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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
31 - 40 of 182
- The (Patho)Biology of SRC Kinase in Platelets and Megakaryocytes(2020)
Authors: Lore De Kock, Kathleen Freson
- Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome(2020)
Authors: Kathleen Freson
Pages: 1956 - 1967 - Unravelling the disease mechanism for TSPYL1 deficiency(2020)
Authors: Gunnar Buyse, Hilde Van Esch, Chris Van Geet, Kathleen Freson
Pages: 3431 - 3442 - Clinical management, ethics and informed consent related to multi-gene panel-based high throughput sequencing testing for platelet disorders: Communication from the SSC of the ISTH(2020)
Authors: Pascal Borry, Chris Van Geet, Kathleen Freson
Pages: 2751 - 2758 - A coagulation defect arising from heterozygous premature termination of tissue factor(2020)
Authors: Kathelijne Peerlinck, Kathleen Freson
Pages: 5302 - 5312 - Strengths and limitations of high-throughput sequencing for the diagnosis of inherited bleeding and platelet disorders(2020)
Authors: Fabienne Ver Donck, Kathleen Freson
Pages: 1839 - 1845 - Whole-genome sequencing of patients with rare diseases in a national health system(2020)
Authors: Kathleen Freson
Pages: 96 - + - The PACAP/VPAC1 system does not contribute to adipose tissue formation in mouse models of nutritionally induced obesity(2020)
Authors: Roger Lijnen, Kathleen Freson, Marc Hoylaerts
Pages: 1 - 5 - Autosomal dominant macrothrombocytopenia caused by a rare GPIBB variant: The importance of DNA sequencing(2020)
Authors: Kathleen Freson
Pages: E98 - E100 - Glanzmann thrombasthenia: genetic basis and clinical correlates(2020)
Authors: Kathleen Freson
Pages: 888 - 894