Publications by authors named "Maya Chrabieh"

Claim this Profile
H
Human LY9 governs CD4 T cell IFN-γ immunity to .
Masato Ogishi, Julia Puchan, Rui Yang, Andrés Augusto Arias, Ji Eun Han, Maya Chrabieh

Sci Immunol· May 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Impaired development of memory B cells and antibody responses in humans and mice deficient in PD-1 signaling.
Masato Ogishi, Koji Kitaoka, Kim L Good-Jacobson, Darawan Rinchai, Baihao Zhang, Maya Chrabieh

Immunity· December 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis.
Masato Ogishi, Rui Yang, Rémy Rodriguez, Dominic P Golec, Emmanuel Martin, Maya Chrabieh

J Exp Med· January 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Impaired IL-23-dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency.
Masato Ogishi, Andrés Augusto Arias, Rui Yang, Ji Eun Han, Peng Zhang, Maya Chrabieh

J Exp Med· October 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin.
András N Spaan, Anna-Lena Neehus, Emmanuel Laplantine, Frederik Staels, Masato Ogishi, Maya Chrabieh

Science· June 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.
Juan Li, Wei-Te Lei, Peng Zhang, Franck Rapaport, Yoann Seeleuthner, Maya Chrabieh

J Exp Med· November 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child.
Masato Ogishi, Rui Yang, Caner Aytekin, David Langlais, Mathieu Bourgey, Maya Chrabieh

Nat Med· September 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance.
Takaki Asano, Joëlle Khourieh, Peng Zhang, Franck Rapaport, András N Spaan, Maya Chrabieh

J Exp Med· August 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Auto-antibodies to type I IFNs can underlie adverse reactions to yellow fever live attenuated vaccine.
Paul Bastard, Eleftherios Michailidis, Hans-Heinrich Hoffmann, Marwa Chbihi, Tom Le Voyer, Maya Chrabieh

J Exp Med· April 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease.
Tom Le Voyer, Anna-Lena Neehus, Rui Yang, Masato Ogishi, Jérémie Rosain, Maya Chrabieh

Proc Natl Acad Sci U S A· April 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Systemic Type I IFN Inflammation in Human ISG15 Deficiency Leads to Necrotizing Skin Lesions.
Marta Martin-Fernandez, María Bravo García-Morato, Conor Gruber, Sara Murias Loza, Muhammad Nasir Hayat Malik, Maya Chrabieh

Cell Rep· May 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genome-wide association study of Buruli ulcer in rural Benin highlights role of two LncRNAs and the autophagy pathway.
Jeremy Manry, Quentin B Vincent, Christian Johnson, Maya Chrabieh, Lazaro Lorenzo

Commun Biol· April 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β.
Juan Li, Marco Ritelli, Cindy S Ma, Geetha Rao, Tanwir Habib, Maya Chrabieh

Sci Immunol· November 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A deep intronic splice mutation of underlies hyper IgE syndrome by negative dominance.
Joëlle Khourieh, Geetha Rao, Tanwir Habib, Danielle T Avery, Alain Lefèvre-Utile, Maya Chrabieh

Proc Natl Acad Sci U S A· August 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency.
Bertrand Boisson, Yoshitaka Honda, Masahiko Ajiro, Jacinta Bustamante, Matthieu Bendavid, Maya Chrabieh

J Clin Invest· February 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Corrigendum: IRAK4 Deficiency in a Patient with Recurrent Pneumococcal Infections: Case Report and Review of the Literature.
Karina S Gobin, Mary Hintermeyer, Bertrand Boisson, Maya Chrabieh, Pegah Ghandil

Front Pediatr· March 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
IRAK4 Deficiency in a Patient with Recurrent Pneumococcal Infections: Case Report and Review of the Literature.
Karina Gobin, Mary Hintermeyer, Bertrand Boisson, Maya Chrabieh, Pegah Ghandil

Front Pediatr· April 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Human Adaptive Immunity Rescues an Inborn Error of Innate Immunity.
Laura Israel, Ying Wang, Katarzyna Bulek, Erika Della Mina, Zhao Zhang, Maya Chrabieh

Cell· February 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Inherited human IRAK-1 deficiency selectively impairs TLR signaling in fibroblasts.
Erika Della Mina, Alessandro Borghesi, Hao Zhou, Salim Bougarn, Sabri Boughorbel, Maya Chrabieh

Proc Natl Acad Sci U S A· January 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations.
Yi Wang, Cindy S Ma, Yun Ling, Aziz Bousfiha, Yildiz Camcioglu, Maya Chrabieh

J Exp Med· October 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Proinflammatory cytokine response toward fungi but not bacteria in chronic granulomatous disease.
Roel P Gazendam, Annemarie van de Geer, John L van Hamme, Leanne Helgers, Jan Rohr, Maya Chrabieh

J Allergy Clin Immunol· September 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Heterozygous Mutations in MAP3K7, Encoding TGF-β-Activated Kinase 1, Cause Cardiospondylocarpofacial Syndrome.
Carine Le Goff, Curtis Rogers, Wilfried Le Goff, Graziella Pinto, Damien Bonnet, Maya Chrabieh

Am J Hum Genet· August 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasia.
Bertrand Boisson, Emmanuel Laplantine, Kerry Dobbs, Aurélie Cobat, Nadine Tarantino, Maya Chrabieh

J Exp Med· June 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Invasive pneumococcal disease in children can reveal a primary immunodeficiency.
Jean Gaschignard, Corinne Levy, Maya Chrabieh, Bertrand Boisson, Cécile Bost-Bru

Clin Infect Dis· July 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency.
Bertrand Boisson, Emmanuel Laplantine, Carolina Prando, Silvia Giliani, Elisabeth Israelsson, Maya Chrabieh

Nat Immunol· December 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis