Evidence map›Paper›PMID 31740812›Full record

ReviewNature neuroscience2020

Neurobiological functions of transcriptional enhancers.

Alex S Nord, Anne E West

Open access · greenAbstract readReview
In one paragraph

Review in Nature neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% of its field
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

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 119 citations in OpenAlex.

  1. Pooled it
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  7. Review
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  14. CTCF regulates global chromatin accessibility and transcription during rod photoreceptor development.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  17. Just a SNP away: The future ofCell insight · 2025
    Review
  18. Review
  19. Review
  20. Article

1 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 1 country.

Alex S NordDepartment of Neurobiology, Physiology, and Behavior, University of California, Davis, Davis, CA, USA. asnord@ucdavis.edu.ORCID http://orcid.org/0000-0003-4259-7514
Anne E WestDepartment of Neurobiology, Duke University School of Medicine, Durham, NC, USA. west@neuro.duke.edu.ORCID http://orcid.org/0000-0003-0846-139X
Duke University · USUniversity of California, Davis · US

Funding

Functional Elucidation of the Sequence-Encoded Regulatory Activity of Enhancers in Vivo in the BrainR35GM119831 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Alexander Nord · 2016 to 2026
$3.9M
Chromatin Mechanisms of Neuronal MaturationR01NS098804 · NINDS · DUKE UNIVERSITY · PI WEST, ANNE ELIZABETH · 2017 to 2021
$2.2M
NIGMS NIH HHS R35 GM119831NINDS NIH HHS R01 NS098804U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM119831
6 · The paper itself

Abstract

Transcriptional enhancers are regulatory DNA elements that underlie the specificity and dynamic patterns of gene expression. Over the past decade, large-scale functional genomics projects have driven transformative progress in our understanding of enhancers. These data have relevance for identifying mechanisms of gene regulation in the CNS, elucidating the function of non-coding regulatory sequences in neurobiology and linking sequence variation within enhancers to genetic risk for neurological and psychiatric disorders. However, the sheer volume and complexity of genomic data presents a challenge to interpreting enhancer function in normal and pathogenic neurobiological processes. Here, to advance the application of genome-scale enhancer data, we offer a primer on current models of enhancer function in the CNS, we review how enhancers regulate gene expression across the neuronal lifespan, and we suggest how emerging findings regarding the role of non-coding sequence variation offer opportunities for understanding brain disorders and developing new technologies for neuroscience.

Indexed as

AnimalsBrainEnhancer Elements, GeneticGene Expression RegulationHumansNeuronsTranscription, Genetic

Identifiers

PMID31740812
PMCPMC7049175
OpenAlexW2983489400

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

None linked

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.