Marie-Claude Addor

Marie-Claude Addor

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Marie-Claude Addor

Marie-Claude Addor

Publications by authors named "Marie-Claude Addor"

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Lamotrigine use in pregnancy and risk of orofacial cleft and other congenital anomalies.

Neurology 2016 05 6;86(18):1716-25. Epub 2016 Apr 6.

From Ulster University (H.D., M.L.), Northern Ireland, UK; University of Groningen (H.W., L.T.W.d.J.-v.d.B.), the Netherlands; Barts and the London School of Medicine and Dentistry (J.M.), UK; Hospital Lillebaelt (E.G.), Kolding, Denmark; Registre Vaudois des Malformations (M.-C.A.), Lausanne, Switzerland; Public Health Division of Gipuzkoa (L.A.), Instituto BIO-Donostia, Basque Government, CIBER Epidemiología y Salud Pública-CIBERESP, Madrid, Spain; University Medical Centre Groningen (M.B.), the Netherlands; Children's University Hospital Zagreb (I.B.), Croatia; Registre des Malformations Congenitales D'Alsace (B.D.), University of Strasbourg, France; Department of Health Information and Research (M.G.), Malta; Swedish National Board of Health and Welfare (K. Kallen), Stockholm, Sweden; Institut National de la Sante et de la Recherche Medicale (B.K.), INSERM, Villejuif, France; Medical Birth Registry of Norway (K. Klungsoyr), Oslo; National Institute for Health & Welfare (A.-M.L.-K.), Helsinki, Finland; Poznan University of Medical Sciences (A.L.-B., J.P.M.), Poland; Provinciaal Instituut voor Hygiene (V.N.), Antwerp, Belgium; Center for Clinical and Epidemiological Research Ferrara (A.N.), Italy; Health Service Executive (M.O.), Kildare, Ireland; Institute of Clinical Physiology-National Research Council (IFC-CNR) (A.P.), Pisa, Italy; Otto-von-Guericke University Magdeburg (A.R.), Germany; Public Health Wales NHS Trust (D.T.), Congenital Anomaly Register and Information Service for Wales; Wessex Clinical Genetics Service (D.W.), Princess Anne Hospital, UK; and University Medical Center of Mainz Birth Registry Mainz Model (A.W.), Germany.

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http://www.neurology.org/content/86/18/1716.full.pdf
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http://www.neurology.org/lookup/doi/10.1212/WNL.000000000000
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http://dx.doi.org/10.1212/WNL.0000000000002540DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854591PMC
May 2016

Selective serotonin reuptake inhibitor antidepressant use in first trimester pregnancy and risk of specific congenital anomalies: a European register-based study.

Eur J Epidemiol 2015 Nov 7;30(11):1187-98. Epub 2015 Jul 7.

WHO Collaborating Centre for the Epidemiologic Surveillance of Congenital Anomalies, Room 12L23, Centre for Maternal, Fetal and Infant Research, Institute of Nursing and Health Research, Ulster University, Shore Road, Newtownabbey, BT37 0QB, UK.

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http://dx.doi.org/10.1007/s10654-015-0065-yDOI Listing
November 2015

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.

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http://dx.doi.org/10.1097/EDE.0000000000000372DOI Listing
November 2015

Evaluation of prenatal diagnosis of congenital heart disease in a regional controlled case study.

Swiss Med Wkly 2014 4;144:w14068. Epub 2014 Dec 4.

Department of Obstetrics and Gynecology, University Hospital of Lausanne (CHUV), Switzerland.

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http://dx.doi.org/10.4414/smw.2014.14068DOI Listing
May 2015

GNAL deletion as a probable cause of dystonia in a patient with the 18p- syndrome.

Parkinsonism Relat Disord 2014 Mar 25;20(3):351-2. Epub 2013 Dec 25.

Department of Clinical Neuroscience, Centre Hospitalier Universitaire Vaudois (CHUV-UNIL), BH13, Rue du Bugnon 21, 1011 Lausanne, Switzerland. Electronic address:

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http://dx.doi.org/10.1016/j.parkreldis.2013.12.005DOI Listing
March 2014

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations.

Nephron Physiol 2012 23;122(1-2):1-6. Epub 2013 Feb 23.

Centre for Nephrology, University College London, London, UK.

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http://dx.doi.org/10.1159/000349989DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782194PMC
October 2013

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.

Authors:
Sébastien Jacquemont Alexandre Reymond Flore Zufferey Louise Harewood Robin G Walters Zoltán Kutalik Danielle Martinet Yiping Shen Armand Valsesia Noam D Beckmann Gudmar Thorleifsson Marco Belfiore Sonia Bouquillon Dominique Campion Nicole de Leeuw Bert B A de Vries Tõnu Esko Bridget A Fernandez Fernando Fernández-Aranda José Manuel Fernández-Real Mònica Gratacòs Audrey Guilmatre Juliane Hoyer Marjo-Riitta Jarvelin R Frank Kooy Ants Kurg Cédric Le Caignec Katrin Männik Orah S Platt Damien Sanlaville Mieke M Van Haelst Sergi Villatoro Gomez Faida Walha Bai-Lin Wu Yongguo Yu Azzedine Aboura Marie-Claude Addor Yves Alembik Stylianos E Antonarakis Benoît Arveiler Magalie Barth Nathalie Bednarek Frédérique Béna Sven Bergmann Mylène Beri Laura Bernardini Bettina Blaumeiser Dominique Bonneau Armand Bottani Odile Boute Han G Brunner Dorothée Cailley Patrick Callier Jean Chiesa Jacqueline Chrast Lachlan Coin Charles Coutton Jean-Marie Cuisset Jean-Christophe Cuvellier Albert David Bénédicte de Freminville Bruno Delobel Marie-Ange Delrue Bénédicte Demeer Dominique Descamps Gérard Didelot Klaus Dieterich Vittoria Disciglio Martine Doco-Fenzy Séverine Drunat Bénédicte Duban-Bedu Christèle Dubourg Julia S El-Sayed Moustafa Paul Elliott Brigitte H W Faas Laurence Faivre Anne Faudet Florence Fellmann Alessandra Ferrarini Richard Fisher Elisabeth Flori Lukas Forer Dominique Gaillard Marion Gerard Christian Gieger Stefania Gimelli Giorgio Gimelli Hans J Grabe Agnès Guichet Olivier Guillin Anna-Liisa Hartikainen Délphine Heron Loyse Hippolyte Muriel Holder Georg Homuth Bertrand Isidor Sylvie Jaillard Zdenek Jaros Susana Jiménez-Murcia Géraldine Joly Helas Philippe Jonveaux Satu Kaksonen Boris Keren Anita Kloss-Brandstätter Nine V A M Knoers David A Koolen Peter M Kroisel Florian Kronenberg Audrey Labalme Emilie Landais Elisabetta Lapi Valérie Layet Solenn Legallic Bruno Leheup Barbara Leube Suzanne Lewis Josette Lucas Kay D MacDermot Pall Magnusson Christian Marshall Michèle Mathieu-Dramard Mark I McCarthy Thomas Meitinger Maria Antonietta Mencarelli Giuseppe Merla Alexandre Moerman Vincent Mooser Fanny Morice-Picard Mafalda Mucciolo Matthias Nauck Ndeye Coumba Ndiaye Ann Nordgren Laurent Pasquier Florence Petit Rolph Pfundt Ghislaine Plessis Evica Rajcan-Separovic Gian Paolo Ramelli Anita Rauch Roberto Ravazzolo Andre Reis Alessandra Renieri Cristobal Richart Janina S Ried Claudine Rieubland Wendy Roberts Katharina M Roetzer Caroline Rooryck Massimiliano Rossi Evald Saemundsen Véronique Satre Claudia Schurmann Engilbert Sigurdsson Dimitri J Stavropoulos Hreinn Stefansson Carola Tengström Unnur Thorsteinsdóttir Francisco J Tinahones Renaud Touraine Louis Vallée Ellen van Binsbergen Nathalie Van der Aa Catherine Vincent-Delorme Sophie Visvikis-Siest Peter Vollenweider Henry Völzke Anneke T Vulto-van Silfhout Gérard Waeber Carina Wallgren-Pettersson Robert M Witwicki Simon Zwolinksi Joris Andrieux Xavier Estivill James F Gusella Omar Gustafsson Andres Metspalu Stephen W Scherer Kari Stefansson Alexandra I F Blakemore Jacques S Beckmann Philippe Froguel

Nature 2011 Aug 31;478(7367):97-102. Epub 2011 Aug 31.

Service of Medical Genetics, Centre Hospitalier Universitaire Vaudois, 1011 Lausanne, Switzerland.

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http://dx.doi.org/10.1038/nature10406DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3637175PMC
August 2011

Congenital hydrocephalus--prevalence, prenatal diagnosis and outcome of pregnancy in four European regions.

Eur J Paediatr Neurol 2010 Mar 2;14(2):150-5. Epub 2009 May 2.

Paediatric Department, Kolding Hospital, DK-6000 Kolding, Denmark.

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http://dx.doi.org/10.1016/j.ejpn.2009.03.005DOI Listing
March 2010

Quantitative sequence analysis of FBN1 premature termination codons provides evidence for incomplete NMD in leukocytes.

Hum Mutat 2009 Sep;30(9):1355-64

Division of Medical Molecular Genetics and Gene Diagnostics, Institute of Medical Genetics, University of Zurich, Zurich, Switzerland.

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http://dx.doi.org/10.1002/humu.21058DOI Listing
September 2009

Uncombable hair syndrome: a clinical report.

Eur J Med Genet 2007 Jul-Aug;50(4):309-14. Epub 2007 Apr 11.

Service de Génétique Médicale, CHUV, rue Pierre Decker, 1011 Lausanne, Switzerland.

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http://dx.doi.org/10.1016/j.ejmg.2007.03.002DOI Listing
September 2007

Season of birth in valvular heart disease.

Paediatr Perinat Epidemiol 2005 May;19(3):246-52

Institute of Social and Preventive Medicine, University of Zurich, Zurich, Switzerland.

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http://doi.wiley.com/10.1111/j.1365-3016.2005.00645.x
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http://dx.doi.org/10.1111/j.1365-3016.2005.00645.xDOI Listing
May 2005

Toward the effective surveillance of hypospadias.

Environ Health Perspect 2004 Mar;112(3):398-402

EUROCAT Central Registry, University of Ulster, Room 15E12, Newtownabbey, County Antrim, Northern Ireland BT37 0QB, UK.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1241874PMC
http://dx.doi.org/10.1289/ehp.6398DOI Listing
March 2004

Distal trisomy 14 (q24 --> qter) and aorto-pulmonary window: a case report and review of the literature.

Ann Genet 2002 Oct-Dec;45(4):173-5

Department of Medical Genetics, CHUV, Lausanne, Switzerland.

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http://dx.doi.org/10.1016/s0003-3995(02)01135-8DOI Listing
November 2003

[Epidemiology of lip-maxilla-palate clefts in the canton of Vaud].

Rev Med Suisse Romande 2003 Aug;123(8):501-5

Service de Génétique Médicale, CHUV, Lausanne.

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August 2003