Gene + body-part link
Learning, talking and behaviour
19 supporting sources
confidence 97%
novelty 55%
The gene ACACA shows up in 13 stories together with learning, talking and behaviour
We read 13 stories that talk about both the gene ACACA and learning, talking and behaviour. That does not prove one causes the other, but they keep showing up together.
How this was derived
This is about what shows up together in the articles. It is not proof that one thing causes the other.
Generated 2026-11-13, last changed
yesterday. Dedup key assoc:ACACA:neurodevelopment.
The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.
Evidence (4 quotes)
Psychosis of Epilepsy: An Update on Clinical Classification and Mechanism
peer_reviewed
· published 2025-01-01
· live page
…ch suggested that some people may be sensitive to the dose changes in genes located in the chromosome 17q12 region. A variable phenotype of epilepsy, intellectual disability, and schizophrenia caused by a 12p13.33-p13.32 terminal microdeletion was identified in a Korean family. Among the six candidate genes in this region…
ESC models of autism with copy-number variations reveal cell-type-specific translational vulnerability
peer_reviewed
· published 2025-01-01
· live page
…number variation in bipolar disorder. Mol. Psychiatry. 2016;21:89-93. doi: 10.1038/mp.2014.174. 9. Mefford H.C., Batshaw M.L., Hoffman E.P. Genomics, Intellectual Disability, and Autism. N. Engl. J. Med. 2012;366:733-743. doi: 10.1056/NEJMra1114194. 10. Srivastava A.K., Schwartz C.E. Intellectual disability and autism spe…
Prenatal Ultrasound–Detected Structural Anomalies Associated with Autism Spectrum Disorder: A Narrative Review
peer_reviewed
· published 2026-01-01
· live page
…4 , 45 ]. Approximately 30-40% of individuals with DiGeorge syndrome meet diagnostic criteria for ASD [ 46 ]. FXS, the most common inherited cause of intellectual disability, is also strongly associated with ASD, with prevalence estimates indicating that around 50% of males and 16% of females with FXS receive an ASD diagn…
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
peer_reviewed
· published 2024-01-01
· live page
…velopmental and epileptic encephalopathies (DEEs, [MIM: 308350]), a severe group of epilepsies characterized by early-onset, intractable seizures and developmental delay. In contrast, genes discovered for the milder, more common forms of epilepsies - genetic generalized epilepsy (GGE [MIM: 600669]) and non-acquired fo…