Evidence map›Paper›PMID 19159391›Full record

ReviewClinical genetics2009

Noncoding RNAs in mental retardation.

K E Szulwach, P Jin, R S Alisch

Abstract readReview
In one paragraph

Review in Clinical genetics, 2009. 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
1.1field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. The role of microRNAs in the biology of rare diseases.International journal of molecular sciences · 2011
    Review
  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

3 authors at 1 institution in 1 country.

K E SzulwachDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA.
P Jin
R S Alisch
Emory University · US

Funding

Dissecting the molecular basis of fragile X syndrome in DrosophilaR01MH076090 · NIMH · EMORY UNIVERSITY · PI JIN, PENG · 2006 to 2010
$1.6M
Dissecting the Molecular Basis of Fragile X Syndrome in DrosophilaR56MH076090 · NIMH · EMORY UNIVERSITY · PI JIN, PENG · 2011 to 2011
$388k
NIMH NIH HHS R01 MH076090NIMH NIH HHS R56 MH076090
6 · The paper itself

Abstract

Recent genome-wide interrogations of transcribed RNA have yielded compelling evidence for pervasive and complex transcription throughout a large majority of the human genome. Tens of thousands of noncoding RNA transcripts have been identified, most of which have yet to be functionally characterized. Along with the revelation that noncoding RNAs in the human genome are surprisingly abundant, there has been a surge in molecular and genetic data showing important and diverse regulatory roles for noncoding RNA. In this report, we summarize the potential roles that noncoding RNAs may play in the molecular pathogenesis of different mental retardation disorders. We suspect that these findings are just the tip of the iceberg, with noncoding RNAs possibly being involved in disease pathogenesis at different levels and through multiple distinct mechanisms.

Indexed as

Chromosomes, Human, Pair 22DiGeorge SyndromeGenome, HumanHumansIntellectual DisabilityMicroRNAsModels, BiologicalPrader-Willi SyndromeRNA, UntranslatedUbiquitin-Protein LigasesMicroRNAsRNA, UntranslatedUbiquitin-Protein Ligases

Identifiers

PMID19159391
PMCPMC3270373
OpenAlexW2104926998

What OpenQuestion 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 OpenQuestion graph.