< Back to previous page
Researcher
Isabelle Meyts
- Disciplines:Innate immunity, Adaptive immunology, Immunogenetics, Inflammation, Transplantation immunology
Affiliations
- Immunogenetics Research Group (Division)
Responsible
From1 Jan 2023 → Today - Inborn Errors of Immunity (Lab)
Responsible
From1 Jan 2019 → Today - Inborn Errors of Immunity (Lab)
Member
From1 Apr 2007 → Today - Interfaculty Centre for Biomedical Ethics and Law (Research institute)
Member
From1 Oct 2000 → 30 Sep 2001
Projects
1 - 10 of 24
- Analysis of pathogenic variants in patients suffering from severe viral infection; unraveling known and novel inborn errors of immunityFrom14 Mar 2023 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- The human genetic and immunological determinants of the clinical manifestations of SARS-CoV-2 infection: Towards personalised medicineFrom1 Jun 2022 → TodayFunding: Horizon Europe - Health
- Next-generation, multi-technology immune-monitoring and easy-access spectral flow cytometryFrom1 May 2022 → TodayFunding: FWO Medium Size Research Infrastructure
- Insights into the susceptibility to viral infections in ADA2 deficiencyFrom26 Apr 2022 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- The studie of the metabolic impact of ADA2 deficiencyFrom6 Sep 2021 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Clinical, Immunological and Functional Study of ADA2 deficiencyFrom2 Aug 2021 → TodayFunding: FWO fellowships
- Clinical, Immunological and genetic study of patients with primary humoral immunodeficiencyFrom22 Feb 2021 → 1 Jul 2023Funding: Own budget, for example: patrimony, inscription fees, gifts
- Multi-omics research applied to Human ADA2 deficiency and beyondFrom1 Jan 2021 → TodayFunding: H2020-EU.1.1. - EXCELLENT SCIENCE - European Research Council (ERC)
- Cytopenia and Autosomal Dominant Polycystic Kidney Disease (ADPKD)From1 Nov 2020 → TodayFunding: FWO fellowships
- Translational research into human adenosine deaminase type 2 deficiencyFrom1 Oct 2020 → TodayFunding: FWO fundamental clinical research fellowship
Publications
1 - 10 of 257
- Wiskott-Aldrich Syndrome: A study on 577 patients defining the genotype as a predictive biomarker for disease severity.(2024)
Authors: Isabelle Meyts
Pages: blood.2023 - Diagnosis of IRAK-4-deficiency by flow cytometric measurement of IκB-α degradation(2024)
Authors: Glynis Frans, Jaan Toelen, Giorgia Bucciol, Leen Moens, Rik Schrijvers, Isabelle Meyts, Xavier Bossuyt
Pages: e102 - e105 - Inborn errors of immunity: A field without frontiers(2024)
Authors: Giorgia Bucciol, Selket Delafontaine, Isabelle Meyts
Pages: 15 - 27 - The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants.(2024)
Authors: Isabelle Meyts, Rik Schrijvers
Pages: eadh4059 - A Novel Heterozygous Variant in AICDA Impairs Ig Class Switching and Somatic Hypermutation in Human B Cells and is Associated with Autosomal Dominant HIGM2 Syndrome(2024)
Authors: Isabelle Meyts
- Long-term and real-world safety and efficacy of retroviral gene therapy for adenosine deaminase deficiency(2024)
Authors: Isabelle Meyts
- Combined deficient response to polysaccharide-based and protein-based vaccines predicts a severe clinical phenotype(2024)
Authors: Rik Schrijvers, Debby Thomas, Giorgia Bucciol, Isabelle Meyts, Xavier Bossuyt
Pages: 138 - 149 - Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.(2024)
Authors: Isabelle Meyts
Pages: 6 - Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children(2024)
Authors: Isabelle Meyts
- Heterozygous mutations in the C-terminal domain of COPA underlie a complex autoinflammatory syndrome.(2024)
Authors: Selket Delafontaine, Daisy Rymen, Katrien Jansen, Djalila Mekahli, Rik Schrijvers, Xavier Bossuyt, Bram Boeckx, Lisa Ehlers, Sebastian Munck, Diether Lambrechts, et al.
Pages: e163604