Researcher
Marjan De Rademaeker
- Keywords:Medicine
Affiliations
- Clinical sciences (Department)
Member
From1 Apr 2017 → 31 Mar 2019 - Reproduction and Genetics (Research group)
Member
From21 Jun 2010 → 31 Mar 2019 - Department of Embryology and Genetics (Department)
Member
From1 Nov 2009 → 31 Oct 2011 - Medical Genetics (Department)
Member
From1 Jan 2008 → 30 Jun 2018
Publications
1 - 10 of 14
- Prenatally detected copy number variants in a national cohort a postnatal follow-up study(2020)
Authors: Joke Muys, Yves Jacquemyn, Bettina Blaumeiser, Laura Bourlard, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Anne De Leener, Marjan De Rademaeker, Julie Désir, et al.
Pages: 1272-1283 - Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder(2019)
Authors: 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.
Pages: 1748-1768 - The ARID1B spectrum in 143 patients(2019)
Authors: 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.
Pages: 1295-1307 - Diagnosing neurodegeneration with brain iron accumulation before iron starts to accumulate.(2019)
Authors: Ine Hoogwijs, Marjan De Rademaeker
- The Belgian MicroArray Prenatal (BEMAPRE) database(2018)
Authors: Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Claude Bandelier, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Winnie Courtens, Anne De Leener, Marjan De Rademaeker, et al.
Pages: 1120-1128 - Risk of malignancy in 22q11.2 deletion syndrome(2017)
Authors: Toer Stevens, Jutte Van Der Werff Ten Bosch, Marjan De Rademaeker, Ann Bogaert, Machiel van den Akker
Pages: 486-490 - An augmented ABCA4 screen targeting noncoding regions reveals a deep intronic founder variant in Belgian Stargardt patients(2015)
Authors: 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.
Pages: 39-42 - Reliable and sensitive detection of fragile x (expanded) alleles in clinical prenatal DNA samples with a fast turnaround time(2012)
Authors: Kristof Endels, Marjan De Rademaeker, Urielle Ullmann, Patrick Haentjens, Sonia Van Dooren
Pages: 560-568 - (0) Save to: more options Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres.(2012)
Authors: Maartje Van Rij, Marjan De Rademaeker, C; Moutou, J. Dreesen, J. Geraedts, C.e.m. De Die-Smulders, Stéphane Viville, Working Group Brumastra Pgd
Pages: 368-375 - Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres.(2012)
Authors: 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
Pages: 368-375