01 · Primary focus

Developmental Neuroscience

Big question

How does the developing brain build the circuits that generate social behavior?

Why it matters

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)
AgRP neurons (red) in the mouse hypothalamus around the third ventricle, with activity-labeled cells (white) after early-life social isolation.
AgRP neurons in the hypothalamus, labeled after early-life social isolation.

Selected publications

All 9 in this area

02 · Body–brain & immunity

Body–Brain Physiology & Neuroimmunology

Big question

How does the body signal to the brain to shape physiology and behavior?

Why it matters

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
Fluorescent mast cells (green) studding the villi of the mouse small intestine, imaged in a mast-cell reporter mouse.
Mast cells (green) throughout the villi of the small intestine — immune sentinels of the gut — imaged in a mast-cell reporter mouse.

Selected publications

All 21 in this area

03 · Armadillo model · reproduction & individuality

Comparative Biology

Big question

What can an extraordinary mammal teach us about how life begins?

Why it matters

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
A nine-banded armadillo (Dasypus novemcinctus) in the Dietrich Lab research colony at Yale.
A nine-banded armadillo in the lab’s research colony.

Selected publications

All 1 in this area

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.

Explore VocalMat