Evidence map›Paper›PMID 33168794›Full record

Trial reportJournal of genetics2020

Methyl-CpG-binding protein 2 gene mutations and its association with epilepsy: a single centre study from the Indian subcontinent.

Payal Kamdar, Maya Thomas, Sangeetha Yoganathan, Karthik Muthusamy, Beena Koshy, Samuel Philip Oommen, Rekha Aaron, Anitha Barney, Suneetha Susan C Abraham, Sumita Danda

Abstract readClinical Trial
PubMed
In one paragraph

Trial report in Journal of genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 87% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 1 institution in 1 country.

Payal KamdarMedical Genetics, Christian Medical College, Vellore 632 004, India. sdanda@cmcvellore.ac.in.
Maya Thomas
Sangeetha Yoganathan
Karthik Muthusamy
Beena Koshy
Samuel Philip Oommen
Rekha Aaron
Anitha Barney
Suneetha Susan C Abraham
Sumita Danda
Christian Medical College, Vellore · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rett syndrome (RTT) is an X-linked disorder caused by mutations in

Indexed as

MutationChild, PreschoolDevelopmental DisabilitiesEpilepsyFemaleHumansIndiaInfantMaleMethyl-CpG-Binding Protein 2PhenotypePrognosisRetrospective StudiesRett SyndromeMECP2 protein, humanMethyl-CpG-Binding Protein 2

Identifiers

PMID33168794
OpenAlexW3093763278

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.