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
351 - 360 of 426
- Recent Developments in the Genetic Factors Underlying Congenital Diaphragmatic Hernia(2011)
Authors: Paul Brady, Koenraad Devriendt, Jean-Pierre Frijns, Jan Deprest, Joris Vermeesch
Pages: 25 - 39 - Circumferential skin creases, cleft palate, typical face, intellectual disability and growth delay: "Circumferential skin creases Kunze type"(2011)
Authors: Vincent Vander Poorten, Koenraad Devriendt, Hilde Van Esch
Pages: 236 - 240 - A Balanced Translocation t(6;14)(q25.3;q13.2) Leading to Reciprocal Fusion Transcripts in a Patient with Intellectual Disability and Agenesis of Corpus Callosum(2011)
Authors: Liesbeth Backx, Eve Seuntjens, Koenraad Devriendt, Joris Vermeesch, Hilde Van Esch
Pages: 135 - 143 - Granulomatous skin lesions complicating Varicella infection in a patient with Rothmund-Thomson syndrome and immune deficiency: case report(2010)
Authors: Lien De Somer, Carine Wouters, Marie Morren, Rita De Vos, Joost van den Oord, Koenraad Devriendt, Isabelle Meyts
- Granulomatous skin lesions complicating Varicella infection in a patient with Rothmund-Thomson syndrome and immune deficiency: case report(2010)
Authors: Lien De Somer, Carine Wouters, Rita De Vos, Joost van den Oord, Koenraad Devriendt, Isabelle Meyts
- A new approach to imprinting mutation detection in GNAS by Sequenom EpiTYPER system(2010)
Authors: Benedetta Izzi, Brigitte Decallonne, Koenraad Devriendt, Roger Bouillon, Dirk Vanderschueren, Elena Levtchenko, Francis de Zegher, Diether Lambrechts, Chris Van Geet, Kathleen Freson
Pages: 2033 - 2039 - Targeted array comparative genomic hybridisation (array CGH) identifies genomic imbalances associated with isolated congenital diaphragmatic hernia (CDH)(2010)
Authors: Paul Brady, Koenraad Devriendt, Jean-Pierre Frijns, Jan Deprest, Joris Vermeesch
Pages: 1198 - 1206 - DISC1 duplication in two brothers with autism and mild mental retardation(2010)
Authors: An Crepel, Jeroen Breckpot, Jean-Pierre Frijns, Wouter De la Marche, Jean Steyaert, Koenraad Devriendt, Hilde Peeters
Pages: 389 - 394 - Structurele chromosoomherschikkingen in autisme spectrum stoornissen(2010)
Authors: An Crepel, Koenraad Devriendt, Hilde Peeters
Number of pages: 172 - Duplication of the TGFBR1 gene causes features of Loeys-Dietz Syndrome(2010)
Authors: Jeroen Breckpot, Werner Budts, Francis de Zegher, Joris Vermeesch, Koenraad Devriendt
Pages: 408 - 410