Alain Hovnanian (A Hovnanian)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 10

Top Venues

Genes, chromosomes & cancer

Science (New York, N.Y.)

The Journal of experimental medicine

Journal of the European Academy of Dermatology and Venereology : JEADV

INSERM

This page only lists publications with an associated author ORCID identifier.

Affiliation History

INSERM Sep 1o 2009

France

Director :: Genetics of skin diseases

Publications

Julie Leclerc, Marie Beaumont, Roseline Vibert, Stéphane Pinson, Catherine Vermaut, Cathy Flament, Tonio Lovecchio, Lucie Delattre, Christophe Demay, Florence Coulet, Erell Guillerm, Nadim Hamzaoui, Patrick R Benusiglio, Afane Brahimi, François Cornelis, Hélène Delhomelle, Sandra Fert-Ferrer, Benjamin Philippe Fournier, Alain Hovnanian, Clémentine Legrand, Alain Lortholary, David Malka, Florence Petit, Jean-Christophe Saurin, Sophie Lejeune, Chrystelle Colas, Marie-Pierre Buisine
AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer. Genes, chromosomes & cancer 62 (4) (2022)
Julie Leclerc, Marie Beaumont, Roseline Vibert, Stéphane Pinson, Catherine Vermaut, Cathy Flament, Tonio Lovecchio, Lucie Delattre, Christophe Demay, Florence Coulet, Erell Guillerm, Nadim Hamzaoui, Patrick R Benusiglio, Afane Brahimi, François Cornelis, Hélène Delhomelle, Sandra Fert-Ferrer, Benjamin Philippe Fournier, Alain Hovnanian, Clémentine Legrand, Alain Lortholary, David Malka, Florence Petit, Jean-Christophe Saurin, Sophie Lejeune, Chrystelle Colas, Marie-Pierre Buisine
AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer. Genes, chromosomes & cancer 62 (4) (2022)
Julie Leclerc, Marie Beaumont, Roseline Vibert, Stéphane Pinson, Catherine Vermaut, Cathy Flament, Tonio Lovecchio, Lucie Delattre, Christophe Demay, Florence Coulet, Erell Guillerm, Nadim Hamzaoui, Patrick R Benusiglio, Afane Brahimi, François Cornelis, Hélène Delhomelle, Sandra Fert-Ferrer, Benjamin Philippe Fournier, Alain Hovnanian, Clémentine Legrand, Alain Lortholary, David Malka, Florence Petit, Jean-Christophe Saurin, Sophie Lejeune, Chrystelle Colas, Marie-Pierre Buisine
AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer. Genes, chromosomes & cancer (2022)
Julie Leclerc, Marie Beaumont, Roseline Vibert, Stéphane Pinson, Catherine Vermaut, Cathy Flament, Tonio Lovecchio, Lucie Delattre, Christophe Demay, Florence Coulet, Erell Guillerm, Nadim Hamzaoui, Patrick R Benusiglio, Afane Brahimi, François Cornelis, Hélène Delhomelle, Sandra Fert-Ferrer, Benjamin Philippe Fournier, Alain Hovnanian, Clémentine Legrand, Alain Lortholary, David Malka, Florence Petit, Jean-Christophe Saurin, Sophie Lejeune, Chrystelle Colas, Marie-Pierre Buisine
AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer. Genes, chromosomes & cancer 62 (4) (2022)
András N Spaan, Anna-Lena Neehus, Emmanuel Laplantine, Frederik Staels, Masato Ogishi, Yoann Seeleuthner, Franck Rapaport, Keenan A Lacey, Erika Van Nieuwenhove, Maya Chrabieh, David Hum, Mélanie Migaud, Araksya Izmiryan, Lazaro Lorenzo, Tatiana Kochetkov, Dani A C Heesterbeek, Bart W Bardoel, Ashley L DuMont, A Kerry Dobbs, Solenne Chardonnet, Søren Heissel, Timour Baslan, Peng Zhang, Jean-Laurent Casanova, Dusan Bogunovic, Herman F Wunderink, Pieter-Jan A Haas, Henrik Molina, Griet Van Buggenhout, Stanislas Lyonnet, Luigi Daniele Notarangelo, Mikko R J Seppänen, Robert Weil, Gisela Seminario, Héctor Gomez-Tello, Carine Wouters, Mehrnaz Mesdaghi, Mohammad Shahrooei, Xavier Bossuyt, Erdal Sağ, Rezan Topaloğlu, Seher Sener, Helen L Leavis, Maarten M J van Eijk, Liliana Bezrodnik, Lizbeth Blancas-Galicia, Alain Hovnanian, Aude Nassif, Brigitte Bader-Meunier, Bénédicte Neven, Isabelle Meyts, Rik Schrijvers, Anne Puel, Jacinta Bustamante, Ivona Aksentijevich, Daniel L Kastner, Victor J Torres, Stephanie Humblet-Baron, Adrian Liston, Laurent Abel, Bertrand Boisson, Jean Laurent Casanova
Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin. Science (New York, N.Y.) 376 (6599) (2022)
Vivien Béziat, Juan Li, Jian-Xin Lin, Cindy S Ma, Peng Li, Aziz Bousfiha, Isabelle Pellier, Samaneh Zoghi, Safa Baris, Sevgi Keles, Paul Gray, Ning Du, Yi Wang, Yoann Zerbib, Romain Levy, Thibaut Leclercq, Frédégonde About, Ai Ing Lim, Geetha Rao, Kathryn J Payne, Simon J Pelham, Danielle T Avery, Elissa K Deenick, Bethany Pillay, Janet Chou, Romain Guery, Aziz Belkadi, Antoine Guérin, Mélanie Migaud, Vimel Rattina, Fatima Ailal, Ibtihal Benhsaien, Matthieu Bouaziz, Tanwir Habib, Damien Chaussabel, Nico Marr, Jamel El-Benna, Bodo Grimbacher, Orli Wargon, Jacinta Bustamante, Bertrand Boisson, Ingrid Müller-Fleckenstein, Bernhard Fleckenstein, Marie-Olivia Chandesris, Matthias Titeux, Sylvie Fraitag, Marie-Alexandra Alyanakian, Marianne Leruez-Ville, Capucine Picard, Isabelle Meyts, James P Di Santo, Alain Hovnanian, Ayper Somer, Ahmet Ozen, Nima Rezaei, Talal A Chatila, Laurent Abel, Warren J Leonard, Stuart G Tangye, Anne Puel, Jean Laurent Casanova
A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity. Science immunology 3 (24) (2019)
Sophie Leducq, S Duchatelet, J Zaragoza, Sarah Ventejou, A de Muret, S Eymieux, Emmanuelle Blanchard, Laurent Machet, Alain Hovnanian, Kervarrec Thibault
A previously unreported frameshift ATP2C1 mutation in a generalized Hailey-Hailey disease. Journal of the European Academy of Dermatology and Venereology : JEADV 34 (3) (2019)
S Gaucher, Su M Lwin, Matthias Titeux, A Abdul-Wahab, N Pironon, Araksya Izmiryan, S Miskinyte, C Ganier, S Duchatelet, Jemima E Mellerio, E Bourrat, John A McGrath, Alain Hovnanian
EBGene trial: patient preselection outcomes for the European GENEGRAFT ex vivo phase I/II gene therapy trial for recessive dystrophic epidermolysis bullosa. The British journal of dermatology 182 (3) (2019)
Raymond J Cho, Ludmil B Alexandrov, Nicoline Y den Breems, Velina S Atanasova, Mehdi Farshchian, Elizabeth Purdom, Tran N Nguyen, Cristian Coarfa, Kimal I Rajapakshe, Marco Prisco, Joya Sahu, Patrick T Tassone, Evan J Greenawalt, Eric A Collisson, Wei Wu, Hui Yao, Xiaoping Su, Christina Guttmann-Gruber, Josefina Piñón Hofbauer, Raabia Hashmi, Ignacia Fuentes, Stephen Charles Benz, Justin Golovato, Erik A Ehli, Christel M Davis, Gareth E Davies, Kyle R Covington, Dedee Frances Murrell, Julio Cesar Salas-Alanis, Francis Palisson, Anna L Bruckner, William Robinson, Cristina Has, Leena Bruckner-Tuderman, Matthias Titeux, Marcel F Jonkman, Elham Rashidghamat, Su M Lwin, Jemima E Mellerio, John A McGrath, Johann W Bauer, Alain Hovnanian, Kenneth Y Tsai, Andrew P South
APOBEC mutation drives early-onset squamous cell carcinomas in recessive dystrophic epidermolysis bullosa. Science translational medicine 10 (455) (2019)
Lucia Pattarini, Coline Trichot, Sofia Bogiatzi, Maximilien Grandclaudon, Stephan Meller, Zela Keuylian, Melanie Durand, Elisabetta Volpe, Stefania Madonna, Andrea Cavani, Andrea Chiricozzi, Marco Romanelli, Toshiyuki Hori, Alain Hovnanian, Bernhard Homey, Vassili Soumelis
TSLP-activated dendritic cells induce human T follicular helper cell differentiation through OX40-ligand. The Journal of experimental medicine 214 (5) (2017)

Alain Hovnanian.css-eqlu8i{font-size:small;padding-left:4px;} (A Hovnanian)

Publication Activity (10 Years)

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Top Venues

Alain Hovnanian (A Hovnanian)