Laurens Hannes
Leuven, VLG, Belgium
Last Updated: 09/26/2026
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Found 8 publications
IBD-linked Genetic Variance in Intestinal Transplantation: A Multicenter Cohort Analysis.
Journal: Annals of surgery
Published: February 21, 2025
Genotype imputation from low-coverage data for medical and population genetic analyses.
Journal: Genome research
Published: October 29, 2024
MIP4IBD: An Easy and Rapid Genotyping-by-Sequencing Assay for the Inflammatory Bowel Diseases Risk Loci.
Journal: Inflammatory bowel diseases
Published: September 23, 2024
Chromosomal analysis and short-term outcome of prenatally diagnosed congenital heart disease.
Journal: Scientific reports
Published: September 05, 2024
The importance of intrafamilial cognitive phenotyping by the case of 22q11.2 deletion, 15q11.2 deletion, and families with inherited copy number variants of unknown significance.
Journal: Journal of neurodevelopmental disorders
Published: May 28, 2024
Germline founder variant c.1998delinsTTCT in the RET oncogene: a cohort study in 15 Belgian families.
Journal: European journal of endocrinology
Published: June 12, 2023
Differential alternative splicing analysis links variation in ZRSR2 to a novel type of oral-facial-digital syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 02, 2023
Triplications of chromosome 1p36.3, including the genes GABRD and SKI, are associated with a developmental disorder and a facial gestalt.
Journal: American journal of medical genetics. Part A
Published: November 28, 2022
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Last Updated: 09/26/2026