Onderzoeker
Tim Van Damme
- Disciplines:Klinische genetica en moleculaire diagnostiek, Epigenetica, Immunogenetica, Genetica
Affiliaties
- Vakgroep Biomoleculaire Geneeskunde (Departement)
Lid
Vanaf1 okt 2018 → 20 sep 2020 - Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf1 sep 2012 → 30 sep 2018
Publicaties
11 - 20 van 30
- Vascular phenotypes in nonvascular subtypes of the Ehlers-Danlos syndrome : a systematic review(2018)
Auteurs: Sanne D'hondt, Tim Van Damme, Fransiska Malfait
Pagina's: 562 - 573 - Knockdown and knockout zebrafish models for the β4GalT7-deficient type of Ehlers-Danlos syndrome reveal distinctive and overlapping phenotypic features(2018)
Auteurs: Sarah Delbaere, Tim Van Damme, Delfien Syx, Sofie Symoens, Andy Willaert, Fransiska Malfait
Aantal pagina's: 1 - Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndrome(2018)
Auteurs: Tim Van Damme, Xiaomeng Pang, Brecht Guillemyn, Sandrine Gulberti, Olivier Kaye, Christine E. M. de Die-Smulders, Rolph Pfundt, Ariana Kariminejad, Sheela Nampoothiri, Genevieve Pierquin, et al.
Pagina's: 3475 - 3487 - Analysis of chromosomal radiosensitivity of healthy BRCA2 mutation carriers and non-carriers in BRCA families with the G2 micronucleus assay(2017)
Auteurs: Annelot Baert, Julie Depuydt, Bruce Poppe, Fransiska Malfait, Tim Van Damme, Sylvia De Nobele, Gianpaolo Perletti
Pagina's: 1379 - 1386 - Zebrafish modeling of the β4GalT7-deficient type of Ehlers-Danlos syndrome(2017)
Auteurs: Sarah Delbaere, Tim Van Damme, Paul Coucke, Sofie Symoens, Delfien Syx, Andy Willaert, Fransiska Malfait
Aantal pagina's: 1 - The 2017 International Classification of the Ehlers-Danlos Syndromes(2017)
Auteurs: Fransiska Malfait, Clair Francomano, Peter Byers, John Belmont, Britta Berglund, James Black, Lara Bloom, Jessica M Bowen, Angela F Brady, Nigel P Burrows, et al.
Pagina's: 8 - 26 - The Ehlers-Danlos syndromes, rare types(2017)
Auteurs: Angela F Brady, Serwet Demirdas, Sylvie Fournel-Gigleux, Neeti Ghali, Cecilia Giunta, Ines Kapferer-Seebacher, Tomoki Kosho, Roberto Mendoza-Londono, Michael F Pope, Marianne Rohrbach, et al.
Pagina's: 70 - 115 - Mutations in ATP6V1E1 or ATP6V1A cause autosomal-recessive cutis laxa(2017)
Auteurs: Tim Van Damme, Thatjana Gardeitchik, Miski Mohamed, Sergio Guerrero-Castillo, Peter Freisinger, Brecht Guillemyn, Ariana Kariminejad, Daisy Dalloyaux, Sanne van Kraaij, Dirk J Lefeber, et al.
Pagina's: 216 - 227 - A homozygous B3GAT3 mutation causes a multisystemic cutis laxa-like syndrome, expanding the phenotype of linkeropathies(2016)
Auteurs: Brecht Guillemyn, Tim Van Damme, Wouter Steyaert, Sheela Nampoothiri, Fransiska Malfait
Aantal pagina's: 1 - Increased chromosomal radiosensitivity in asymptomatic carriers of a heterozygous BRCA1 mutation(2016)
Auteurs: Annelot Baert, Julie Depuydt, Bruce Poppe, Fransiska Malfait, Katrien Storm, Jenneke van den Ende, Tim Van Damme, Sylvia De Nobele, Gianpaolo Perletti