Researchers used two sets of data: RNA in post-mortem brain tissue and intracranial EEG (iEEG) data from epilepsy patients. They then measure RNA as a proxy for gene expression in the brain.
"Quantifying RNA in the brain requires extracting RNA from the brain tissue itself. Thus, we are limited to accessing brain tissue post-mortem, or in rare occasions can obtain tissue from surgical resections of the brain," researchers said.
"This is very exciting because the identification of these gene-to-behaviour relationships opens up new research avenues for testing the role of these genes in specific aspects of memory function and dysfunction," said Genevieve Konopka of University of Texas Southwestern in the US.
The study is part of the nascent but growing field of "imaging genetics," which aims to relate genetic variation to variation in brain anatomy and function.
"We have identified a window into the molecular pathways important for normal memory function that are at risk from a genetic perspective in autism," Konopka said.
"Genes shape the anatomy and functional organisation of the brain, and these structural and functional characteristics of the brain give rise to the observable behaviours," said Evelina Fedorenko of Harvard University in the US.
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