Research
What we study
Our science spans three connected pillars — from the neural circuits that build social behavior in early life, to how the body and immune system communicates with the brain, to what an extraordinary mammal can reveal about reproduction and individuality.
01 · Primary focus
Developmental Neuroscience
How does the developing brain build the circuits that generate social behavior?
The circuits wired in infancy and adolescence shape social and emotional health for the rest of life.
The developing brain must assemble brain circuits that generate social behavior, and these circuits are surprisingly dynamic. We study how the young brain builds and re-tunes neural circuits across two sensitive windows: infancy, when an animal is fully dependent on a caregiver, and adolescence, when relationships with peers can shape mental and physical health for years to come.
A recurring theme is that social behavior is regulated much like hunger or thirst — all needs that are regulated by the brain. When young animals are deprived of social contact, the brain registers a state of social need and boosts the drive to reconnect.
Across these projects we treat behavior as a developmental phenomenon: the same brain circuit can mean different things at different ages.
Key techniques
- Fiber photometry in pups & juveniles
- Two-photon microendoscopy (GRIN lens)
- Optogenetics & chemogenetics
- Whole-brain Fos mapping & viral tracing
- Activity-dependent neuronal tagging (TRAP)
- Ultrasonic-vocalization analysis (VocalMat, SqueakOut)

Selected publications
All 9 in this areaAge-specific regulation of sociability by hypothalamic Agrp neurons (opens in new tab)
Current Biology 35(18):4522–4536.e6 · doi:10.1016/j.cub.2025.08.014 (opens in new tab)
Erratic maternal care induces avoidant-like attachment deficits in a mouse model of early life adversity (opens in new tab)
eNeuro 12(11) · doi:10.1523/ENEURO.0249-25.2025 (opens in new tab)
Neurons for infant social behaviors in the mouse zona incerta (opens in new tab)
Science 385(6707):409–416 · doi:10.1126/science.adk7411 (opens in new tab)
Development of "Hunger Neurons" and the unanticipated relationship between energy metabolism and mother–infant interactions (opens in new tab)
Biological Psychiatry 91(10):907–914 · doi:10.1016/j.biopsych.2022.02.962 (opens in new tab)
AgRP neurons control structure and function of the medial prefrontal cortex (opens in new tab)
Molecular Psychiatry 27(10):3951–3960 · doi:10.1038/s41380-022-01691-8 (opens in new tab)
02 · Body–brain & immunity
Body–Brain Physiology & Neuroimmunology
How does the body signal to the brain to shape physiology and behavior?
Seeing conditions like food allergy as brain problems, not only immune problems, opens new ways to understand and treat them.
The brain does not act in isolation: peripheral organs and the immune system continuously signal to the brain, which reads those signals and coordinates physiology and behavior. We study this two-way conversation — the body–brain axis and the dialogue between immunity and the nervous system.
A central project asks how the brain participates in food allergy. We are currently dissecting how allergen detection in the gut is relayed to the brain, focusing on hindbrain hubs that turn an allergic reaction into a coordinated, whole-body response.
A complementary line asks how metabolic state — and the circuits that represent hunger and satiety — can reprogram long-lived, tissue-resident immune cells, and how early-life experience shapes the brain’s opioid and stress systems. The unifying question is how signals originating in the body are read by the brain and translated into physiology and behavior.
Key techniques
- Mouse models of food allergy
- Gut-compartment & vagal/spinal pathway manipulation
- Two-photon imaging of hindbrain neurons
- Activity-dependent labeling (Fos/TRAP) & chemogenetics
- Multiplexed in situ hybridization
- Tissue clearing & light-sheet imaging

Selected publications
All 21 in this areaImmune sensing of food allergens promotes avoidance behaviour (opens in new tab)
Nature 620(7974):643–650 · doi:10.1038/s41586-023-06362-4 (opens in new tab)
Deciphering an AgRP-serotoninergic neural circuit in distinct control of energy metabolism from feeding (opens in new tab)
Nature Communications 12(1):3525 · doi:10.1038/s41467-021-23846-x (opens in new tab)
Ketogenic diet restrains aging-induced exacerbation of coronavirus infection in mice (opens in new tab)
eLife 10:e66522 · doi:10.7554/eLife.66522 (opens in new tab)
AgRP neurons control compulsive exercise and survival in an activity-based anorexia model (opens in new tab)
Nature Metabolism 2(11):1204–1211 · doi:10.1038/s42255-020-00300-8 (opens in new tab)
Regulation of substrate utilization and adiposity by Agrp neurons (opens in new tab)
Nature Communications 10(1):311 · doi:10.1038/s41467-018-08239-x (opens in new tab)
03 · Armadillo model · reproduction & individuality
Comparative Biology
What can an extraordinary mammal teach us about how life begins?
Armadillo diapause and identical quadruplets illuminate human reproduction, quiescence, and the origins of individuality.
The classic Krogh principle states that some questions can only be answered in the right organism. To this end, we have spent more than a decade establishing the nine-banded armadillo (Dasypus novemcinctus) as a modern research model in Yale’s Department of Comparative Medicine — home to what we believe is the only academic armadillo research colony of its kind. A member of the ancient Xenarthra lineage, the armadillo has two extraordinary features that make it a rare window into how life begins:
1. Reproduction and suspended development. Like many mammals, the armadillo can pause its pregnancy through embryonic diapause (delayed implantation) — but it does so to an extreme found nowhere else, holding an early embryo in a suspended state for years. We study how development is halted and later reawakened, and the molecular signals from the embryo, uterus, ovaries, and nervous system that place life on hold. These mechanisms bear on human reproductive challenges such as infertility and pregnancy loss, and on broader questions of cellular dormancy and aging.
2. The origins of individuality. The armadillo always gives birth to genetically identical quadruplets: a single fertilized egg reliably splits into four embryos (obligate polyembryony), essentially unique among mammals. This provides a natural experiment to test how four individuals arise from one genome. We probe this question with single-cell and spatial genomics, epigenomics, lineage tracing, and stem-cell models, with implications reaching into stem-cell biology and the neurobiology of individuality.
Key techniques
- Single-cell & spatial transcriptomics
- Epigenomic profiling (ATAC-seq, ChIP-seq)
- Whole-genome sequencing & lineage tracing
- Embryonic & induced pluripotent stem cells
- In vitro implantation & twinning models
- Uterine-fluid proteomics & metabolomics

Selected publications
All 1 in this areaWhat makes each of us unique? The nine-banded armadillo as a model to study individuality (opens in new tab)
Frontiers in Mammal Science 3:1450655 · doi:10.3389/fmamm.2024.1450655 (opens in new tab)
Methods & tools
Open tools we build
We build and share the tools our science needs — including VocalMat, an open framework for detecting and classifying mouse ultrasonic vocalizations.