Koenraad Devriendt

23PUBLICATIONS

206CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsDevelopmental genetics (incl. sex determination)Cardiology (incl. cardiovascular diseases)Clinical nutrition

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Publications (23)

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|Jul 09, 2026

Copy number variant analysis by exome sequencing is an effective approach to optimize diagnostic yield for developmental disorders-the DDD-Africa study.

|Jun 03, 2026

Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment.

|Mar 27, 2026

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Jhih-Rong Lin, Daniella Miller, Dana Luong

|Aug 12, 2025

Non-isolated tetralogy of fallot (TOF+): exome sequencing efficacy and phenotypic expansions.

Julia Volpi, Xiaonan Zhao, Nichole Owen

|Jul 17, 2025

Growth Hormone Treatment in Patients With KBG Syndrome: Novel Insights, Challenges and Recommendations From Six New Patients and Literature Review.

Sietse M Aukema, Kim Vandenput, Emanuela Scarano

|Jan 10, 2024

Expanding the phenotype of copy number variations involving NR0B1 (DAX1).

Nathalie Veyt, Griet Van Buggenhout, Koen Devriendt

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Frequent Collaborators

4 joint publications

Jeroen Breckpot

3 joint publications

Joris Robert Vermeesch

Gholson J Lyon

Matthew E Hurles

Jill A Rosenfeld

Himanshu Goel

Bernice E Morrow

Anne S Bassett

Huiwen Che

Bernard Thienpont

Frequent Collaborators

4 joint publications

Jeroen Breckpot

3 joint publications

Joris Robert Vermeesch

2 joint publications

Gholson J Lyon

2 joint publications

Matthew E Hurles