Marie‐Laure Moutard
Sorbonne Université(FR)Hôpitaux Universitaires Paris-Ouest(FR)
Publications by Year
Research Areas
Fetal and Pediatric Neurological Disorders, Neonatal and fetal brain pathology, Prenatal Screening and Diagnostics, Genomics and Rare Diseases, Hereditary Neurological Disorders
Most-Cited Works
- → Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1(2015)601 cited
- → Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome(2007)445 cited
- → Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A)(2007)231 cited
- → Congenital cerebral malformations and dysfunction in fetuses and newborns following the 2013 to 2014 Zika virus epidemic in French Polynesia(2016)218 cited
- → Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities(2012)202 cited
- → Changes in Electroencephalogram and Autonomic Cardiovascular Activity during Induction of Anesthesia with Sevoflurane Compared with Halothane in Children(1999)167 cited