Evidence map›Paper›PMID 31915469›Full record

ArticleDisease markers2019

Association of Common Variants in HNF1A Gene with Serum AFP Level in Healthy Chinese Individuals and HCC Patients.

Xue-Jun Li, Dong-Hua Shao, Mei-Lin He, Guo-Wei Liang

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Integrated bioinformatic analysis of HNF1A in human cancers.The Journal of international medical research · 2021
    Article
  10. [Carcinoembryonic type specific markers and liver cancer immunotherapy].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2020
    Review
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

4 authors at 1 institution in 1 country.

Xue-Jun LiDepartment of Clinical Laboratory, Aerospace Center Hospital, No. 15 Yuquan Road, Haidian District, Beijing 100049, China.ORCID https://orcid.org/0000-0001-9283-8238
Dong-Hua ShaoDepartment of Clinical Laboratory, Aerospace Center Hospital, No. 15 Yuquan Road, Haidian District, Beijing 100049, China.ORCID https://orcid.org/0000-0003-1260-1404
Mei-Lin HeDepartment of Clinical Laboratory, Aerospace Center Hospital, No. 15 Yuquan Road, Haidian District, Beijing 100049, China.ORCID https://orcid.org/0000-0002-2070-8247
Guo-Wei LiangDepartment of Clinical Laboratory, Aerospace Center Hospital, No. 15 Yuquan Road, Haidian District, Beijing 100049, China.ORCID https://orcid.org/0000-0003-3910-1290
Aerospace Center Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although alpha-fetoprotein (AFP) is a widely used tumor marker in hepatocellular carcinoma (HCC), 40% of newly diagnosed patients do not have an elevated AFP level. Research has revealed that mutations in the HNF1A binding site of the AFP gene promoter cause significantly elevated serum AFP levels in patients with hereditary persistence of AFP. This study investigated the relationship between HNF1A genetic variants and serum AFP levels. We examined the association between the HNF1A-rs1169288 (A/C), rs2464196 (G/A), and rs1169310 (C/T) polymorphisms and AFP levels in a healthy Chinese population (

Indexed as

Polymorphism, Single NucleotideAdultalpha-FetoproteinsBiomarkers, TumorCarcinoma, HepatocellularCase-Control StudiesDiagnosis, DifferentialFemaleGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHepatocyte Nuclear Factor 1-alphaHumansLiver NeoplasmsMaleMiddle AgedAFP protein, humanalpha-FetoproteinsBiomarkers, TumorHepatocyte Nuclear Factor 1-alphaHNF1A protein, human

Identifiers

PMID31915469
PMCPMC6935455
OpenAlexW2989105033

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.