Evidence map›Paper›PMID 36940239›Full record

ArticleeLife2023

Native functions of short tandem repeats.

Shannon E Wright, Peter K Todd

Open access · goldFull text read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
6.4field-weighted citation impact, top 2% 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

29 citing papers in PubMed, 43 citations in OpenAlex.

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  13. The human intelligence evolved from proximalQuantitative biology (Beijing, China) · 2025
    Article
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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 1 institution in 1 country.

Shannon E WrightDepartment of Neurology, University of Michigan-Ann Arbor, Ann Arbor, United States.ORCID 0000-0002-7388-1617
Peter K ToddDepartment of Neurology, University of Michigan-Ann Arbor, Ann Arbor, United States.ORCID 0000-0003-4781-6376
University of Michigan · US

Funding

The FMR1 CGG repeat as functional element and therapeutic target in Fragile X associated disordersP50HD104463 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI TODD, PETER K · 2020 to 2024
$9.0M
Hexanucleotide repeat translation in ALS and Frontotemporal DementiaR01NS099280 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Peter K Todd · 2016 to 2026
$4.9M
CGG repeat associated translation in Fragile X-associated Tremor/Ataxia Syndrome-Diversity SupplementR01NS086810 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TODD, PETER K · 2014 to 2024
$4.1M
Early Stage Training in the NeurosciencesT32NS076401 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Carol Fuzeti Elias, LESLIE S. SATIN · 2011 to 2026
$3.1M
Repeat associated neurodegeneration in CANVASR21NS129096 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TODD, PETER K · 2022 to 2022
$425k
CGG repeat associated translation in Fragile X gene function and diseaseF31NS113513 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WRIGHT, SHANNON · 2020 to 2022
$84k
BLRD VA I01 BX004842NICHD NIH HHS P50 HD104463NICHD NIH HHS P50HD104463NINDS NIH HHS F31 NS113513NINDS NIH HHS F31NS113513NINDS NIH HHS R01 NS086810NINDS NIH HHS R01NS086810NINDS NIH HHS R01 NS099280NINDS NIH HHS R01NS099280NINDS NIH HHS R21 NS129096NINDS NIH HHS T32 NS076401VA BX004842
6 · The paper itself

Abstract

Over a third of the human genome is comprised of repetitive sequences, including more than a million short tandem repeats (STRs). While studies of the pathologic consequences of repeat expansions that cause syndromic human diseases are extensive, the potential native functions of STRs are often ignored. Here, we summarize a growing body of research into the normal biological functions for repetitive elements across the genome, with a particular focus on the roles of STRs in regulating gene expression. We propose reconceptualizing the pathogenic consequences of repeat expansions as aberrancies in normal gene regulation. From this altered viewpoint, we predict that future work will reveal broader roles for STRs in neuronal function and as risk alleles for more common human neurological diseases.

Indexed as

Genome, HumanMicrosatellite RepeatsGene Expression RegulationHumansautismdisease mechanismFragile Xgene expressiongeneticsgenomic instabilitygenomicsneurodegeneration

Identifiers

PMID36940239
PMCPMC10027321
OpenAlexW4327892846

What OpenQuestion holds

Textfull text, public
LicenceCC0
measurements read18
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.