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
11.
Sy M, Chauhan J, Prescott K, Imam A, Kraus A, Beleza A, et al.
Am J Med Genet A
. 2022 Sep;
188(12):3492-3504.
PMID: 36135330
Esophageal atresia/tracheoesophageal fistula (EA/TEF) is a life-threatening birth defect that often occurs with other major birth defects (EA/TEF+). Despite advances in genetic testing, a molecular diagnosis can only be made...
12.
Che H, Jatsenko T, Lannoo L, Stanley K, Dehaspe L, Vancoillie L, et al.
NPJ Genom Med
. 2022 Sep;
7(1):55.
PMID: 36100603
The early detection of tissue and organ damage associated with autoimmune diseases (AID) has been identified as key to improve long-term survival, but non-invasive biomarkers are lacking. Elevated cell-free DNA...
13.
Hardcastle A, Berry A, Campbell I, Zhao X, Liu P, Gerard A, et al.
Am J Med Genet A
. 2022 Jul;
188(10):2958-2968.
PMID: 35904974
Congenital diaphragmatic hernia (CDH) can occur in isolation or in conjunction with other birth defects (CDH+). A molecular etiology can only be identified in a subset of CDH cases. This...
14.
Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge
Lannoo L, van Straaten K, Breckpot J, Brison N, De Catte L, Dimitriadou E, et al.
Eur J Hum Genet
. 2022 Jul;
30(12):1323-1330.
PMID: 35896702
Non-invasive prenatal testing has been introduced for the detection of Trisomy 13, 18, and 21. Using genome-wide screening also other "rare" autosomal trisomies (RATs) can be detected with a frequency...
15.
Che H, Jatsenko T, Lenaerts L, Dehaspe L, Vancoillie L, Brison N, et al.
Clin Chem
. 2022 Jun;
68(9):1164-1176.
PMID: 35769009
Background: Cell-free DNA (cfDNA) analysis holds great promise for non-invasive cancer screening, diagnosis, and monitoring. We hypothesized that mining the patterns of cfDNA shallow whole-genome sequencing datasets from patients with...
16.
Lannoo L, Lenaerts L, Van den Bogaert K, Che H, Brison N, Devriendt K, et al.
Prenat Diagn
. 2021 Aug;
41(10):1264-1272.
PMID: 34405430
Cancer is diagnosed in one in 1000 to 1500 pregnancies. Most frequently encountered malignancies during pregnancy are breast cancer, hematological cancer, cervical cancer and malignant melanoma. Maternal cancer is associated...
17.
Lantoine J, Brysse A, Dideberg V, Claes K, Symoens S, Coucke W, et al.
JMIR Med Inform
. 2021 Jul;
9(7):e27980.
PMID: 34255700
Background: Participation in quality controls, also called external quality assessment (EQA) schemes, is required for the ISO15189 accreditation of the Medical Centers of Human Genetics. However, directives on the minimal...
18.
Lenaerts L, Brison N, Maggen C, Vancoillie L, Che H, Vandenberghe P, et al.
EClinicalMedicine
. 2021 May;
35:100856.
PMID: 34036251
Background: Implausible false positive results in non-invasive prenatal testing (NIPT) have been occasionally associated with the detection of occult maternal malignancies. Hence, there is a need for approaches allowing accurate...
19.
van Riel M, Brison N, Baetens M, Blaumeiser B, Boemer F, Bourlard L, et al.
Obstet Gynecol
. 2021 May;
137(6):1102-1108.
PMID: 33957658
Objective: To evaluate the accuracy and diagnostic value of genome-wide noninvasive prenatal testing (NIPT) for the detection of fetal aneuploidies in multiple gestations, with a focus on dichorionic-diamniotic twin pregnancies....
20.
Domaradzka J, Deperas M, Obersztyn E, Kucinska-Chahwan A, Brison N, Van den Bogaert K, et al.
Mol Cytogenet
. 2021 Mar;
14(1):18.
PMID: 33722255
Background: Non-invasive prenatal testing (NIPT) is a rapidly developing and widely used method in the prenatal screening. Recently, the widespread use of the NIPT caused a neglecting of the limitations...