Evidence map›Paper›PMID 28346832›Full record

ArticleGenetic testing and molecular biomarkers2017

TCF21 rs12190287 Polymorphisms Are Associated with Ventricular Septal Defects in a Chinese Population.

Liping Yang, Xiaobo Gao, Haiyan Luo, Qiuyu Huang, Dongmei Su, Xinyu Tan, Cailing Lu

Abstract read
In one paragraph

Article in Genetic testing and molecular biomarkers, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 37% 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, 9 citations in OpenAlex.

  1. International journal of medical sciences · 2024
    Article
  2. Review
  3. Association BetweenInternational journal of general medicine · 2022
    Article
  4. TCF21: a critical transcription factor in health and cancer.Journal of molecular medicine (Berlin, Germany) · 2020
    Review
  5. 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

7 authors at 3 institutions in 1 country.

Liping Yang1 Department of Cardiovascular Surgery, Union Hospital, Fujian Medical University , Fuzhou, China .
Xiaobo Gao2 Department of Genetics, National Research Institute for Family Planning , Beijing, China .
Haiyan Luo2 Department of Genetics, National Research Institute for Family Planning , Beijing, China .
Qiuyu Huang1 Department of Cardiovascular Surgery, Union Hospital, Fujian Medical University , Fuzhou, China .
Dongmei Su2 Department of Genetics, National Research Institute for Family Planning , Beijing, China .
Xinyu Tan3 CAS Key Laboratory of Genome Sciences and Information, Chinese Academy of Sciences, Beijing Institute of Genomics , Beijing, China .
Cailing Lu2 Department of Genetics, National Research Institute for Family Planning , Beijing, China .
Fujian Medical University · CNChinese Academy of Sciences · CNPeking Union Medical College Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsTCF21 knockout mice display cardiac defects, including ventricular septal defects (VSDs). Functional rs12190287 polymorphisms located within the 3' untranslated region (3'-UTR) of TCF21 were associated with a risk of coronary heart disease in the European and Eastern populations. However, whether rs12190287 polymorphisms in the TCF21-3'UTR confer predisposition to congenital heart disease (CHD) is unclear.

methodsA case-control study was designed consisting of 781 nonsyndromic VSD patients and 867 non-CHD control subjects. The genotype frequency of rs12190287 polymorphisms was determined by real-time polymerase chain reaction.

resultsThere were significant differences in the genotype and allele frequencies of rs12190287 between the cases and controls in a Chinese population. Allele G of rs12190287 was significantly associated with an increased risk of VSD in a Chinese population.

conclusionsOur results demonstrate that rs12190287 polymorphisms confer predisposition to VSDs in the Chinese population studied here.

Indexed as

3' Untranslated RegionsAdolescentAllelesAsian PeopleBasic Helix-Loop-Helix ProteinsCase-Control StudiesChildChild, PreschoolChinaCoronary Artery DiseaseFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHeart Defects, Congenital3' Untranslated RegionsBasic Helix-Loop-Helix ProteinsTCF21 protein, humanrs12190287susceptibilityTCF21ventricular septal defect

Identifiers

PMID28346832
PMCPMC5444416
OpenAlexW2614086613

What OpenQuestion holds

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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.