Marion Gérard‐Blanluet

Author

Also Known As

Gérard-Blanluet Marion, Gérard-Blanluet, M., M Gérard-Blanluet, M. Gerard‐Blanluet, M. Gérard-Blanluet, M. Gérard‐Blanluet, Marion Gerard-Blanluet, Marion Gerard‐Blanluet, Marion Gérard-Blanluet, Marion Gérard‐Blanluet

Publications

749

Citations

H-Index

Concepts

All Affiliations

Hôpital Robert-Debré Assistance Publique – Hôpitaux de Paris Hôpital Intercommunal de Créteil Sorbonne Université Inserm

About

Marion Gérard‐Blanluet is an author at Hôpital Robert-Debré specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	140
2	Public Health	2	2	55
3	Data Science	2	2	55
4	Engineering	1	1	32
5	Anatomy	1	1	28

Marion Gérard‐Blanluet

Publications

584

Citations

H-Index

Page 1

	Year	Citations
Alternating Hemiplegia of Childhood: Early Characteristics and Evolution of a Neurodevelopmental Syndrome Matthew Sweney, Kenneth Silver, Marion Gérard‐Blanluet, PEDIATRICS	2009	145
CNS malformations in Knobloch syndrome with splice mutation in <i>COL18A1</i> gene Boris Keren, Oscar Suzuki, Marion Gérard‐Blanluet, American Journal of Medical Genetics Part A Developmental AnomalyCns MalformationsGenetic DisorderMedicineGenetics	2007	40
Binder phenotype: clinical and etiological heterogeneity of the so‐called Binder maxillonasal dysplasia in prenatally diagnosed cases, and review of the literature J. M. Levaillant, D. Moeglin, K. Zouiten, Prenatal Diagnosis	2009	37
Specific osseous spurs in a lethal form of hypophosphatasia correlated with 3D prenatal ultrasonographic images M Sinico, J. M. Levaillant, A. Vergnaud, Prenatal Diagnosis	2007	32
CEMARA an information system for rare diseases Paul Landais, Claude Messiaen, Ana Rath, Studies in health technology and informatics EngineeringLabelled Reference CentresInformation SystemDisease ClassificationPrimary Care	2010	32
Intrafamilial segregation analysis of the p.E148Q MEFV allele in familial Mediterranean fever Dimitri Tchernitchko, Marion Gérard‐Blanluet, Marie Legendre, Annals of the Rheumatic Diseases	2006	31
Prenatal phenotypic overlap of Costello syndrome and severe Noonan syndrome by tri‐dimensional ultrasonography Jean‐Marc Levaillant, Marion Gérard‐Blanluet, Muriel Holder‐Espinasse, Prenatal Diagnosis Suspected SyndromeDermatoglyphicPathologyCostello SyndromeAnatomy	2006	28
Bilateral periventricular heterotopias in an X‐linked dominant transmission in a family with two affected males Marion Gérard‐Blanluet, Volney Sheen, Kalotina Machinis, American Journal of Medical Genetics Part A	2006	27
Genomic imbalances detected by array-CGH in patients with syndromal ocular developmental anomalies Andrée Delahaye‐Duriez, Pierre Bitoun, Séverine Drunat, European Journal of Human Genetics Developmental AnomalyGenomic ImbalancesDevelopmental BiologyMendelian DisorderOphthalmology	2012	24
Hypophosphatasia: molecular testing of 19 prenatal cases and discussion about genetic counseling Brigitte Simon‐Bouy, A. Taillandier, Delphine Fauvert, Prenatal Diagnosis	2008	24

Page 1