Marie‐Christine de Blois

Author

Hôpital Necker-Enfants Malades

Also Known As

M-C de Blois, Marie-Christine de Blois, Marie‐Christine De Blois, Marie‐Christine de Blois, de Blois, Marie-Christine

Publications

964

Citations

H-Index

Concepts

All Affiliations

Hôpital Necker-Enfants Malades Hôpital des Enfants Université Paris Cité Inserm Institut Necker Enfants Malades

About

Marie‐Christine de Blois is an author at Hôpital Necker-Enfants Malades specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	485
2	Neuroscience	2	2	86
3	Neurology	1	1	75
4	Obstetrics	1	1	11
5	Pathology	1	1	119

Marie‐Christine de Blois

Publications

701

Citations

H-Index

Page 1

	Year	Citations
Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome Hélène De Leersnyder, Marie‐Christine de Blois, Bruno Claustrat, The Journal of Pediatrics ChronobiologyMedicinePineal GlandCircadian RhythmSmith-magenis Syndrome	2001	185
Overgrowth and trisomy 15q26.1-qter including the IGF1 receptor gene: report of two families and review of the literature Laurence Faivre, Philippe Gosset, Valérie Cormier‐Daire, European Journal of Human Genetics Developmental BiologyGenetic DisorderGeneticsIgf1 Receptor GenePathology	2002	119
Neurobehavioral Profile and Brain Imaging Study of the 22q13.3 Deletion Syndrome in Childhood Anne Philippe, Nathalie Boddaert, Laurence Vaivre‐Douret, PEDIATRICS	2008	109
A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation Laurence Colleaux, Marlène Rio, S. Heuertz, European Journal of Human Genetics Developmental AnomalyPsychiatryIdiopathic Mental RetardationGeneticsPediatrics	2001	95
Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation Marlène Rio, Florence Molinari, S. Heuertz, Journal of Medical Genetics GeneticsEpigeneticsClinical GeneticsMendelian DisorderPsychiatric Genetics	2002	75
DNA polymorphism analysis in families with recurrence of free trisomy 21 Constantinos Pángalos, C. Conover Talbot, John G. Lewis, PubMed	1992	62
Ebstein anomaly associated with rearrangements of chromosomal region 11q Pascale de Lonlay-Debeney, Marie‐Christine de Blois, Damien Bonnet, American Journal of Medical Genetics	1998	32
Werner mesomelic dysplasia with Hirschsprung disease Alice Goldenberg, Mathieu Milh, Pascal de Lagausie, American Journal of Medical Genetics Part A	2003	13
17q21.31 Microdeletion: Brain Anomalies Leading to Prenatal Diagnosis Matthieu Egloff, Férechté Encha‐Razavi, Cathérine Garel, Cytogenetic and Genome Research Developmental AnomalyDevelopmental BiologySevere VentriculomegalyBrain DevelopmentFetal Medicine	2014	11

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