Evidence map›Paper›PMID 30275311›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Early adolescent Rai1 reactivation reverses transcriptional and social interaction deficits in a mouse model of Smith-Magenis syndrome.

Wei-Hsiang Huang, David C Wang, William E Allen, Matthew Klope, Hailan Hu, Mehrdad Shamloo, Liqun Luo

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
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  6. Article
  7. Review
  8. Article
  9. Critical periods and Autism Spectrum Disorders, a role for sleep.Neurobiology of sleep and circadian rhythms · 2023
    Article
  10. Loss ofProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Review
  12. Development of prefrontal cortex.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Review
  13. Article
  14. Article
  15. Lysergic acid diethylamide (LSD) promotes social behavior through mTORC1 in the excitatory neurotransmission.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. Article
  17. Review
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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

7 authors at 3 institutions in 2 countries.

Wei-Hsiang HuangHoward Hughes Medical Institute, Stanford University, Stanford, CA 94305; weihsiah@stanford.edu lluo@stanford.edu.
David C WangHoward Hughes Medical Institute, Stanford University, Stanford, CA 94305.
William E AllenHoward Hughes Medical Institute, Stanford University, Stanford, CA 94305.
Matthew KlopeStanford Behavioral and Functional Neuroscience Laboratory, Stanford University School of Medicine, Stanford, CA 94305.
Hailan HuInterdisciplinary Institute of Neuroscience and Technology, Zhejiang University, 310012 Hangzhou, People's Republic of China.ORCID 0000-0002-0425-5057
Mehrdad ShamlooStanford Behavioral and Functional Neuroscience Laboratory, Stanford University School of Medicine, Stanford, CA 94305.
Liqun LuoHoward Hughes Medical Institute, Stanford University, Stanford, CA 94305; weihsiah@stanford.edu lluo@stanford.edu.ORCID 0000-0001-5467-9264
Howard Hughes Medical Institute · USStanford University · USZhejiang University · CN

Funding

The Neural Functions of Rai1, the Causal Gene for Smith-Magenis SyndromeK99HD092545 · NICHD · STANFORD UNIVERSITY · PI HUANG, WEI-HSIANG · 2017 to 2018
$202k
NICHD NIH HHS K99 HD092545
6 · The paper itself

Abstract

Haploinsufficiency of

Indexed as

Disease Models, AnimalHaploinsufficiencyInterpersonal RelationsAdolescentAnimalsDendritic SpinesHeterozygoteHumansMaleMiceMutationPhenotypeSmith-Magenis SyndromeSocial Behavior DisordersTrans-ActivatorsRai1 protein, mouseTrans-Activatorsautism spectrum disorderschromatincopy number variationSmith–Magenis syndromesocial behavior

Identifiers

PMID30275311
PMCPMC6196530
OpenAlexW2895485733

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.