Elisabeth Tournier‐Lasserve

Author

Also Known As

Alice Poisson, CAA study group, Deborah A Nickerson, E TOURNIER-LASSERVE, E Tournier Lasserve, E Tournier-Lasserve, E. TOURNIER‐LASSERVE, E. Tournier Lasserve, E. Tournier-Lasserve, E. Tournier-lasserve

356

Publications

25.8K

Citations

H-Index

159

Concepts

All Affiliations

Inserm Hôpital Lariboisière Assistance Publique – Hôpitaux de Paris Université Paris Cité Délégation Paris 7

About

Elisabeth Tournier‐Lasserve is an author at Inserm specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	47	80	12.3K
2	Social Sciences	13	13	3.3K
3	Public Health	9	9	412
4	Health Sciences	5	5	295
5	Natural Sciences	4	4	398

Elisabeth Tournier‐Lasserve

168

Publications

19.7K

Citations

H-Index

Page 1

	Year	Citations
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia Anne Joutel, Christophe Corpechot, Anne Ducros, Nature Neurobiology Of DiseaseNotch3 MutationsMendelian DisorderGenetic DisorderGenetics	1996	2K
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients Anne Joutel, Katayoun Vahedi, Christophe Corpechot, The Lancet Somatic VariantNotch3 MutationsGenetic DisorderGeneticsHematology	1997	678
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12 Elisabeth Tournier‐Lasserve, Anne Joutel, Judith Melki, Nature Genetics Subcortical InfarctsNeurological DisorderBrain InjuryNeurologyLeukoencephalopathy Maps	1993	676
Clinical spectrum of CADASIL: a study of 7 families Hugues Chabriat, Katayoun Vahedi, M G Bousser, The Lancet Family MedicineClinical FindingHistopathologyClinical EvidenceCase Series	1995	667
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients Anne Joutel, F. Andreux, Swann Gaulis, Journal of Clinical Investigation Notch3 Receptor AccumulatesAngiogenesisSignal TransductionEpendymaPathology	2000	591
Role of COL4A1 in Small-Vessel Disease and Hemorrhagic Stroke Douglas B. Gould, F. Campbell Phalan, Saskia E. van Mil, New England Journal of Medicine Vascular DiseaseEnvironmental StressPathologyCerebral Vascular RegulationNeuroinflammation	2006	565
The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel Anne Ducros, Christian Denier, Anne Joutel, New England Journal of Medicine	2001	555
<i>Notch3</i> is required for arterial identity and maturation of vascular smooth muscle cells Valérie Domenga, Peggy Fardoux, Pierre Lacombe, Genes & Development	2004	523
Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas Sophie Laberge, Hans H. Jung, Pierre Labauge, Nature Genetics GeneticsVascular MalformationPathologyCongenital Heart AnomalyMedicine	1999	477
EndMT contributes to the onset and progression of cerebral cavernous malformations Luigi Maddaluno, Noemi Rudini, Roberto Cuttano, Nature NeuroanatomyVascular MalformationCerebral Cavernous MalformationsNeurologyNeuroscience	2013	475

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