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
31 - 40 of 41
- Is there a role for the nuclear export factor 2 gene in male infertility?(2008)
Authors: Katrien Stouffs, H Tournaye, Josiane Van Der Elst, Willy Lissens
Pages: 1787-91 - Is beta-glucuronidase a clinical useful biomarker for an acute organophosphorus poisoning?(2008)
Authors: Marc Sabbe, D. Desruelles, Willy Lissens
Pages: 431-433 - A New Missense Mutation in the CASR Gene in Familial Interstitial Lung Disease with Hypocalciuric Hypercalcemia and Defective Granulocyte Function.(2008)
Authors: Maurits Demedts, Willy Lissens, Wim Wuyts, Gert Matthijs, Michiel Thomeer, Roger Bouillon
Pages: 558-559 - Molecular diagnosis of Krabbe disease(2008)
Authors: Willy Lissens
- Retinitis pigmentosa and adult-onset neurological deterioration revealing Sanfilippo A disease.(2008)
Authors: Marie-Cécile Nassogne, A. Jeanjean, C. Kestens, C. Grandin, Marie-Françoise Vincent, Willy Lissens
Pages: 114-114 - N-Acetylamino aciduria: a benign biochemical finding!(2008)
Authors: J. Calvin, R.a. Wevers, U. Engelke, Willy Lissens, J. Perrier, T.g. Giardina, Joél Smet, S. Hogg, L. Abulhoul, V. Puthi, et al.
Pages: 4-4 - Fluorescent visualization of the mitochondrial membrane potential gradient identifies oxidative phosphorylation defects in fibroblasts.
Authors: Rudy Van Coster, Boél De Paepe, Joél Smet, Willy Lissens, Linda De Meirleir, R. Rodenburg
Pages: 159-159 - Identification of two de novo mutations responsible for type I antithrombin deficiency.
Authors: Willy Lissens, Daniele Hasaerts
Pages: 187-189 - Complex III staining in blue native polyacrylamide gels.
Authors: Joél Smet, Boél De Paepe, Sara Seneca, Willy Lissens, H. Kotarsky, Linda De Meirleir, V. Fellman, Rudy Van Coster
Pages: 741-747 - Mutation analysis of three genes in patients with maturation arrest of spermatogenesis and couples with recurrent miscarriages
Authors: D Vandermaelen, Willy Lissens
Pages: 65-71