Christel Depienne - Concepedia

Author

Christel Depienne

Also Known As

A.-S. Denommé-Pichon, Bruce Poppe, C Depienne, C. Depienne, Carla Marini, Caroline Demilly, Christel Depienne, Csaba Barta, DDD Study, Daniel Brandeis

314

Publications

17.9K

Citations

H-Index

150

Concepts

All Affiliations

Inserm Sorbonne Université Assistance Publique – Hôpitaux de Paris Centre National de la Recherche Scientifique Pitié-Salpêtrière Hospital

About

Christel Depienne is an author at Inserm specializing in medicine, genetics, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	37	63	7.8K
2	Health Sciences	5	5	335
3	Natural Sciences	2	2	91
4	Public Health	2	2	2K
5	Education	1	1	103

Christel Depienne

141

Publications

13.3K

Citations

H-Index

Page 1

	Year	Citations
Analysis of shared heritability in common disorders of the brain Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Science Brain FunctionPsychiatric DisordersGeneticsGenetic EpidemiologyNeuropsychiatry	2018	2K
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders Phil H. Lee, Verneri Anttila, Hyejung Won, Cell PsychiatryPsychiatric DisordersGenetic DisorderGeneticsPsychiatric Genetics	2019	1.4K
Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females Christel Depienne, Delphine Bouteiller, Boris Keren, PLoS Genetics Mainly Affects FemalesDravet SyndromeMendelian DisorderGenetic DisorderMedicine	2009	368
The phenotypic spectrum of <i>SCN8A</i> encephalopathy Jan Larsen, Gemma L. Carvill, Elena Gardella, Neurology	2015	282
<i>GRIN2B</i> encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects Konrad Platzer, Hongjie Yuan, Hannah M. Schutz, Journal of Medical Genetics	2017	249
Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration Giovanni Stévanin, Hamid Azzedine, Paola S. Denora, Brain	2007	246
De novo mutations in HCN1 cause early infantile epileptic encephalopathy Caroline Nava, Carine Dalle, Agnès Rastetter, Nature Genetics Genetic DisorderGeneticsNeuroscienceNeurologyNeuropathology	2014	230
De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome Arvid Suls, Johanna A. Jaehn, Angéla Kecskés, The American Journal of Human Genetics Chd2 CauseDravet SyndromeMolecular NeuroscienceNeurobiology Of DiseaseGenetic Disorder	2013	219
Delineating the <i>GRIN1</i> phenotypic spectrum Johannes R. Lemke, Kirsten Geider, Katherine L. Helbig, Neurology	2016	202
Annonacin, a Natural Mitochondrial Complex I Inhibitor, Causes Tau Pathology in Cultured Neurons Myriam Escobar-Khondiker, Matthias Höllerhage, Marie‐Paule Muriel, Journal of Neuroscience Cultured NeuronsMitophagyNadh OxidationNatural Mitochondrial ComplexLipid Peroxidation	2007	201

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