Publications by authors named "Liesbeth Rooms"

27Publications

Impaired GABAergic inhibition in the hippocampus of Fmr1 knockout mice.

Neuropharmacology 2017 04 21;116:71-81. Epub 2016 Dec 21.

Laboratory of Biological Psychology, KU Leuven, Leuven, Belgium. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.neuropharm.2016.12.010DOI Listing
April 2017

Thoracic dimples and dysmorphic features associated with a partial duplication and triplication of chromosome 12q24.

Clin Dysmorphol 2016 Oct;25(4):167-73

Departments of aPediatrics bMedical Genetics, Antwerp University Hospital, University of Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://content.wkhealth.com/linkback/openurl?sid=WKPTLP:land
Publisher Site
http://dx.doi.org/10.1097/MCD.0000000000000141DOI Listing
October 2016

Haploinsufficiency of CMIP in a girl with autism spectrum disorder and developmental delay due to a de novo deletion on chromosome 16q23.2.

Autism Res 2012 Aug 11;5(4):277-81. Epub 2012 Jun 11.

Department of Medical Genetics, University and University Hospital of Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/aur.1240DOI Listing
August 2012

A de novo balanced t(2;6)(p15;p22.3) in a patient with West Syndrome disrupts a lnc-RNA.

Epilepsy Res 2012 May 13;99(3):346-9. Epub 2012 Jan 13.

Department of Medical Genetics, University of and University Hospital of Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.eplepsyres.2011.12.009DOI Listing
May 2012

Advances in understanding fragile X syndrome and related disorders.

Curr Opin Pediatr 2011 Dec;23(6):601-6

Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/MOP.0b013e32834c7f1aDOI Listing
December 2011

Array-based MLPA to detect recurrent copy number variations in patients with idiopathic mental retardation.

Am J Med Genet A 2011 Feb 14;155A(2):343-8. Epub 2011 Jan 14.

Department of Medical Genetics, University of Antwerp and University Hospital, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/ajmg.a.33810
Publisher Site
http://dx.doi.org/10.1002/ajmg.a.33810DOI Listing
February 2011

CNV-WebStore: online CNV analysis, storage and interpretation.

BMC Bioinformatics 2011 Jan 5;12. Epub 2011 Jan 5.

Department of Medical Genetics, University Hospital Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1471-2105-12-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024943PMC
January 2011

Involvement and therapeutic potential of the GABAergic system in the fragile X syndrome.

ScientificWorldJournal 2010 Nov 4;10:2198-206. Epub 2010 Nov 4.

Department of Medical Genetics, University of Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1100/tsw.2010.211DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763973PMC
November 2010

Diverse chromosome breakage mechanisms underlie subtelomeric rearrangements, a common cause of mental retardation.

Hum Mutat 2007 Feb;28(2):177-82

Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/humu.20421
Publisher Site
http://dx.doi.org/10.1002/humu.20421DOI Listing
February 2007

A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.

Eur J Med Genet 2006 Sep-Oct;49(5):402-13. Epub 2006 Jan 30.

Department of Medical Genetics, University Hospital Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejmg.2006.01.001DOI Listing
November 2006

A subterminal deletion of the long arm of chromosome 10: a clinical report and review.

Am J Med Genet A 2006 Feb;140(4):402-9

Department of Medical Genetics, University Hospital Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.31053DOI Listing
February 2006

Subtelomeric rearrangements in the mentally retarded: a comparison of detection methods.

Hum Mutat 2005 Jun;25(6):513-24

Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/humu.20185DOI Listing
June 2005

Screening for subtelomeric rearrangements using genetic markers in 70 patients with unexplained mental retardation.

Ann Genet 2004 Jan-Mar;47(1):53-9

Department of Medical Genetics, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.anngen.2003.10.001DOI Listing
December 2004