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
11 - 20 of 257
- Proposal for a Disease Activity Score and Disease Damage Score for ADA2 Deficiency: the DADA2AI and DADA2DI(2024)
Authors: Giorgia Bucciol, Isabelle Meyts
- Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome(2024)
Authors: Bethany Pillay, Lisa Ehlers, Selket Delafontaine, Xavier Bossuyt, Stefaan Soenen, Giorgia Bucciol, Stephanie Humblet-Baron, Leen Moens, Isabelle Meyts
- Human adenosine deaminase type 2 deficiency: Novel insights into a multifaceted disease(2023)
Authors: Isabelle Meyts
- Leukopenia in autosomal dominant polycystic kidney disease: a single-center cohort of kidney transplant candidates with post-transplantation follow-up(2023)
Authors: Elisabet Van Loon, Maarten Coemans, Isabelle Meyts, Rudi Vennekens, Dirk Kuypers, Djalila Mekahli, Bert Bammens
Pages: 2578 - 2586 - CLINICAL AND NEUROLOGICAL OUTCOME IN PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENT CHILDREN AFTER ALLOGENEIC HSCT - A MULTI-CENTER STUDY(2023)
Authors: Isabelle Meyts
Pages: 79 - 80 - A Narrative Review of the Neurological Manifestations of Human Adenosine Deaminase 2 Deficiency(2023)
Authors: Mariia Dzhus, Lisa Ehlers, Katrien Jansen, Rik Schrijvers, Lien De Somer, Steven Vanderschueren, Marco Baggio, Leen Moens, Rik Lories, Giorgia Bucciol, et al.
Pages: 1916 - 1926 - Haploidentical Stem Cell Transplantation with Post-transplantation Cyclophosphamide in High-Risk Chronic Granulomatous Disease Patient with Invasive Mucormycosis(2023)
Authors: Giorgia Bucciol, Isabelle Meyts
Pages: 1758 - 1765 - An International Survey of Allogeneic Hematopoietic Cell Transplantation for X-Linked Agammaglobulinemia(2023)
Authors: Giorgia Bucciol, Isabelle Meyts
Pages: 1827 - 1839 - Activated phosphoinositide 3-kinase d syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity(2023)
Authors: Giorgia Bucciol, Isabelle Meyts
- Rituximab and improved nodular regenerative hyperplasia-associated non-cirrhotic liver disease in common variable immunodeficiency: a case report and literature study(2023)
Authors: Willem Roosens, Stephanie Humblet-Baron, Isabelle Meyts, Chris Verslype, Hannah van Malenstein, Schalk Van der Merwe, Wim Laleman, Rik Schrijvers