Evidence map›Paper›PMID 32555415›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2020

Correction: Phenotate: crowdsourcing phenotype annotations as exercises in undergraduate classes.

Willie H Chang, Pouria Mashouri, Alexander X Lozano, Brittney Johnstone, Mia Husić, Annie Olry, Sylvie Maiella, Tugce B Balci, Sarah L Sawyer, Peter N Robinson and 2 more

Abstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2020. 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
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.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Willie H ChangCentre for Computational Medicine, The Hospital For Sick Children, Toronto, ON, Canada.
Pouria MashouriCentre for Computational Medicine, The Hospital For Sick Children, Toronto, ON, Canada.
Alexander X LozanoCentre for Computational Medicine, The Hospital For Sick Children, Toronto, ON, Canada.
Brittney JohnstoneCentre for Computational Medicine, The Hospital For Sick Children, Toronto, ON, Canada.
Mia HusićCentre for Computational Medicine, The Hospital For Sick Children, Toronto, ON, Canada.
Annie OlryOrphanet, Institut national de la santé et de la recherche médicale, Paris, France.
Sylvie MaiellaOrphanet, Institut national de la santé et de la recherche médicale, Paris, France.
Tugce B BalciMedical Genetics Program of Southwestern Ontario, London Health Sciences Centre, London, ON, Canada.
Sarah L SawyerDepartment of Genetics, Children's Hospital of Eastern Ontario and Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.
Peter N RobinsonThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Ana RathOrphanet, Institut national de la santé et de la recherche médicale, Paris, France.
Michael BrudnoCentre for Computational Medicine, The Hospital For Sick Children, Toronto, ON, Canada. brudno@cs.toronto.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Identifiers

PMID32555415

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.