Evidence map›Paper›PMID 31180027›Full record

ArticleLancet (London, England)2019

Genotype-phenotype association in patients with SCN4A mutation - Authors' reply.

Emma Matthews, Roope Männikkö, Elijah Behr, Michael G Hanna

Open access · bronzeAbstract readLetterComment
PubMed Publisher
In one paragraph

Article in Lancet (London, England), 2019. 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 96% 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

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Emma MatthewsMRC Centre for Neuromuscular Diseases, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery, Queen Square, London, WC1N 3BG, UK. Electronic address: emma.matthews@ucl.ac.uk.
Roope MännikköMRC Centre for Neuromuscular Diseases, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery, Queen Square, London, WC1N 3BG, UK.
Elijah BehrCardiology Clinical Academic Group, St George's University of London, London, UK; St George's University Hospitals NHS Foundation Trust, London, UK.
Michael G HannaMRC Centre for Neuromuscular Diseases, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery, Queen Square, London, WC1N 3BG, UK.
National Hospital for Neurology and Neurosurgery · GBSt George's, University of London · GB

Funding

British Heart Foundation FS/13/78/30520Medical Research Council G0802760Medical Research Council G1001253Medical Research Council G108/638Medical Research Council MR/K000608/1Medical Research Council MR/S01165X/1The Dunhill Medical Trust R605/0717Wellcome Trust 209583/Z/17/Z
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genetic Association StudiesHumansMutationNAV1.4 Voltage-Gated Sodium ChannelNAV1.4 Voltage-Gated Sodium ChannelSCN4A protein, human

Identifiers

PMID31180027
OpenAlexW2948189049

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.