Researcher
Willy Lissens
- Keywords:Medicine, Language and literature (incl. information, documentation, library and archive sciences)
Affiliations
- Communication Sciences (Department)
Member
From1 Jan 2019 → 30 Sep 2020 - Clinical sciences (Department)
Member
From1 Jan 2014 → 30 Jun 2014 - Reproduction and Genetics (Research group)
Member
From21 Jun 2010 → 30 Sep 2020 - Department of Embryology and Genetics (Department)
Member
From1 Jan 2010 → 31 Dec 2013 - Department of Embryology and Genetics (Department)
Member
From1 Oct 2003 → 30 Sep 2013
Projects
1 - 4 of 4
- SRP (Groeiers): Development of an in vitro testing strategy for epigenetic susceptibility of the oocyte: understanding long term effects on adult healthFrom1 Mar 2014 → 28 Feb 2019Funding: BOF - Concerted Research Project from 1994
- Development of diagnostic, biochemical and molecular methods, the prevention and the study of treatment of OXPHOS deficiency.From1 Jan 2010 → 31 Dec 2013Funding: FWO research project (including WEAVE projects)
- Research at the interface between human genetics and reproduction.From1 Jan 2009 → TodayFunding: Methusalem
- Analysis of genes involved in male infertilityFrom1 Jan 2008 → 31 Dec 2011Funding: FWO research project (including WEAVE projects)
Publications
11 - 20 of 41
- Characterization of CoQ₁₀ biosynthesis in fibroblasts of patients with primary and secondary CoQ₁₀ deficiency(2014)
Authors: Nuria Buján, Angela Arias, Raquel Montero, Judit García-Villoria, Willy Lissens, Sara Seneca, Carmen Espinós, Plácido Navas, Linda De Meirleir, Rafael Artuch, et al.
Pages: 53-62 - A new double substitution mutation in the MEN1 gene: a limited penetrance and a specific phenotype(2013)
Authors: Urielle Ullmann, David Unuane, Brigitte Velkeniers-Hoebanckx, Willy Lissens, Wim Wuyts, Maryse Bonduelle
Pages: 695-697 - Genetic causes of spermatogenic failure(2012)
Authors: Annelien Massart, Willy Lissens, Herman Tournaye, Katrien Stouffs
Pages: 40-48 - Array comparative genomic hybridization in male infertility.(2012)
Authors: Katrien Stouffs, Deborah Vandermaelen, A. Massart, B. Menten, Sarah Vergult, Herman Tournaye, Willy Lissens
Pages: 921-929 - Krabbe leukodystrophy in a selected population with high rate of late onset forms: longer survival linked to c.121G>A (p.Gly41Ser) mutation(2011)
Authors: Agata Fiumara, , Alessia Arena, , Willy Lissens, , Giovanni Sorge
Pages: 452-458 - Discordance for retinitis pigmentosa in two monozygotic twin pairs(2011)
Authors: Berghmans Lv, De Mendonça Rh, , , Takahashi Wy, Willy Lissens, E. De Baere, Bart Leroy
Pages: 1164-1169 - Novel variants of beta-subunits of sodium channel genes in Brugada Syndrome(2011)
Authors: Evrim Komurcu-Bayrak, Kristof Endels, Willy Lissens, Sara Seneca, F. Bayrak, Andrea Sarkozy, Pedro Brugada, Maryse Bonduelle, Sonia Van Dooren
Pages: 276-276 - Facilitating the Fragile X post- and prenatal genetic diagnostic testing workflow by use of the Abbott FMR1 TP-PCR and FMR1 sizing PCR products.(2011)
Authors: Sonia Van Dooren, Sara Seneca, Kristof Endels, K. Keymolen, Marjan De Rademaeker, Van Berkel Kim, Willy Lissens, Maryse Bonduelle
Pages: 178-178 - A novel Brugada syndrome variant shown to be causal based on segregation analysis and familial genotypic-phenotypic correlation(2011)
Authors: Sonia Van Dooren, Willy Lissens, Sara Seneca, Liszl Peirsman, Urielle Ullmann, Andrea Sarkozy, Pedro Brugada, Maryse Bonduelle
Pages: 394-394 - Screening for nuclear genetic defects in the ATP synthase-associated genes TMEM70, ATP12 and ATP5E in patients with 3-methylglutaconic aciduria.(2011)
Authors: F Tort, M Del Toro, Willy Lissens, J Montoya, M Fernandez-Burriel, A. Font, N. Bujan, A. Navarro-Sastre, E; Lopez-Gallardo, Ja Arranz, et al.
Pages: 297-300