Previous studies have shown that face-specific recognition ability (FRA) is heritable; however, the neural basis of this heritability is unclear. Candidate gene studies have suggested that the catechol-Omethyltransferase (COMT) rs4680 polymorphism is related to face perception. Here, using a partial least squares (PLS) method, we examined the multivariate association between 12 genotypes of 4 COMT polymorphisms (rs6269-rs4633-rs4818-rs4680) and multimodal MRI phenotypes in the human fusiform face area (FFA), which selectively responds to face stimuli, in 338 Han Chinese adults (mean age 20.45 years; 135 males). The MRI phenotypes included gray matter volume (GMV), resting-state fractional amplitude of low-frequency fluctuations (fALFF), and face-selective blood-oxygen-level-dependent (BOLD) responses (FS). We found that the first COMT-variant component (PLS1) was positively associated with the FS but negatively associated with the fALFF in the FFA. Moreover, participants with the COMT heterozygous-HEA-haplotype showed higher PLS1 FFA-MRI scores, which were positively associated with the FRA in an old/new face recognition task, than those with the COMT homozygous HEA haplotype and HEA non-carriers, suggesting that individuals with an appropriate (intermediate) level of dopamine activity in the FFA might have better FRA. In summary, our study provides empirical evidence for the genetic and neural basis for the heritability of face recognition and informs the formation of neural module functional specificity.Face recognition is a highly developed skill in humans that shows considerable variability between individuals 1-5 . Previous behavioral genetic studies have shown that face recognition ability is heritable 4,6 ; however, the neural basis for this heritability is unclear. One candidate cortical region underlying inter-individual variability in face recognition is the human fusiform face area (FFA) especially in the right hemisphere, which shows more significant responses to visual face stimuli than to other non-face stimuli 7 and represents a critical hub in the face network 8-10 . More importantly, features of the FFA are associated with face-specific recognition ability (FRA) 2,3 . However, information about the effects of genetic variability on FFA structure and function and their relationship with face recognition ability remain limited.Previous twin studies have demonstrated the higher intra-pair similarity of cortical structure 11 and functional magnetic resonance imaging (fMRI) responses 11,12 in the occipitotemporal cortex encompassing the FFA in monozygotic twins than dizygotic twins. Additionally, neural responses to facial expressions are modulated by common genetic variance in a set of regions constituting the face network that include the FFA 13 . These studies suggest that the FFA may be modulated by genetic variations. However, previous studies have not specifically localized the FFA, and it is unclear whether the observed genetic effects are derived from changes in the FFA or other regions. Notab...