Meyts,James P. Di Santo,James P. Di Santo,Alain Hovnanian,Alain Hovnanian,Ayper Somer,Ahmet Ozen,Nima Rezaei,Nima Rezaei,Talal A. Chatila,Talal A. Chatila,Laurent Abel,Laurent Abel,Laurent Abel,Warren J. Leonard,Stuart G. Tangye,Stuart G. Tangye,Anne Puel,Anne Puel,Anne Puel,Jean-Laurent Casanova +92 more
TL;DR: Patients with an autosomal recessive form of HIES due to loss-of-function mutations of a previously uncharacterized gene, ZNF341 are described, revealing a Previously unappreciated layer of transcriptional regulation controlling JAK-STAT signaling.
Journal ArticleDOI
Inherited p40phox deficiency differs from classic chronic granulomatous disease
Annemarie van de Geer,Alejandro Nieto-Patlán,Alejandro Nieto-Patlán,Alejandro Nieto-Patlán,Douglas B. Kuhns,Anton T.J. Tool,Andrés Augusto Arias,Matthieu Bouaziz,Matthieu Bouaziz,Martin de Boer,José Luis Franco,Roel P. Gazendam,John L. van Hamme,Michel van Houdt,Karin van Leeuwen,Paul Verkuijlen,Timo K. van den Berg,Timo K. van den Berg,Juan F. Alzate,Carlos Andrés Arango-Franco,Vritika Batura,Andrea Bernasconi,Barbara Boardman,Claire Booth,Siobhan O. Burns,Siobhan O. Burns,Felipe Cabarcas,Felipe Cabarcas,Nadine Cerf–Bensussan,Nadine Cerf–Bensussan,Fabienne Charbit-Henrion,Anniek Corveleyn,Caroline Deswarte,Caroline Deswarte,María Esnaola Azcoiti,María Esnaola Azcoiti,Dirk Foell,John I. Gallin,Carlos Garcés,Margarida Guedes,Claas Hinze,Steven M. Holland,Stephen M. Hughes,Patricio Ibañez,Harry L. Malech,Isabelle Meyts,Marcela Moncada-Vélez,Kunihiko Moriya,Kunihiko Moriya,Esmeralda Neves,Matías Oleastro,Laura Perez,Vimel Rattina,Vimel Rattina,Carmen Oleaga-Quintas,Carmen Oleaga-Quintas,Neil Warner,Aleixo M. Muise,Jeanet Serafín López,Eunice Trindade,Júlia Vasconcelos,Severine Vermeire,Helmut Wittkowski,Austen Worth,Laurent Abel,Laurent Abel,Laurent Abel,Mary C. Dinauer,Peter D. Arkwright,Dirk Roos,Jean-Laurent Casanova,Taco W. Kuijpers,Taco W. Kuijpers,Jacinta Bustamante,Jacinta Bustamante +74 more
TL;DR: In inherited p40phox deficiency underlies a distinctive condition, resembling a mild, atypical form of CGD, which suffers from hyperinflammation and peripheral infections, but does not have any of the invasive bacterial or fungal infections seen in CGD.
Journal ArticleDOI
The human CIB1-EVER1-EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses.
Sarah Jill De Jong,Amandine Crequer,Irina Matos,David Hum,Vignesh Gunasekharan,Lazaro Lorenzo,Lazaro Lorenzo,Fabienne Jabot-Hanin,Fabienne Jabot-Hanin,E. Imahorn,Andrés Augusto Arias,Hassan Vahidnezhad,Hassan Vahidnezhad,Leila Youssefian,Leila Youssefian,Janet Markle,Etienne Patin,Aurelia D’Amico,Claire Q.F. Wang,Florian Full,Armin Ensser,Tina M. Leisner,Leslie V. Parise,Matthieu Bouaziz,Matthieu Bouaziz,Nataly Portilla Maya,Xavier Rueda Cadena,Bayaki Saka,Amir Hossein Saeidian,Nessa Aghazadeh,Sirous Zeinali,Peter Itin,James G. Krueger,Lou Laimins,Laurent Abel,Laurent Abel,Laurent Abel,Elaine Fuchs,Jouni Uitto,José Luis Franco,Bettina Burger,Gérard Orth,Emmanuelle Jouanguy,Emmanuelle Jouanguy,Emmanuelle Jouanguy,Jean-Laurent Casanova +45 more
TL;DR: It is suggested that the disruption of CIB1-EVER1–EVER2-dependent keratinocyte-intrinsic immunity underlies the selective susceptibility to &bgr;-HPVs of EV patients.
Journal ArticleDOI
IRF4 haploinsufficiency in a family with Whipple’s disease
Antoine Guérin,Antoine Guérin,Gaspard Kerner,Gaspard Kerner,Nico Marr,Janet Markle,Florence Fenollar,Natalie Wong,Natalie Wong,Sabri Boughorbel,Danielle T. Avery,Danielle T. Avery,Cindy S. Ma,Cindy S. Ma,Salim Bougarn,Matthieu Bouaziz,Matthieu Bouaziz,Vivien Béziat,Vivien Béziat,Erika Della Mina,Erika Della Mina,Carmen Oleaga-Quintas,Carmen Oleaga-Quintas,Tomi Lazarov,Lisa Worley,Lisa Worley,Tina Nguyen,Tina Nguyen,Etienne Patin,Etienne Patin,Caroline Deswarte,Caroline Deswarte,Rubén Martínez-Barricarte,Soraya Boucherit,Soraya Boucherit,Xavier Ayral,Sophie Edouard,Stéphanie Boisson-Dupuis,Stéphanie Boisson-Dupuis,Stéphanie Boisson-Dupuis,Vimel Rattina,Vimel Rattina,Benedetta Bigio,Guillaume Vogt,Frederic Geissmann,Frederic Geissmann,Lluis Quintana-Murci,Lluis Quintana-Murci,Damien Chaussabel,Stuart G. Tangye,Stuart G. Tangye,Didier Raoult,Laurent Abel,Laurent Abel,Laurent Abel,Jacinta Bustamante,Jean-Laurent Casanova +56 more
TL;DR: It is found that IRF4 had evolved under purifying selection, and can underlie WD by haploinsufficiency, with age-dependent incomplete penetrance.