Anorexia nervosa is a complex eating disorder with genetic, metabolic, and psychosocial underpinnings. Using genome-wide methods, recent studies have associated many genes with the disorder. We characterized these genes by projecting them into reference transcriptomic atlases of the prenatal and adult human brain to determine where these genes are expressed in fine detail. We found that genes from an induced stem cell study of anorexia nervosa cases are expressed at higher levels in the lateral parabrachial nucleus. Although weaker, expression enrichment of the adult lateral parabrachial is also found with genes from independent genetic studies. Candidate causal genes from the largest genetic study of anorexia nervosa to date were enriched for expression in the arcuate nucleus of the hypothalamus. We also found an enrichment of anorexia nervosa associated genes in the adult and fetal raphe and ventral tegmental areas. Motivated by enrichment of these feeding circuits, we tested if these genes respond to fasting in mice hypothalami, which highlighted the differential expression of Rps26 and Dalrd3. This work improves our understanding of the neurobiology of anorexia nervosa by suggesting disturbances in subcortical appetitive circuits. Anorexia nervosa is a complex eating disorder that primarily occurs in women with onset often occurring during adolescence. While a portion of anorexia nervosa patients sustain a full recovery, a substantial fraction suffer from protracted partial recovery or are afflicted with a chronic disease course 1. Currently, there are few effective treatments, and the standard-of-care is broadly aimed at psychological and nutritional recovery 2,3. Specifically, for youth, family-based treatment has been shown to be beneficial 4. Due to self-starvation and suicide, anorexia nervosa is consistently reported to be among psychiatric disorders with the highest all-cause mortality ratios 5,6. Our understanding of the neuroanatomical circuits involved in anorexia nervosa is limited. MRI studies of people affected with the illness are only able to examine large structures, and such studies find broad volume reductions and white matter alterations 7-9. Diffusion tensor imaging studies have found changes in several white matter tracts 10. Due to the coarse resolution of MR images, these studies cannot detect structural or functional changes at the microcircuit level. In addition, it is difficult to identify structural alterations that may underlie the disorder due to a lack of studies initiated prior to the onset of symptoms. While subjects with anorexia nervosa are noted to have widespread cortical thinning and decreased volume, recent studies report that measured alterations in brain structure reflect changes in nutritional status and that weight restoration can rapidly reverse these changes in younger patients 11-13. Regional analyses have found stronger differences in reward and somatosensory regions. The identification of the reward areas was hypothesized to mark aberrant reward responses to food...