Evidence map›Paper›PMID 16943798›Full record

ArticleGenes and immunity2006

A family-based study does not confirm the association of MYO9B with celiac disease in the Italian population.

M Giordano, C Marano, M Mellai, M G Limongelli, E Bolognesi, F Clerget-Darpoux, P Momigliano-Richiardi, L Greco

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Genes and immunity, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

2 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. MYO9B polymorphisms in multiple sclerosis.European journal of human genetics : EJHG · 2009
    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

8 authors at 3 institutions in 2 countries.

M GiordanoDepartment of Medical Sciences, University of Eastern Piedmont and Interdisciplinary Research Center for Autoimmune Diseases (IRCAD), Novara, Italy. giordano@med.unipmn.it
C Marano
M Mellai
M G Limongelli
E Bolognesi
F Clerget-Darpoux
P Momigliano-Richiardi
L Greco
Università degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITUniversity of Naples Federico II · ITInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Association between Myosin IXB (MYO9B) gene polymorphisms and celiac disease (CD) was recently detected by a case-control association study in the Dutch, but not confirmed in the British and Swedish/Norwegian populations. We tested the association between CD and the three most associated single nucleotide polymorphisms (SNPs) in the Dutch study by the transmission disequilibrium test in the Italian population. A total of 252 pediatric patients and 504 parents were genotyped. No transmission distortion was detected either for the single SNPs or for their haplotypic combinations. Control allele frequencies, calculated from untransmitted alleles, were significantly different from those of the Dutch control population. Conversely, allele frequencies were very similar in Italian, British, Swedish/Norwegian and Dutch patients. In conclusion, MYO9B is not involved in CD susceptibility in the Italian population. The difference with the Dutch result might be explained by an imperfect selection of the Dutch controls.

Indexed as

AdultAllelesCase-Control StudiesCeliac DiseaseChildFamilyFemaleGene FrequencyHumansItalyLinkage DisequilibriumMaleMyosinsNetherlandsPolymorphism, Single Nucleotidemyosin IXBMyosins

Identifiers

PMID16943798
OpenAlexW2027458061

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.