Christine Verellen-Dumoulin

Christine Verellen-Dumoulin

UNVERIFIED PROFILE

Are you Christine Verellen-Dumoulin?   Register this Author

Register author
Christine Verellen-Dumoulin

Christine Verellen-Dumoulin

Publications by authors named "Christine Verellen-Dumoulin"

Are you Christine Verellen-Dumoulin?   Register this Author

35Publications

-Reads

Dissociating emotional and cognitive empathy in pre-clinical and clinical Huntington's disease.

Psychiatry Res 2016 Mar 28;237:103-8. Epub 2016 Jan 28.

Department of Adult Psychiatry, Saint-Luc University Hospital, 10 Avenue Hippocrate, B-1200 Brussels, Belgium.

View Article
March 2016

The Association of H1N1 Pandemic Influenza with Congenital Anomaly Prevalence in Europe: An Ecological Time Series Study.

Epidemiology 2015 Nov;26(6):853-61

From the aInstitute of Nursing Research/School of Nursing, University of Ulster, Newtownabbey, United Kingdom; bDivision of Medical Genetics, Lausanne, Switzerland; cPublic Health Division of Gipuzkoa, Instituto BIO-Donostia, Basque Government, CIBER Epidemiología y Salud Pública-CIBERESP, Madrid, Spain; dUnit of Epidemiology, Institute of Clinical Physiology, Pisa, Italy; eDepartment of Paediatrics, Hospital Lillebaelt, Kolding, Denmark; fINSERM U953, Paris, France; gProvinciaal Instituut voor Hygiene, Antwerp, Belgium; hIMER Registry-Azienda Ospedaliero-Universitaria di Ferrara, Ferrara, Italy; iUniversity Medical Center of the Johannes Gutenberg University, Mainz, Germany; jInstitute of Health & Society, Newcastle University, Newcastle-upon-Tyne, United Kingdom; kNational Perinatal Epidemiology Unit, University of Oxford, Oxford, United Kingdom; lInstitut de Pathologie et de Génétique, Charleroi, Belgium; mDepartment of Genetics, University Medical Center Groningen, University of Groningen, Eurocat, Groningen, The Netherlands; nWessex Clinical Genetics Service, Princess Anne Hospital, Southampton, United Kingdom; oSchool of Clinical Sciences, University of Bristol, Bristol, United Kingdom; pOMNI-Net for Children, Rivne Medical Diagnostic Center, Rivne, Ukraine; qDivision of Pharmacy, Department of Pharmacoepidemiology and Pharmacoeconomics, University of Groningen, Groningen, The Netherlands; and rCentre for Environmental and Preventive Medicine, Queen Mary University of London, London, United Kingdom.

View Article
November 2015

A three generation X-linked family with Kabuki syndrome phenotype and a frameshift mutation in KDM6A.

Am J Med Genet A 2014 May 24;164A(5):1289-92. Epub 2014 Mar 24.

Center for Human Genetics, IPG, Charleroi, (Gosselies), Belgium.

View Article
May 2014

Intron 22 homologous regions are implicated in exons 1-22 duplications of the F8 gene.

Eur J Hum Genet 2013 Sep 9;21(9):970-6. Epub 2013 Jan 9.

Center of Human Genetics UCLouvain, Cliniques Universitaires Saint-Luc, Bruxelles, Belgium.

View Article
September 2013

Atypical findings in three patients with Pai syndrome and literature review.

Am J Med Genet A 2012 Nov 17;158A(11):2899-904. Epub 2012 Sep 17.

Center for Human Genetics, IPG, Charleroi (Gosselies), Belgium.

View Article
November 2012

Discordant monozygotic twins for macrocephaly-capillary malformation.

Am J Med Genet A 2012 Jun 14;158A(6):1509-11. Epub 2012 May 14.

Center For Human Genetics, IPG, Charleroi (Gosselies), Belgium.

View Article
June 2012

NF1 microduplication first clinical report: association with mild mental retardation, early onset of baldness and dental enamel hypoplasia?

Eur J Hum Genet 2008 Mar 9;16(3):305-11. Epub 2008 Jan 9.

Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.

View Article
March 2008

Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population.

Eur J Hum Genet 2005 Nov;13(11):1239-42

Laboratory of Human Molecular Genetics, Christian de Duve Institute of Cellular Pathology and University of Louvain Medical School, Brussels, Belgium.

View Article
November 2005

Congenital diaphragmatic eventration and bilateral uretero-hydronephrosis in a patient with neonatal Marfan syndrome caused by a mutation in exon 25 of the FBN1 gene and review of the literature.

Eur J Pediatr 2004 Jan 30;163(1):33-7. Epub 2003 Oct 30.

Center for Human Genetics and Medical Genetics Unit, Cliniques universitaires Saint-Luc and Université catholique de Louvain, Av. Mounier 5220, 1200 Brussels, Belgium.

View Article
January 2004

Free fetal DNA concentration in maternal plasma during normal labour at term.

Prenat Diagn 2003 Dec;23(13):1077-82

Department of Obstetrics, Université Catholique de Louvain, Cliniques Universitaires Saint Luc, Bruxelles, Belgium.

View Article
December 2003

Polymicrogyria in chromosome 22q11 deletion syndrome.

Eur J Paediatr Neurol 2002 ;6(1):73-7

Department of Pediatric Neurology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

View Article
August 2002