Evidence map›Paper›PMID 34573249›Full record

ArticleBrain sciences2021

Sleep Abnormalities in the Synaptopathies-

Constance Smith-Hicks, Damien Wright, Aisling Kenny, Robert C Stowe, Maria McCormack, Andrew C Stanfield, J Lloyd Holder

Open access · goldAbstract read
In one paragraph

Article in Brain sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
6.9field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 46 citations in OpenAlex.

  1. Effects of ganaxolone on non-seizure outcomes in CDKL5 Deficiency Disorder: Double-blind placebo-controlled randomized trial.European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society · 2024
    Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Subjective sleep assessment in individuals withJournal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Context-dependent hyperactivity inFrontiers in molecular neuroscience · 2024
    Article
  12. Developmental outcome of electroencephalographic findings inFrontiers in cell and developmental biology · 2024
    Article
  13. Adult Phenotype ofNeurology. Genetics · 2023
    Article
  14. Article
  15. Mouse models ofProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  16. Updated consensus guidelines on the management of Phelan-McDermid syndrome.American journal of medical genetics. Part A · 2023
    Review
  17. Article
  18. Mouse models ofbioRxiv : the preprint server for biology · 2023
    Article
  19. Review
  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 5 institutions in 2 countries.

Constance Smith-HicksDivision of Neurogenetics Kennedy Krieger Institute, 1741 Ashland Avenue Rm 526, Baltimore, MD 21205, USA.
Damien WrightPatrick Wild Centre, University of Edinburgh, Edinburgh EH8 9YL, UK.
Aisling KennyPatrick Wild Centre, University of Edinburgh, Edinburgh EH8 9YL, UK.
Robert C StoweDepartment of Neurology, Division of Epilepsy and Clinical Neurophysiology, Boston Children's Hospital, Boston, MA 02115, USA.
Maria McCormackJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital 1250 Moursund, Suite 925, Houston, TX 77030, USA.
Andrew C StanfieldPatrick Wild Centre, University of Edinburgh, Edinburgh EH8 9YL, UK.
J Lloyd HolderJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital 1250 Moursund, Suite 925, Houston, TX 77030, USA.
University of Edinburgh · GBAshland (United States) · USBaylor College of Medicine · USHarvard University · USTexas Children's Hospital · US

Funding

Bridge the Gap: SYNGAP1 Education and Research Foundation Center of Excellence
6 · The paper itself

Abstract

Neurodevelopmental disorders are frequently associated with sleep disturbances. One class of neurodevelopmental disorders, the genetic synaptopathies, is caused by mutations in genes encoding proteins found at the synapse. Mutations in these genes cause derangement of synapse development and function. We utilized a validated sleep instrument, Children's Sleep Habits Questionnaire (CSHQ) to examine the nature of sleep abnormalities occurring in individuals with two synaptopathies-Phelan-McDermid syndrome (PMD) (N = 47, male = 23, female = 24, age 1-46 years) and

Indexed as

Children’s Sleep Habits QuestionnairePhelan–Mcdermid syndromepolysomnographySYNGAP1

Identifiers

PMID34573249
PMCPMC8472329
OpenAlexW3200631480

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.