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Researcher
Chris Van Geet
- Disciplines:Cardiac and vascular medicine not elsewhere classified, Molecular diagnostics, Hematology, Paediatrics
Affiliations
- Centre for Molecular and Vascular Biology (Division)
Member
From1 Jan 2012 → Today
Projects
1 - 10 of 20
- Ondersteuning van systemen voor vroegtijdige waarschuwing en op de natuur gebaseerde oplossingen met behulp van opportunistische regenvalmonitoring in RwandaFrom1 Sep 2024 → TodayFunding: VLIR-UOS TEAM
- Omics and cell-based disease models to explore novel causes of inherited bleedingFrom1 Oct 2023 → TodayFunding: BOF - projects
- Genome medicine for bleeding, thrombotic and platelet disordersFrom1 Oct 2019 → 30 Sep 2023Funding: BOF - projects
- Improved prevention and treatment of non-Typhoidal Salmonella disease in Africa trough understanding the role of human carriersFrom1 Jan 2018 → 31 Dec 2019Funding: VLIR-UOS South Initiatives
- 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
- DIAGNOSIS AND TREATMENT BY HYDROXYUREA OF CHILDREN WITH SICKLE CELL ANEMIA IN THE DEMOCRATIC REPUBLIC OF CONGO.From1 Jan 2017 → 25 Mar 2023Funding: Own budget, for example: patrimony, inscription fees, gifts
- 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
- (Epi)Genetic studies and system biology approaches to characterize rare inherited bleeding and platelet disorders: from patient studies to basic biology to cl inical applicationsFrom1 Oct 2014 → 30 Sep 2018Funding: BOF - Concerted Research Project from 1994
- Functional platelet studies and (epi)genetics to unravel the molecular basis of autism spectrum disorders.From1 Oct 2014 → 31 May 2015Funding: FWO fellowships
- Lessons from pseudo(pseudo)hypoparathyroidism using platelets: (epi)genetic defects within and outside the imprinted GNAS cluster.From1 Jan 2014 → 31 Dec 2017Funding: FWO research project (including WEAVE projects)
Publications
1 - 10 of 131
- Multigene panel for thrombophilia testing in venous thromboembolism(2025)Published in: JOURNAL OF THROMBOSIS AND HAEMOSTASISISSN: 1538-7933Issue: 6Volume: 23Pages: 1838 - 1849
- Blood Group O Does Not Increase the Risk of Inhibitors in Severe Haemophilia A: Data from the PedNet Study Group(2025)Published in: HAEMOPHILIAISSN: 1351-8216Issue: 3Volume: 31Pages: 419 - 423
- Functional assessment of genetic variants in thrombomodulin detected in patients with bleeding and thrombosis(2025)Published in: BLOODISSN: 0006-4971Issue: 17Volume: 145Pages: 1929 - 1942
- Genetic Modulators of Diversity in the Biological Expression of Sickle Cell Anemia in Patients from Democratic Republic of Congo: Role of βs-globin Haplotypes(2025)Published in: Mediterranean Journal Of Hematology And Infectious DiseasesISSN: 2035-3006Issue: 1Volume: 17
- Bleeding control improves after switching to emicizumab: Real-world experience of 177 children in the PedNet registry(2024)Published in: HAEMOPHILIAISSN: 1351-8216Issue: 3Volume: 30Pages: 685 - 692
- Clinical and biological profile of Sickle Cell Anemia children in a rural area in Central Africa(2023)Published in: Hematology (Amsterdam, Netherlands)ISSN: 1024-5332Issue: 1Volume: 28
- Hydroxyurea treatment for adult sickle cell anemia patients in Kinshasa(2023)Published in: EJHaemISSN: 2688-6146Issue: 3Volume: 4Pages: 595 - 601
- Ribosome dysfunction underlies SLFN14-related thrombocytopenia(2023)Published in: BLOODISSN: 0006-4971Issue: 18Volume: 141Pages: 2261 - 2274
- Clinical application of multigene panel testing for bleeding, thrombotic, and platelet disorders: a 3-year Belgian experience(2023)Published in: JOURNAL OF THROMBOSIS AND HAEMOSTASISISSN: 1538-7933Issue: 4Volume: 21Pages: 887 - 895
- DIAGNOSIS AND TREATMENT BY HYDROXYUREA OF CHILDREN WITH SICKLE CELL ANEMIA IN THE DEMOCRATIC REPUBLIC OF CONGO.(2023)