Christelle Lenoir
Paris, France
Last Updated: 09/26/2026
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Found 29 publications
Genetic and molecular approaches for patients with familial hemophagocytic lymphohistiocytosis: a multi-center experience from Mexico.
Journal: Frontiers in immunology
Published: April 07, 2026
Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndrome.
Journal: The Journal of allergy and clinical immunology
Published: March 23, 2023
Role of IL-27 in Epstein-Barr virus infection revealed by IL-27RA deficiency.
Journal: Nature
Published: November 11, 2022
NBEAL2 deficiency in humans leads to low CTLA-4 expression in activated conventional T cells.
Journal: Nature communications
Published: September 08, 2022
Lymphoma as an Exclusion Criteria for CVID Diagnosis Revisited.
Journal: Journal of clinical immunology
Published: July 05, 2022
Gain-of-function IKZF1 variants in humans cause immune dysregulation associated with abnormal T/B cell late differentiation.
Journal: Science immunology
Published: March 25, 2022
Identification of Germline Non-coding Deletions in XIAP Gene Causing XIAP Deficiency Reveals a Key Promoter Sequence.
Journal: Journal of clinical immunology
Published: September 28, 2021
Inherited TNFSF9 deficiency causes broad Epstein-Barr virus infection with EBV+ smooth muscle tumors.
Journal: The Journal of experimental medicine
Published: August 06, 2021
Corrigendum to: Diagnostic Yield of Next-Generation Sequencing in Very Early-Onset Inflammatory Bowel Diseases: A Multicenter Study.
Journal: Journal of Crohn's & colitis
Published: September 08, 2020
DEF6 deficiency, a mendelian susceptibility to EBV infection, lymphoma, and autoimmunity.
Journal: The Journal of allergy and clinical immunology
Published: December 16, 2019
Last Updated: 09/26/2026