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Journal of Virology|June 7, 2002
Turnover of hepatitis B virus X protein is regulated by damaged DNA-binding complexFrançoise Bergametti, Delphine Sitterlin, Catherine TransyEuropean Journal of Human Genetics : EJHG|July 16, 2015
Can whole-exome sequencing data be used for linkage analysis?Steven Gazal, Simon Gosset, Edgard Verdura, et al.Annals of Neurology|October 17, 2006
Genotype-phenotype correlations in cerebral cavernous malformations patientsChristian Denier, Pierre Labauge, Françoise Bergametti, et al.Stroke|March 20, 2014
Cerebral cavernous malformations arise independent of the heart of glass receptorXiangjian Zheng, Florence Riant, Françoise Bergametti, et al.European Journal of Human Genetics : EJHG|June 22, 2017
Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in CaucasiansStéphanie Guey, Markus Kraemer, Dominique Hervé, et al.Stroke|March 26, 2019
Clinical and Molecular Features of 5 European Multigenerational Families With Moyamoya AngiopathyLou Grangeon, Stéphanie Guey, Jan Claudius Schwitalla, et al.Journal of Medical Genetics|January 16, 2020
Novel CCM2 missense variants abrogating the CCM1-CCM2 interaction cause cerebral cavernous malformationsFrançoise Bergametti, Geraldine Viot, Christophe Verny, et al.Journal of Medical Genetics|March 27, 2017
De novo mutations in CBL causing early-onset paediatric moyamoya angiopathyStéphanie Guey, Lou Grangeon, Francis Brunelle, et al.Human Genomics|March 21, 2023
Biallelic variants in NOS3 and GUCY1A3, the two major genes of the nitric oxide pathway, cause moyamoya cerebral angiopathyStéphanie Guey, Dominique Hervé, Manoëlle Kossorotoff, et al.Stroke|January 2, 2026
<i>COL4A1</i> and <i>COL4A2</i> Gene Duplication or Triplication as a Genetic Cause of Cerebral Small Vessel Disease in AdultsDominique Hervé, Saskia A J Lesnik Oberstein, Eva Pipiras, et al.Pageof 2