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
11 - 20 of 21
- Prevalence and incidence of pulmonary arterial hypertension (PAH) in congenital heart disease (CHD) in Belgium; developing detection methods of preclinical PAH; and influencing clinical outcome by early treatment of pulmonary vascular disease.From1 Oct 2013 → 31 Dec 2017Funding: IWT personal funding - strategic basic research grants
- Breakpoint variability as an explanation for phenotypical variation in 22q11DS.From1 Aug 2013 → 11 Jun 2020Funding: IWT personal funding - strategic basic research grants
- Variability in expression of the 15q11.2 microdeletion syndrome: genetic modifiers in the FMRP network.From1 Mar 2012 → 20 Feb 2015Funding: Foreign foundations, funds with scientific view
- A functional human genome project: integrated research of human congenital disorders.From1 Oct 2011 → 30 Sep 2016Funding: BOF - Concerted Research Project from 1994
- Aetiological Genetic and Occupational Risk factors for Anomalies in childrenFrom1 Oct 2010 → 28 Feb 2021Funding: Own budget, for example: patrimony, inscription fees, gifts
- A functional human genome project: integrated research of human congenital disorders.From1 Oct 2010 → 30 Sep 2012Funding: BOF - Concerted Research Project from 1994
- Identification of novel genes causing microcephaly using genomic approaches.From1 Aug 2010 → 31 Jul 2014Funding: BOF - Doctoral projects
- The FMRP- pathway and Autism Spectrum Disorders: a genetic studyFrom1 Aug 2010 → 1 Jan 2016Funding: Private funding of national origin - undefined
- Prenatal Chromosomal Microarray Analysis and Identification of Genetic Variants in Congenital Diaphragmatic Hernia.From1 Jun 2009 → 14 Apr 2014Funding: Own budget, for example: patrimony, inscription fees, gifts
- Autism: phenotype to genotype. The use of phenotypical, neurocognitive and neurobiological data in understanding the genetic structure of autism.From1 Jun 2009 → 31 May 2013Funding: BOF - Other initiatives
Publications
1 - 10 of 426
- Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age.(2024)
Authors: Ann Swillen, Jeroen Breckpot, Joris Vermeesch, Koenraad Devriendt
Pages: 368.e1 - 368.e12 - Deciphering Developmental Disorders in Africa (DDD-Africa) -the first ∼100 cases from South Africa(2024)
Authors: Koenraad Devriendt
Pages: 471 - 472 - CHD8 missense variants cause a variable neurodevelopmental disorder with incomplete penetrance(2024)
Authors: Koenraad Devriendt
Pages: 721 - 721 - Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles(2024)
Authors: Koenraad Devriendt, Kris Van Den Bogaert, Joris Vermeesch
Pages: 31 - 36 - Clinical and biological profile of Sickle Cell Anemia children in a rural area in Central Africa(2023)
Authors: Gloire Mbayabo, Gert Matthijs, Koenraad Devriendt, Chris Van Geet
- IMPLEMENTATION OF GENOME-WIDE CELL-FREE DNA SEQUENCING FOR THE EARLY IDENTIFICATION AND EFFICIENT MANAGEMENT OF HIGH-RISK PREGNANCIES(2023)
Authors: Lore Lannoo, Kristel Van Calsteren, Kris Van Den Bogaert, Koenraad Devriendt
- What helps define outcomes in persistent uninterpretable non-invasive prenatal testing: Maternal factors, fetal fraction or quality scores?(2023)
Authors: Lore Lannoo, Nathalie Brison, Kris Van Den Bogaert, Joris Vermeesch, Koenraad Devriendt, Kristel Van Calsteren
Pages: 1333 - 1343 - Fetal-onset Alexander disease with radiological-neuropathological correlation(2023)
Authors: Koenraad Devriendt, Jute Richter, Katrien Jansen, Marcella Baldewijns, Dietmar Thal, Michael Aertsen
Pages: 2149 - 2153 - Cell-free DNA methylome analysis for early preeclampsia prediction(2023)
Authors: Marie De Borre, Lore Lannoo, Kobe De Ridder, Mio Aerden, Jeroen Breckpot, Koenraad Devriendt, Joris Vermeesch, Kristel Van Calsteren, Bernard Thienpont
Pages: 2206 - + - Usefulness of automated image analysis for recognition of the fragile X syndrome gestalt in Congolese subjects(2023)
Authors: Koenraad Devriendt