Evidence map›Paper›PMID 37961304›Full record

ArticlebioRxiv : the preprint server for biology2025

Functional characterization of the disease-associated

Feroz Akhtar, Joselin Hernandez Ruiz, Ya-Guang Liu, Roy G Resendez, Denis Feliers, Liza D Morales, Alvaro Diaz-Badillo, Donna M Lehman, Rector Arya, Juan Carlos Lopez-Alvarenga and 3 more

Open access · greenAbstract readPreprint
PubMed Full text at PMC Publisher
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 1 country.

Feroz AkhtarDepartment of Health and Behavioral Sciences, Texas A&M University- San Antonio, Texas, USA.
Joselin Hernandez RuizUtah Center for Genetic Discovery, Department of Human Genetics, University of Utah, Salt Lake City, Utah, USA.
Ya-Guang LiuDepartment of Pathology, School of Medicine, University of Texas Health San Antonio, San Antonio, Texas, USA.
Roy G ResendezDepartment of Health and Behavioral Sciences, Texas A&M University- San Antonio, Texas, USA.
Denis FeliersDepartment of Medicine, School of Medicine, University of Texas Health San Antonio, San Antonio, Texas, USA.
Liza D MoralesSouth Texas Diabetes and Obesity Institute, Department of Genetics, School of Medicine, University of Texas Rio Grande Valley, Brownsville, Texas, USA.
Alvaro Diaz-BadilloDepartment of Health and Behavioral Sciences, Texas A&M University- San Antonio, Texas, USA.
Donna M LehmanDepartment of Health and Behavioral Sciences, Texas A&M University- San Antonio, Texas, USA.
Rector AryaDepartment of Health and Behavioral Sciences, Texas A&M University- San Antonio, Texas, USA.
Juan Carlos Lopez-AlvarengaDepartment of Population Health and Biostatistics, School of Medicine, University of Texas Rio Grande Valley, Harlingen, Texas, USA.ORCID 0000-0002-0966-8766
John BlangeroSouth Texas Diabetes and Obesity Institute, Department of Genetics, School of Medicine, University of Texas Rio Grande Valley, Brownsville, Texas, USA.ORCID 0000-0001-6250-5723
Ravindranath DuggiralaDepartment of Health and Behavioral Sciences, Texas A&M University- San Antonio, Texas, USA.
Srinivas MummidiDepartment of Health and Behavioral Sciences, Texas A&M University- San Antonio, Texas, USA.
Texas A&M University – San Antonio · USThe University of Texas Rio Grande Valley · USThe University of Texas Health Science Center at San Antonio · USUniversity of Utah · US

Funding

Impact of disease associated noncoding polymorphisms on post-transcriptional gene regulationR01AI119131 · NIAID · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI MUMMIDI, SRINIVAS · 2016 to 2019
$1.5M
NIAID NIH HHS R01 AI119131
6 · The paper itself

Abstract

CC-chemokine ligand 2 (CCL2) is involved in the pathogenesis of several diseases associated with monocyte/macrophage recruitment, such as HIV-associated neurocognitive disorder (HAND), tuberculosis, and atherosclerosis. The rs1024611 (alleles: A>G; G is the risk allele) polymorphism in the

Identifiers

PMID37961304
PMCPMC10635030
OpenAlexW4388208984

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.