Michiel Vanneste

Leuven, VLG, Belgium

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 14 publications

Shared genetic basis and structure of syndromic and normal facial variation.

Shared genetic basis and structure of syndromic and normal facial variation.

Journal: American journal of human genetics

Published: November 07, 2025

A 3D Clinical Face Phenotype Space of Genetic Syndromes Using a Triplet-Based Singular Geometric Autoencoder.

A 3D Clinical Face Phenotype Space of Genetic Syndromes Using a Triplet-Based Singular Geometric Autoencoder.

Journal: IEEE access : practical innovations, open solutions

Published: August 14, 2025

Advancing Genotype-Phenotype Analysis through 3D Facial Morphometry: Insights from Cri-du-Chat Syndrome.

Advancing Genotype-Phenotype Analysis through 3D Facial Morphometry: Insights from Cri-du-Chat Syndrome.

Journal: medRxiv : the preprint server for health sciences

Published: June 10, 2025

Advancing genotype-phenotype analysis through 3D facial morphometry: insights from Cri-du-Chat syndrome.

Advancing genotype-phenotype analysis through 3D facial morphometry: insights from Cri-du-Chat syndrome.

Journal: Journal of medical genetics

Published: May 20, 2025

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

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

Journal: American journal of medical genetics. Part A

Published: April 14, 2025

Attenuated Clinical Forms of Tubulinopathies in Children and Adults: A Series of 24 Individuals.

Attenuated Clinical Forms of Tubulinopathies in Children and Adults: A Series of 24 Individuals.

Journal: Pediatric neurology

Published: October 31, 2024

Mapping genes for human face shape: exploration of univariate phenotyping strategies.

Mapping genes for human face shape: exploration of univariate phenotyping strategies.

Journal: bioRxiv : the preprint server for biology

Published: June 19, 2024

Toward 3D facial analysis for recognizing Mendelian causes of autism spectrum disorder.

Toward 3D facial analysis for recognizing Mendelian causes of autism spectrum disorder.

Journal: Clinical genetics

Published: April 28, 2024

Mapping genes for human face shape: Exploration of univariate phenotyping strategies.

Mapping genes for human face shape: Exploration of univariate phenotyping strategies.

Journal: PLoS computational biology

Published: April 07, 2024

Syndrome-informed phenotyping identifies a polygenic background for achondroplasia-like facial variation in the general population.

Syndrome-informed phenotyping identifies a polygenic background for achondroplasia-like facial variation in the general population.

Journal: bioRxiv : the preprint server for biology

Published: December 18, 2023

Syndrome-informed phenotyping identifies a polygenic background for achondroplasia-like facial variation in the general population.

Syndrome-informed phenotyping identifies a polygenic background for achondroplasia-like facial variation in the general population.

Journal: Nature communications

Published: November 29, 2023

In vivo quantification of the 3D kinematics and coupling of the thumb base joints.

In vivo quantification of the 3D kinematics and coupling of the thumb base joints.

Journal: Medical engineering & physics

Published: March 23, 2022

Showing 1-12 of 14

Last Updated: 09/26/2026