Evidence map›Paper›PMID 42787119›Full record

ArticleFrontiers in cellular neuroscience2026

Deciphering the impact of genetic variants on vulnerability to Opioid Use Disorder.

Rajashree Chakraborty, Chittibabu Guda, Avinash Veerappa

Abstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Rajashree ChakrabortyDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, United States.
Chittibabu GudaDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, United States.
Avinash VeerappaDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, United States.

Funding

UNMC Structural Biology CoreP20GM103427 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Heather Colleen Jensen-Smith · 2012 to 2026
$59.2M
UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI James Eudy · 1985 to 2026
$55.0M
NCI NIH HHS P30 CA036727NIGMS NIH HHS P20 GM103427
6 · The paper itself

Abstract

Introduction: Opioid Use Disorder (OUD) is a chronic condition characterized by compulsive opioid intake that drives widespread health, social, and economic burdens. Methods: To elucidate molecular contributors to addiction susceptibility, we conducted a comprehensive RNA-sequencing analysis of postmortem nucleus accumbens (NAc) tissue from individuals with OUD and matched controls. Results: Cohort-concordance filtering identified 17 candidate missense variants and one candidate stop-gain variant across 16 genes detected in OUD samples; these RDEVs require DNA-based validation. Missense variants could disrupt key protein domains, and five of these identified variants ( Discussion: Together, these findings provide an integrated view of candidate genetic and transcriptomic alterations in OUD and identify lncRNA-centered regulatory networks and candidate variant-bearing genes as hypothesis-generating leads for future functional and DNA-based validation studies.

Indexed as

differential gene expressionexonic variantsgenetic variantslong non-coding RNAnucleus accumbensOioid Use DisorderRNA sequencingZNF117

Identifiers

PMID42787119
PMCPMC13600877

What OpenQuestion holds

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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.