Sandra D. Janssens

Gent, VLG, Belgium

Last Updated: 09/26/2026

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Found 69 publications

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

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

Integrating PGT-A into PGT-M protocols in young ART-naïve patients undergoing single embryo transfer.

Integrating PGT-A into PGT-M protocols in young ART-naïve patients undergoing single embryo transfer.

Journal: Reproductive biomedicine online

Published: December 07, 2025

ERN GENTURIS guideline on counselling on reproductive options for individuals with a cancer predisposition syndrome (including genturis).

ERN GENTURIS guideline on counselling on reproductive options for individuals with a cancer predisposition syndrome (including genturis).

Journal: European journal of human genetics : EJHG

Published: October 22, 2025

Risk management and the further use of gametes from a donor with a known pathogenic variant.

Risk management and the further use of gametes from a donor with a known pathogenic variant.

Journal: Journal of medical ethics

Published: October 22, 2025

Unexpected High Prevalence of Focal Facial Dermal Dysplasia (FFDD) Type IV Is Linked to a Founder Effect in the Belgian Population.

Unexpected High Prevalence of Focal Facial Dermal Dysplasia (FFDD) Type IV Is Linked to a Founder Effect in the Belgian Population.

Journal: Clinical genetics

Published: December 06, 2024

Advancing diagnosis and early risk assessment of preeclampsia through noninvasive cell-free DNA methylation profiling.

Advancing diagnosis and early risk assessment of preeclampsia through noninvasive cell-free DNA methylation profiling.

Journal: Clinical epigenetics

Published: August 09, 2024

Full characterization of unresolved structural variation through long-read sequencing and optical genome mapping.

Full characterization of unresolved structural variation through long-read sequencing and optical genome mapping.

Journal: Scientific reports

Published: July 20, 2024

Should we use expanded carrier screening in gamete donation?

Should we use expanded carrier screening in gamete donation?

Journal: Fertility and sterility

Published: May 29, 2024

Managing risks for genetic conditions in donor sperm treatment: current practices in Belgian fertility clinics.

Managing risks for genetic conditions in donor sperm treatment: current practices in Belgian fertility clinics.

Journal: Reproductive biomedicine online

Published: April 25, 2024

CHD7 Disorder-Not CHARGE Syndrome-Presenting as Isolated Cochleovestibular Dysfunction.

CHD7 Disorder-Not CHARGE Syndrome-Presenting as Isolated Cochleovestibular Dysfunction.

Journal: Genes

Published: March 29, 2024

Aligning genotyping and copy number data in single trophectoderm biopsies for aneuploidy prediction: uncovering incomplete concordance.

Aligning genotyping and copy number data in single trophectoderm biopsies for aneuploidy prediction: uncovering incomplete concordance.

Journal: Human reproduction open

Published: July 07, 2023

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Last Updated: 09/26/2026