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Orthodontics & Craniofacial Research|June 25, 2021
Automated landmarking for palatal shape analysis using geometric deep learningBalder Croquet, Harold Matthews, Jules Mertens, et al.
Genome Research|March 3, 2004
Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide arrayHajime Matsuzaki, Halina Loi, Shoulian Dong, et al.
American Journal of Respiratory Cell and Molecular Biology|January 10, 2006
Novel polymorphisms in the myosin light chain kinase gene confer risk for acute lung injuryLi Gao, Audrey Grant, Indrani Halder, et al.
JAMA Pediatrics|June 7, 2017
Association Between Prenatal Alcohol Exposure and Craniofacial Shape of Children at 12 Months of AgeEvelyne Muggli, Harold Matthews, Anthony Penington, et al.
IEEE Access : Practical Innovations, Open Solutions|August 14, 2025
A 3D Clinical Face Phenotype Space of Genetic Syndromes Using a Triplet-Based Singular Geometric AutoencoderSoha S Mahdi, Eduarda Caldeira, Harold Matthews, et al.
Journal of Medical Genetics|November 20, 2025
Advancing genotype-phenotype analysis through 3D facial morphometry: insights from Cri-du-Chat syndromeMichiel Vanneste, Harold Matthews, Yoeri Sleyp, et al.
Medrxiv : the Preprint Server for Health Sciences|June 10, 2025
Advancing Genotype-Phenotype Analysis through 3D Facial Morphometry: Insights from Cri-du-Chat SyndromeMichiel Vanneste, Harold Matthews, Yoeri Sleyp, et al.
Proceedings. Biological Sciences|April 29, 2016
Sexual selection on male vocal fundamental frequency in humans and other anthropoidsDavid A Puts, Alexander K Hill, Drew H Bailey, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
Leveraging the genetics of human face shape boosts the discovery of orofacial cleft risk lociNoah Herrick, Seppe Goovaerts, Alexandra Manchel, et al.
American Journal of Human Genetics|September 13, 2003
Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effectLinda L Bachinski, Bjarne Udd, Giovanni Meola, et al.
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