Marie‐Claude Addor

Author

Marie‐Claude Addor

Inserm

Also Known As

Abutheraa, Anna Pierini, Dominique Bonneau, Marie-Claude Addor, Marie‐Claude Addor, Marie–Claude Addor, Tiffany Busa

Publications

6.1K

Citations

H-Index

Concepts

All Affiliations

Inserm University of Ulster Health Service Executive University Medical Center Groningen University of Groningen

About

Marie‐Claude Addor is an author at Inserm specializing in medicine, pediatrics, and prenatal diagnosis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	17	2.6K
2	Public Health	5	5	805
3	Cell Biology	3	3	607
4	Epidemiology	3	3	234
5	Family Medicine	1	1	82

Marie‐Claude Addor

Publications

5.7K

Citations

H-Index

Page 1

	Year	Citations
Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis Ian T. Fiddes, Gerrald A. Lodewijk, Meghan Mooring, Cell Cortical NeurogenesisDevelopmental BiologyNeural Stem CellMolecular NeurobiologyMedicine	2018	539
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Nature Gene DosageGeneticsHuman PolymorphismMolecular GeneticsChromosome 16P11.2	2011	474
Twenty-year trends in the prevalence of Down syndrome and other trisomies in Europe: impact of maternal age and prenatal screening Maria Loane, Joan K. Morris, Marie‐Claude Addor, European Journal of Human Genetics Down SyndromeMaternal AgeGenetic EpidemiologyPediatricsGynecology	2012	364
Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study M McGivern, Kate Best, Judith Rankin, Archives of Disease in Childhood Fetal & Neonatal	2014	307
Long term trends in prevalence of neural tube defects in Europe: population based study Babak Khoshnood, Maria Loane, Hermien E. K. de Walle, BMJ	2015	243
Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data Breidge Boyle, Marie‐Claude Addor, Larraitz Arriola, Archives of Disease in Childhood Fetal & Neonatal	2017	210
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe Diana Wellesley, Helen Dolk, Patricia A. Boyd, European Journal of Human Genetics Prenatal Diagnosis RatesDevelopmental AnomalyGenetic EpidemiologyPediatricsGynecology	2012	206
Epidemiology of small intestinal atresia in Europe: a register-based study Kate Best, Peter W. G. Tennant, Marie‐Claude Addor, Archives of Disease in Childhood Fetal & Neonatal	2012	167
Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in Europe Ingeborg Barišić, Ljubica Odak, Maria Loane, European Journal of Human Genetics Developmental AnomalyPediatricsGynecologyMaternal HealthDiagnosis	2014	150
Congenital hydrocephalus – prevalence, prenatal diagnosis and outcome of pregnancy in four European regions Ester Garne, Maria Loane, Marie‐Claude Addor, European Journal of Paediatric Neurology Pediatric HydrocephalusPediatricsGynecologyMaternal HealthEuropean Regions	2009	138

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