Mathijs B. van der Lei
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Autism Spectrum Disorder Research, MicroRNA in disease regulation, Neuroscience and Neuropharmacology Research, Alzheimer's disease research and treatments
Most-Cited Works
- → Deletion of Fmr1 in parvalbumin-expressing neurons results in dysregulated translation and selective behavioral deficits associated with fragile X syndrome(2022)39 cited
- → Cognitive deficits in human ApoE4 knock-in mice: A systematic review and meta-analysis(2024)7 cited
- → Therapeutic potential of GABAA receptor subunit expression abnormalities in fragile X syndrome(2022)4 cited
- → From Discovery to Innovative Translational Approaches in 80 Years of Fragile X Syndrome Research(2025)2 cited
- → A Novel Adnp Frameshift Variant Disrupts Wnt Signaling Leading To Chromatocytoskeletal Defects and Autism-Related Behavior in Mice(2025)2 cited
- → CMIP as a novel candidate gene for neurodevelopmental and neuropsychiatric disorders(2026)
- → Deletion of <i>Fmr1</i> in Parvalbumin Inhibitory Neurons Leads to Dysregulated Translation and Selective Behavioral Deficits Associated with Fragile X Syndrome(2021)