Epigenome-wide analysis identifies DNA methylation signatures associated with the infant pupillary light reflex, a candidate intermediate phenotype for autism.

Saved in:
Bibliographic Details
Title: Epigenome-wide analysis identifies DNA methylation signatures associated with the infant pupillary light reflex, a candidate intermediate phenotype for autism.
Authors: Fish, Laurel A.1,2 (AUTHOR), Gliga, Teodora3 (AUTHOR), Gui, Anna4,5 (AUTHOR), Ali, Jannath Begum5 (AUTHOR), Mason, Luke5 (AUTHOR), Johnson, Mark H.5,6 (AUTHOR), Charman, Tony7 (AUTHOR), Falck-Ytter, Terje8,9 (AUTHOR), Jones, Emily J. H.5,10 (AUTHOR), Kandaswamy, Radhika2 (AUTHOR), Happé, Francesca2 (AUTHOR), Wong, Chloe C. Y.2,11 (AUTHOR) Chloe.wong@kcl.ac.uk
Source: Scientific Reports. 1/8/2026, Vol. 16 Issue 1, p1-10. 10p.
Database: Academic Search Ultimate
Full text is not displayed to guests.
Description
ISSN:20452322
DOI:10.1038/s41598-025-31651-5