Koenraad Devriendt - Genetic Mutations

Author Information

Koenraad Devriendt is affiliated with the Center for Human Genetics at the University Hospital Leuven and KU Leuven, located in Leuven, Belgium. His extensive research focuses on various genetic disorders and their implications.

Research Contributions

Koenraad Devriendt has made significant contributions to the field of genetics through his research on a wide range of topics. His recent papers cover various areas such as DNA testing for sickle cell anemia in Africa, genome-wide analysis for cancer prediction, and the genetic basis of congenital heart disease, autism spectrum disorder, and primary microcephaly. His work is notable for its integrative approach, combining genomic data with clinical insights to uncover new associations and potential diagnostic tools.

Aliases

Koenraad Devriendt is also known by several aliases, including K. Devriendt, K Devriendt, and Koen Devriendt. These variations may appear in different publications and databases.

Publication and Citation Metrics

Metric	Value
Citation Count	25,838
h-index	80
Paper Count	953

Publications:

DNA testing for sickle cell anemia in Africa: Implementation choices for the Democratic Republic of Congo.

DOI: 10.1002/jcla.24398

Year: 2022

Comprehensive genome-wide analysis of routine non-invasive test data allows cancer prediction: A single-center retrospective analysis of over 85,000 pregnancies

DOI: 10.1016/j.eclinm.2021.100856

Year: 2021

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

DOI: 10.1371/journal.pgen.1009679

Year: 2021

MO021ENHANCED MCP-1 RELEASE IN EARLY AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE

DOI: 10.1093/NDT/GFAB081.003

Year: 2021

Oculo‐Auriculo‐Vertebral Spectrum

DOI: 10.1002/9780470893159.CH39

Year: 2021

Extraocular muscle hypoplasia associated with Axenfeld-Rieger syndrome

DOI: 10.1080/09273972.2021.1987926

Year: 2021

8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder.

DOI: 10.1007/s10048-021-00635-8

Year: 2021

60 Comprehensive genome-wide analysis of non-invasive test data allows accurate cancer prediction: a retrospective analysis of over 85.000 pregnancies

DOI: 10.1136/ijgc-2021-esgo.235

Year: 2021

Phenotypes and genotypes in outbred and inbred Primary microcephaly: high incidence of epilepsy

DOI: 10.22541/au.160978661.19941555/v1

Year: 2021

Usefulness of Automated Image Analysis for Recognition of the Fragile X Syndrome Gestalt in Congolese Subjects

DOI: 10.21203/rs.3.rs-1082768/v1

Year: 2021

What are the ethical considerations of using ZFNs?

How Do Microarrays Work?

How Does the Mutation Occur?

What Are the Challenges in Pharmacogenomics?

What is Genetic Research?

What Causes CNVs?

How Does the Neutral Theory Affect Our Understanding of Genetic Diversity?

What is Third Generation Sequencing?

Why is Sequencing Important for Studying Genetic Mutations?

What are the Challenges in Populace Genomics?

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