Evidence map›Paper›PMID 31491999›Full record

ArticleGenes2019

Previously Identified Genetic Variants in

Sabin A Marquardt, Callie V Wilcox, Erin N Burns, Janel A Peterson, Carrie J Finno

Open access · goldAbstract read
In one paragraph

Article in Genes, 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
0.1field-weighted citation impact, top 46% 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, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

5 authors at 1 institution in 1 country.

Sabin A MarquardtDepartment of Population, Health and Reproduction at the University of California, Davis, Davis, CA 95616, USA. samarquardt@ucdavis.edu.
Callie V WilcoxDepartment of Population, Health and Reproduction at the University of California, Davis, Davis, CA 95616, USA. cvwilcox@ucdavis.edu.
Erin N BurnsDepartment of Population, Health and Reproduction at the University of California, Davis, Davis, CA 95616, USA. enburns@ucdavis.edu.ORCID 0000-0002-8007-6552
Janel A PetersonDepartment of Population, Health and Reproduction at the University of California, Davis, Davis, CA 95616, USA. janel.peterson@bcm.edu.
Carrie J FinnoDepartment of Population, Health and Reproduction at the University of California, Davis, Davis, CA 95616, USA. cjfinno@ucdavis.edu.ORCID 0000-0001-5924-0234
University of California, Davis · US

Funding

NCATS NIH HHS L40 TR001136
6 · The paper itself

Abstract

Equine neuroaxonal dystrophy/equine degenerative myeloencephalopathy (eNAD/EDM) is a neurologic disease that has been reported in young horses from a wide range of breeds. The disease is inherited and associated with vitamin E deficiency during the first two years of life, resulting in bilateral symmetric ataxia. A missense mutation (chr3:71,917,591 C > T) within adhesion G protein-coupled receptor L3 (

Indexed as

Polymorphism, Single NucleotideAnimalsHorse DiseasesHorsesMutation, MissenseNeuroaxonal DystrophiesReceptors, G-Protein-CoupledReceptors, Peptidealpha-latrotoxin receptorReceptors, G-Protein-CoupledReceptors, Peptideequine neuroaxonal dystrophyhorsevitamin E

Identifiers

PMID31491999
PMCPMC6770705
OpenAlexW2971851300

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.