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Researcher
Koenraad Devriendt
- Disciplines:Genetics, Systems biology, Medical imaging and therapy, Molecular and cell biology, Other paramedical sciences
Affiliations
- Laboratory for Genetics of Human Development (Division)
Responsible
From1 Jan 2008 → Today - Department of Human Genetics (Department)
Member
From1 Oct 1999 → Today
Projects
1 - 10 of 21
- Training teams to decipher developmental disorders in AfricaFrom1 Sep 2023 → TodayFunding: VLIR-UOS International Training Program (ITP)
- DECIPHERING DEVELOPMENTAL DISORDERS IN CENTRAL AFRICAFrom18 Feb 2021 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- A network for research and multidisciplinary medical care for oculocutaneous albinism in the DR CongoFrom1 Jan 2020 → 31 Aug 2022Funding: VLIR-UOS South Initiatives
- IMPLEMENTATION OF GENOME-WIDE CELL-FREE DNA SEQUENCING FOR THE EARLY IDENTIFICATION AND EFFICIENT MANAGEMENT OF HIGH-RISK PREGNANCIESFrom1 Nov 2019 → 10 Oct 2023Funding: Own budget, for example: patrimony, inscription fees, gifts
- Deep familial phenotyping and genotyping to resolve phenotypic variability of inherited pathogenic genetic variantsFrom1 Oct 2019 → 30 Sep 2023Funding: BOF - projects
- Long Read Sequencing for the detection of cryptic Structural Variation in patients with intellectual disability and congenital anomaliesFrom1 Oct 2019 → 30 Sep 2023Funding: FWO Applied Biomedical Research (TBM)
- Genetic origin of congenital heart defects in Tunisian population ( a clinical and laboratory approach)From1 Sep 2018 → 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
- Identification of genetic and genomic causes of syndromic and non-syndromic tooth agenesis (TA).From1 Mar 2016 → 28 Feb 2021Funding: Own budget, for example: patrimony, inscription fees, gifts
- Human genetics in the Democratic Republic of Congo.From1 Oct 2013 → 31 Dec 2015Funding: VLIR-UOS International Conferences (INCO)
Publications
11 - 20 of 426
- Induced Pluripotent Stem Cell-based Cardiac Tissue Modeling Of Mitogenic Cardiomyopathy In Alstrom Syndrome(2023)
Authors: Samaneh Ekhteraeitousi, Koenraad Devriendt
- Hydroxyurea treatment for adult sickle cell anemia patients in Kinshasa.(2023)
Authors: Gert Matthijs, Chris Van Geet, Koenraad Devriendt
Pages: 595 - 601 - BAFfling: Microduplications of ARID1A and ARID1B cause a novel clinical and epigenetic distinct BAFopathy(2023)
Authors: Koenraad Devriendt
Pages: 449 - 450 - Methylome analysis of cfDNA to predict preeclampsia presymptomatically(2023)
Authors: Lore Lannoo, Jeroen Breckpot, Koenraad Devriendt, Kristel Van Calsteren, Bernard Thienpont
Pages: 47 - 47 - Machine learning-based detection of immune-mediated diseases from genome-wide cell-free DNA sequencing datasets(2023)
Authors: Lore Lannoo, Koenraad Devriendt, Ellen De Langhe, Bram Verstockt, Kristel Van Calsteren
Pages: 45 - 46 - BeSolveRD: The Belgian genome resource to resolve rare diseases(2023)
Authors: Koenraad Devriendt, Jeroen Luyten, Gert Matthijs
Pages: 573 - 574 - Multicentric longitudinal performance monitoring of different non-invasive prenatal screening technologies used in Belgium(2023)
Authors: Koenraad Devriendt
Pages: 46 - 47 - NID1-related autosomal dominant Dandy-Walker malformation with occipital cephalocele in three generations(2023)
Authors: Koenraad Devriendt, Gunnar Buyse, Frank Van Calenbergh
- Diagnosis and treatment by hydroxyurea of adults with sickle cell disease in DR Congo(2023)
Authors: Paul Lumbala Kabuyi, Koenraad Devriendt, Prosper Lukusa-Tshilobo
- DIAGNOSIS AND TREATMENT BY HYDROXYUREA OF CHILDREN WITH SICKLE CELL ANEMIA IN THE DEMOCRATIC REPUBLIC OF CONGO.(2023)
Authors: Gloire Mbayabo, Chris Van Geet, Koenraad Devriendt, Prosper Lukusa-Tshilobo