Juliette Nectoux - Concepedia

Author

Juliette Nectoux

Inserm ORCID

Also Known As

François Petit, J Nectoux, J. Nectoux, J.U.L. Nectoux, Juliette Nectoux, Nectoux, Juliette, Romane Muletier

122

Publications

2.2K

Citations

H-Index

Concepts

All Affiliations

Inserm Université Paris Cité Hôpital Cochin Assistance Publique – Hôpitaux de Paris Institut Cochin

About

Juliette Nectoux is an author at Inserm specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	20	1K
2	Social Sciences	4	4	87
3	Natural Sciences	3	3	218
4	Public Health	2	2	38
5	Health Sciences	1	1	111

Juliette Nectoux

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
Key clinical features to identify girls with CDKL5 mutations Nadia Bahi‐Buisson, Juliette Nectoux, Haydeé Rosas‐Vargas, Brain Cdkl5-associated EncephalopathyDevelopmental AnomalyMendelian DisorderKey Clinical FeaturesRefractory Epilepsy	2008	285
Update on fluoroquinolone resistance in Helicobacter pylori: new mutations leading to resistance and first description of a gyrA polymorphism associated with hypersusceptibility Vincent Cattoir, Juliette Nectoux, Christine Lascols, International Journal of Antimicrobial Agents Antimicrobial Resistance GeneHealth SciencesGeneticsPathogenesisResistance Mutation (Virology)	2007	111
Novel <i>FOXG1</i> mutations associated with the congenital variant of Rett syndrome Maria Antonietta Mencarelli, Ariele Spanhol-Rosseto, Rosangela Artuso, Journal of Medical Genetics	2009	108
A quantitative gene expression study suggests a role for angiopoietins in focal nodular hyperplasia Valérie Paradis, Ivan Bièche, Delphine Dargère, Gastroenterology Radiation OncologyAngiogenesisDevelopmental BiologyFocal Nodular HyperplasiaNatural Sciences	2003	106
Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant Nadia Bahi‐Buisson, Juliette Nectoux, Benôıt Girard, Neurogenetics Developmental AnomalyNovel CasesDevelopmental BiologyFoxg1 MutationsGenetic Disorder	2009	83
Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization Gina O’Grady, Heather Best, Tamar E. Sztal, The American Journal of Human Genetics Internalized NucleiMyofibrillar DisorganizationBiochemistryNatural SciencesPhysiology	2016	82
Targeted next-generation sequencing for differential diagnosis of neurofibromatosis type 2, schwannomatosis, and meningiomatosis Camille Louvrier, Éric Pasmant, Audrey Briand‐Suleau, Neuro-Oncology	2018	65
Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes Chloé Delépine, Hamid Méziane, Juliette Nectoux, Human Molecular Genetics	2015	60
Droplet digital PCR combined with minisequencing, a new approach to analyze fetal DNA from maternal blood: application to the non-invasive prenatal diagnosis of achondroplasia Lucie Orhant, Olivia Anselem, Mélanie Fradin, Prenatal Diagnosis	2016	60
A new titinopathy Rafael de Cid, Rabah Ben Yaou, Carinne Roudaut, Neurology	2015	56

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