Evidence map›Paper›PMID 33897766›Full record

ArticleFrontiers in genetics2021

Case Report: Compound Heterozygous Variants in

Qi Tian, Yang Cao, Li Shu, Yongjun Chen, Ying Peng, Yaqin Wang, Yuanyuan Chen, Hua Wang, Xiao Mao

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

Article in Frontiers in genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Molybdenum Cofactor Deficiency in Humans.Molecules (Basel, Switzerland) · 2022
    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

9 authors at 4 institutions in 1 country.

Qi TianDepartment of Medical Genetics, Maternal and Child Health Hospital of Hunan Province, Changsha, China.
Yang CaoDepartment of Radiology, Chenzhou First People's Hospital, Chenzhou, China.
Li ShuDepartment of Medical Genetics, Maternal and Child Health Hospital of Hunan Province, Changsha, China.
Yongjun ChenDepartment of Neurology, Nanhua Affiliated Hospital, University of South China, Hengyang, China.
Ying PengDepartment of Medical Genetics, Maternal and Child Health Hospital of Hunan Province, Changsha, China.
Yaqin WangHealth Management Center, The Third Xiangya Hospital, Central South University, Changsha, China.
Yuanyuan ChenReproductive Center of Maternal and Child Health Hospital of Hunan Province, Changsha, China.
Hua WangDepartment of Medical Genetics, Maternal and Child Health Hospital of Hunan Province, Changsha, China.
Xiao MaoDepartment of Medical Genetics, Maternal and Child Health Hospital of Hunan Province, Changsha, China.
Hunan Provincial Maternal and Child Health Hospital · CNCentral South University · CNChenzhou First People's Hospital · CNUniversity of South China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

MOCS3molybdenum cofactor deficiencyneurodevelopmental outcomesulfite oxidasewhole exome sequencing

Identifiers

PMID33897766
PMCPMC8060434
OpenAlexW3156252318

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.