Marijke Bauters

发表

Detection of genomic copy number changes in patients with idiopathic mental retardation by high‐resolution X‐array‐CGH: important role for increased gene dosage of XLMR genes

P. Marynen, K. Devriendt, J. Vermeesch, 2007, Human mutation.

Encephalopathy and bilateral cataract in a boy with an interstitial deletion of Xp22 comprising the CDKL5 and NHS genes

H. Van Esch, J. Fryns, A. Jansen, 2007, American journal of medical genetics. Part A.

Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia

Rob Pieters, Frank Speleman, Peter Marynen, 2007, Nature Genetics.

Detection and validation of copy number variation in X-linked mental retardation

P. Marynen, H. Van Esch, H. Esch, 2009, Cytogenetic and Genome Research.

X chromosome array-CGH for the identification of novel X-linked mental retardation genes.

P. Marynen, H. Van Esch, G. Froyen, 2005, European journal of medical genetics.

Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair.

P. Marynen, R. Stevenson, C. Schwartz, 2008, Genome research.

architecture-driven DNA breaks and break-induced replication duplications mediated by genomicMECP 2 Nonrecurrent Material Supplemental

P. Marynen, R. Stevenson, C. Schwartz, 2008 .

X-linked mental retardation and epigenetics

P. Marynen, T. Voet, G. Froyen, 2006, Journal of cellular and molecular medicine.

Ubiquitin Ligase HUWE1 Regulates Axon Branching through the Wnt/β-Catenin Pathway in a Drosophila Model for Intellectual Disability

Bassem A. Hassan, Marion Langen, P. Verstreken, 2013, PloS one.

BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome.

Y. Moreau, L. Tranchevent, K. Devriendt, 2012, European journal of medical genetics.

Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.

Peter Marynen, Rodney Scott, Patrick S Tarpey, 2008, American journal of human genetics.

Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males.

J. Gécz, P. Marynen, H. Van Esch, 2005, American journal of human genetics.

Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region

J. Gécz, P. Marynen, H. Ropers, 2007, Human Genetics.

Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1

Y. Moreau, L. Tranchevent, K. Devriendt, 2012, American journal of medical genetics. Part A.

ZIC1 gene expression is controlled by DNA and histone methylation in mesenchymal proliferations

R. Sciot, S. Tejpar, J. Cassiman, 2007, FEBS letters.