Bauters M - Search Results

1

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

Van Esch H, Bauters M, Ignatius J, Jansen M, Raynaud M, Hollanders K, Lugtenberg D, Bienvenu T, Jensen LR, Gecz J, Moraine C, Marynen P, Fryns JP, Froyen G. Van Esch H, et al. Among authors: bauters m. Am J Hum Genet. 2005 Sep;77(3):442-53. doi: 10.1086/444549. Epub 2005 Jul 29. Am J Hum Genet. 2005. PMID: 16080119 Free PMC article.

2

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

Bauters M, Van Esch H, Marynen P, Froyen G. Bauters M, et al. Eur J Med Genet. 2005 Jul-Sep;48(3):263-75. doi: 10.1016/j.ejmg.2005.04.008. Eur J Med Genet. 2005. PMID: 16179222

3

X-linked mental retardation and epigenetics.

Froyen G, Bauters M, Voet T, Marynen P. Froyen G, et al. Among authors: bauters m. J Cell Mol Med. 2006 Oct-Dec;10(4):808-25. doi: 10.1111/j.1582-4934.2006.tb00526.x. J Cell Mol Med. 2006. PMID: 17125586 Free PMC article. Review.

4

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

Van Esch H, Jansen A, Bauters M, Froyen G, Fryns JP. Van Esch H, et al. Among authors: bauters m. Am J Med Genet A. 2007 Feb 15;143(4):364-9. doi: 10.1002/ajmg.a.31572. Am J Med Genet A. 2007. PMID: 17256798

5

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.

Froyen G, Bauters M, Boyle J, Van Esch H, Govaerts K, van Bokhoven H, Ropers HH, Moraine C, Chelly J, Fryns JP, Marynen P, Gecz J, Turner G. Froyen G, et al. Among authors: bauters m. Hum Genet. 2007 Jun;121(5):539-47. doi: 10.1007/s00439-007-0343-1. Epub 2007 Feb 28. Hum Genet. 2007. PMID: 17333282

6

Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia.

Lahortiga I, De Keersmaecker K, Van Vlierberghe P, Graux C, Cauwelier B, Lambert F, Mentens N, Beverloo HB, Pieters R, Speleman F, Odero MD, Bauters M, Froyen G, Marynen P, Vandenberghe P, Wlodarska I, Meijerink JP, Cools J. Lahortiga I, et al. Among authors: bauters m. Nat Genet. 2007 May;39(5):593-5. doi: 10.1038/ng2025. Epub 2007 Apr 15. Nat Genet. 2007. PMID: 17435759

7

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.

Froyen G, Van Esch H, Bauters M, Hollanders K, Frints SG, Vermeesch JR, Devriendt K, Fryns JP, Marynen P. Froyen G, et al. Among authors: bauters m. Hum Mutat. 2007 Oct;28(10):1034-42. doi: 10.1002/humu.20564. Hum Mutat. 2007. PMID: 17546640

8

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

Froyen G, Corbett M, Vandewalle J, Jarvela I, Lawrence O, Meldrum C, Bauters M, Govaerts K, Vandeleur L, Van Esch H, Chelly J, Sanlaville D, van Bokhoven H, Ropers HH, Laumonnier F, Ranieri E, Schwartz CE, Abidi F, Tarpey PS, Futreal PA, Whibley A, Raymond FL, Stratton MR, Fryns JP, Scott R, Peippo M, Sipponen M, Partington M, Mowat D, Field M, Hackett A, Marynen P, Turner G, Gécz J. Froyen G, et al. Among authors: bauters m. Am J Hum Genet. 2008 Feb;82(2):432-43. doi: 10.1016/j.ajhg.2007.11.002. Epub 2008 Jan 24. Am J Hum Genet. 2008. PMID: 18252223 Free PMC article.

9

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

Bauters M, Van Esch H, Friez MJ, Boespflug-Tanguy O, Zenker M, Vianna-Morgante AM, Rosenberg C, Ignatius J, Raynaud M, Hollanders K, Govaerts K, Vandenreijt K, Niel F, Blanc P, Stevenson RE, Fryns JP, Marynen P, Schwartz CE, Froyen G. Bauters M, et al. Genome Res. 2008 Jun;18(6):847-58. doi: 10.1101/gr.075903.107. Epub 2008 Apr 2. Genome Res. 2008. PMID: 18385275 Free PMC article.

10

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

Bauters M, Weuts A, Vandewalle J, Nevelsteen J, Marynen P, Van Esch H, Froyen G. Bauters M, et al. Cytogenet Genome Res. 2008;123(1-4):44-53. doi: 10.1159/000184691. Epub 2009 Mar 11. Cytogenet Genome Res. 2008. PMID: 19287138 Review.

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