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In recent years, considerable advances have been made toward our understanding of the genetic architecture of behavior and the physical, mental, and environmental influences that underpin behavioral processes.
Background: The "temporal architecture" of behavior is a construct that can be used to quantify the structure of behavioral sequences in the temporal domain for example, by using a two-choice prediction task to investigate how past responses, stimuli, and outcomes influence the decision-making process.
The implications of this finding, and the other insights into the genetic architecture of behavior we have discussed, become clear when we turn to look at the second focus of our review.
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Although there is a heritable basis for many animal behaviors, the genetic architecture of behavioral variation in natural populations remains mostly unknown, particularly in vertebrates.
Comparative studies of social responsiveness, an ability that is impaired in autism spectrum disorders, can inform our understanding of both autism and the cognitive architecture of social behavior.
Williams syndrome (WS), a genetic disorder resulting from hemizygous microdeletion of chromosome 7q11.23, has emerged as a model for identifying the genetic architecture of socioemotional behavior.
Findings from a large selection of the twin and adoption studies that have investigated the genetic and environmental architecture of aggressive behavior are summarized.
Using this task, previous investigations of the temporal architecture of the behavior in schizophrenic patients have identified an increased frequency of alternating highly predictable and highly unpredictable response sequences in the same test session in the same patient.
In conclusion, our study expands the understanding of the neural architecture of impulsive behavior.
Our results indicate that the genetic architecture of social behavior includes both highly connected and conserved components as well as loosely connected and evolutionarily labile components.
We further investigated the genetic architecture of escape behavior by focusing on two strains, a wild Hawaii-derived strain, and the commonly used laboratory N2 strain.
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