The complex phenotype of Prader-Willi syndrome (PWS) includes neurodevelopmental delay, psychiatric features, and multiple physical and behavioral characteristics, including obesity secondary to hyperphagia and reduced metabolism. We are using transcranial magnetic stimulation (TMS) and functional neuroimaging to test the involvement of a novel network, the cerebellar-VS circuit, in regulating food intake in PWS, representing cutting-edge development in the circuit basis of hyperphagia in PWS.

We are currently recruiting for this study. If you believe you may be eligible, click here.


Individuals with ARFID severely restrict their food intake – by volume and/or variety – due to reasons that often overlap including fear of aversive consequences, lack of interest in eating or food, and sensory sensitivity. We propose that dysfunctional endocrine signaling acts on neural circuitry to produce observable behavioral symptoms that comprise the three ARFID phenotypes. Through a combination of clinical interviews, endocrine signal monitoring, and functional neuroimaging, we hope to advance precision medicine in ARFID.

We are currently recruiting for this study. If you believe you may be eligible, click here. We are also recruiting healthy controls; if you believe you may be eligible click here.


This study is an innovative project that will yield a more refined understanding of the role of discrete amygdala nuclei groups in women with restrictive eating disorders. Our project will leverage a 7T MRI scanner to acquire high-resolution structural, functional MRI data and metabolic-targeted proteomics from women with and without restrictive eating disorders (R-ED). Informed by our prior work, we hypothesize smaller volumes of the basolateral and centromedial amygdala volume in R-ED compared to HC groups.

We are currently recruiting both participants with restrictive eating disorders and healthy controls. If you believe you are eligible for either group, click here.


Cognitive behavioral therapy (CBT) is a leading evidence-based treatment for other eating disorders but has yet to be rigorously tested for children with ARFID. Our team has developed a manualized cognitive-behavioral therapy for ARFID, wherein the active ingredient is exposure based on inhibitory learning. To test the efficacy of this new treatment, we are conducting a randomized control trial to evaluate behavioral (clinical symptoms) and neural (fear circuitry) correlates of adolescents aged 10-18 with ARFID after having received nutritional counseling versus CBT-AR.

We are currently recruiting for this study. If you believe you or your child may be eligible, click here.


We propose a model that identifies the cerebellar-VS circuit as a critical network involved in regulating reward-based satiation and food intake. This experiment conducts a TMS circuit manipulation experiment to test the hypothesis that targeting the cerebellum can alter activity in response to food cues to advance the understanding of this novel brain circuit involved in feeding behavior. We combine neuroimaging with clinical assessments, food-related behavioral tasks, and food consumption to evaluate appetite reward response after TMS circuit modulation.

We are not currently recruiting participants for this study.