Maya Chrabieh

Inserm — France

Immunology and Microbiology · Life Sciences

33h-index11.6kcitations44works11.52yr avg
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Research Topics

Immunodeficiency and Autoimmune Disorders(24), Immune Response and Inflammation(13), Immune Cell Function and Interaction(9), NF-κB Signaling Pathways(9), T-cell and B-cell Immunology(7)

Publications42 total

Human LY9 governs CD4 <sup>+</sup> T cell IFN-γ immunity to <i>Mycobacterium tuberculosis</i>
Science Immunology·2025· 6 citedOpen Access
Impaired development of memory B cells and antibody responses in humans and mice deficient in PD-1 signaling
Immunity·2024· 17 citedOpen Access
Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis
The Journal of Experimental Medicine·2022· 24 citedOpen Access
Impaired IL-23–dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency
The Journal of Experimental Medicine·2022· 61 citedOpen Access
Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin
Science·2022· 59 citedOpen Access
Biochemically deleterious human <i>NFKB1</i> variants underlie an autosomal dominant form of common variable immunodeficiency
The Journal of Experimental Medicine·2021· 52 citedOpen Access
Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child
Nature Medicine·2021· 104 citedOpen Access
Human <i>STAT3</i> variants underlie autosomal dominant hyper-IgE syndrome by negative dominance
The Journal of Experimental Medicine·2021· 59 citedOpen Access
Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease
Proceedings of the National Academy of Sciences·2021· 81 citedOpen Access
Auto-antibodies to type I IFNs can underlie adverse reactions to yellow fever live attenuated vaccine
The Journal of Experimental Medicine·2021· 224 citedOpen Access
Systemic Type I IFN Inflammation in Human ISG15 Deficiency Leads to Necrotizing Skin Lesions
Cell Reports·2020· 78 citedOpen Access
Genome-wide association study of Buruli ulcer in rural Benin highlights role of two LncRNAs and the autophagy pathway
Communications Biology·2020· 20 citedOpen Access
Genome-wide association study of Buruli ulcer in rural Benin
2019Open Access
Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β
Science Immunology·2019· 51 citedOpen Access
A deep intronic splice mutation of <i>STAT3</i> underlies hyper IgE syndrome by negative dominance
Proceedings of the National Academy of Sciences·2019· 29 citedOpen Access
Rescue of recurrent deep intronic mutation underlying cell type–dependent quantitative NEMO deficiency
Journal of Clinical Investigation·2018· 52 citedOpen Access
Corrigendum: IRAK4 Deficiency in a Patient with Recurrent Pneumococcal Infections: Case Report and Review of the Literature
Frontiers in Pediatrics·2018Open Access
IRAK4 Deficiency in a Patient with Recurrent Pneumococcal Infections: Case Report and Review of the Literature
Frontiers in Pediatrics·2017· 35 citedOpen Access
Human Adaptive Immunity Rescues an Inborn Error of Innate Immunity
Cell·2017· 80 citedOpen Access
Inherited human IRAK-1 deficiency selectively impairs TLR signaling in fibroblasts
Proceedings of the National Academy of Sciences·2017· 56 citedOpen Access
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Frequent Co-authors

Jean‐Laurent Casanova(38), Anne Puel(32), Laurent Abel(29), Capucine Pïcard(27), Jacinta Bustamante(16), Bertrand Boisson(14), Stéphanie Boisson‐Dupuis(12), Vivien Béziat(10), Nico Marr(10), László Maródi(8), Laura Israël(8), Rui Yang(8), Emmanuelle Jouanguy(7), Luigi D. Notarangelo(7), Shen‐Ying Zhang(7), Lazaro Lorenzo(7), Stuart G. Tangye(7), Masato Ogishi(7), Peng Zhang(7), Pegah Ghandil(6)