Margaux Gerbaux

Leuven, VLG, Belgium

Last Updated: 09/26/2026

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Found 18 publications

Identification of a novel hypomorphic variant in CYBB underlying an adult presentation of X-linked recessive Mendelian susceptibility to mycobacterial disease.

Identification of a novel hypomorphic variant in CYBB underlying an adult presentation of X-linked recessive Mendelian susceptibility to mycobacterial disease.

Journal: Clinical immunology (Orlando, Fla.)

Published: January 16, 2026

Biological Anti-Tumoral Mechanisms of Metformin in Head and Neck Squamous Cell Carcinomas: A Systematic Review.

Biological Anti-Tumoral Mechanisms of Metformin in Head and Neck Squamous Cell Carcinomas: A Systematic Review.

Journal: Journal of clinical medicine

Published: April 06, 2025

Systems vaccinology identifies immunological correlates of SARS-CoV-2 vaccine response in solid organ transplant recipients.

Systems vaccinology identifies immunological correlates of SARS-CoV-2 vaccine response in solid organ transplant recipients.

Journal: NPJ vaccines

Published: October 16, 2024

Homozygosity for the Common IL23R R381Q Variant Associates with Increased Susceptibility to Chronic Mucocutaneous Candidiasis.

Homozygosity for the Common IL23R R381Q Variant Associates with Increased Susceptibility to Chronic Mucocutaneous Candidiasis.

Journal: European journal of immunology

Published: August 10, 2024

Author Correction: Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects.

Author Correction: Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects.

Journal: Cellular & molecular immunology

Published: December 05, 2022

DNA replication-associated inborn errors of immunity.

DNA replication-associated inborn errors of immunity.

Journal: The Journal of allergy and clinical immunology

Published: September 13, 2022

Homozygous DBF4 mutation as a cause of severe congenital neutropenia.

Homozygous DBF4 mutation as a cause of severe congenital neutropenia.

Journal: The Journal of allergy and clinical immunology

Published: September 08, 2022

OTULIN haploinsufficiency predisposes to environmentally directed inflammation.

OTULIN haploinsufficiency predisposes to environmentally directed inflammation.

Journal: Frontiers in immunology

Published: July 01, 2022

Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations.

Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations.

Journal: Frontiers in immunology

Published: June 20, 2022

Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects.

Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects.

Journal: Cellular & molecular immunology

Published: April 28, 2022

A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial Disease.

A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial Disease.

Journal: Journal of clinical immunology

Published: March 28, 2022

CTLA4-Ig Effectively Controls Clinical Deterioration and Immune Condition in a Murine Model of Foxp3 Deficiency.

CTLA4-Ig Effectively Controls Clinical Deterioration and Immune Condition in a Murine Model of Foxp3 Deficiency.

Journal: Journal of clinical immunology

Published: February 02, 2022

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Last Updated: 09/26/2026