Evidence map›Paper›PMID 29912702›Full record

ArticleEmerging infectious diseases2018

Diagnosis of Methionine/Valine Variant Creutzfeldt-Jakob Disease by Protein Misfolding Cyclic Amplification.

Daisy Bougard, Maxime Bélondrade, Charly Mayran, Lilian Bruyère-Ostells, Sylvain Lehmann, Chantal Fournier-Wirth, Richard S Knight, Robert G Will, Alison J E Green

Open access · diamondAbstract read
In one paragraph

Article in Emerging infectious diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  8. Variant CJD: Reflections a Quarter of a Century on.Pathogens (Basel, Switzerland) · 2021
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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

9 authors at 4 institutions in 2 countries.

Daisy Bougard
Maxime Bélondrade
Charly Mayran
Lilian Bruyère-Ostells
Sylvain Lehmann
Chantal Fournier-Wirth
Richard S Knight
Robert G Will
Alison J E Green
Hôpital Arnaud de Villeneuve · FRÉtablissement Français du Sang · FRUniversity of Edinburgh · GBInstitute for Regenerative Medicine & Biotherapy · FR

Funding

Department of Health PRST061400008Medical Research Council MR/L016400/1
6 · The paper itself

Abstract

A patient with a heterozygous variant of Creutzfeldt-Jakob disease (CJD) with a methionine/valine genotype at codon 129 of the prion protein gene was recently reported. Using an ultrasensitive and specific protein misfolding cyclic amplification-based assay for detecting variant CJD prions in cerebrospinal fluid, we discriminated this heterozygous case of variant CJD from cases of sporadic CJD.

Indexed as

Creutzfeldt-Jakob SyndromeGenotypeHumansMethioninePrion ProteinsProteostasis DeficienciesSensitivity and SpecificityValineMethioninePrion ProteinsValinecerebrospinal fluidCJDCreutzfeldt-Jakob diseaseCSFdiagnosisgCJDgenetic Creutzfeldt-Jakob diseasemethionine/valine variantPMCAprions and related diseasesprotein misfolding cyclic amplificationsCJDsporadic Creutzfeldt-Jakob diseasevariant Creutzfeldt-Jakob diseasevCJD

Identifiers

PMID29912702
PMCPMC6038758
OpenAlexW2807628815

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.