An open‑access Nature study indicates that diagnostic timing in autism reflects partially distinct genetic and developmental pathways—reshaping screening, comorbidity assessment and lifespan care.
New genomic data suggest autism is not one line but many intersecting constellations; embracing that plurality can deepen clinical care and social understanding.
A Cambridge‑led Nature report shows partially distinct genetic architectures for early‑ versus late‑diagnosed autism, with implications for screening and adolescent services.
Distinct polygenic trajectories in autism carry practical consequences for screening calendars, referral routes and clinic design—moving services toward precision neurodevelopment.