Evidence map›Paper›PMID 25189242›Full record

ArticleJournal of genetics2014

Spectrum of GJB2 mutations in Cypriot nonsyndromic hearing loss subjects.

Vassos Neocleous, Constantina Costi, Christos Shammas, Elena Spanou, Violetta Anastasiadou, George A Tanteles, Leonidas A Phylactou

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of genetics, 2014. 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
0.3field-weighted citation impact, top 47% 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, 7 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

7 authors at 2 institutions in 1 country.

Vassos NeocleousDepartment of Molecular Genetics, Function and Therapy, The Cyprus Institute of Neurology and Genetics, 1683 Nicosia, Cyprus. laphylac@cing.ac.cy.
Constantina Costi
Christos Shammas
Elena Spanou
Violetta Anastasiadou
George A Tanteles
Leonidas A Phylactou
Cyprus Institute of Neurology and Genetics · CYArchbishop Makarios III Hospital · CY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Base SequenceConnexin 26ConnexinsCyprusDeafnessDNA Mutational AnalysisGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHearing Loss, SensorineuralHumansMutation, MissenseSequence DeletionConnexin 26ConnexinsGJB2 protein, human

Identifiers

PMID25189242
OpenAlexW2015769407

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.