Margaux Gerbaux

Rega Institute for Medical Research — Belgium

Immunology and Microbiology · Life Sciences

8h-index268citations25works0.62yr avg
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Research Topics

Immunodeficiency and Autoimmune Disorders(9), Immune Cell Function and Interaction(6), SARS-CoV-2 and COVID-19 Research(5), COVID-19 Clinical Research Studies(4), Antifungal resistance and susceptibility(4)

Publications24 total

Biological Anti-Tumoral Mechanisms of Metformin in Head and Neck Squamous Cell Carcinomas: A Systematic Review
Journal of Clinical Medicine·2025Open Access
Systems vaccinology identifies immunological correlates of SARS-CoV-2 vaccine response in solid organ transplant recipients
npj Vaccines·2025Open Access
Homozygosity for the Common IL23R R381Q Variant Associates with Increased Susceptibility to Chronic Mucocutaneous Candidiasis
European Journal of Immunology·2025Open Access
Author response for "Homozygosity for the Common IL23R R381Q Variant Associates with Increased Susceptibility to Chronic Mucocutaneous Candidiasis"
2025
Author response for "Homozygosity for the Common IL23R R381Q Variant Associates with Increased Susceptibility to Chronic Mucocutaneous Candidiasis"
2025
Author response for "Homozygosity for the Common IL23R R381Q Variant Associates with Increased Susceptibility to Chronic Mucocutaneous Candidiasis"
2025
OTULIN haploinsufficiency predisposes to environmentally directed inflammation
Frontiers in Immunology·2024· 5 citedOpen Access
Systems vaccinology identifies clinical and immunological correlates of SARS-CoV-2 vaccine response in solid-organ transplant recipients
2024Open Access
Systems Vaccinology Identifies Clinical and Immunological Correlates of SARS-CoV-2 Vaccine Response in Solid-Organ Transplant Recipients
SSRN Electronic Journal·2024Open Access
CTLA4-Ig Effectively Controls Clinical Deterioration and Immune Condition in a Murine Model of Foxp3 Deficiency
Journal of Clinical Immunology·2023· 6 citedOpen Access
Homozygous DBF4 mutation as a cause of severe congenital neutropenia
Journal of Allergy and Clinical Immunology·2023· 8 citedOpen Access
Author Correction: Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects
Cellular and Molecular Immunology·2022Open Access
DNA replication–associated inborn errors of immunity
Journal of Allergy and Clinical Immunology·2022· 8 citedOpen Access
Disrupted Ca2+ homeostasis and immunodeficiency in patients with functional IP3 receptor subtype 3 defects
Cellular and Molecular Immunology·2022· 22 citedOpen Access
Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations
Frontiers in Immunology·2022· 5 citedOpen Access
A Novel Homozygous Stop Mutation in IL23R Causes Mendelian Susceptibility to Mycobacterial Disease
Journal of Clinical Immunology·2022· 21 citedOpen Access
Insights From Early Clinical Trials Assessing Response to mRNA SARS-CoV-2 Vaccination in Immunocompromised Patients
Frontiers in Immunology·2022· 10 citedOpen Access
Monogenic Adult-Onset Inborn Errors of Immunity
Frontiers in Immunology·2021· 45 citedOpen Access
Unstable regulatory T cells, enriched for naïve and Nrp1<sup>neg</sup>cells, are purged after fate challenge
Science Immunology·2021· 31 citedOpen Access
Disrupted Ca <sup>2+</sup> homeostasis and immunodeficiency in patients with functional Inositol 1,4,5-trisphosphate receptor subtype 3 defects
2021· 1 citedOpen Access
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Frequent Co-authors

Stéphanie Humblet‐Baron(21), Adrian Liston(20), Mathijs Willemsen(19), Julika Neumann(18), Frederik Staels(15), Rik Schrijvers(13), Leoni Bücken(9), Teresa Prezzemolo(7), Susan Schlenner(6), Isabelle Meyts(6), Carlos P. Roca(5), Erika Van Nieuwenhove(5), Lize Van Meerbeeck(5), John S. Barber(4), Isabelle Desombere(4), Pieter Pannus(4), Arnaud Marchant(4), Willem Roosens(4), Oliver T. Burton(3), Lara E. Terry(3)