Evidence map›Paper›PMID 33568421›Full record

ArticleCold Spring Harbor molecular case studies2021

A novel variant of

Shenghai Yang, Weishi Yu, Qian Chen, Xiaodong Wang

Open access · diamondAbstract read
In one paragraph

Article in Cold Spring Harbor molecular case studies, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Heterozygous Med13l mice recapitulate a developmental growth delay and craniofacial anomalies seen in MED13L syndrome.Developmental dynamics : an official publication of the American Association of Anatomists · 2026
    Article
  2. Article
  3. 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

4 authors at 2 institutions in 1 country.

Shenghai YangChildren's Hospital, Capital Institute of Pediatrics, Beijing, China.
Weishi YuCipher Gene Ltd., Beijing, China.
Qian ChenChildren's Hospital, Capital Institute of Pediatrics, Beijing, China.
Xiaodong WangCipher Gene Ltd., Beijing, China.ORCID 0000-0002-5374-0235
Children's Hospital of Capital Institute of Pediatrics · CNCipher Gene (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infantile spasms are a potentially catastrophic form of epilepsy syndrome that are usually associated with substantial developmental delay and commonly occur in children younger than 1 yr. Recent reports on four cases revealed that variants harbored in a novel gene

Indexed as

Genetic VariationCyclin-Dependent KinasesEpileptic SyndromesExome SequencingHumansInfantMaleMutation, MissenseNeurodevelopmental DisordersPedigreePhenotypeSeizuresSpasms, InfantileCDK19 protein, humanCyclin-Dependent Kinasesepileptic encephalopathyinfantile spasmssevere global developmental delay

Identifiers

PMID33568421
PMCPMC8040737
OpenAlexW3128950735

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.