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Researcher
Kathleen Freson
- Disciplines:Cardiac and vascular medicine, Molecular and cell biology
Affiliations
- Centre for Molecular and Vascular Biology (Division)
Responsible
From1 Jul 2016 → Today - Centre for Molecular and Vascular Biology (Division)
Member
From1 Oct 1999 → Today
Projects
1 - 10 of 21
- Omics and cell-based disease models to explore novel causes of bleedingFrom23 Nov 2023 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Omics and cell-based disease models to explore novel causes of inherited bleedingFrom1 Oct 2023 → TodayFunding: BOF - projects
- Whole genome and RNA sequencing for platelet disordersFrom3 Nov 2021 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Improved disease modelling and genetics for inherited platelet disordersFrom1 Oct 2021 → TodayFunding: FWO fellowships
- Improved disease modelling and genetics for inherited platelet disordersFrom1 Jan 2021 → TodayFunding: FWO research project (including WEAVE projects)
- Genome medicine for bleeding, thrombotic and platelet disordersFrom1 Oct 2019 → 30 Sep 2023Funding: BOF - projects
- Pathophysiological characterization of megakaryopoiesis and erythropoiesis: whole genome sequencing and functional studiesFrom4 Sep 2017 → 2 Sep 2021Funding: Own budget, for example: patrimony, inscription fees, gifts
- Blood cell counts in human and animal researchFrom1 Oct 2016 → 30 Sep 2018Funding: Fund Recuperation Fiscal Exemption
- Interdiscplinary Training in High-Troughput Sequencing, Bioinformatics and Model Systems: Moving towards Clinical applications of GenomicsFrom1 Jan 2016 → 31 Dec 2018Funding: H2020-EU.4. - Spreading excellence and widening participation
- The study of granule biogenesis during megakaryopoiesis from insights of known and novel genetic granule deficienciesFrom1 Oct 2015 → 31 Aug 2020Funding: FWO Strategic Basic Research Grant
Publications
11 - 20 of 182
- Loss of APOLD1: a new vascular bleeding disorder?(2023)
Authors: Kathleen Freson
Pages: 665 - 667 - Genetic association analysis of 77,539 genomes reveals rare disease etiologies(2023)
Authors: Kathleen Freson
Pages: 679 - + - Diagnostic value of multigene sequencing for inherited thrombocytopenia(2022)
Authors: Kathleen Freson
Pages: 645 - 646 - Methylome analysis for haemophilia A intron 22 inversion patients with and without inhibitors: A pilot study(2022)
Authors: Veerle Labarque, Chris Van Geet, Kathelijne Peerlinck, Kathleen Freson
Pages: E248 - E250 - A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger(2022)
Authors: Kathleen Freson
- The Analysis of the Human Megakaryocyte and Platelet Coding Transcriptome in Healthy and Diseased Subjects(2022)
Authors: Koen De Wispelaere, Kathleen Freson
- F11 Gene Duplication Causes Elevated FXI Plasma Levels and Is a Risk for Venous Thrombosis(2022)
Authors: Kathelijne Peerlinck, Marc Jacquemin, Veerle Labarque, Kathleen Freson
Pages: 1 - 3 - A novel RUNX1 exon 3-7 deletion causing a familial platelet disorder(2022)
Authors: Kathleen Freson
Pages: 320 - 323 - Combined transcriptome and proteome profiling of SRC kinase activity in healthy and E527K defective megakaryocytes(2021)
Authors: Lore De Kock, Fabienne Ver Donck, Chris Van Geet, Kathleen Freson
Pages: 3206 - 3210 - Hemostatic phenotypes and genetic disorders(2021)
Authors: Fabienne Ver Donck, Veerle Labarque, Kathleen Freson