Evidence map›Paper›PMID 41437782›Full record

ReviewGenome biology and evolution2026

Evolutionary Balancing of Genetic Consequence and Innovation in Mammals Through Variable Number Tandem Repeats.

Petar Pajic, Omer Gokcumen

Abstract readReview
In one paragraph

Review in Genome biology and evolution, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

2 authors.

Petar PajicDepartment of Chemistry, Yale University, New Haven, CT 06511, USA.ORCID 0000-0002-6791-294X
Omer GokcumenDepartment of Biological Sciences, University at Buffalo, The State University of New York, Buffalo, NY 14260, USA.ORCID 0000-0003-4371-679X

Funding

Evolutionary and functional impact of common genomic structural variationsR35GM156519 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Omer Gokcumen · 2025 to 2026
$887k
National Institute of Health R35-GM156519National Science Foundation 2049947National Science Foundation 2123284National Science Foundation 2508185NIGMS NIH HHS R35 GM156519
6 · The paper itself

Abstract

Understanding genomic function has historically relied on sequence conservation across evolutionary time. However, advances in genomics have revealed that functional innovations often arise from rapidly evolving, nonconserved elements that are frequently overlooked by conservation-based approaches. Among these, variable number tandem repeats (VNTRs) act as engines of both functional innovation and phenotypic consequence. VNTRs are repetitive genomic sequences whose copy numbers can vary significantly between individuals and species, influencing gene regulation, protein structure, and eventually, phenotypic diversity. Recent long-read assemblies and pangenomes now resolve VNTR loci accurately, enabling robust evolutionary reconstruction and functional associations. Here, we synthesize emerging insights into the functional and evolutionary impact of VNTRs in mammals. Specifically, we outline pressing questions on the mutational mechanisms driving VNTR evolution in humans, the selective forces maintaining their structural heterogeneity, and propose a theoretical framework for their persistence through evolutionary tradeoffs.

Indexed as

Evolution, MolecularMammalsMinisatellite RepeatsAnimalsHumansdisease susceptibilityfunctionmucinsselectiontradeoffs

Identifiers

PMID41437782
PMCPMC12776774

What OpenQuestion holds

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LicenceCC BY
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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.