Evidence map›Paper›PMID 26806084›Full record

ArticleAsian journal of andrology

A missense mutation in the androgen receptor gene causing androgen insensitivity syndrome in a Chinese family.

Lin Li, Wen-Miao Liu, Mei-Xin Liu, Shu-Qi Zheng, Ji-Xia Zhang, Feng-Yuan Che, Shi-Guo Liu

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

Article in Asian journal of andrology. 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
0.3field-weighted citation impact, top 36% 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, 6 citations in OpenAlex.

  1. [Complete androgen insensitivity syndrome: diagnosis and multidisciplinary management].Revista medica del Instituto Mexicano del Seguro Social · 2023
    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

7 authors at 2 institutions in 1 country.

Lin LiDepartment of Genetics Counseling, Genetics Institute of Linyi People's Hospital, Linyi 276003, Shandong, China.
Wen-Miao LiuDepartment of Clinical Laboratory Diagnosis, Medical College of Qingdao University, Qingdao 266003, Shandong, China.
Mei-Xin LiuDepartment of Ultrasonography, The Affiliated Hospital of Qingdao University, Qingdao 266003, Shandong, China.
Shu-Qi ZhengDepartment of Genetics Counseling, Genetics Institute of Linyi People's Hospital, Linyi 276003, Shandong, China.
Ji-Xia ZhangDepartment of Genetics Counseling, Genetics Institute of Linyi People's Hospital, Linyi 276003, Shandong, China.
Feng-Yuan CheDepartment of Neurology, Linyi People's Hospital, Linyi 276003, Shandong, China.
Shi-Guo LiuDepartment of Prenatal Diagnosis Center, The Affiliated Hospital of Qingdao University, Qingdao 266003, Shandong, China.
Linyi People's Hospital · CNQingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Mutation, MissenseAndrogen-Insensitivity SyndromeAsian PeopleChinaHomozygoteHumansMaleReceptors, AndrogenReceptors, Androgen

Identifiers

PMID26806084
PMCPMC5312231
OpenAlexW2411488522

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.