Willy Lissens
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Explore the profile of Willy Lissens including associated specialties, affiliations and a list of published articles.
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68
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984
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Recent Articles
1.
Gheldof A, Seneca S, Stouffs K, Lissens W, Jansen A, Laeremans H, et al.
Mol Genet Genomic Med
. 2018 Dec;
7(2):e00527.
PMID: 30548430
Background: The diagnostic workup in patients with a clinical suspicion of lysosomal storage diseases (LSD) is often difficult due to the variability in the clinical phenotype. The gold standard for...
2.
Vandervore L, Stouffs K, Tanyalcin I, Vanderhasselt T, Roelens F, Holder-Espinasse M, et al.
J Med Genet
. 2017 Mar;
54(6):432-440.
PMID: 28258187
Background: Collagens are one of the major constituents of the pial membrane, which plays a crucial role in neuronal migration and cortical lamination during brain development. Type III procollagen, the...
3.
Harvengt J, Wanty C, De Paepe B, Sempoux C, Revencu N, Smet J, et al.
Mol Genet Metab Rep
. 2016 Nov;
1:223-231.
PMID: 27896091
A 1-year-old girl born to consanguineous parents presented with unexplained liver failure, leading to transplantation at 19 months. Subsequent partial splenectomy for persistent cytopenia showed the presence of foamy cells,...
4.
Tanyalcin I, Stouffs K, Daneels D, Al Assaf C, Lissens W, Jansen A, et al.
BMC Bioinformatics
. 2016 Oct;
17(1):425.
PMID: 27760515
Background: Predict whether a mutation is deleterious based on the custom 3D model of a protein. Results: We have developed MODICT, a mutation prediction tool which is based on per...
5.
Stouffs K, Gheldof A, Tournaye H, Vandermaelen D, Bonduelle M, Lissens W, et al.
Biomed Res Int
. 2016 Mar;
2016:6191307.
PMID: 26925412
Sertoli cell-only syndrome is defined by the complete absence of germ cells in testicular tissues and always results in male infertility. The aetiology often remains unknown. In this paper, we...
6.
Tanyalcin I, Al Assaf C, Gheldof A, Stouffs K, Lissens W, Jansen A
Bioinformatics
. 2015 Oct;
32(3):447-9.
PMID: 26454277
Summary: Today's genome browsers and protein databanks supply vast amounts of information about proteins. The challenge is to concisely bring together this information in an interactive and easy to generate...
7.
Bissay V, Van Malderen S, Keymolen K, Lissens W, Peeters U, Daneels D, et al.
Eur J Hum Genet
. 2015 Jun;
24(3):400-7.
PMID: 26036855
SCN5A mutations involving the α-subunit of the cardiac voltage-gated muscle sodium channel (NaV1.5) result in different cardiac channelopathies with an autosomal-dominant inheritance such as Brugada syndrome. On the other hand,...
8.
Orlando C, Heylen O, Lissens W, Jochmans K
Thromb Res
. 2015 Apr;
135(6):1179-85.
PMID: 25837307
Background: Hereditary antithrombin (AT) deficiency is a rare autosomal dominant disorder characterised by decreased AT activity in plasma and predisposition to recurrent venous thromboembolism (VTE). Thrombotic risk is thought to...
9.
Vancampenhout K, Caljon B, Spits C, Stouffs K, Jonckheere A, De Meirleir L, et al.
PLoS One
. 2014 Nov;
9(11):e112950.
PMID: 25383547
The advent of massive parallel sequencing (MPS) has revolutionized the field of human molecular genetics, including the diagnostic study of mitochondrial (mt) DNA dysfunction. The analysis of the complete mitochondrial...
10.
Stouffs K, Seneca S, Lissens W
Ann Endocrinol (Paris)
. 2014 Apr;
75(2):109-11.
PMID: 24768008
Male infertility, affecting around half of the couples with a problem to get pregnant, is a very heterogeneous condition. Part of patients are having a defect in spermatogenesis of which...