Evidence map›Paper›PMID 31020005›Full record

ArticleAnnals of clinical and translational neurology2019

Dominant

Reem A Alkhater, Peixiang Wang, Alessandra Ruggieri, Lori Israelian, Susan Walker, Stephen W Scherer, Mary Lou Smith, Berge A Minassian

Open access · goldAbstract readCase Reports
In one paragraph

Article in Annals of clinical and translational neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

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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

8 authors at 4 institutions in 4 countries.

Reem A AlkhaterProgram in Genetics and Genome Biology The Hospital for Sick Children Toronto Ontario Canada.
Peixiang WangProgram in Genetics and Genome Biology The Hospital for Sick Children Toronto Ontario Canada.
Alessandra RuggieriNeuromuscular Diseases and Neuroimmunology Unit Fondazione IRCCS Istituto Neurologico Carlo Besta Milan Italy.ORCID 0000-0002-2777-6226
Lori IsraelianProgram in Genetics and Genome Biology The Hospital for Sick Children Toronto Ontario Canada.
Susan WalkerProgram in Genetics and Genome Biology The Hospital for Sick Children Toronto Ontario Canada.
Stephen W SchererProgram in Genetics and Genome Biology The Hospital for Sick Children Toronto Ontario Canada.
Mary Lou SmithDepartment of Psychology University of Toronto Mississauga Mississauga Ontario Canada.
Berge A MinassianProgram in Genetics and Genome Biology The Hospital for Sick Children Toronto Ontario Canada.
Hospital for Sick Children · CAUniversity of Toronto · CAFondazione IRCCS Istituto Neurologico Carlo Besta · ITSaudi Aramco Medical Services Organization · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mis-secreted glycoproteins (LGI1, reelin) are emerging causes of epilepsy. LMAN2L belongs to a glycoprotein secretion chaperone family. One recessive

Indexed as

ChildChild, PreschoolEpilepsyHumansIntellectual DisabilityLectinsMaleMembrane Transport ProteinsMiddle AgedMutationPedigreePhenotypeReelin ProteinLectinsLMAN2L protein, humanMembrane Transport ProteinsReelin ProteinRELN protein, human

Identifiers

PMID31020005
PMCPMC6469342
OpenAlexW2921970117

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.