Hilde Peeters
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Explore the profile of Hilde Peeters including associated specialties, affiliations and a list of published articles.
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88
Citations
2343
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Recent Articles
1.
Yuan M, Goovaerts S, Lee M, Devine J, Richmond S, Walsh S, et al.
Brief Bioinform
. 2025 Mar;
26(2).
PMID: 40062617
Genotype-phenotype (G-P) analyses for complex morphological traits typically utilize simple, predetermined anatomical measures or features derived via unsupervised dimension reduction techniques (e.g. principal component analysis (PCA) or eigen-shapes). Despite the...
2.
Geysens M, Huremagic B, Souche E, Breckpot J, Devriendt K, Peeters H, et al.
Genome Med
. 2025 Jan;
17(1):1.
PMID: 39789644
Background: A subset of developmental disorders (DD) is characterized by disease-specific genome-wide methylation changes. These episignatures inform on the underlying pathogenic mechanisms and can be used to assess the pathogenicity...
3.
Verhelst P, Janssens S, Matthews H, Begnoni G, Claes P, Shaheen E, et al.
Sci Rep
. 2025 Jan;
15(1):664.
PMID: 39753589
Condylar resorption is a feared complication of orthognathic surgery. This study investigated condylar resorption in a cohort of 200 patients This allowed for a powerful update on incidence and risk...
4.
Vanneste M, Hoskens H, Goovaerts S, Matthews H, Devine J, Aponte J, et al.
Nat Commun
. 2024 Dec;
15(1):10458.
PMID: 39622794
Human craniofacial shape is highly variable yet highly heritable with numerous genetic variants interacting through multiple layers of development. Here, we hypothesize that Mendelian phenotypes represent the extremes of a...
5.
Yuan M, Goovaerts S, Vanneste M, Matthews H, Hoskens H, Richmond S, et al.
PLoS Comput Biol
. 2024 Dec;
20(12):e1012617.
PMID: 39621772
Human facial shape, while strongly heritable, involves both genetic and structural complexity, necessitating precise phenotyping for accurate assessment. Common phenotyping strategies include simplifying 3D facial features into univariate traits such...
6.
Andreoli L, Peeters H, Van Steen K, Dierickx K
Eur J Hum Genet
. 2024 Nov;
33(3):266-280.
PMID: 39580561
Polygenic Risk Scores (PRS) are statistical methods estimating part of an individual's genetic susceptibility to various disease phenotypes. Their potential clinical applications to enhance the prediction, prevention, and risk management...
7.
Vervoort L, Dierckxsens N, Sousa Santos M, Meynants S, Souche E, Cools R, et al.
Genome Res
. 2024 Nov;
PMID: 39537358
The 22q11.2 deletion syndrome (22q11.2DS) is the most common microdeletion disorder. Why the incidence of 22q11.2DS is much greater than that of other genomic disorders remains unknown. Short-read sequencing cannot...
8.
Sleyp Y, Matthews H, Vanneste M, Vandenhove L, Delanote V, Hoskens H, et al.
Clin Genet
. 2024 Jul;
106(5):603-613.
PMID: 39056288
Recognizing Mendelian causes is crucial in molecular diagnostics and counseling for patients with autism spectrum disorder (ASD). We explored facial dysmorphism and facial asymmetry in relation to genetic causes in...
9.
Yuan M, Goovaerts S, Vanneste M, Matthews H, Hoskens H, Richmond S, et al.
bioRxiv
. 2024 Jun;
PMID: 38895298
Author Summary: Advancements linking variation in the human genome to phenotypes have rapidly evolved in recent decades and have revealed that most human traits are influenced by genetic variants to...
10.
Vervoort L, Dierckxsens N, Sousa Santos M, Meynants S, Souche E, Cools R, et al.
bioRxiv
. 2024 Apr;
PMID: 38562770
The 22q11.2 deletion syndrome (22q11.2DS) is the most common microdeletion disorder. Why the incidence of 22q11.2DS is much greater than that of other genomic disorders remains unknown. Short read sequencing...