Top-down knowledge rapidly acquired through abstract rule learning biases subsequent visual attention in 9-month-old infants.

Visual attention is an information-gathering mechanism that supports the emergence of complex perceptual and cognitive capacities. Yet, little is known about how the infant brain learns to direct attention to information that is most relevant for learning and behavior. Here we address this gap by examining whether learning a hierarchical rule structure, where there is a higher-order feature that organizes visual inputs into predictable sequences, subsequently biases 9-month-old infants' visual attention to the higher-order visual feature. In Experiment 1, we found that individual differences in infants' ability to structure simple visual inputs into generalizable rules was related to the change in infants' attention biases towards higher-order features. In Experiment 2, we found that increased functional connectivity between the PFC and visual cortex was related to the efficacy of rule learning. Moreover, Granger causality analyses provided exploratory evidence that increased functional connectivity reflected PFC influence over visual cortex. These findings provide new insights into how the infant brain learns to flexibly select features from the cluttered visual world that were previously relevant for learning and behavior.

Brain-derived neurotrophic factor as a model system for examining gene by environment interactions across development.

There has been a dramatic rise in gene x environment studies of human behavior over the past decade that have moved the field beyond simple nature versus nurture debates. These studies offer promise in accounting for more variability in behavioral and biological phenotypes than studies that focus on genetic or experiential factors alone. They also provide clues into mechanisms of modifying genetic risk or resilience in neurodevelopmental disorders. Yet, it is rare that these studies consider how these interactions change over the course of development. In this paper, we describe research that focuses on the impact of a polymorphism in a brain-derived neurotrophic factor (BDNF) gene, known to be involved in learning and development. Specifically we present findings that assess the effects of genotypic and environmental loadings on neuroanatomic and behavioral phenotypes across development. The findings illustrate the use of a genetic mouse model that mimics the human polymorphism, to constrain the interpretation of gene-environment interactions across development in humans.