Evidence map›Paper›PMID 37077812›Full record

ReviewFrontiers in pharmacology2023

Non-coding and intergenic genetic variants of human arylamine

Kyung U Hong, Kennedy M Walls, David W Hein

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Guideline
  2. PharmVar GeneFocus: NAT2-Genetic Variation and Updated Nomenclature.Clinical pharmacology and therapeutics · 2026
    Review
  3. Article
  4. Article
  5. Investigation on regulation ofFrontiers in pharmacology · 2024
    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

3 authors at 1 institution in 1 country.

Kyung U HongDepartment of Pharmacology & Toxicology, Brown Cancer Center, University of Louisville School of Medicine, Louisville, KY, United States.
Kennedy M WallsDepartment of Pharmacology & Toxicology, Brown Cancer Center, University of Louisville School of Medicine, Louisville, KY, United States.
David W HeinDepartment of Pharmacology & Toxicology, Brown Cancer Center, University of Louisville School of Medicine, Louisville, KY, United States.
University of Louisville · US

Funding

University of Louisville Center for Integrative Environmental Health SciencesP30ES030283 · NIEHS · UNIVERSITY OF LOUISVILLE · PI Amanda Jo LeBlanc · 2020 to 2026
$10.0M
Study of Environmental Risk Factors of MS After Conditioning on Genetic FactorR21ES015564 · NIEHS · MARSHFIELD CLINIC RESEARCH FOUNDATION · PI ROLAK, LOREN A · 2007 to 2008
$297k
NIEHS NIH HHS P30 ES030283NIEHS NIH HHS R21 ES015564
6 · The paper itself

Abstract

Arylamine N-acetyltransferase 2 (NAT2) is a phase II metabolic enzyme, best known for metabolism of aromatic amines and hydrazines. Genetic variants occurring in the NAT2 coding region have been well-defined and are known to affect the enzyme activity or protein stability. Individuals can be categorized into rapid, intermediate, and slow acetylator phenotypes that significantly alter their ability to metabolize arylamines, including drugs (e.g., isoniazid) and carcinogens (e.g., 4-aminobiphenyl). However, functional studies on non-coding or intergenic variants of

Indexed as

arylamine N-acetyltransferase 2cholesteroldyslipidemiafatty acidsGWAShaplotypetriglyceride

Identifiers

PMID37077812
PMCPMC10106703
OpenAlexW4362585986

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.