Evidence map›Paper›PMID 36110215›Full record

ArticleFrontiers in genetics2022

Clinical and Genetic Analysis of a Patient With Coexisting 17a-Hydroxylase/17,20-Lyase Deficiency and Moyamoya Disease.

Jiaming Huang, Danli Zhou, Nan Dong, Chenzhao Ding, Yan Liu, Fangping Li

Open access · goldAbstract read
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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. 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

6 authors at 2 institutions in 1 country.

Jiaming HuangDepartment of Endocrinology, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
Danli ZhouDepartment of Endocrinology, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
Nan DongDepartment of Scientific Research Center, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
Chenzhao DingDepartment of Endocrinology, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
Yan LiuDepartment of Scientific Research Center, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
Fangping LiDepartment of Endocrinology, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
Sun Yat-sen University · CNThe Seventh Affiliated Hospital of Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

17a-Hydroxylase/17,20-lyase deficiency (17OHD) is caused by pathogenic mutations in

Indexed as

17a-hydroxylase/1720-lyase deficiencyCNOT3 geneCYP17A1 geneHLA-DRB1 genemoyamoya diseasePCNT gene

Identifiers

PMID36110215
PMCPMC9468450
OpenAlexW4293537663

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.