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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
21 - 30 of 182
- Consensus recommendations on flow cytometry for the assessment of inherited and acquired disorders of platelet number and function: Communication from the ISTH SSC Subcommittee on Platelet Physiology(2021)
Authors: Kathleen Freson
Pages: 3193 - 3202 - GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis(2021)
Authors: Kathleen Freson
Pages: 2612 - 2617 - The brain-derived neurotrophic factor prompts platelet aggregation and secretion(2021)
Authors: Kathleen Freson
Pages: 3568 - 3580 - Pathophysiological characterization of megakaryopoiesis and erythropoiesis: whole genome sequencing and functional studies(2021)
Authors: Lore De Kock, Kathleen Freson, Chris Van Geet
- Macrothrombocytopenia and stomatocytosis in sitosterolaemia(2021)
Authors: Kathleen Freson
Pages: 804 - 804 - Illustrated State-of-the-Art Capsules of the ISTH 2021 Congress(2021)
Authors: Kathleen Freson
- The EHA Research Roadmap: Platelet Disorders(2021)
Authors: Kathleen Freson, Chris Van Geet
- ThromboGenomics implementation in Belgium(2021)
Authors: Marc Jacquemin, Kathelijne Peerlinck, Kathleen Freson
Pages: 99 - 105 - Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function(2021)
Authors: Marilena Crescente, Kathleen Freson
Pages: 1423 - 1432 - Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel(2021)
Authors: Kathleen Freson
Pages: 414 - 431