Evidence map›Paper›PMID 15931377›Full record

ReviewThe Journal of clinical investigation2005

Linkage disequilibrium maps and association mapping.

Newton E Morton

Abstract readReview
In one paragraph

Review in The Journal of clinical investigation, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–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

11 citing papers in PubMed.

  1. Genetic Variation and Haplotype Structure ofLife (Basel, Switzerland) · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Genotype matrix mapping: searching for quantitative trait loci interactions in genetic variation in complex traits.DNA research : an international journal for rapid publication of reports on genes and genomes · 2007
    Article
  7. Article
  8. Article
  9. Article
  10. Microarray technology in obstetrics and gynecology: a guide for clinicians.American journal of obstetrics and gynecology · 2006
    Review
  11. Mapping the new frontier: complex genetic disorders.The Journal of clinical investigation · 2005
    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

1 author.

Newton E MortonHuman Genetics Division, Southampton General Hospital, Southampton, United Kingdom. nem@soton.ac.uk

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The causal chain between a gene and its effect on disease susceptibility cannot be understood until the effect has been localized in the DNA sequence. Recently, polymorphisms incorporated in the HapMap Project have made linkage disequilibrium (LD) the most powerful tool for localization. The genetics of LD, the maps and databases that it provides, and their use for association mapping, as well as alternative methods for gene localization, are briefly described.

Indexed as

Genome, HumanLinkage DisequilibriumPhysical Chromosome MappingPolymorphism, Single NucleotideDatabases, GeneticGenetic Predisposition to DiseaseHumans

Identifiers

PMID15931377
PMCPMC1137007

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.