Kris Van den Bogaert
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Explore the profile of Kris Van den Bogaert including associated specialties, affiliations and a list of published articles.
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48
Citations
575
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Recent Articles
1.
Verbeke M, Hannes L, Devriendt K, Van den Bogaert K, Cools B, De Catte L, et al.
Sci Rep
. 2025 Jan;
15(1):3923.
PMID: 39890866
Congenital structural heart disease (CHD) is the leading cause of infant death from birth defects. Postnatal survival primarily depends on the type and severity of the defect. In addition, worse...
2.
Geysens M, Huremagic B, Souche E, Breckpot J, Devriendt K, Peeters H, et al.
Genome Med
. 2025 Jan;
17(1):1.
PMID: 39789644
Background: A subset of developmental disorders (DD) is characterized by disease-specific genome-wide methylation changes. These episignatures inform on the underlying pathogenic mechanisms and can be used to assess the pathogenicity...
3.
Lannoo L, Van den Bogaert K, Brison N, Dehaspe L, Dimitriadou E, Fieuws S, et al.
N Engl J Med
. 2024 Jul;
391(2):184-185.
PMID: 38986064
No abstract available.
4.
Stanley K, Jatsenko T, Tuveri S, Sudhakaran D, Lannoo L, Van Calsteren K, et al.
Nat Commun
. 2024 Mar;
15(1):2220.
PMID: 38472221
Circulating cell-free DNA (cfDNA) fragments have characteristics that are specific to the cell types that release them. Current methods for cfDNA deconvolution typically use disease tailored marker selection in a...
5.
Veyt N, Van Buggenhout G, Devriendt K, Van den Bogaert K, Brison N
Eur J Hum Genet
. 2024 Jan;
32(4):421-425.
PMID: 38200083
46,XY gonadal dysgenesis (GD) is a disorder of sex development due to incomplete gonadal differentiation into testes, resulting in female to ambiguous external genitalia. Duplications at the Xp21.2 locus involving...
6.
Lannoo L, Van Camp J, Brison N, Parijs I, Vancoillie L, Van den Bogaert K, et al.
Prenat Diagn
. 2023 Aug;
43(10):1333-1343.
PMID: 37592442
Objectives: To assess maternal characteristics and comorbidities in patients with persistent uninterpretable non-invasive prenatal testing (NIPT) and to evaluate the association with adverse pregnancy outcome in a general risk population....
7.
Zagnoli-Vieira G, Brazina J, Van den Bogaert K, Huybrechts W, Molenaers G, Caldecott K, et al.
Hum Genet
. 2023 Aug;
142(9):1417-1427.
PMID: 37558815
Mutations in TDP2, encoding tyrosyl-DNA phosphodiesterase 2, have been associated with a syndromal form of autosomal recessive spinocerebellar ataxia, type 23 (SCAR23). This is a very rare and progressive neurodegenerative...
8.
Parijs I, Brison N, Vancoillie L, Baetens M, Blaumeiser B, Boulanger S, et al.
Eur J Hum Genet
. 2023 Apr;
32(1):31-36.
PMID: 37029316
Maternally inherited 15q11-q13 duplications are generally found to cause more severe neurodevelopmental anomalies compared to paternally inherited duplications. However, this assessment is mainly inferred from the study of patient populations,...
9.
Dietvorst S, Devriendt K, Lambert J, Boogaerts A, Van den Bogaert K, Buyse G, et al.
Eur J Med Genet
. 2023 Jan;
66(4):104713.
PMID: 36702440
The combination of Dandy-Walker malformation and occipital cephalocele is a rare autosomal dominant condition, known as ADDWOC, and caused by mutations in NID1 or LAMC1. We present a three-generation family...
10.
Cospain A, Rivera-Barahona A, Dumontet E, Gener B, Bailleul-Forestier I, Meyts I, et al.
Genet Med
. 2022 Oct;
24(12):2475-2486.
PMID: 36197437
Purpose: We aimed to investigate the molecular basis of a novel recognizable neurodevelopmental syndrome with scalp and enamel anomalies caused by truncating variants in the last exon of the gene...