Evidence map›Paper›PMID 31850070›Full record

ArticleFrontiers in genetics2019

The Precise Diagnosis of Wolfram Syndrome Type 1 Based on Next-Generation Sequencing.

Dan-Dan Wang, Fang-Yuan Hu, Feng-Juan Gao, Sheng-Hai Zhang, Ping Xu, Guo-Hong Tian, Ji-Hong Wu

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

Article in Frontiers in genetics, 2019. 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
0.3field-weighted citation impact, top 42% 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, 7 citations in OpenAlex.

  1. Wolfram syndrome type 1: a case series.Orphanet journal of rare diseases · 2023
    Article
  2. 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.

Dan-Dan WangEye Institute, Eye and ENT Hospital, College of Medicine, Fudan University, Shanghai, China.
Fang-Yuan HuEye Institute, Eye and ENT Hospital, College of Medicine, Fudan University, Shanghai, China.
Feng-Juan GaoEye Institute, Eye and ENT Hospital, College of Medicine, Fudan University, Shanghai, China.
Sheng-Hai ZhangEye Institute, Eye and ENT Hospital, College of Medicine, Fudan University, Shanghai, China.
Ping XuEye Institute, Eye and ENT Hospital, College of Medicine, Fudan University, Shanghai, China.
Guo-Hong TianEye Institute, Eye and ENT Hospital, College of Medicine, Fudan University, Shanghai, China.
Ji-Hong WuEye Institute, Eye and ENT Hospital, College of Medicine, Fudan University, Shanghai, China.
Eye & ENT Hospital of Fudan University · CNScience and Technology Commission of Shanghai Municipality · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

diabetes mellitusnext-generation sequencingoptic atrophyprecise diagnosisWFS1wolfram syndrome

Identifiers

PMID31850070
PMCPMC6887651
OpenAlexW2991050331

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.