Evidence map›Paper›PMID 37736838›Full record

ArticleEuropean journal of human genetics : EJHG2023

Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown-Rahman syndrome.

Candy Kumps, Erika D'haenens, Jennifer Kerkhof, Haley McConkey, Marielle Alders, Bekim Sadikovic, Olivier M Vanakker

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

Article in European journal of human genetics : EJHG, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

7 authors at 2 institutions in 2 countries.

Candy KumpsCenter for Medical Genetics, Ghent University Hospital, Gent, Belgium. candy.kumps@ugent.be.ORCID 0000-0002-0574-5138
Erika D'haenensCenter for Medical Genetics, Ghent University Hospital, Gent, Belgium.
Jennifer KerkhofClinical Genome Centre, London Health Sciences Centre, London, ON, Canada.ORCID 0000-0003-1245-6606
Haley McConkeyClinical Genome Centre, London Health Sciences Centre, London, ON, Canada.
Marielle AldersClinical Genome Centre, London Health Sciences Centre, London, ON, Canada.
Bekim SadikovicClinical Genome Centre, London Health Sciences Centre, London, ON, Canada.ORCID 0000-0001-6363-0016
Olivier M VanakkerCenter for Medical Genetics, Ghent University Hospital, Gent, Belgium.
London Health Sciences Centre · CAGhent University Hospital · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Abnormalities, MultipleIntellectual DisabilityAdultDNA (Cytosine-5-)-MethyltransferasesDNA MethylationDNA Methyltransferase 3AHumansMethylationDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNMT3A protein, human

Identifiers

PMID37736838
PMCPMC10689817
OpenAlexW4386944270

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.