K Devriendt
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Explore the profile of K Devriendt including associated specialties, affiliations and a list of published articles.
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229
Citations
3515
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Recent Articles
1.
Devriendt K, Van Mieghem P
Phys Rev E
. 2018 Jan;
96(5-1):052314.
PMID: 29347672
We propose an approximation framework that unifies and generalizes a number of existing mean-field approximation methods for the susceptible-infected-susceptible (SIS) epidemic model on complex networks. We derive the framework, which...
2.
Van Mieghem P, Devriendt K, Cetinay H
Phys Rev E
. 2018 Jan;
96(3-1):032311.
PMID: 29346956
Determining a set of "important" nodes in a network constitutes a basic endeavor in network science. Inspired by electrical flows in a resistor network, we propose the best conducting node...
3.
Lewyllie A, Roosenboom J, Indencleef K, Claes P, Swillen A, Devriendt K, et al.
J Dent Res
. 2017 Jul;
96(12):1386-1391.
PMID: 28732176
The 22q11.2 deletion syndrome (22q11.2DS) is one of the most frequent microdeletion syndromes and presents with a highly variable phenotype. In most affected individuals, specific but subtle facial features can...
4.
Mbuyi-Musanzayi S, Tshilombo Katombe F, Lukusa Tshilobo P, Kalenga Mwenze Kayamba P, Devriendt K, Reychler H
Int J Oral Maxillofac Surg
. 2017 Jun;
46(10):1338-1345.
PMID: 28629945
One hundred and one patients with complete or incomplete cleft lip underwent the anatomical subunit approximation technique for repair. The patients were followed up prospectively for 1year. The objective of...
5.
Lumaka A, Cosemans N, Lulebo Mampasi A, Mubungu G, Mvuama N, Lubala T, et al.
Clin Genet
. 2016 Dec;
92(2):166-171.
PMID: 27925162
The evaluation of facial dysmorphism is a critical step toward reaching a diagnostic. The aim of the present study was to evaluate the ability to interpret facial morphology in African...
6.
Khandelwal K, Ishorst N, Zhou H, Ludwig K, Venselaar H, Gilissen C, et al.
J Dent Res
. 2016 Nov;
96(2):179-185.
PMID: 27834299
Common variants in interferon regulatory factor 6 ( IRF6) have been associated with nonsyndromic cleft lip with or without cleft palate (NSCL/P) as well as with tooth agenesis (TA). These...
7.
Odent S, Casteels I, Cassiman C, Dieltiens M, Hua M, Devriendt K
Ophthalmic Genet
. 2016 Apr;
38(2):167-170.
PMID: 27096414
We present a newborn diagnosed with posterior amorphous corneal dystrophy (PACD). PACD is a rare disorder with partial or complete posterior lamellar corneal opacification. Genetic screening showed a deletion of...
8.
Roosenboom J, Claes P, Devriendt K, Dormaar T, Peeters H, Saey I, et al.
B-ENT
. 2015 Nov;
11(3):173-82.
PMID: 26601549
Cleft lip and/or palate (CL/P) is one of the most frequent congenital malformations, with a frequency of 1 in 700 live births. Non-syndromic orofacial clefting is a multifactorial condition, with...
9.
Rathe M, Rayyan M, Schoenaers J, Dormaar J, Breuls M, Verdonck A, et al.
Int J Pediatr Otorhinolaryngol
. 2015 Jun;
79(8):1206-12.
PMID: 26092549
Objectives: To review early clinical manifestations of Pierre Robin sequence (PRS) and their management during the first year of life in the University Hospitals Leuven. Methods: Retrospective series of 48...
10.
Roosenboom J, Saey I, Peeters H, Devriendt K, Claes P, Hens G
Biomed Res Int
. 2015 Jun;
2015:863429.
PMID: 26064961
Evidence exists for the presence of a specific facial phenotype in nonaffected first-degree relatives of persons with CL/P. An increased risk for olfactory dysfunction has also been reported in CL/P-relatives....