Evidence map›Paper›PMID 22377486›Full record

ReviewEuropean journal of medical genetics2012

Seizures and X-linked intellectual disability.

Roger E Stevenson, Kenton R Holden, R Curtis Rogers, Charles E Schwartz

Open access · greenAbstract readReview
In one paragraph

Review in European journal of medical genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Emerging roles for E3 ubiquitin ligases in neural development and disease.Frontiers in cell and developmental biology · 2025
    Review
  2. X-Linked Epilepsies: A Narrative Review.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Epilepsy, cognitive deficits and neuroanatomy in males with ZDHHC9 mutations.Annals of clinical and translational neurology · 2015
    Article
  5. 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

4 authors at 1 institution in 1 country.

Roger E StevensonGreenwood Genetic Center, 106 Gregor Mendel Circle, Greenwood, SC 29646, USA. res@ggc.org
Kenton R Holden
R Curtis Rogers
Charles E Schwartz
Greenwood Genetic Center · US

Funding

X-LINKED MENTAL RETARDATION: LINKAGE &CLINICAL STUDIESR01HD026202 · NICHD · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI SCHWARTZ, CHARLES E · 1990 to 2006
$7.9M
INFRASTRUCTURE FOR RESEARCH ON MENTAL DISABILITIESR24MH057840 · NIMH · GREENWOOD GENETIC CENTER · PI STEVENSON, ROGER EUGENE · 1999 to 2003
$1.4M
Identification of Novel X-linked Intellectual Disability GenesR01NS073854 · NINDS · GREENWOOD GENETIC CENTER · PI SCHWARTZ, CHARLES E, WANG, TAO · 2011 to 2013
$1.4M
NICHD NIH HHS R01 HD026202NIMH NIH HHS R24 MH057840NINDS NIH HHS R01 NS073854
6 · The paper itself

Abstract

Intellectual disability occurs as an isolated X-linked trait and as a component of recognizable X-linked syndromes in the company of somatic, metabolic, neuromuscular, or behavioral abnormalities. Seizures accompany intellectual disability in almost half of these X-linked disorders. The spectrum of seizures found in the X-linked intellectual disability syndromes is broad, varying in time of onset, type of seizure, and response to anticonvulsant therapy. The majority of the genes associated with XLID and seizures have now been identified.

Indexed as

Abnormalities, MultipleBrainEpilepsyHumansMetabolism, Inborn ErrorsPhenotypeSyndromeX-Linked Intellectual Disability

Identifiers

PMID22377486
PMCPMC3531238
OpenAlexW2021050524

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.