Florence Riant - Concepedia

Author

Florence Riant

Assistance Publique – Hôpitaux de Paris ORCID

Also Known As

F Riant, F. Riant, Florence Cave-Riant, Florence Cavé-Riant, Florence Cavé-Riant, Florence Cavé‐Riant, Florence Riant, Riant Florence, Richard Redon, the Société Française de Neurochirurgie

112

Publications

4.5K

Citations

H-Index

Concepts

All Affiliations

Assistance Publique – Hôpitaux de Paris Inserm Université Paris Cité Hôpital Fernand-Widal Hôpital Lariboisière

About

Florence Riant is an author at Assistance Publique – Hôpitaux de Paris specializing in medicine, neurology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	25	1.4K
2	Social Sciences	4	4	232
3	Public Health	2	2	145
4	Health Sciences	1	1	12
5	Biology	1	1	56

Florence Riant

Publications

3.5K

Citations

H-Index

Page 1

	Year	Citations
Genotype–phenotype correlations in cerebral cavernous malformations patients Christian Denier, Pierre Labauge, Françoise Bergametti, Annals of Neurology	2006	264
Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis Anne Joutel, Pascal Favrole, Pierre Labauge, The Lancet MedicineSurgical PathologyHistopathologyImmunologyPathology	2001	250
Pathogenic Mutations Associated with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Differently Affect Jagged1 Binding and Notch3 Activity via the RBP/JK Signaling Pathway Anne Joutel, Marie Monet, Valérie Domenga, The American Journal of Human Genetics Rbp/jk Signaling PathwayVascular DiseaseSubcortical InfarctsAutophagyImmunology	2004	158
Defective membrane expression of the Na <sup>+</sup> -HCO <sub>3</sub> <sup>−</sup> cotransporter NBCe1 is associated with familial migraine Masashi Suzuki, Wim Van Paesschen, Ingeborg Stalmans, Proceedings of the National Academy of Sciences	2010	147
De novo mutations in <i>ATP1A2</i> and <i>CACNA1A</i> are frequent in early-onset sporadic hemiplegic migraine Florence Riant, Anne Ducros, Claire Ploton, Neurology	2010	131
<i>PRRT2</i> mutations cause hemiplegic migraine Florence Riant, Emmanuel Roze, Cécile Barbance, Neurology	2012	128
JAML, a novel protein with characteristics of a junctional adhesion molecule, is induced during differentiation of myeloid leukemia cells Christel Moog‐Lutz, Florence Riant, Florence C. Guibal, Blood	2003	127
Clinical features of cerebral cavernous malformations patients with <i>KRIT1</i> mutations Christian Denier, Pierre Labauge, L. Brunereau, Annals of Neurology	2003	122
A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies Marie Coutelier, Giulia Coarelli, Marie‐Lorraine Monin, Brain NeurogenomicsNeurological DisorderGeneticsGenetic EpidemiologyDisease Gene Identification	2017	111
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy Katayoun Vahedi, Pascale Massin, Jean‐Pierre Guichard, Neurology	2003	104

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