Bert L. Callewaert

26656Ghent University
Gent, VLG 2665, Belgium

Last Updated: 09/26/2026

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Found 170 publications

Evaluation of the Diagnostic Yield of Exome-Based Panels for Congenital Heart Defects in Different Clinical Settings.

Evaluation of the Diagnostic Yield of Exome-Based Panels for Congenital Heart Defects in Different Clinical Settings.

Journal: Circulation. Genomic and precision medicine

Published: July 01, 2026

Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Journal: European journal of human genetics : EJHG

Published: April 02, 2026

Unmasking NF1 mosaicism: optical genome mapping identifies a novel t(15;17) translocation in melanocytes.

Unmasking NF1 mosaicism: optical genome mapping identifies a novel t(15;17) translocation in melanocytes.

Journal: Journal of medical genetics

Published: January 23, 2026

Prevention of Heart Failure in Women: An Expert Consensus Statement on Sex-Specific Risk Factors.

Prevention of Heart Failure in Women: An Expert Consensus Statement on Sex-Specific Risk Factors.

Journal: European journal of heart failure

Published: January 20, 2026

Diagnosis in children with Marfan syndrome: red flags for early identification.

Diagnosis in children with Marfan syndrome: red flags for early identification.

Journal: Archives of disease in childhood

Published: January 11, 2026

Multicentric Longitudinal Performance Monitoring of Different Prenatal Cell-Free DNA Screening Technologies in Belgium.

Multicentric Longitudinal Performance Monitoring of Different Prenatal Cell-Free DNA Screening Technologies in Belgium.

Journal: Prenatal diagnosis

Published: December 26, 2025

Classifying novel DSG1 variants on disease severity in SAM syndrome and palmoplantar keratoderma.

Classifying novel DSG1 variants on disease severity in SAM syndrome and palmoplantar keratoderma.

Journal: Journal of dermatological science

Published: October 17, 2025

Smad3 deficiency attenuates disease severity in a zebrafish model for Smad6-related aortic disease.

Smad3 deficiency attenuates disease severity in a zebrafish model for Smad6-related aortic disease.

Journal: Angiogenesis

Published: October 08, 2025

RBMX functional retrocopy safeguards brain development in a species-dependent context.

RBMX functional retrocopy safeguards brain development in a species-dependent context.

Journal: Brain : a journal of neurology

Published: September 11, 2025

Autosomal Dominant Transmission Reframes Reproductive Counseling in Myhre Syndrome: A Novel Family and Literature Review.

Autosomal Dominant Transmission Reframes Reproductive Counseling in Myhre Syndrome: A Novel Family and Literature Review.

Journal: American journal of medical genetics. Part C, Seminars in medical genetics

Published: July 03, 2025

Evaluating variants of uncertain significance in adult zebrafish via prime editing: a proof of concept with a COL1A2 variant.

Evaluating variants of uncertain significance in adult zebrafish via prime editing: a proof of concept with a COL1A2 variant.

Journal: BMC medical genomics

Published: June 27, 2025

Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND).

Characterization of the genotypic and phenotypic spectrum of TCF7L2-related neurodevelopmental disorder (TRND).

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 23, 2025

Showing 1-12 of 170

Last Updated: 09/26/2026