Evidence map›Paper›PMID 27933089›Full record

ArticleFrontiers in genetics2016

A Rare Inherited 15q11.2-q13.1 Interstitial Duplication with Maternal Somatic Mosaicism, Renal Carcinoma, and Autism.

Nora Urraca, Brian Potter, Rachel Hundley, Eniko K Pivnick, Kathryn McVicar, Ronald L Thibert, Christopher Ledbetter, Reed Chamberlain, Leticia Miravalle, Carissa L Sirois and 2 more

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. 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

12 authors at 5 institutions in 1 country.

Nora UrracaDepartment of Neurology, University of Tennessee Health Science CenterMemphis, TN, USA; Pediatric Clinical Research Unit, Le Bonheur Children's HospitalMemphis, TN, USA.
Brian PotterDepartment of Pediatrics, University of Tennessee Health Science CenterMemphis, TN, USA; Neuroscience Institute, Le Bonheur Children's HospitalMemphis, TN, USA.
Rachel HundleyDivision of Developmental Medicine, Department of Pediatrics, Vanderbilt University School of Medicine Nashville, TN, USA.
Eniko K PivnickDepartment of Pediatrics, University of Tennessee Health Science CenterMemphis, TN, USA; Department of Ophthalmology, University of Tennessee Health Science CenterMemphis, TN, USA.
Kathryn McVicarDepartment of Pediatrics, University of Tennessee Health Science Center Memphis, TN, USA.
Ronald L ThibertDepartment of Neurology, Massachusetts General Hospital Boston, MA, USA.
Christopher LedbetterDepartment of Urology, University of Tennessee Health Science Center Memphis, TN, USA.
Reed ChamberlainGenetics Associates Inc., Nashville, TN USA.
Leticia MiravalleGenetics Associates Inc., Nashville, TN USA.
Carissa L SiroisDepartment of Genetics and Genome Sciences, University of Connecticut Health Center Farmington, CT, USA.
Stormy ChamberlainDepartment of Genetics and Genome Sciences, University of Connecticut Health Center Farmington, CT, USA.
Lawrence T ReiterDepartment of Neurology, University of Tennessee Health Science CenterMemphis, TN, USA; Department of Pediatrics, University of Tennessee Health Science CenterMemphis, TN, USA.
University of Tennessee Health Science Center · USInsight Genetics (United States) · USUConn Health · USMassachusetts General Hospital · USVanderbilt University · US

Funding

Tooth pulp as a source for neuronal precursor cells to study neurogenetic disordeR21NS075709 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI REITER, LAWRENCE T · 2012 to 2013
$404k
NINDS NIH HHS R21 NS075709
6 · The paper itself

Abstract

Chromosome 15q11-q13.1 duplication is a common copy number variant associated with autism spectrum disorder (ASD). Most cases are

Indexed as

15q duplicationautismgrowth competition assayrenal carcinomasomatic mosaicismstem cells

Identifiers

PMID27933089
PMCPMC5122884
OpenAlexW2551887390

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.