Evidence map›Paper›PMID 28770012›Full record

ArticleMobile DNA2017

Discovery of rare, diagnostic

Julie Feusier, David J Witherspoon, W Scott Watkins, Clément Goubert, Thomas A Sasani, Lynn B Jorde

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Mobile DNA, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. AnNAR genomics and bioinformatics · 2022
    Article
  4. Review
  5. Article
  6. Article
  7. Contribution of unfixed transposable element insertions to human regulatory variation.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Article
  8. Article
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

6 authors.

Julie FeusierDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT USA.ORCID 0000-0002-1266-087X
David J WitherspoonDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT USA.
W Scott WatkinsDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT USA.
Clément GoubertDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT USA.
Thomas A SasaniDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT USA.
Lynn B JordeDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT USA.

Funding

POPULATION GENETICS OF MOBILE ELEMENTSR01GM059290 · NIGMS · UNIVERSITY OF UTAH · PI BATZER, MARK A, FESCHOTTE, CEDRIC · 1999 to 2018
$8.5M
Human Genetic Variation and DiseaseR35GM118335 · NIGMS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI JORDE, LYNN · 2016 to 2025
$5.1M
VAAST+: Tool for variant prioritization, risk assessment and disease-gene findingR01GM104390 · NIGMS · UNIVERSITY OF UTAH · PI JORDE, LYNN, YANDELL, MARK DOUGLAS · 2013 to 2017
$2.2M
NIGMS NIH HHS R01 GM059290NIGMS NIH HHS R01 GM104390NIGMS NIH HHS R35 GM118335
6 · The paper itself

Abstract

backgroundPolymorphic human

resultsWe identified 5,288 putative

conclusionCurrent

Indexed as

Ancestry informative markersHuman ancestryMobilomePolymorphismPopulation geneticsRetrotransposon

Identifiers

PMID28770012
PMCPMC5531096

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.