Ethan B. Richman

Ethan B. Richman

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Ethan B. Richman

Human Neural Circuitry program, Stanford University, Stanford, CA, USA

Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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18 December 2020 in Science
Verified
Journal Article
Closed access
JKJustus M. Kebschull
Justus M. Kebschull
EREthan B. Richman
Ethan B. Richman
NRNoam Ringach
Noam Ringach
DFDrew Friedmann
Drew Friedmann
EAEddy Albarran
Eddy Albarran
LLLiqun Luo
Liqun Luo
Cerebellar evolution: Cerebellar nuclei, substructures of the cerebellum, transfer information from the cerebellum to other parts of the brain. Using single-cell transcriptomics, Kebschull et al. have now identified a conserved pattern of cerebellar nuclei structure that has been repeated through evolution (see the Perspective by Hatten). Ranging from mice to chickens to humans, cerebellar nuclei are made up of region-specific excitatory neurons and region-invariant inhibitory neurons. In humans, a facet connecting the cerebellum to the frontal cortex is enhanced. Science , this issue p. eabd5059 ; see also p. 1411

29 May 2025 in Science
Verified
Journal Article
Open access
IKIsaac Kauvar
Isaac Kauvar
EREthan B. Richman
Ethan B. Richman
TLTony X. Liu
Tony X. Liu
CLChelsea Li
Chelsea Li
SVSam Vesuna
Sam Vesuna
KDKarl Deisseroth
Karl Deisseroth
Emotional responses to sensory experience are central to the human condition in health and disease. We hypothesized that principles governing the emergence of emotion from sensation might be discoverable through their conservation across the mammalian lineage. We therefore designed a cross-species neural activity screen, applicable to humans and mice, combining precise affective behavioral measurements, clinical medication administration, and brain-wide intracranial electrophysiology. This screen revealed conserved biphasic dynamics in which emotionally salient sensory signals are swiftly broadcast throughout the brain and followed by a characteristic persistent activity pattern. Medication-based interventions that selectively blocked persistent dynamics while preserving fast broadcast selectively inhibited emotional responses in humans and mice. Mammalian emotion appears to emerge as a specifically distributed neural context, driven by persistent dynamics and shaped by a global intrinsic timescale.