Evidence map›Paper›PMID 36506311›Full record

ArticleFrontiers in genetics2022

Case report: Identification of a frameshift mutation in GC enrichment and the GCC repeat region of the androgen insensitivity receptor (AR) gene in a patient with complete androgen insensitivity syndrome by whole-exome sequencing (WES) combined with specific PCR and deep sequencing.

Xiaojing He, Qingya Ma, Qiaoli Zhang, Xutao Hong, Ming Qi, Yongkai Li, Xiaodong Li

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

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 51% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 5 institutions in 2 countries.

Xiaojing HeDepartment of Obstetrics and Gynaecology, The Second Hospital of Hebei Medical University, Shijiazhuang, China.
Qingya MaDepartment of Gynecology, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Qiaoli ZhangDepartment of Human Reproductive Medicine, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, China.
Xutao HongZhejiang University Medical School Affiliated SRRS Hospital, Zhejiang, China.
Ming QiZhejiang University Medical School Affiliated SRRS Hospital, Zhejiang, China.
Yongkai LiDepartment of Gynecology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Xiaodong LiDepartment of Gynecology, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Hebei Medical University · CNCapital Medical University · CNFirst Affiliated Hospital of Xinjiang Medical University · CNSir Run Run Shaw Hospital · CNUniversity of Rochester Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

androgen receptorcomplete androgen insensitivity syndromedeep sequencingreproductive chimerismwhole-exome sequencing

Identifiers

PMID36506311
PMCPMC9732716
OpenAlexW4310039714

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.