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
391 - 400 of 426
- Improving our Insight in the Genetic Origin of Congenital Heart defects using Array Comparative Genome Hybridization.(2009)
Authors: Bernard Thienpont, Koenraad Devriendt, Joris Vermeesch
- Network analysis of differential expression for the identification of disease-causing genes(2009)
Authors: Léon-Charles Tranchevent, Bernard Thienpont, Lieven Thorrez, Hilde Van Esch, Koenraad Devriendt, Yves Moreau
- Nail-patella syndrome, infantile nephrotic syndrome: complete remission with antiproteinuric treatment(2009)
Authors: Koenraad Devriendt
Pages: 1335 - 1338 - Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant(2009)
Authors: Femke Hannes, Thomy de Ravel de l'Argentière, Jean-Pierre Frijns, Koenraad Devriendt, Griet Van Buggenhout, Annick Vogels, Joris Vermeesch
Pages: 223 - 232 - Early detection of chromosome 9q22.32q31.1 microdeletion and the nevoid basal cell carcinoma syndrome(2009)
Authors: Thomy de Ravel de l'Argentière, Joris Vermeesch, Koenraad Devriendt
Pages: 145 - 147 - Early detection of chromosome 9q22.32q31.1 microdeletion and the nevoid basal cell carcinoma syndrome(2009)
Authors: Thomy de Ravel de l'Argentière, Liliane Ameye, Katleen Ballon, Martine Borghgraef, Joris Vermeesch, Koenraad Devriendt
Pages: 145 - 147 - Elements of morphology: standard terminology for the lips, mouth, and oral region(2009)
Authors: Koenraad Devriendt
Pages: 77 - 92 - Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1(2009)
Authors: Bernard Thienpont, Eftychia Dimitriadou, Jeroen Breckpot, Joris Vermeesch, Koenraad Devriendt
Pages: 393 - 7 - Nature en nurture(2009)
Authors: Koenraad Devriendt
Pages: 29 - 29Number of pages: 1 - The C20orf133 gene is disrupted in a patient with Kabuki syndrome.(2009)
Authors: Koenraad Devriendt, Jean-Pierre Frijns, Joris Vermeesch
Pages: bcr06.2009