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 19
- 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
- Functional platelet studies and (epi)genetics to unravel the molecular basis of autism spectrum disorders.From1 Oct 2014 → 31 May 2015Funding: FWO fellowships
- (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
- 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)
- Pathofysiological characterization of megakarypoiesis using next generation sequencingFrom1 Sep 2013 → 13 Sep 2017Funding: BOF - Doctoral projects
Publications
31 - 40 of 134
- PIGO deficiency: palmoplantar keratoderma and novel mutations(2017)
Authors: Chris Van Geet, Kathleen Freson
Pages: 101 - The transcription factor GATA1 regulates NBEAL2 expression through a long-distance enhancer(2017)
Authors: Anouck Wijgaerts, Timothy Devos, Kathelijne Peerlinck, Chris Van Geet, Kathleen Freson
Pages: 695 - 706 - 3D Multi-segment foot kinematics in children: A developmental study in typically developing boys(2017)
Authors: Kevin Deschamps, Filip Staes, Kathelijne Peerlinck, Chris Van Geet, Giovanni Matricali
Pages: 40 - 44 - Pituitary adenylate cyclase-activating polypeptide (PACAP) in zebrafish models of nephrotic syndrome(2017)
Authors: Mohamed Ibrahim, Bert van den Heuvel, Laleh Khodaparast, Ladan Khodaparast, Chris Van Geet, Kathleen Freson, Elena Levtchenko
- GATA1 gene variants associated with thrombocytopenia and anemia(2017)
Authors: Kathleen Freson, Anouck Wijgaerts, Chris Van Geet
Pages: 731 - 734 - Platelet abnormalities in nephrotic syndrome(2016)
Authors: Benedicte Eneman, Elena Levtchenko, Bert van den Heuvel, Chris Van Geet, Kathleen Freson
Pages: 1267 - 1279 - A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss(2016)
Authors: Chris Van Geet, Kathleen Freson
Pages: 2903 - 2914 - A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders(2016)
Authors: Kathelijne Peerlinck, Chris Van Geet, Kathleen Freson
Pages: 2791 - 2803 - A comprehensive high-throughput sequencing test for the diagnosis of inherited bleeding, thrombotic and platelet disorders(2016)
Authors: Kathelijne Peerlinck, Chris Van Geet, Kathleen Freson
Pages: 307 - 307 - A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies(2016)
Authors: Anouck Wijgaerts, Kathelijne Peerlinck, Marc De Maeyer, Chris Van Geet, Kathleen Freson
Pages: 328