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Neurology|November 24, 2012
A novel hereditary extensive vascular leukoencephalopathy mapping to chromosome 20q13Dominique Hervé, Hugues Chabriat, Mélanie Rigal, et al.
Brain : a Journal of Neurology|June 12, 2015
Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel diseaseEdgard Verdura, Dominique Hervé, Eva Scharrer, et al.
Annals of Neurology|October 4, 2021
End-Truncated LAMB1 Causes a Hippocampal Memory Defect and a LeukoencephalopathyChaker Aloui, Dominique Hervé, Gaelle Marenne, et al.
Brain : a Journal of Neurology|March 26, 2026
SCN2A variants are associated with familial and sporadic hemiplegic migraineFlorence Riant, Christopher H Thompson, Syed M A Wafa, et al.
European Journal of Medical Genetics|October 14, 2018
Further refinement of COL4A1 and COL4A2 related cortical malformationsMara Cavallin, Manuele Mine, Marion Philbert, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2019
The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathyAmélie Pinard, Stéphanie Guey, Dongchuan Guo, et al.
Annals of Neurology|September 27, 2016
Disruption of a miR-29 binding site leading to COL4A1 upregulation causes pontine autosomal dominant microangiopathy with leukoencephalopathyEdgard Verdura, Dominique Hervé, Françoise Bergametti, et al.
Developmental Cell|January 28, 2015
Regulation of β1 integrin-Klf2-mediated angiogenesis by CCM proteinsMarc Renz, Cécile Otten, Eva Faurobert, et al.
Brain : a Journal of Neurology|July 16, 2021
Heterozygous HTRA1 nonsense or frameshift mutations are pathogenicThibault Coste, Dominique Hervé, Jean Philippe Neau, et al.
EMBO Molecular Medicine|September 6, 2018
Systematic pharmacological screens uncover novel pathways involved in cerebral cavernous malformationsCécile Otten, Jessica Knox, Gwénola Boulday, et al.
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