Evidence map›Paper›PMID 27343258›Full record

ArticleBrain : a journal of neurology2016

Reply: Aberrant splicing induced by the most common EPG5 mutation in an individual with Vici syndrome.

Susan Byrne, Thomas Cullup, Manolis Fanto, Mathias Gautel, Heinz Jungbluth

Open access · bronzeAbstract readLetterComment
PubMed Publisher
In one paragraph

Article in Brain : a journal of neurology, 2016. 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
0.5field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 5 institutions in 1 country.

Susan Byrne1 Department of Paediatric Neurology, Neuromuscular Service, Evelina's Children Hospital, Guy's & St. Thomas' Hospital NHS Foundation Trust, London, UK.
Thomas Cullup2 Regional Molecular Genetics Laboratory, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Manolis Fanto3 Department of Clinical and Basic Neuroscience, IoPPN, King's College, London, UK.
Mathias Gautel4 Randall Division of Cell and Molecular Biophysics, King's College London, British Heart Foundation Centre of Excellence, London, UK 5 Cardiovascular Division, King's College London, British Heart Foundation Centre of Excellence, London, UK.
Heinz Jungbluth1 Department of Paediatric Neurology, Neuromuscular Service, Evelina's Children Hospital, Guy's & St. Thomas' Hospital NHS Foundation Trust, London, UK 3 Department of Clinical and Basic Neuroscience, IoPPN, King's College, London, UK 4 Randall Division of Cell and Molecular Biophysics, King's College London, British Heart Foundation Centre of Excellence, London, UK Heinz.Jungbluth@gstt.nhs.uk.
British Heart Foundation · GBGreat Ormond Street Hospital for Children NHS Foundation Trust · GBGuy's and St Thomas' NHS Foundation Trust · GBKing's College London · GBSt Thomas' Hospital · GB

Funding

British Heart Foundation PG/11/127/29322Medical Research Council G0600251Medical Research Council G1002186
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Agenesis of Corpus CallosumCataractHumansMutation

Identifiers

PMID27343258
OpenAlexW2474376679

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.