Evidence map›Paper›PMID 35692839›Full record

ArticleFrontiers in genetics2022

A Novel Mutation c.3392G>T of

Lihong Fan, Longfei Ji, Yuqing Xu, Guosong Shen, Kefeng Tang, Zhi Li, Sisi Ye, Xueping Shen

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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.7field-weighted citation impact, top 18% 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, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. [Growth plate regulation and short stature: mechanistic insights and therapeutic advances].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
    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

8 authors at 3 institutions in 1 country.

Lihong FanCenter of Prenatal Diagnosis, Huzhou Maternity & Child Health Care Hospital, Huzhou, China.
Longfei JiDepartment of Clinical Laboratory, The First People's Hospital of Huzhou, Huzhou, China.
Yuqing XuDepartment of Reproductive Genetics, Women's Hospital, School of Medicine Zhejiang University, Hangzhou, China.
Guosong ShenCenter of Prenatal Diagnosis, Huzhou Maternity & Child Health Care Hospital, Huzhou, China.
Kefeng TangCenter of Prenatal Diagnosis, Huzhou Maternity & Child Health Care Hospital, Huzhou, China.
Zhi LiCenter of Prenatal Diagnosis, Huzhou Maternity & Child Health Care Hospital, Huzhou, China.
Sisi YeCenter of Prenatal Diagnosis, Huzhou Maternity & Child Health Care Hospital, Huzhou, China.
Xueping ShenCenter of Prenatal Diagnosis, Huzhou Maternity & Child Health Care Hospital, Huzhou, China.
Huzhou Women and Children's Hospital · CNThird People's Hospital of Huzhou · CNWomen's Hospital, School of Medicine, Zhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spondyloepiphyseal dysplasia congenital (SEDC) is a rare chondrodysplasia caused by dominant pathogenic variants in

Indexed as

COL2A1in-frame deletionminigenenext-generation sequencingprenatal diagnosisspondyloepiphyseal dysplasia congenital

Identifiers

PMID35692839
PMCPMC9174977
OpenAlexW4223914341

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.