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• W2039878956 abstract "Abstract Our study investigates the dependence of response monitoring and error detection on genetic influences modulating the serotonergic system. This was done using the event‐related potentials (ERPs) after error (Ne/ERN) and correct trials (Nc/CRN). To induce a sufficient amount of errors, a standard flanker task was used. The subjects ( N = 94) were genotyped for the functional 5‐HT1A C(−1019)G polymorphism. The results show that the 5‐HT1A C(−1019)G polymorphism specifically modulates error detection. Neurophysiological modulations on error detection were paralleled by a similar modulation of response slowing after an error, reflecting the behavioral adaptation. The 5‐HT1A −1019 CC genotype group showed a larger Ne and stronger posterror slowing than the CG and GG genotype groups. More general processes of performance monitoring, as reflected in the Nc/CRN, were not affected. The finding that error‐specific processes, but not general response monitoring processes, are modulated by the 5‐HT1A C(−1019)G polymorphism is underlined by a wavelet analysis. In summary, the results suggest a specific effect of the 5‐HT1A C(−1019)G polymorphism on error monitoring, as reflected in the Ne, and suggest a neurobiological dissociation between processes of error monitoring and general response monitoring at the level of the serotonin 1A receptor system. Hum Brain Mapp, 2010. © 2009 Wiley‐Liss, Inc." @default.
• W2039878956 created "2016-06-24" @default.
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• W2039878956 date "2010-03-10" @default.
• W2039878956 modified "2023-10-16" @default.
• W2039878956 title "Functional 5-HT1a receptor polymorphism selectively modulates error-specific subprocesses of performance monitoring" @default.
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• W2039878956 doi "https://doi.org/10.1002/hbm.20892" @default.
• W2039878956 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6870701" @default.
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