Nils Peeters
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Explore the profile of Nils Peeters including associated specialties, affiliations and a list of published articles.
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17
Citations
177
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Recent Articles
1.
Boudewyns A, Van den Ende J, Peeters N, Van Camp G, Hofkens-Van den Brandt A, Van Schil K, et al.
Otol Neurotol
. 2023 Feb;
44(4):360-366.
PMID: 36804529
Objective: To investigate the diagnostic yield of targeted next-generation sequencing using hearing loss panels and to identify patient-related factors that are associated with a definite genetic cause. Study Design: Retrospective...
2.
Kumar A, Loeys B, Van De Beek G, Peeters N, Wuyts W, Van Laer L, et al.
Bioinformatics
. 2022 Nov;
39(1).
PMID: 36440912
Motivation: Computational identification of copy number variants (CNVs) in sequencing data is a challenging task. Existing CNV-detection methods account for various sources of variation and perform different normalization strategies. However,...
3.
Van Gucht I, Krebsova A, Diness B, Laga S, Adlam D, Kempers M, et al.
Int J Mol Sci
. 2021 Jul;
22(13).
PMID: 34281165
Thoracic aortic aneurysm and dissection (TAAD) is a major cause of cardiovascular morbidity and mortality. Loss-of-function variants in , encoding the extracellular matrix crosslinking enzyme lysyl oxidase, have been reported...
4.
Boudewyns A, Van den Ende J, Declau F, Wuyts W, Peeters N, Hofkens-Van den Brandt A, et al.
Otol Neurotol
. 2020 Sep;
41(9):1240-1248.
PMID: 32925850
Background: Confirmation of permanent hearing loss in a newborn should be followed by a search for an underlying etiology because this may impact hearing loss management and counselling. Methods: Retrospective...
5.
Luyckx I, MacCarrick G, Kempers M, Meester J, Geryl C, Rombouts O, et al.
Eur J Hum Genet
. 2019 Feb;
27(7):1044-1053.
PMID: 30796334
Progressive dilatation of the thoracic aorta leads to thoracic aortic aneurysm (TAA), which is often asymptomatic but predisposes to lethal aortic dissections and ruptures. TAA is a common complication in...
6.
Cannaerts E, Kempers M, Maugeri A, Marcelis C, Gardeitchik T, Richer J, et al.
J Med Genet
. 2018 Jul;
56(4):220-227.
PMID: 29967133
Background: Missense variants in , encoding a key transcriptional regulator of transforming growth factor beta signalling, were recently reported to cause arterial aneurysmal disease. Objectives: The aims of the study...
7.
Role of Targeted Next Generation Sequencing in the Etiological Work-Up of Congenitally Deaf Children
Boudewyns A, Van den Ende J, Sommen M, Wuyts W, Peeters N, Van de Heyning P, et al.
Otol Neurotol
. 2018 Jun;
39(6):732-738.
PMID: 29889784
Objectives: The purpose of this study is to report the results of a comprehensive etiological work-up for congenitally deaf children including targeted next generation sequencing. Study Design: Retrospective case review....
8.
JanssensdeVarebeke S, Van Camp G, Peeters N, Elinck E, Widdershoven J, Cox T, et al.
Eur J Hum Genet
. 2018 Feb;
26(4):587-591.
PMID: 29449721
Pathogenic variant in COCH are a known cause of DFNA9 autosomal dominant progressive hearing loss and vestibular dysfunction with adult onset. Hitherto, only dominant nonsynonymous variants and in-frame deletions with...
9.
Proost D, Vandeweyer G, Meester J, Salemink S, Kempers M, Ingram C, et al.
Hum Mutat
. 2015 Apr;
36(8):808-14.
PMID: 25907466
At least 14 causative genes have been identified for both syndromic and nonsyndromic forms of thoracic aortic aneurysm/dissection (TAA), an important cause of death in the industrialized world. Molecular confirmation...
10.
Wischmeijer A, Van Laer L, Tortora G, Bolar N, Van Camp G, Fransen E, et al.
Am J Med Genet A
. 2013 Apr;
161A(5):1028-35.
PMID: 23554019
Recently, mutations in the SMAD3 gene were found to cause a new autosomal dominant aneurysm condition similar to Loeys-Dietz syndrome (LDS), mostly with osteoarthritis, called aneurysms-osteoarthritis syndrome (AOS). Our 3-year-old...