Chantal Lagresle-Peyrou (C Lagresle)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 8

Top Venues

The Journal of experimental medicine

Blood advances

Nature medicine

INSERM

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

Affiliation History

INSERM Jan 1o 2009

France

PhD :: Clinical investigation center in biotherapy

Publications

Romane Thouenon, Loïc Chentout, Nidia Carolina Moreno-Corona, Lucie Poggi, Emilia Puig Lombardi, Bénédicte Hoareau-Coudert, Yohann Schmitt, Chantal Lagresle-Peyrou, Jacinta Bustamante, Isabelle André-Schmutz, Marina Cavazzana, Anne Durandy, Jean Laurent Casanova, Lionel Galicier, Jehane Fadlallah, Alain Fischer, Sven Kracker
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiency. The Journal of experimental medicine 220 (6) (2023)
Romane Thouenon, Loïc Chentout, Nidia Carolina Moreno-Corona, Lucie Poggi, Emilia Puig Lombardi, Bénédicte Hoareau-Coudert, Yohann Schmitt, Chantal Lagresle-Peyrou, Jacinta Bustamante, Isabelle André-Schmutz, Marina Cavazzana, Anne Durandy, Jean Laurent Casanova, Lionel Galicier, Jehane Fadlallah, Alain Fischer, Sven Kracker
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiency. The Journal of experimental medicine 220 (6) (2023)
Romane Thouenon, Loïc Chentout, Nidia Carolina Moreno-Corona, Lucie Poggi, Emilia Puig Lombardi, Bénédicte Hoareau-Coudert, Yohann Schmitt, Chantal Lagresle-Peyrou, Jacinta Bustamante, Isabelle André-Schmutz, Marina Cavazzana, Anne Durandy, Jean Laurent Casanova, Lionel Galicier, Jehane Fadlallah, Alain Fischer, Sven Kracker
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiency. The Journal of experimental medicine 220 (6) (2023)
Romane Thouenon, Loïc Chentout, Nidia Carolina Moreno-Corona, Lucie Poggi, Emilia Puig Lombardi, Bénédicte Hoareau-Coudert, Yohann Schmitt, Chantal Lagresle-Peyrou, Jacinta Bustamante, Isabelle André-Schmutz, Marina Cavazzana, Anne Durandy, Jean Laurent Casanova, Lionel Galicier, Jehane Fadlallah, Alain Fischer, Sven Kracker
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiency. The Journal of experimental medicine 220 (6) (2023)
Romane Thouenon, Loïc Chentout, Nidia Carolina Moreno-Corona, Lucie Poggi, Emilia Puig Lombardi, Bénédicte Hoareau-Coudert, Yohann Schmitt, Chantal Lagresle-Peyrou, Jacinta Bustamante, Isabelle André-Schmutz, Marina Cavazzana, Anne Durandy, Jean Laurent Casanova, Lionel Galicier, Jehane Fadlallah, Alain Fischer, Sven Kracker
A neomorphic mutation in the interferon activation domain of IRF4 causes a dominant primary immunodeficiency. The Journal of experimental medicine 220 (6) (2023)
A Magnani, M Semeraro, Frédéric Adam, C Booth, L Dupré, Emma Catherine Morris, A Gabrion, C Roudaut, D Borgel, Antoine Toubert, Emmanuel Clave, C Abdo, G Gorochov, R Petermann, M Guiot, M Miyara, D Moshous, E Magrin, A Denis, F Suarez, Chantal Lagresle-Peyrou, A M Roche, J Everett, A Trinquand, M Guisset, J Xu Bayford, S Hacein-Bey-Abina, Alexandre Kauskot, R Elfeky, C Rivat, S Abbas, H B Gaspar, Elizabeth A Macintyre, C Picard, Frederic D Bushman, A Galy, Alain Fischer, Emmanuelle Six, Adrian J Thrasher, Marina Cavazzana
Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott-Aldrich syndrome. Nature medicine 28 (1) (2022)
Ornellie Bernadin, Fouzia Amirache, Anais Girard-Gagnepain, Ranjita Devi Moirangthem, Camille Lévy, Kuiying Ma, Caroline Costa, Didier Nègre, Christian Reimann, David Fenard, Agata Cieslak, Vahid Asnafi, Hanem Sadek, Rana Mhaidly, Marina Cavazzana, Chantal Lagresle-Peyrou, François-Loïc Cosset, Isabelle André, Els Verhoeyen
Baboon envelope LVs efficiently transduced human adult, fetal, and progenitor T cells and corrected SCID-X1 T-cell deficiency. Blood advances 3 (3) (2020)
Tayebeh Soheili, Amandine Durand, Fernando E Sepulveda, Julie Rivière, Chantal Lagresle-Peyrou, Hanem Sadek, Geneviève de Saint Basile, Samia Martin, Fulvio Mavilio, Marina Cavazzana, Isabelle André-Schmutz
Gene transfer into hematopoietic stem cells reduces HLH manifestations in a murine model of Munc13-4 deficiency. Blood advances 1 (27) (2017)

Chantal Lagresle-Peyrou.css-eqlu8i{font-size:small;padding-left:4px;} (C Lagresle)

Publication Activity (10 Years)

Top Topics

Top Venues

Chantal Lagresle-Peyrou (C Lagresle)