Evidence map›Paper›PMID 32648047›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2021

A de novo mutation in SMC1A gene identified in a Chinese infant with nonclassical Cornelia de Lange syndrome and drug-resistant epilepsy.

Hongjun Fang, Xi Zhang, Bo Xiao, Lily Zhang, Hongyu Long

Abstract readCase ReportsLetter
PubMed Publisher
In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2021. 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 43% 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. 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

5 authors at 2 institutions in 1 country.

Hongjun Fang *Neurology Department, Hunan Children's Hospital, Changsha, China.
Xi Zhang *Neurology Department, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Bo XiaoNeurology Department, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.
Lily ZhangNeurology Department, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China. zhanglily@csu.edu.cn.
Hongyu LongNeurology Department, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China. longhongyu@csu.edu.cn.ORCID 0000-0001-5641-8850
Central South University · CNHunan Children's Hospital · CN

Funding

Hunan Provincial Science and Technology Department 2019SK1012National Natural Science Foundation of China Grant nos. 81974206the Scientific Research project of Hunan Provincial Commission of Health C2019010
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Cell Cycle ProteinsChromosomal Proteins, Non-HistoneDe Lange SyndromeEpilepsyPharmaceutical PreparationsChinaHumansInfantMutationPhenotypeStructural Maintenance of Chromosome Protein 1Cell Cycle ProteinsChromosomal Proteins, Non-HistonePharmaceutical PreparationsStructural Maintenance of Chromosome Protein 1

Identifiers

PMID32648047
OpenAlexW3041768423

What OpenQuestion holds

Textmetadata
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.