Evidence map›Paper›PMID 28835471›Full record

ArticleGenetics2017

Genetic Screen for Postembryonic Development in the Zebrafish (

Katrin Henke, Jacob M Daane, M Brent Hawkins, Christopher M Dooley, Elisabeth M Busch-Nentwich, Derek L Stemple, Matthew P Harris

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 69 citations in OpenAlex.

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  13. Zebrafish: an important model for understanding scoliosis.Cellular and molecular life sciences : CMLS · 2022
    Review
  14. Article
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  16. A Baseline for Skeletal Investigations in Medaka (Frontiers in endocrinology · 2022
    Review
  17. Article
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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

7 authors at 3 institutions in 2 countries.

Katrin HenkeDepartment of Orthopedic Research, Boston Children's Hospital, Massachusetts 02115 khenke@genetics.med.harvard.edu harris@genetics.med.harvard.edu.
Jacob M DaaneDepartment of Orthopedic Research, Boston Children's Hospital, Massachusetts 02115.
M Brent HawkinsDepartment of Orthopedic Research, Boston Children's Hospital, Massachusetts 02115.
Christopher M DooleyWellcome Trust Sanger Institute, Hinxton, CB10 1SA, UK.
Elisabeth M Busch-NentwichWellcome Trust Sanger Institute, Hinxton, CB10 1SA, UK.
Derek L StempleWellcome Trust Sanger Institute, Hinxton, CB10 1SA, UK.
Matthew P HarrisDepartment of Orthopedic Research, Boston Children's Hospital, Massachusetts 02115 khenke@genetics.med.harvard.edu harris@genetics.med.harvard.edu.
Boston Children's Hospital · USWellcome Sanger Institute · GBHarvard University · US

Funding

Anatomical atlas and transgenic toolkit for late skull formation in zebrafishU01DE024434 · NIDCR · UNIVERSITY OF PENNSYLVANIA · PI FISHER, SHANNON, HARRIS, MATTHEW P · 2014 to 2018
$3.3M
NIDCR NIH HHS U01 DE024434
6 · The paper itself

Abstract

Large-scale forward genetic screens have been instrumental for identifying genes that regulate development, homeostasis, and regeneration, as well as the mechanisms of disease. The zebrafish,

Indexed as

Genes, DominantMutagenesisAnimalsBone DevelopmentHaplotypesPhenotypeSkin PigmentationZebrafishZebrafish ProteinsZebrafish Proteinsdominant screenmappingpigmentpostembryonicskeletogenesiszebrafish

Identifiers

PMID28835471
PMCPMC5629327
OpenAlexW2749398233

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.