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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 22
- Clinical, pathological and genetic characteristics of breast cancer in Congolese womenFrom13 Oct 2025 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Training teams to decipher developmental disorders in AfricaFrom1 Sep 2023 → TodayFunding: VLIR-UOS International Training Program (ITP)
- Deciphering Developmental Disorders in Central Africa: Clinical and Genetic studiesFrom18 Feb 2021 → 8 Sep 2025Funding: 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
- 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)
- Deep familial phenotyping and genotyping to resolve phenotypic variability of inherited pathogenic genetic variantsFrom1 Oct 2019 → 30 Sep 2023Funding: BOF - projects
- 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
Publications
1 - 10 of 431
- Growth Hormone Treatment in Patients With KBG Syndrome: Novel Insights, Challenges and Recommendations From Six New Patients and Literature Review(2025)Published in: American Journal of Medical Genetics AISSN: 1552-4825Issue: 12Volume: 197
- Deciphering Developmental Disorders in Central Africa: Clinical and Genetic studies(2025)
- Genotype imputation from low-coverage data for medical and population genetic analyses(2025)Published in: Genome ResearchISSN: 1088-9051Issue: 9Volume: 35Pages: 1929 - 1941
- Non-isolated tetralogy of fallot (TOF plus ): exome sequencing efficacy and phenotypic expansions(2025)Published in: EUROPEAN JOURNAL OF HUMAN GENETICSISSN: 1018-4813
- Persistent Uninterpretable or Failed Prenatal Cell-Free DNA Screening Indicates a High-Risk Pregnancy and is Associated With Biological Factors Interfering With cfDNA-Analysis: A Prospective Cohort Study(2025)Published in: Prenatal DiagnosisISSN: 0197-3851Issue: 5Volume: 45Pages: 581 - 590
- Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndrome(2025)Published in: Genome ResearchISSN: 1088-9051Issue: 4Volume: 35Pages: 786 - 797
- Chromosomal analysis and short-term outcome of prenatally diagnosed congenital heart disease(2025)Published in: Scientific ReportsISSN: 2045-2322Issue: 1Volume: 15
- Clinical evaluation of long-read sequencing-based episignature detection in developmental disorders(2025)Published in: Genome MedicineISSN: 1756-994XIssue: 1Volume: 17
- Genetic Modulators of Diversity in the Biological Expression of Sickle Cell Anemia in Patients from Democratic Republic of Congo: Role of βs-globin Haplotypes(2025)Published in: Mediterranean Journal Of Hematology And Infectious DiseasesISSN: 2035-3006Issue: 1Volume: 17
- Microduplications of ARID1A and ARID1B cause a novel clinical and epigenetic distinct BAFopathy(2025)Published in: Genetics in MedicineISSN: 1098-3600Issue: 1Volume: 27