Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia.
Research Articles
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.
Early developmental regression in autism spectrum disorder: evidence from an international multiplex sample.
Does bilateral damage to the human amygdala produce autistic symptoms?
Fragile X mental retardation protein is required for synapse elimination by the activity-dependent transcription factor MEF2.
Live face-to-face interaction during fMRI : A new tool for social cognitive neuroscience.
Mutations in PNKP cause microcephaly, seizures and defects in DNA repair.
Clinical genetic testing for patients with autism spectrum disorders.
Prenatal polycyclic aromatic hydrocarbon exposure leads to behavioral deficits and downregulation of receptor tyrosine kinase, MET.
Impaired hippocampal-prefrontal synchrony in a genetic mouse model of schizophrenia.
- Previous Page
- Viewing
- Next Page