Elisabeth Tournier-Lasserve

Research.com Recognitions

• 2019 - The Brain Prize, Lundbeck Foundation for more than 30 years spent describing, understanding and diagnosing the most common inherited form of stroke, CADASIL

Overview

Best Publications

• Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

  Anne Joutel;Christophe Corpechot;Anne Ducros;Katayoun Vahedi

  2440
  Citations

• The Control of Vascular Integrity by Endothelial Cell Junctions: Molecular Basis and Pathological Implications

  Elisabetta Dejana;Elisabeth Tournier-Lasserve;Elisabeth Tournier-Lasserve;Brant M. Weinstein

  930
  Citations

• Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

  Anne Joutel;Katayoun Vahedi;Christophe Corpechot;Alain Troesch

  812
  Citations

• Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12

  E Tournier-Lasserve;A Joutel;J Melki;J Weissenbach

  795
  Citations

• The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients

  Anne Joutel;Fréderic Andreux;Swann Gaulis;Valérie Domenga

  676
  Citations

• The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel

  Anne Ducros;Christian Denier;Anne Joutel;Michaëlle Cecillon

  675
  Citations

• Notch3 is required for arterial identity and maturation of vascular smooth muscle cells

  Valérie Domenga;Peggy Fardoux;Pierre Lacombe;Marie Monet

  615
  Citations

• Role of COL4A1 in small-vessel disease and hemorrhagic stroke.

  Douglas B Gould;F Campbell Phalan;Saskia E van Mil;John P Sundberg

  592
  Citations

• EndMT contributes to the onset and progression of cerebral cavernous malformations

  Luigi Maddaluno;Noemi Rudini;Roberto Cuttano;Luca Bravi

  488
  Citations

• A gene for familial hemiplegic migraine maps to chromosome 19.

  Anne Joutel;Marie-Germaine Bousser;Valérie Biousse;Pierre Labauge

  472
  Citations

• Synopsis of Guidelines for the Clinical Management of Cerebral Cavernous Malformations: Consensus Recommendations Based on Systematic Literature Review by the Angioma Alliance Scientific Advisory Board Clinical Experts Panel.

  Amy Akers;Rustam Al-Shahi Salman;Issam A. Awad;Kristen Dahlem

  456
  Citations

• Genetics of cavernous angiomas.

  Pierre Labauge;Christian Denier;Francoise Bergametti;Francoise Bergametti;Elisabeth Tournier-Lasserve;Elisabeth Tournier-Lasserve

  441
  Citations

• Patterns of MRI lesions in CADASIL

  H. Chabriat;C. Levy;H. Taillia;M.-T. Iba-Zizen

  405
  Citations

• Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families

  Pierre Labauge;Sophie Laberge;L Brunereau;C Levy

  327
  Citations

• Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis.

  Anne Joutel;Pascal Favrole;Pierre Labauge;Hugues Chabriat

  319
  Citations

• Genotype–phenotype correlations in cerebral cavernous malformations patients

  Christian Denier;Pierre Labauge;Françoise Bergametti;Françoise Bergametti;Florence Marchelli

  307
  Citations

• Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.

  Elizabeth Tournier-Lasserve;Marie-Thérèse Iba-Zizen;Norma Romero;Marie-Germaine Bousser

  275
  Citations

• Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity.

  Anne Ducros;Anne Joutel Md;Michaëlle Cecillon;Elisabeth Tournier-Lasserve

  271
  Citations

• Notch signalling pathway and human diseases.

  Anne Joutel;Elisabeth Tournier-Lasserve

  265
  Citations

• Transgenic Mice Expressing Mutant Notch3 Develop Vascular Alterations Characteristic of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

  Marie Magdeleine Ruchoux;Valérie Domenga;Peggy Brulin;Jacqueline Maciazek

  249
  Citations