Bjorn Menten
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Explore the profile of Bjorn Menten including associated specialties, affiliations and a list of published articles.
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Articles
151
Citations
4005
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Recent Articles
1.
Verlee M, Dhaenens E, De Cock L, Mosquera L, De Groote K, Vandekerckhove K, et al.
Eur J Hum Genet
. 2025 Jan;
PMID: 39870876
The etiology of congenital heart disease (CHD) is complex, comprising both genetic and environmental factors. Despite documented familial occurrences, the genetic etiology remains largely elusive. Trio exome sequencing identified a...
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.
Leger L, Aalders J, Heymans N, Van Acker-Verberckt K, De Bleeckere L, Coucke P, et al.
Stem Cell Res
. 2024 Sep;
81:103537.
PMID: 39217685
Arrhythmogenic cardiomyopathy is a severe genetic heart muscle disease characterized by fibro-fatty replacement of the myocardium. Pathogenic variants causal for this disease are mainly located in desmosomal genes, including desmoplakin...
6.
Maria Del Rocio P, Palomares Bralo M, Vanhooydonck M, Hamerlinck L, Dhaene E, Leimbacher S, et al.
medRxiv
. 2024 Aug;
PMID: 39148819
8q21.11 microdeletions encompassing the gene encoding transcription factor ZFHX4, have previously been associated by us with a syndromic form of intellectual disability, hypotonia, decreased balance and hearing loss. Here, we...
7.
Ingels J, De Cock L, Stevens D, Mayer R, Thery F, Sanchez Sanchez G, et al.
Cell Rep Med
. 2024 Apr;
5(5):101516.
PMID: 38626769
Non-small cell lung cancer (NSCLC) is known for high relapse rates despite resection in early stages. Here, we present the results of a phase I clinical trial in which a...
8.
Christodoulaki A, He H, Zhou M, De Roo C, Baetens M, De Pretre T, et al.
Hum Reprod Open
. 2024 Mar;
2024(1):hoae009.
PMID: 38425578
Study Question: Is pronuclear transfer (PNT) capable of restoring embryo developmental arrest caused by cytoplasmic inferiority of -grown (IVG) mouse oocytes? Summary Answer: PNT to matured cytoplasm significantly improved embryo...
9.
Perez Baca M, Jacobs E, Vantomme L, LeBlanc P, Bogaert E, Dheedene A, et al.
Am J Hum Genet
. 2024 Feb;
111(3):509-528.
PMID: 38412861
Neurodevelopmental disorders (NDDs) result from impaired development and functioning of the brain. Here, we identify loss-of-function (LoF) variation in ZFHX3 as a cause for syndromic intellectual disability (ID). ZFHX3 is...
10.
Popovic M, Borot L, Lorenzon A, Lopes A, Sakkas D, Lledo B, et al.
Hum Reprod
. 2023 Oct;
39(1):258-274.
PMID: 37873575
Study Question: Does the diagnosis of mosaicism affect ploidy rates across different providers offering preimplantation genetic testing for aneuploidies (PGT-A)? Summary Answer: Our analysis of 36 395 blastocyst biopsies across...