Evidence map›Paper›PMID 26022164›Full record

ReviewPediatric clinics of North America2015

Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.

Louisa Kalsner, Stormy J Chamberlain

Registry-linked trialAbstract readReview
In one paragraph

Review in Pediatric clinics of North America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03848481 (Cannabidivarin), which is not on this map. Cited by 87 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 2 pooled it
–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.

NCT03848481 phase2terminatednot on this mapstarted 2020, after this paper: background citation

Cannabidivarin (CBDV) vs. Placebo in Children and Adults up to Age 30 With Prader-Willi Syndrome (PWS)

TypeinterventionalSponsorEric HollanderRan2020 to 2024Enrolled6ConditionsPrader-Willi SyndromeArmsCBDV Compound, Placebo
3 · Its place in the literature

Who cites it

87 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. RO4938581, a GABAMolecular psychiatry · 2026
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Pituitary Gland Duplication Syndrome: An International Imaging Analysis.AJNR. American journal of neuroradiology · 2025
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

27 more citing papers are in PubMed but not listed here.

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

2 authors.

Louisa KalsnerDepartment of Pediatrics, Connecticut Children's Medical Center, University of Connecticut School of Medicine, 505 Farmington Avenue, Farmington, CT 06032, USA; Department of Neurology, Connecticut Children's Medical Center, University of Connecticut School of Medicine, 505 Farmington Avenue, Farmington, CT 06032, USA. Electronic address: Lkalsner@connecticutchildrens.org.
Stormy J ChamberlainDepartment of Pediatrics, Connecticut Children's Medical Center, University of Connecticut School of Medicine, 505 Farmington Avenue, Farmington, CT 06032, USA; Departments of Genetics and Genome Sciences and Pediatrics, Connecticut Children's Medical Center, University of Connecticut Health Center, 400 Farmington Avenue, Farmington, CT 06030-6403, USA. Electronic address: chamberlain@uchc.edu.

Funding

Regulation of UBE3A genomic imprinting by tissue-specific alternative splicingR01HD068730 · NICHD · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI CHAMBERLAIN, STORMY JO · 2011 to 2015
$1.3M
NICHD NIH HHS R01 HD068730
6 · The paper itself

Abstract

Three distinct neurodevelopmental disorders arise primarily from deletions or duplications that occur at the 15q11-q13 locus: Prader-Willi syndrome, Angelman syndrome, and 15q11-q13 duplication syndrome. Each of these disorders results from the loss of function or overexpression of at least 1 imprinted gene. This article discusses the clinical background, genetic cause, diagnostic strategy, and management of each of these 3 disorders.

Indexed as

Angelman SyndromeChildChromosome AberrationsChromosomes, Human, Pair 15DNA MethylationEpigenesis, GeneticGene DosageGene DuplicationGene ExpressionHumansIntellectual DisabilityPrader-Willi SyndromeAngelman syndromeChromosome 15q11-q13 duplicationCopy number variationDNA methylationGenomic imprintingPrader-Willi syndromeSNRPNUBE3A

Identifiers

PMID26022164
PMCPMC4449422

What OpenQuestion holds

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Registered trials

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.