Andrée Delahaye‐Duriez

Author

Also Known As

A DELAHAYE, A Delahaye, A Delahaye‐Duriez, A. Delahaye, A. Delahaye‐Duriez, A. Hiance Delahaye, Andre Delahaye, Andree Delahaye, Andree Delahaye-Duriez, Andree Delahaye‐Duriez

122

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

Inserm Université Paris Cité Assistance Publique – Hôpitaux de Paris Hôpital Jean-Verdier Université Sorbonne Paris Nord

About

Andrée Delahaye‐Duriez is an author at Inserm specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	18	1K
2	Social Sciences	5	5	437
3	Health Sciences	1	1	41
4	Public Health	1	1	31
5	Behavioral Sciences	1	1	22

Andrée Delahaye‐Duriez

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
Systems genetics identifies a convergent gene network for cognition and neurodevelopmental disease Michael R. Johnson, Kirill Shkura, Sarah R. Langley, Nature Neuroscience Neurodevelopmental DisordersBrain StructureDevelopmental Cognitive NeuroscienceMedicineGenetics	2015	138
Decreased microglial Wnt/β-catenin signalling drives microglial pro-inflammatory activation in the developing brain Juliette Van Steenwinckel, Anne‐Laure Schang, Michelle L. Krishnan, Brain Glial BiologyBrain DevelopmentImmunologyDeveloping BrainSynaptic Signaling	2019	136
A systems-level framework for drug discovery identifies Csf1R as an anti-epileptic drug target Prashant K. Srivastava, Jonathan van Eyll, Patrice Godard, Nature Communications	2018	102
Haploinsufficiency of<i>SOX5</i>at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features Allen N. Lamb, Jill A. Rosenfeld, Nicholas J. Neill, Human Mutation Brain DevelopmentGeneticsLanguage DevelopmentGenomic MechanismAtypical Language Development	2012	101
16p13.11 microduplication in 45 new patients: refined clinical significance and genotype–phenotype correlations Laïla El Khattabi, Solveig Heide, Jean‐Hubert Caberg, Journal of Medical Genetics	2018	93
Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery Andrée Delahaye‐Duriez, Prashant K. Srivastava, Kirill Shkura, Genome biology	2016	86
Clinical and molecular findings in 39 patients with KBG syndrome caused by deletion or mutation of <i>ANKRD11</i> Alice Goldenberg, Florence Riccardi, Aude Tessier, American Journal of Medical Genetics Part A Developmental AnomalyDevelopmental BiologyMolecular FindingsShort StatureGenetic Disorder	2016	85
Genome-wide analysis of differential RNA editing in epilepsy Prashant K. Srivastava, Marta Bagnati, Andrée Delahaye‐Duriez, Genome Research Generalized EpilepsyDifferential Rna EditingGeneticsLong Non-coding RnaGene Editing	2017	82
Haploinsufficiency for ANKRD11-flanking genes makes the difference between KBG and 16q24.3 microdeletion syndromes: 12 new cases Francesca Novara, Berardo Rinaldi, Sanjay M. Sisodiya, European Journal of Human Genetics	2017	80
<i>WWOX</i>-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation Cyril Mignot, Laëtitia Lambert, Laurent Pasquier, Journal of Medical Genetics	2014	79

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