Evidence map›Paper›PMID 12140746›Full record

ArticleGenes and immunity2002

A genome-wide screen for linkage in Nordic sib-pairs with multiple sclerosis.

E Akesson, A Oturai, J Berg, S Fredrikson, O Andersen, H F Harbo, M Laaksonen, K M Myhr, H I Nyland, L P Ryder and 8 more

Abstract read
PubMed Publisher
In one paragraph

Article in Genes and immunity, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. The genetic aspects of multiple sclerosis.Annals of Indian Academy of Neurology · 2009
    Article
  9. Review
  10. Article
  11. Article
  12. Gluten: a two-edged sword. Immunopathogenesis of celiac disease.Springer seminars in immunopathology · 2005
    Review
  13. A high-density screen for linkage in multiple sclerosis.American journal of human genetics · 2005
    Article
  14. Article
  15. A second-generation genomic screen for multiple sclerosis.American journal of human genetics · 2004
    Article
  16. Article
  17. Article
  18. Looking back and looking forward.Genes and immunity · 2003
    Article
  19. Article
  20. Genetic analysis of multiple sclerosis.Current neurology and neuroscience reports · 2002
    Review
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

18 authors.

E AkessonUniversity of Cambridge, Neurology unit, Addenbrooke's Hospital, UK. eva.akesson@neurotec.ki.se
A Oturai
J Berg
S Fredrikson
O Andersen
H F Harbo
M Laaksonen
K M Myhr
H I Nyland
L P Ryder
M Sandberg-Wollheim
P S Sorensen
A Spurkland
A Svejgaard
P Holmans
A Compston
J Hillert
S Sawcer

Funding

Medical Research Council G9810900
6 · The paper itself

Abstract

Genetic factors influence susceptibility to multiple sclerosis but the responsible genes remain largely undefined, association with MHC class II alleles being the only established genetic feature of the disease. The Nordic countries have a high prevalence of multiple sclerosis, and to further explore the genetic background of the disease, we have carried out a genome-wide screen for linkage in 136 sibling-pairs with multiple sclerosis from Denmark, Finland, Norway and Sweden by typing 399 microsatellite markers. Seventeen regions where the lod score exceeds the nominal 5% significance threshold (0.7) were identified-1q11-24, 2q24-32, 3p26.3, 3q21.1, 4q12, 6p25.3, 6p21-22, 6q21, 9q34.3, 10p15, 10p12-13, 11p15.5, 12q21.3, 16p13.3, 17q25.3, 22q12-13 and Xp22.3. Although none of these regions reaches the level of genome-wide significance, the number observed exceeds the 10 that would be expected by chance alone. Our results significantly add to the growing body of linkage data relating to multiple sclerosis.

Indexed as

Genetic LinkageDenmarkFemaleFinlandGenes, MHC Class IIGenetic MarkersGenome, HumanHLA-DR AntigensHLA-DR Serological SubtypesHumansLod ScoreMaleMultiple SclerosisNorwaySwedenGenetic MarkersHLA-DR15 antigenHLA-DR AntigensHLA-DR Serological Subtypes

Identifiers

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.