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Exploratory VLSM analyses linked this heightened temporal impulsivity to damage in the vmPFC (areas 13 and 25) and the ventral striatum.
Exploratory VLSM analyses linked this heightened temporal impulsivity to damage in the vmPFC (areas 13 and 25) and the ventral striatum.
mPFC damage also led to greater baseline temporal impulsivity (i.e., steeper discounting of future rewards) compared to HCs, without affecting preference uncertainty.
mPFC damage also led to greater baseline temporal impulsivity (i.e., steeper discounting of future rewards) compared to HCs, without affecting preference uncertainty.
VLSM analysis revealed that this enhanced susceptibility to impulsive (vs patient) social influence was specifically associated with damage to the dmPFC (including area 9).
VLSM analysis revealed that this enhanced susceptibility to impulsive (vs patient) social influence was specifically associated with damage to the dmPFC (including area 9).
We examined their susceptibility to social influence using signed Kullback-Leibler (KL) divergence.
We found that participants with mPFC damage were more influenced by impulsive (vs patient) others, compared to HCs.
We examined their susceptibility to social influence using signed Kullback-Leibler (KL) divergence.
We found that participants with mPFC damage were more influenced by impulsive (vs patient) others, compared to HCs.