Onderzoeker
Annelies Dheedene
- Disciplines:Pediatrie en neonatologie, Moleculaire en celbiologie, Systeembiologie, Verpleegkunde, Genetica
Affiliaties
- Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf16 jul 2007 → 24 sep 2017
Publicaties
21 - 30 van 53
- Preimplantation genetic diagnosis (PGD) for translocation carriers using whole genome screening by microarray analysis at the blastocyst stage(2016)Volume: 31
Auteurs: CHRISTODOULOS CHRISTODOULOU, Annelies Dheedene, Ilse De Croo, Björn Heindryckx, Lieselot Deleye, Filip Van Nieuwerburgh, Dieter Deforce, Petra De Sutter, Björn Menten, Etienne Van den Abbeel
Pagina's: 386 - 387 - Performance of a TthPrimPol-based whole genome amplification kit for copy number alteration detection using massively parallel sequencing(2016)
Auteurs: Lieselot Deleye, Dieter De Coninck, Annelies Dheedene, Dieter Deforce, Filip Van Nieuwerburgh
- Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method(2015)
Auteurs: Lieselot Deleye, Dieter De Coninck, CHRISTODOULOS CHRISTODOULOU, Tom Sante, Annelies Dheedene, Dieter Deforce, Filip Van Nieuwerburgh
- Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta(2015)
Auteurs: M Huckert, C Stoetzel, S Morkmued, V Laugel-Haushalter, V Geoffroy, J Muller, F Clauss, MK Prasad, F Obry, JL Raymond, et al.
Pagina's: 3038 - 3049 - Redefining the MED13L syndrome(2015)
Auteurs: Abidemi Adegbola, Luciana Musante, Bert Callewaert, Patricia Maciel, Hao Hu, Bertrand Isidor, Sylvie Picker-Minh, Cedric Le Caignec, Barbara Delle Chiaie, Olivier Vanakker, et al.
Pagina's: 1308 - 1317 - Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts(2015)
Auteurs: Lieselot Deleye, Annelies Dheedene, Dieter De Coninck, Tom Sante, CHRISTODOULOS CHRISTODOULOU, Dieter Deforce, Filip Van Nieuwerburgh
Pagina's: 1276 - 1285 - Role of CGH array in the diagnosis of autosomal recessive disease : a case of Ellis-van Creveld syndrome(2015)
Auteurs: Valentina D'Ambrosio, Carmela Votino, Teresa Cos, Sebastien Boulanger, Annelies Dheedene, Jacques Jani, Kathelijn Keymolen
Pagina's: 97 - 99 - Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges(2014)
Auteurs: Olivier Vanakker, Catheline Vilain, Katrien Janssens, Nathalie Van der Aa, Guillaume Smits, Claude Bandelier, Bettina Blaumeiser, Saskia Bulk, Jean-Hubert Caberg, Anne De Leener, et al.
Pagina's: 151 - 156 - Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humans(2013)
Auteurs: Fransiska Malfait, Sanne D'hondt, Bert Callewaert, Annelies Dheedene, Wouter Steyaert, Hans Peter Bächinger, Hulya Kayserili
- The need for transparency and good practices in the qPCR literature(2013)
Auteurs: Stephen A Bustin, Vladimir Benes, Jeremy Garson, Jan Hellemans, Jim Huggett, Mikael Kubista, Reinhold Mueller, Tania Nolan, Michael W Pfaffl, Gregory Shipley, et al.
Pagina's: 1063 - 1067