Evidence map›Paper›PMID 19953286›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2010

BRD2 and TAP-1 genes and juvenile myoclonic epilepsy.

Samia Layouni, Catherine Buresi, Pierre Thomas, Alain Malafosse, Mohamed Dogui

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In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 27% 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, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Genetic and epigenetic mechanisms of epilepsy: a review.Neuropsychiatric disease and treatment · 2017
    Review
  6. Article
  7. Article
  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

5 authors at 4 institutions in 4 countries.

Samia LayouniLaboratoire de Physiologie, Faculté de Médecine de Monastir, Monastir, Tunisia.
Catherine Buresi
Pierre Thomas
Alain Malafosse
Mohamed Dogui
University of Monastir · TNBelorusneft (Belarus) · BYCentre Hospitalier Universitaire de Nice · FRHôpital Beau-Séjour · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Juvenile myoclonic epilepsy (JME) is a genetically determined common subtype of idiopathic generalized epilepsy. Linkage of JME to the chromosomal region 6p21.3 has been reported. An association has been previously observed between JME and the positional candidate, 6p21.3 linked, BRD2. Another candidate in this region is the TAP-1 gene encoding the Transporter Associated with Antigen Processing. The aim of the present study is to determine whether these two genes modulate the vulnerability to JME. While no difference was observed in the allele and genotype frequencies of BRD2 between JME and controls, an association was found between a TAP-1 haplotype and JME, suggesting that this gene may be another 6p21.3 linked vulnerability factor to JME.

Indexed as

Genetic Predisposition to DiseasePolymorphism, GeneticAdultATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily B, Member 2Bromodomain Containing ProteinsFemaleFranceGene FrequencyGenetic Association StudiesGenotypeHaplotypesHumansMaleMyoclonic Epilepsy, JuvenilePolymorphism, Single NucleotideATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily B, Member 2BRD2 protein, humanBromodomain Containing ProteinsProtein Serine-Threonine KinasesTAP1 protein, humanTranscription Factors

Identifiers

PMID19953286
OpenAlexW2019458028

What OpenQuestion holds

Textmetadata
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.