Emilie Mugniery - Concepedia

Author

Emilie Mugniery

Hôpital Necker-Enfants Malades

Also Known As

E. Mugniery, Emilie Mugniery

Publications

649

Citations

H-Index

Concepts

All Affiliations

Hôpital Necker-Enfants Malades Inserm Université Paris Cité Centre National de la Recherche Scientifique Délégation Paris 7

About

Emilie Mugniery is an author at Hôpital Necker-Enfants Malades specializing in medicine, genetics, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	337
2	Natural Sciences	2	2	112
3	Biochemistry	1	1	59
4	Biology	1	1	53
5	Biomedical Engineering	1	1	199

Emilie Mugniery

Publications

649

Citations

H-Index

Page 1

	Year	Citations
Evaluation of the Therapeutic Potential of a CNP Analog in a Fgfr3 Mouse Model Recapitulating Achondroplasia Florence Lorget, Nabil Kaci, Jeff Peng, The American Journal of Human Genetics Regenerative MedicineTherapeutic PotentialCnp AnalogFibroblast Growth FactorCytoskeleton	2012	199
Temporal-spatial changes in Sonic Hedgehog expression and signaling reveal different potentials of ventral mesencephalic progenitors to populate distinct ventral midbrain nuclei Sandra Blaess, Gabriela O. Bodea, Anna Kabanova, Neural Development	2011	136
FGFR3 mutation causes abnormal membranous ossification in achondroplasia Federico Di Rocco, Martin Biosse Duplan, Yann Heuzé, Human Molecular Genetics	2014	84
Synthesis and biological evaluation of a triazole-based library of pyrido[2,3-d]pyrimidines as FGFR3 tyrosine kinase inhibitors Laurent Le Corre, Anne‐Lise Girard, J Aubertin, Organic & Biomolecular Chemistry Combinatorial ChemistryBioorganic ChemistryPharmaceutical ChemistryMedicinal ChemistryReceptor Tyrosine Kinase	2010	59
Zebrafish midbrain slow-amplifying progenitors exhibit high levels of transcripts for nucleotide and ribosome biogenesis Gaëlle Recher, Julia Jouralet, Alessandro Brombin, Development GeneticsMolecular GeneticsGanglion CellRetinaTransparent Embryo Midbrain	2013	53
A novel tyrosine kinase inhibitor restores chondrocyte differentiation and promotes bone growth in a gain-of-function Fgfr3 mouse model Aurélie Jonquoy, Emilie Mugniery, Catherine Benoist-Lasselin, Human Molecular Genetics	2011	46
An activating Fgfr3 mutation affects trabecular bone formation via a paracrine mechanism during growth Emilie Mugniery, Romain Dacquin, Caroline Marty, Human Molecular Genetics	2012	46
Delayed bone age due to a dual effect of FGFR3 mutation in Achondroplasia Stéphanie Pannier, Emilie Mugniery, Aurélie Jonquoy, Bone Bone DiseaseBone Morphogenic ProteinGeneticsFgfr3 MutationBone Remodeling	2010	26

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