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
21 - 30 of 426
- A cross-country comparison of pregnant women's decision-making and perspectives when opting for non-invasive prenatal testing in the Netherlands and Belgium(2023)
Authors: Lore Lannoo, Luc De Catte, Koenraad Devriendt, Kristel Van Calsteren, Neeltje Crombag
Pages: 294 - 303 - Clinical and laboratory characterization of adult sickle cell anemia patients in Kinshasa(2022)
Authors: Gloire Mbayabo, Gert Matthijs, Chris Van Geet, Koenraad Devriendt
- Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge(2022)
Authors: Lore Lannoo, Jeroen Breckpot, Nathalie Brison, Luc De Catte, Eftychia Dimitriadou, Eric Legius, Hilde Peeters, Olga Tsuiko, Joris Vermeesch, Griet Van Buggenhout, et al.
Pages: 1323 - 1330 - FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects(2022)
Authors: Isabelle Meyts, Wim Wuyts, Leen Moens, Selket Delafontaine, Kris Van Den Bogaert, Koenraad Devriendt
Pages: 2475 - 2486 - An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome(2022)
Authors: Jeroen Breckpot, Koenraad Devriendt
Pages: 1867 - 1884 - Machine learning-based detection of immune-mediated diseases from genome-wide cell-free DNA sequencing datasets(2022)
Authors: Huiwen Che, Lore Lannoo, Nathalie Brison, Kris Van Den Bogaert, Koenraad Devriendt, Ellen De Langhe, Séverine Vermeire, Bram Verstockt, Kristel Van Calsteren, Joris Vermeesch
- PERCHING syndrome: Clinical presentation in the first African patient confirmed by clinical whole genome sequencing(2022)
Authors: Koenraad Devriendt
Pages: 2825 - 2831 - Value of DNA testing in the diagnosis of sickle-cell anemia in childhood in an environment with a high prevalence of other causes of anemia(2022)
Authors: Gloire Mbayabo, Gert Matthijs, Koenraad Devriendt, Chris Van Geet
- Loss-of-function variants in SRRM2 cause a neurodevelopmental disorder(2022)
Authors: Koenraad Devriendt
Pages: 1774 - 1780 - Increasing African genomic data generation and sharing to resolve rare and undiagnosed diseases in Africa: a call-to-action by the H3Africa rare diseases working group(2022)
Authors: Koenraad Devriendt