Evidence map›Paper›PMID 36159989›Full record

ArticleFrontiers in genetics2022

A novel mutation in

Yu Wang, Hanqing Song, Lingling Yu, Nan Wu, Xiaodong Zheng, Bo Liang, Peiguang Wang

Abstract 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. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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.

  1. Netherton Syndrome Masquerading as Pustular Psoriasis.Indian dermatology online journal · 2026
    Article
  2. Review
  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.

Yu WangDepartment of Dermatology, The First Affiliated Hospital, Anhui Medical University, Hefei, China.
Hanqing SongDepartment of Dermatology, The First Affiliated Hospital, Anhui Medical University, Hefei, China.
Lingling YuDepartment of Dermatology, The First Affiliated Hospital, Anhui Medical University, Hefei, China.
Nan WuDepartment of Dermatology, The First Affiliated Hospital, Anhui Medical University, Hefei, China.
Xiaodong ZhengDepartment of Dermatology, The First Affiliated Hospital, Anhui Medical University, Hefei, China.
Bo LiangDepartment of Dermatology, The First Affiliated Hospital, Anhui Medical University, Hefei, China.
Peiguang WangDepartment of Dermatology, The First Affiliated Hospital, Anhui Medical University, Hefei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Netherton syndrome (NS, OMIM #256500) is a rare autosomal recessive disease characterized by a triad of congenital ichthyosiform erythroderma (CIE) or ichthyosis linearis circumflexa (ILC), trichorrhexis invaginata (TI), and atopic predisposition. The disease is caused by a mutation in the

Indexed as

congenital ichthyosiform erythrodermamutationNetherton syndromephenotypeSPINK5

Identifiers

PMID36159989
PMCPMC9500337

What OpenQuestion holds

Textmetadata
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.