Evidence map›Paper›PMID 31570502›Full record

ArticleG3 (Bethesda, Md.)2019

Natural Genetic Variation Screen in

Rebecca A S Palu, Elaine Ong, Kaitlyn Stevens, Shani Chung, Katie G Owings, Alan G Goodman, Clement Y Chow

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. A recombinantbioRxiv : the preprint server for biology · 2026
    Article
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  5. Review
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  14. AeLife · 2020
    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 2 institutions in 1 country.

Rebecca A S PaluDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT 84112.ORCID 0000-0001-9444-8815
Elaine OngDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT 84112.
Kaitlyn StevensDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT 84112.
Shani ChungDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT 84112.
Katie G OwingsDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT 84112.
Alan G GoodmanSchool of Molecular Biosciences, and.ORCID 0000-0001-6394-332X
Clement Y ChowDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT 84112, cchow@genetics.utah.edu.ORCID 0000-0002-3104-7923
University of Utah · USWashington State University · US

Funding

TRAINING PROGRAM IN GENETICST32GM007464 · NIGMS · UNIVERSITY OF UTAH · PI GRUNWALD, DAVID J., STANFIELD, GILLIAN · 1985 to 2020
$6.1M
Investigating the impact of genetic variation on the ER stress response, protein folding, and diseaseR35GM124780 · NIGMS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Clement Chow · 2017 to 2026
$4.0M
University of Utah Interdisciplinary Training Program in Computational Approaches to Diabetes and Metabolism ResearchT32DK110966 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Karen Louise Eilbeck, Marcus Guy Pezzolesi · 2016 to 2026
$2.6M
Identifying host genetic determinants of Coxiella burnetii pathogenesisR21AI128103 · NIAID · WASHINGTON STATE UNIVERSITY · PI GOODMAN, ALAN GABRIEL · 2017 to 2018
$421k
NIAID NIH HHS R21 AI128103NIDDK NIH HHS T32 DK110966NIGMS NIH HHS R35 GM124780NIGMS NIH HHS T32 GM007464
6 · The paper itself

Abstract

Apoptosis is the primary cause of degeneration in a number of neuronal, muscular, and metabolic disorders. These diseases are subject to a great deal of phenotypic heterogeneity in patient populations, primarily due to differences in genetic variation between individuals. This creates a barrier to effective diagnosis and treatment. Understanding how genetic variation influences apoptosis could lead to the development of new therapeutics and better personalized treatment approaches. In this study, we examine the impact of the natural genetic variation in the

Indexed as

Genetic VariationAnimalsApoptosisDrosophilaDrosophila ProteinsEyeGene Regulatory NetworksGenome-Wide Association StudyHomeostasisMitochondriaOrgan SizeOxidation-ReductionTumor Suppressor Protein p53Wnt Signaling PathwayDrosophila ProteinsTumor Suppressor Protein p53apoptosisDrosophilagenetic variationmodifier genes

Identifiers

PMID31570502
PMCPMC6893197
OpenAlexW2977969847

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.