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
41 - 50 of 426
- Outcome of publicly funded nationwide first-tier noninvasive prenatal screening(2021)
Authors: Kris Van Den Bogaert, Lore Lannoo, Nathalie Brison, Koenraad Devriendt, Joris Vermeesch
Pages: 1137 - 1142 - Enhanced MCP-1 Release in Early Autosomal Dominant Polycystic Kidney Disease(2021)
Authors: Jean-Paul Decuypere, Dorien Van Giel, Jaak Billen, Luc De Catte, Marcella Baldewijns, Koenraad Devriendt, Bert Bammens, Isabelle Meyts, Rudi Vennekens, Djalila Mekahli
Pages: 1687 - 1698 - Comprehensive genome-wide analysis of routine non-invasive test data allows cancer prediction: A single-center retrospective analysis of over 85,000 pregnancies(2021)
Authors: Liesbeth Lenaerts, Nathalie Brison, Charlotte Maggen, Huiwen Che, Peter Vandenberghe, Daan Dierickx, Lucienne Michaux, Barbara Dewaele, Patrick Neven, Beppe Floris, et al.
- Dental and Craniofacial Characteristics in Patients With 14Q22.1-Q22.2 Deletion: A Case Series(2021)
Authors: Koenraad Devriendt, Maria Cadenas de Llano Perula, Guy Willems, Anna Verdonck
Pages: 505 - 513 - 8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder(2021)
Authors: Nele Cosemans, Jarymke Maljaars, Annick Vogels, Koenraad Devriendt, Jean Steyaert, Kris Van Den Bogaert, Ilse Noens, Hilde Peeters
Pages: 207 - 213 - Clinical presentation and evolution of Xia-Gibbs syndrome due to p.Gly375ArgfsTer3 variant in a patient from DR Congo (Central Africa)(2021)
Authors: Koenraad Devriendt
Pages: 990 - 994 - Phenotypic spectrum of the RBM10-mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome features(2021)
Authors: Koenraad Devriendt
Pages: 449 - 456 - A BBS1 SVA F retrotransposon insertion is a frequent cause of Bardet-Biedl syndrome(2021)
Authors: Koenraad Devriendt
Pages: 318 - 324 - The broad phenotypic spectrum of PPP2R1A-related neurodevelopmental disorders correlates with the degree of biochemical dysfunction(2021)
Authors: Saar Reynhout, Iris Verbinnen, Koenraad Devriendt, Veerle Janssens
- DNA Methylation Profiling and Genomic Analysis in 20 Children with Short Stature Who Were Born Small for Gestational Age(2020)
Authors: Koenraad Devriendt, Francis de Zegher