Published August 31, 2022 | Version v1
Journal article Open

Development of the pupillary light reflex from 9 to 24 months: association with common ASD genetic liability and 3-year ASD diagnosis

Creators

Description

Although autism spectrum disorder (ASD) is heritable, the mechanisms through which genes contribute to symptom emergence remain unclear. Investigating candidate intermediate phenotypes such as the pupillary light reflex (PLR) prospectively from early in development could bridge genotype and behavioural phenotype.

Notes

The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results. Any views expressed are those of the author(s) and not necessarily those of the funders.

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Funding

European Commission
AIMS-2-TRIALS – Autism Innovative Medicine Studies – 2 – Trials 777394
European Commission
EU-AIMS – European Autism Interventions - A Multicentre Study for Developing New Medications 115300
European Commission
BRAINVIEW – Integrated view on disruptions of early brain development 642996