Evidence map›Paper›PMID 28019661›Full record

ArticleAnnals of neurology2017

KCNA2 mutations are rare in hereditary spastic paraplegia.

Ziv Gan-Or, Grace Yoon, Oksana Suchowersky, Nicolas Dupré, Guy A Rouleau

Open access · greenAbstract readLetterComment
PubMed Publisher
In one paragraph

Article in Annals of neurology, 2017. 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

5 · Who and what money

Authors and funding

5 authors at 4 institutions in 1 country.

Ziv Gan-OrMontreal Neurological Institute and Hospital, McGill University, Montreal, Quebec.ORCID 0000-0003-0332-234X
Grace YoonDivision of Neurology, Department of Pediatrics, University of Toronto, Hospital for Sick Children, Toronto, Ontario.
Oksana SuchowerskyDivision of Neurology, University of Alberta, Edmonton, Alberta.
Nicolas DupréDivision of Neurology, University Hospital Center of Quebec and Faculty of Medicine, Laval University, Quebec City, Quebec, Canada.
Guy A RouleauMontreal Neurological Institute and Hospital, McGill University, Montreal, Quebec.
Montreal Neurological Institute and Hospital · CAUniversité Laval · CAUniversity of Alberta · CAUniversity of Toronto · CA

Funding

CIHR
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Spastic Paraplegia, HereditaryAtaxiaDatabases, GeneticHumansKv1.2 Potassium ChannelMutationKCNA2 protein, humanKv1.2 Potassium Channel

Identifiers

PMID28019661
OpenAlexW2567485069

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.