Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by J.V. Warner
Genotyping FOXG1 Mutations in Patients With Clinical Evidence of the FOXG1 Syndrome
Molecular Syndromology
Genetics
Related publications
FOXG1 Dose in Brain Development
Frontiers in Pediatrics
Child Health
Pediatrics
Perinatology
Platelet Defects in Congenital Variant of Rett Syndrome Patients With FOXG1 Mutations or Reduced Expression Due to a Position Effect at 14q12
European Journal of Human Genetics
Genetics
Visual Impairment in FOXG1-mutated Individuals and Mice
Neuroscience
Neuroscience
FOXG1 Orchestrates Neocortical Organization and Cortico-Cortical Connections
Neuron
Neuroscience
Partial Monosomy14q Involving FOXG1 and NOVA1 in an Infant With Microcephaly, Seizures and Severe Developmental Delay
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
Deep Genotyping of the IDS Gene in Colombian Patients With Hunter Syndrome
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
The Transcription Factor Foxg1 Regulates Telencephalic Progenitor Proliferation Cell Autonomously, in Part by Controlling Pax6 Expression Levels
Neural Development
Developmental Neuroscience
MicroRNA-9 Modulates Cajal-Retzius Cell Differentiation by Suppressing Foxg1 Expression in Mouse Medial Pallium
Journal of Neuroscience
Neuroscience
Mutations inRIT1cause Noonan Syndrome - Additional Functional Evidence and Expanding the Clinical Phenotype
Clinical Genetics
Genetics