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
1 - 10 of 41
- Clinical implementation of gene panel testing for lysosomal storage diseases(2019)
Authors: Alexander Gheldof, Sara Seneca, Katrien Stouffs, Willy Lissens, Anna C Jansen, Hilde Laeremans, Patrick Verloo, An-Sofie Schoonjans, Marije Meuwissen, Diana Barca, et al.
- Bi-allelic variants in COL3A1 encoding the ligand to GPR56 are associated with cobblestone-like cortical malformation, white matter changes and cerebellar cysts(2017)
Authors: Laura Vandervore, Katrien Stouffs, Ibrahim Tanyalcin, Tim Vanderhasselt, Filip Roelens, Muriel Holder-Espinasse, Agnete Jørgensen, Melanie G Pepin, Florence Petit, Philippe Khau Van Kien, et al.
Pages: 432-440 - SCN4A variants and Brugada syndrome(2016)
Authors: Véronique Bissay, Sophie Van Malderen, K. Keymolen, Willy Lissens, Uschi Peeters, Dorien Daneels, Anna C Jansen, Gudrun Pappaert, Pedro Brugada, Jacques De Keyser, et al.
Pages: 400-407 - Convert your favorite protein modeling program into a mutation predictor: "MODICT"(2016)
Authors: Ibrahim Tanyalcin, Katrien Stouffs, Dorien Daneels, Carla Al Assaf, Willy Lissens, Anna C Jansen, Alexander Gheldof
- I-PV: a CIRCOS module for interactive protein sequence visualization(2016)
Authors: Ibrahim Tanyalcin, Carla Al Assaf, Alexander Gheldof, Katrien Stouffs, Willy Lissens, Anna C Jansen
Pages: 447-449 - Sertoli Cell-Only Syndrome: Behind the Genetic Scenes(2016)
Authors: Katrien Stouffs, Alexander Gheldof, H Tournaye, Deborah Vandermaelen, Maryse Bonduelle, Willy Lissens, Sara Seneca
- Antithrombin heparin binding site deficiency: A challenging diagnosis of a not so benign thrombophilia(2015)
Authors: Christelle Orlando, Olivier Heylen, Willy Lissens, Kristin Jochmans
Pages: 1179-1185 - Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?(2015)
Authors: Sara Seneca, Kim Vancampenhout, Rudy Van Coster, Joél Smet, Willy Lissens, A. Vanlander, Boel De Paepe, An Jonckheere, Katrien Stouffs, Linda De Meirleir
Pages: 41-48 - A bumpy ride on the diagnostic bench of massive parallel sequencing, the case of the mitochondrial genome(2014)
Authors: Kim Vancampenhout, Ben Caljon, C Spits, Katrien Stouffs, An Jonckheere, Linda De Meirleir, Willy Lissens, A. Vanlander, Joél Smet, Boel De Paepe, et al.
- Clinical variability in neurohepatic syndrome due to combined mitochondrial DNA depletion and Gaucher disease(2014)
Authors: Julie Harvengt, Catherine Wanty, Boel De Paepe, Christine Sempoux, Nicole Revencu, Joél Smet, Rudy Van Coster, Willy Lissens, Sara Seneca, Laurent Weekers, et al.
Pages: 223-231