Non-human primates (NHP) provide crucial research models. Their strong similarities to humans make them particularly valuable for understanding complex behavioral traits and brain structure and function. We report here the genetic mapping of an NHP nervous system biologic trait, the cerebrospinal fluid (CSF) concentration of the dopamine metabolite homovanillic acid (HVA), in an extended inbred vervet monkey (Chlorocebus aethiops sabaeus) pedigree. CSF HVA is an index of CNS dopamine activity, which is hypothesized to contribute substantially to behavioral variations in NHP and humans. For quantitative trait locus (QTL) mapping, we carried out a two-stage procedure. We first scanned the genome using a first-generation genetic map of short tandem repeat markers. Subsequently, using >100 SNPs within the most promising region identified by the genome scan, we mapped a QTL for CSF HVA at a genome-wide level of significance (peak logarithm of odds score >4) to a narrow well delineated interval (<10 Mb). The SNP discovery exploited conserved segments between human and rhesus macaque reference genome sequences. Our findings demonstrate the potential of using existing primate reference genome sequences for designing high-resolution genetic analyses applicable across a wide range of NHP species, including the many for which full genome sequences are not yet available. Leveraging genomic information from sequenced to nonsequenced species should enable the utilization of the full range of NHP diversity in behavior and disease susceptibility to determine the genetic basis of specific biological and behavioral traits.comparative genomics ͉ genetic mapping ͉ homovanillic acid ͉ vervet T he genetic investigation of non-human primates (NHPs) has the potential to generate enormous insights into the development, degeneration, and structure of the human brain and the biological basis of human behavior. Like humans, NHPs experience a prolonged period of postnatal development, together with strong family ties and complex social relationships. Furthermore, most features of human behavior have recognizable counterparts in NHPs, enabling the examination of traits such as anxiety and impulsivity, which are central components of human behavioral disorders. The pronounced interindividual variability observed in such traits within pedigreed primate colonies has stimulated interest in identifying genetic variants associated with these variable traits.There are several advantages in genetically investigating behavior-related traits in NHPs compared with humans. It is feasible to assess systematically a given trait in all members of large multigenerational NHP pedigrees, providing power to detect genetic variants of relatively small effect. It is also possible to obtain measures related to brain structure and function in