Evidence map›Paper›PMID 25705109›Full record

ArticleAdvances in genomics and genetics

Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromes.

Merlin G Butler, Kun Wang, Jan D Marshall, Jürgen K Naggert, Jasmine A Rethmeyer, Sumedha S Gunewardena, Ann M Manzardo

Open access · diamondAbstract read
In one paragraph

Article in Advances in genomics and genetics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.4field-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

25 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Obesity-Related Ciliopathies: Focus on Advances of Biomarkers.International journal of molecular sciences · 2024
    Review
  4. Genetics and epigenetics in the obesity phenotyping scenario.Reviews in endocrine & metabolic disorders · 2023
    Review
  5. Review
  6. Review
  7. The Potential Role of Small Nucleolar RNAs in Cancers - An Evidence Map.International journal of general medicine · 2022
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

7 authors at 3 institutions in 2 countries.

Merlin G ButlerDepartment of Psychiatry and Behavioral Sciences, University of Kansas Medical Center, Kansas City, KS, USA ; Department of Pediatrics, University of Kansas Medical Center, Kansas City, KS, USA.
Kun WangDepartment of Psychiatry and Behavioral Sciences, University of Kansas Medical Center, Kansas City, KS, USA.
Jan D MarshallThe Jackson Laboratory, Bar Harbor, ME, USA.
Jürgen K NaggertThe Jackson Laboratory, Bar Harbor, ME, USA.
Jasmine A RethmeyerDepartment of Psychiatry and Behavioral Sciences, University of Kansas Medical Center, Kansas City, KS, USA.
Sumedha S GunewardenaDepartment of Biostatistics, Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS, USA.
Ann M ManzardoDepartment of Psychiatry and Behavioral Sciences, University of Kansas Medical Center, Kansas City, KS, USA.
University of Kansas Medical Center · USInstitute of Behavioral Sciences · JPJackson Laboratory · US

Funding

Research Design and Analysis Core (RDAC)P30HD002528 · NICHD · UNIVERSITY OF KANSAS LAWRENCE · PI DURHAM, DIANNE NONE · 1985 to 2015
$22.1M
Training and Career Development ComponentU54HD061222 · NICHD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PERCY, ALAN KENNETH · 2009 to 2019
$12.4M
MOLECULAR GENETIC CHARACTERIZATION OF ALSTROM SYNDROMER01HD036878 · NICHD · JACKSON LABORATORY · PI NAGGERT, JUERGEN K. · 1998 to 2011
$4.2M
Early Prevention of Aberrant Behavior in Neurodevelopmental Disorders in PeruR21HD060500 · NICHD · UNIVERSITY OF KANSAS LAWRENCE · PI SCHROEDER, STEPHEN ROBERT · 2010 to 2011
$261k
NICHD NIH HHS P30 HD002528NICHD NIH HHS R01 HD036878NICHD NIH HHS R21 HD060500NICHD NIH HHS U54 HD061222
6 · The paper itself

Abstract

Obesity is accompanied by hyperphagia in several classical genetic obesity-related syndromes that are rare, including Prader-Willi syndrome (PWS) and Alström syndrome (ALMS). We compared coding and noncoding gene expression in adult males with PWS, ALMS, and nonsyndromic obesity relative to nonobese males using readily available lymphoblastoid cells to identify disease-specific molecular patterns and disturbed mechanisms in obesity. We found 231 genes upregulated in ALMS compared with nonobese males, but no genes were found to be upregulated in obese or PWS males and 124 genes were downregulated in ALMS. The metallothionein gene (

Indexed as

exon expressiongenehyperphagiamicroarray analysismiRNA expressionobesity

Identifiers

PMID25705109
PMCPMC4334166
OpenAlexW2119855077

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.