Evidence map›Paper›PMID 38105698›Full record

ArticleZhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences2023

Genetic analysis of novel pathogenic gene

Xinghan Wu, Xiangyun Peng, Yu Zheng, Shuju Zhang, Yu Peng, Hua Wang

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

Article in Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 35% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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 1 institution in 1 country.

Xinghan WuDepartment of Medical Genetics, Hunan Children's Hospital, Changsha 410007, China. 930409377@qq.com.
Xiangyun PengDepartment of Endocrinology, Hunan Children's Hospital, Changsha 410007, China.
Yu ZhengDepartment of Medical Genetics, Hunan Children's Hospital, Changsha 410007, China.
Shuju ZhangDepartment of Medical Genetics, Hunan Children's Hospital, Changsha 410007, China.
Yu PengDepartment of Medical Genetics, Hunan Children's Hospital, Changsha 410007, China.
Hua WangDepartment of Medical Genetics, Hunan Children's Hospital, Changsha 410007, China. wanghua213@aliyun.com.
Hunan Children's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 13-year and 6-month-old girl attended the Hunan Children's Hospital due to delayed menarche. The laboratory test results indicated increased follicle-stimulating hormone and luteinizing hormone, decreased anti-Mullerian hormone, and pelvic ultrasound showed a cord-like uterus and absence of bilateral ovaries. Her 11-year and 5-month-old younger sister had the same laboratory and imaging findings, and both girls were diagnosed with primary ovarian insufficiency. Whole exome sequencing and Sanger sequencing confirmed that the proband and her sister carried heterozygous variants of

Indexed as

Primary Ovarian InsufficiencyChildEstradiolFemaleHumansInfantLuteinizing HormoneEstradiolLuteinizing HormoneCase reportDNA damage repairHomologous recombinationHROB genePrimary ovarian insufficiencyWhole exome sequencing

Identifiers

PMID38105698
PMCPMC10764178
OpenAlexW4389805341

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.