Evidence map›Paper›PMID 34377013›Full record

ArticleInternational journal of general medicine2021

Variant of TSHR is Not a Frequent Cause of Congenital Hypothyroidism in Chinese Han Patients.

Peng Xue, Yuqi Yang, Qi Yun, Yue Cui, Bin Yu, Wei Long

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in International journal of general medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 48% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. InvestigatingFrontiers in endocrinology · 2025
    Article
  2. Article
  3. 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

6 authors at 2 institutions in 1 country.

Peng XueDepartment of Pediatrics, Changzhou Children's Hospital, Changzhou, People's Republic of China.
Yuqi YangDepartment of Medical Genetics, Affiliated Changzhou Women and Children's Hospital, Nanjing Medical University, Changzhou, People's Republic of China.
Qi YunDepartment of Pediatrics, Changzhou Children's Hospital, Changzhou, People's Republic of China.
Yue CuiDepartment of Pediatrics, Changzhou Children's Hospital, Changzhou, People's Republic of China.
Bin YuDepartment of Medical Genetics, Affiliated Changzhou Women and Children's Hospital, Nanjing Medical University, Changzhou, People's Republic of China.ORCID 0000-0001-7796-7314
Wei LongDepartment of Medical Genetics, Affiliated Changzhou Women and Children's Hospital, Nanjing Medical University, Changzhou, People's Republic of China.ORCID 0000-0001-7744-4521
Hangzhou Children's Hospital · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo screen variants of the thyroid stimulating hormone receptor ( PATIENTS AND

methodsWe conducted a genetic screening of the

resultsA total of 11

conclusionThe prevalence of

Indexed as

congenital hypothyroidismprevalencethyroid stimulating hormone receptorvariant

Identifiers

PMID34377013
PMCPMC8349214
OpenAlexW3192286478

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.