Evidence map›Paper›PMID 12119603›Full record

ArticleAmerican journal of human genetics2002

A major susceptibility gene for asthma maps to chromosome 14q24.

Hakon Hakonarson, Unnur S Bjornsdottir, Eva Halapi, Snaebjorn Palsson, Elva Adalsteinsdottir, David Gislason, Gudmundur Finnbogason, Thorarinn Gislason, Kristleifur Kristjansson, Thor Arnason and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 4 pooled it
9.4field-weighted citation impact, top 1% 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

34 citing papers in PubMed, 4 syntheses or guidelines pooled it, 127 citations in OpenAlex.

  1. Pooled it
  2. A genome-wide association study on African-ancestry populations for asthma.The Journal of allergy and clinical immunology · 2010
    Pooled it
  3. Pooled it
  4. Pooled it
  5. Article
  6. Article
  7. Article
  8. Review
  9. Genetics of allergic diseases.Immunology and allergy clinics of North America · 2015
    Review
  10. An understanding of the genetic basis of asthma.The Indian journal of medical research · 2011
    Review
  11. Regulating the Regulators: microRNA and Asthma.The World Allergy Organization journal · 2011
    Article
  12. Genomewide association studies in allergy and the influence of ethnicity.Current opinion in allergy and clinical immunology · 2010
    Review
  13. Article
  14. Acute cobalt-induced lung injury and the role of hypoxia-inducible factor 1alpha in modulating inflammation.Toxicological sciences : an official journal of the Society of Toxicology · 2010
    Article
  15. Article
  16. Article
  17. Article
  18. Integrating genomic and clinical medicine: searching for susceptibility genes in complex lung diseases.Translational research : the journal of laboratory and clinical medicine · 2008
    Review
  19. Asthma from a pharmacogenomic point of view.British journal of pharmacology · 2008
    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

15 authors at 2 institutions in 1 country.

Hakon HakonarsondeCODE Genetics, Inc., Reykjavik, Iceland. hakonh@decode.is
Unnur S Bjornsdottir
Eva Halapi
Snaebjorn Palsson
Elva Adalsteinsdottir
David Gislason
Gudmundur Finnbogason
Thorarinn Gislason
Kristleifur Kristjansson
Thor Arnason
Illugi Birkisson
Michael L Frigge
Augustine Kong
Jeffrey R Gulcher
Kari Stefansson
deCODE Genetics (Iceland) · ISNational University Hospital of Iceland · IS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Asthma is a complex genetic disorder with a heterogeneous phenotype, largely attributed to the interactions among many genes and between these genes and the environment. Numerous loci and candidate genes have been reported to show linkage and association to asthma and atopy. Although some studies reporting these observations are compelling, no gene has been mapped that confers a sufficiently high risk of asthma to meet the stringent criteria for genomewide significance. Using 175 extended Icelandic families that included 596 patients with asthma, we performed a genomewide scan with 976 microsatellite markers. The families were identified by cross-matching a list of patients with asthma from the Department of Allergy/Pulmonary Medicine of the National University Hospital of Iceland with a genealogy database of the entire Icelandic nation. We detected linkage of asthma to chromosome 14q24, with an allele-sharing LOD score of 2.66. After we increased the marker density within the locus to an average of one microsatellite every 0.2 cM, the LOD score rose to 4.00. We designate this locus "asthma locus one" (AS1). Taken together, these results provide evidence of a novel susceptibility gene for asthma on chromosome 14q24.

Indexed as

Chromosome MappingGenetic Predisposition to DiseaseAllelesAsthmaChromosomes, Human, Pair 14Databases, FactualFemaleHumansIcelandLod ScoreMaleMicrosatellite RepeatsPedigreeRespiratory Function Tests

Identifiers

PMID12119603
PMCPMC379187
OpenAlexW2004725730

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.