All Stories

  1. Characterisation of CASPR2 deficiency disorder - a syndrome involving autism, epilepsy and language impairment
  2. Retinoic Acid Signaling: A New Piece in the Spoken Language Puzzle
  3. A novel approach identifies the first transcriptome networks in bats: a new genetic model for vocal communication
  4. A chromosomal rearrangement in a child with severe speech and language disorder separates FOXP2 from a functional enhancer
  5. Genetics and the Language Sciences
  6. FOXP2 drives neuronal differentiation by interacting with retinoic acid signaling pathways
  7. Genome wide identification of Fruitless targets suggests a role in upregulating genes important for neural circuit formation
  8. A direct molecular link between the autism candidate gene RORa and the schizophrenia candidate MIR137
  9. Shining a light on CNTNAP2: complex functions to complex disorders
  10. FOXP2 Targets Show Evidence of Positive Selection in European Populations
  11. Genetic Pathways Implicated in Speech and Language
  12. Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain
  13. Functional Genomic Dissection of Speech and Language Disorders
  14. Unravelling neurogenetic networks implicated in developmental language disorders
  15. Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia
  16. A Functional Genetic Link between Distinct Developmental Language Disorders
  17. Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human Brain
  18. High-Throughput Analysis of Promoter Occupancy Reveals Direct Neural Targets of FOXP2, a Gene Mutated in Speech and Language Disorders
  19. Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits