Danielle Seilhean - Concepedia

Author

Danielle Seilhean

Also Known As

Catherine Lubetzki, Charles Duyckaerts, D D Seilhean, D Seilhean, D. Seilhean, Danielle D Seilhean, Danielle D. Seilhean, Danielle Seilhan, Danielle Seilhean, Danielle Seilhean<sup>2</sup>

270

Publications

14.7K

Citations

H-Index

159

Concepts

All Affiliations

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

About

Danielle Seilhean is an author at Sorbonne Université specializing in medicine, neurology, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	38	64	6.5K
2	Health Sciences	5	5	336
3	Natural Sciences	3	3	268
4	Education	1	1	12
5	Engineering	1	1	34

Danielle Seilhean

119

Publications

12.3K

Citations

H-Index

Page 1

	Year	Citations
Neuroinvasion of SARS-CoV-2 in human and mouse brain Eric Song, Ce Zhang, Benjamin Israelow, The Journal of Experimental Medicine Long CovidNeurovirologyMedicineCovid-19 PandemicViral Pathogenesis	2020	1K
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions Vivianna M. Van Deerlin, Patrick Sleiman, María Martínez-Lage, Nature Genetics Frontotemporal Lobar DegenerationAllelic VariantGenetic DisorderGeneticsTdp-43 Inclusions	2010	597
Dyslipidemia is a protective factor in amyotrophic lateral sclerosis Luc Dupuis, P. Corcia, Anissa Fergani, Neurology	2008	531
Staging of Neurofibrillary Pathology in Alzheimer's Disease: A Study of the BrainNet Europe Consortium Irina Alafuzoff, Thomas Arzberger, Safa Al‐Sarraj, Brain Pathology Neurofibrillary PathologyPathologyNeuro-oncologyAlzheimer's DiseaseStepwise Progression	2008	468
Hallucinations, REM sleep, and Parkinson’s disease Isabelle Arnulf, Muriel Bonnet, Philippe Damier, Neurology	2000	436
Inhibition of the mTORC Pathway in the Antiphospholipid Syndrome Guillaume Canaud, Frank Bienaimé, Fanny Tabarin, New England Journal of Medicine	2014	342
Activation of the subventricular zone in multiple sclerosis: Evidence for early glial progenitors Brahim Nait‐Oumesmar, Nathalie Picard-Riéra, Christophe Kerninon, Proceedings of the National Academy of Sciences	2007	316
<i>SOD1</i>, <i>ANG</i>, <i>VAPB</i>, <i>TARDBP</i>, and <i>FUS</i> mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations Stéphanie Millecamps, François Salachas, C. Cazeneuve, Journal of Medical Genetics	2010	292
Perforin-Dependent Brain-Infiltrating Cytotoxic CD8+ T Lymphocytes Mediate Experimental Cerebral Malaria Pathogenesis Josianne Nitcheu, Olivia Bonduelle, Christophe Combadière, The Journal of Immunology	2003	278
Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology Elisa Teyssou, Takahiro Takeda, Vincent Lebon, Acta Neuropathologica Neurodegenerative DiseasesAmyotrophic Lateral SclerosisGeneticsExperimental NeuropathologyNeuroscience	2013	228

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