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Publications by Nathalie Boddaert

Mutations in KEOPS-complex Genes Cause Nephrotic Syndrome With Primary Microcephaly

Nature Genetics
Genetics
2017English

A Missense Mutation Within the Fork-Head Domain of the Forkhead Box G1 Gene (FOXG1) Affects Its Nuclear Localization

Human Mutation
Genetics
2010English

Magnetic Resonance Imaging Arterial-Spin-Labelling Perfusion Alterations in Childhood Migraine With Atypical Aura: A Case-Control Study

Developmental Medicine and Child Neurology
Child HealthDevelopmental NeurosciencePediatricsPerinatologyNeurology
2016English

Neural and Behavioral Signature of Human Social Perception

Scientific Reports
Multidisciplinary
2019English

Mutations in TCF4, Encoding a Class I Basic Helix-Loop-Helix Transcription Factor, Are Responsible for Pitt-Hopkins Syndrome, a Severe Epileptic Encephalopathy Associated With Autonomic Dysfunction

American Journal of Human Genetics
Genetics
2007English

Thalamic Tumors in Children: A Reappraisal

Journal of Neurosurgery: Pediatrics
Child HealthPerinatologyNeurologyMedicinePediatricsSurgery
2007English

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