Sandra Janssens
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Explore the profile of Sandra Janssens including associated specialties, affiliations and a list of published articles.
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75
Citations
1526
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Recent Articles
1.
Beyens A, Van de Voorde S, Guerreiro Santano Ramos Da Silva M, De Meulemeester S, Devriendt K, Goeteyn M, et al.
Clin Genet
. 2025 Jan;
PMID: 39828664
Focal facial dermal dysplasia (FFDD) type IV is a rare inherited facial defect caused by biallelic variants in CYP26C1. This study reports two novel Belgian FFDD type IV cases, both...
2.
Baetens M, Van Gaever B, Deblaere S, De Koker A, Meuris L, Callewaert N, et al.
Clin Epigenetics
. 2024 Dec;
16(1):182.
PMID: 39695764
Background: Aberrant embryo implantation and suboptimal placentation can lead to (severe) complications such as preeclampsia and fetal growth restriction later in pregnancy. Current identification of high-risk pregnancies relies on a...
3.
De Clercq G, Vantomme L, Dewaele B, Callewaert B, Vanakker O, Janssens S, et al.
Sci Rep
. 2024 Nov;
14(1):29142.
PMID: 39587234
Structural variants (SVs) are important contributors to human disease. Their characterization remains however difficult due to their size and association with repetitive regions. Long-read sequencing (LRS) and optical genome mapping...
4.
De Witte L, Baetens M, Tilleman K, Vanden Meerschaut F, Janssens S, Van Tongerloo A, et al.
Hum Reprod Open
. 2024 Oct;
2024(4):hoae056.
PMID: 39391861
Study Question: To what extent can genotype analysis aid in the classification of (mosaic) aneuploid embryos diagnosed through copy number analysis of a trophectoderm (TE) biopsy? Summary Answer: In a...
5.
Accoe D, Pennings G, Tilleman K, Vanden Meerschaut F, Janssens S, Mertes H
Reprod Biomed Online
. 2024 Aug;
49(5):104352.
PMID: 39213985
Research Question: How do fertility clinics in Belgium manage risks for genetic conditions in donor sperm treatment? Design: An electronic questionnaire was distributed to all fertility clinics in Belgium in...
6.
Capalbo A, Pla J, Janssens S, Accoe D, Pennings G, Mertes H
Fertil Steril
. 2024 Jun;
122(2):220-227.
PMID: 38934980
No abstract available.
7.
Driesen J, Van Hoecke H, Maes L, Janssens S, Acke F, De Leenheer E
Genes (Basel)
. 2024 May;
15(5).
PMID: 38790272
CHARGE syndrome, characterized by a distinct set of clinical features, has been linked primarily to mutations in the gene. Initially defined by specific clinical criteria, including coloboma, heart defects, choanal...
8.
Van Tongerloo A, Verdin H, Steyaert W, Coucke P, Janssens S
J Genet Couns
. 2024 Apr;
34(1):e1899.
PMID: 38610077
Rapidly evolving genomic technologies have made genetic expanded carrier screening (ECS) possible for couples considering a pregnancy. The aim of ECS is to identify couples at risk of having a...
9.
Wilderman A, Dhaene E, Baetens M, Yankee T, Winchester E, Glidden N, et al.
Nat Commun
. 2024 Jan;
15(1):136.
PMID: 38167838
Craniofacial abnormalities account for approximately one third of birth defects. The regulatory programs that build the face require precisely controlled spatiotemporal gene expression, achieved through tissue-specific enhancers. Clusters of coactivated...
10.
Vanbelleghem E, Muyshond V, Colman R, Vanden Meerschaut F, Stoop D, Janssens S, et al.
Reprod Biomed Online
. 2023 May;
47(2):103224.
PMID: 37244865
Research Question: What are the incidence of and indications for sperm donor restriction due to suspected/confirmed disease risk, and the future treatment choices of patients using these sperm donors? Design:...