Evidence map›Paper›PMID 41703343›Full record

ArticleMolecular neurobiology2026

Single-Cell Transcriptomic Analysis of Macaque LGN Neurons Reveals Novel Subpopulations.

Shi Hai Sun, Kai T Renshaw, John S Pezaris

Abstract read
In one paragraph

Article in Molecular neurobiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Shi Hai Sun *Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.
Kai T Renshaw *Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA.
John S PezarisDepartment of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA. pezaris.john@mgh.harvard.edu.

Funding

Finessing the details: subclasses of LGN neurons and the richness of spatial transcriptomicsR21EY037012 · NEI · MASSACHUSETTS GENERAL HOSPITAL · PI PEZARIS, JOHN S. · 2025 to 2025
$454k
NEI NIH HHS R21 EY037012NIH HHS EY027888
6 · The paper itself

Abstract

Neurons in the lateral geniculate nucleus (LGN) provide a pivotal role in the visual system by modulating and relaying signals from the retina to the visual cortex. Although the primate LGN, with its distinct divisions (magnocellular, M; parvocellular, P; and koniocellular, K), has been extensively characterized, the intrinsic heterogeneity of LGN neurons has remained unexplained. With the development of high-throughput single-cell transcriptomics, researchers can rapidly isolate and profile large sets of neuronal nuclei, revealing a surprising diversity of genetic expression within the nervous system, such as two types of K neurons (as reported by Bakken et al., eLife, 10, e64875, 2021). Here, we analyzed the transcriptomes of individual cells belonging to macaque LGN using raw data from a public database to explore the heterogeneity of LGN neurons. Using statistical analyses, we found additional subpopulations within the LGN transcriptomic population, whose gene expressions imply functional differences. Our results suggest the existence of a more nuanced complexity in LGN processing beyond the classic view of the three cell types and highlight a need to combine transcriptomic and functional assessments. A complete account of the cell type diversity of the primate LGN is critical to understanding how vision works.

Indexed as

Gene Expression ProfilingGeniculate BodiesNeuronsSingle-Cell AnalysisTranscriptomeAnimalsMacacaSingle-Cell Gene Expression AnalysisLateral Geniculate NucleusNonhuman primatescRNA-seqTranscriptomicsVisual pathways

Identifiers

PMID41703343
PMCPMC12913271

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.