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In contrast, no systematic effect of cTBS to the AG (or to the PMC) upon decision latencies in auditory trials was found. Response times were sensitive to the chances of winning (F(2)?=?3.75, p?=?.03, ��p2?=?.12), but not significantly influenced by the stimulation condition (main effect of Stimulation Condition: F(2)?=?1.76, p?=?.18, ��p2?=?.06, interaction term: F(4)?=?1.13, p?=?.34, ��p2?=?.04, see Fig.?3B). Betting behavior was not systematically influenced by cTBS to the AG. No significant main effect of Stimulation Condition was found for either risk adjustment (F(2)?=?.76, p?=?.47, ��p2?=?.03) or overall betting (F(2)?=?.58, CPI-637 nmr p?=?.92, ��p2?=?.01). Betting behavior was similar in visual and auditory trials: No significant main effect of Trial Type (risk adjustment: F(1)?=?.02, p?=?.89, ��p2?=?.01, overall betting: F(1)?=?.14, p?=?.71, ��p2?=?.01) CASK or Trial Type???Stimulation Condition interaction effects (risk adjustment: F(2)?OICR-9429 cell line for visuospatial attention, while auditory trials provided the same information without a visuospatial component. cTBS to the AG significantly and systematically affected decision-making behavior in visual trials. Without stimulation, and following cTBS to the control region, deliberation times reflected the chances of winning (see also Studer et al., 2012?and?Studer and Clark, 2011), however, this was no longer the case following cTBS to the AG. Inhibitory TMS to the AG thus disrupted the relationship between decision latencies and the probability of winning/losing. In contrast, we found no systematic effect of cTBS to the AG upon decision-making in auditory trials. We note that average decision latencies were overall higher in visual than auditory trials.