Onderzoeker
Marjan De Rademaeker
- Trefwoorden:Geneeskunde
Affiliaties
- Observerende Klinische wetenschappen (Departement)
Lid
Vanaf1 apr 2017 → 31 mrt 2019 - Reproductie en Genetica (Onderzoeksgroep)
Lid
Vanaf21 jun 2010 → 31 mrt 2019 - Embryologie en Menselijke Genetica (Departement)
Lid
Vanaf1 nov 2009 → 31 okt 2011 - Medische genetica (Departement)
Lid
Vanaf1 jan 2008 → 30 jun 2018
Publicaties
1 - 10 van 14
- Prenatally detected copy number variants in a national cohort a postnatal follow-up study(2020)
Auteurs: Joke Muys, Yves Jacquemyn, Bettina Blaumeiser, Laura Bourlard, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Anne De Leener, Marjan De Rademaeker, Julie Désir, et al.
Pagina's: 1272-1283 - Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder(2019)
Auteurs: Suzanna G M Frints, Aysegul Ozanturk, Germán Rodríguez Criado, Ute Grasshoff, Bas de Hoon, Michael Field, Sylvie Manouvrier-Hanu, Scott E Hickey, Molka Kammoun, Karen W Gripp, et al.
Pagina's: 1748-1768 - The ARID1B spectrum in 143 patients(2019)
Auteurs: Eline P J van der Sluijs, Sandra Jansen, Samantha A Vergano, Miho Adachi-Fukuda, Yasemin Alanay, Adila AlKindy, Anwar Baban, Allan Bayat, Stefanie Beck-Wödl, Katherine Berry, et al.
Pagina's: 1295-1307 - Diagnosing neurodegeneration with brain iron accumulation before iron starts to accumulate.(2019)
Auteurs: Ine Hoogwijs, Marjan De Rademaeker
- The Belgian MicroArray Prenatal (BEMAPRE) database(2018)
Auteurs: Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Claude Bandelier, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Winnie Courtens, Anne De Leener, Marjan De Rademaeker, et al.
Pagina's: 1120-1128 - Risk of malignancy in 22q11.2 deletion syndrome(2017)
Auteurs: Toer Stevens, Jutte Van der Werff Ten Bosch, Marjan De Rademaeker, Ann Bogaert, Machiel van den Akker
Pagina's: 486-490 - An augmented ABCA4 screen targeting noncoding regions reveals a deep intronic founder variant in Belgian Stargardt patients(2015)
Auteurs: Miriam Bauwens, Julie De Zaeytijd, Nicole Weisschuh, Susanne Kohl, Françoise Meire, Karin Dahan, Fanny Depasse, Sarah De Jaegere, Thomy de Ravel, Marjan De Rademaeker, et al.
Pagina's: 39-42 - Reliable and sensitive detection of fragile x (expanded) alleles in clinical prenatal DNA samples with a fast turnaround time(2012)
Auteurs: Kristof Endels, Marjan De Rademaeker, Urielle Ullmann, Patrick Haentjens, Sonia Van Dooren
Pagina's: 560-568 - Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres.(2012)
Auteurs: M.c. Van Rij, Marjan De Rademaeker, C; Moutou, J. Dreesen, J.p. Geraedts, C.e.m. De Die-Smulders, S. Viville, Working Group Brumastra Pgd
Pagina's: 368-375 - (0) Save to: more options Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres.(2012)
Auteurs: Maartje Van Rij, Marjan De Rademaeker, C; Moutou, J. Dreesen, J. Geraedts, C.e.m. De Die-Smulders, Stéphane Viville, Working Group Brumastra Pgd
Pagina's: 368-375