Evidence map›Paper›PMID 10330361›Full record

ArticleAmerican journal of human genetics1999

Linkage-disequilibrium mapping of disease genes by reconstruction of ancestral haplotypes in founder populations.

S K Service, D W Lang, N B Freimer, L A Sandkuijl

Open access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
9.1field-weighted citation impact, top 2% 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

33 citing papers in PubMed, 112 citations in OpenAlex.

  1. Article
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  9. Haplotype thinking in lung disease.Proceedings of the American Thoracic Society · 2007
    Review
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  17. Prospects for whole genome linkage disequilibrium mapping in domestic dog breeds.Mammalian genome : official journal of the International Mammalian Genome Society · 2003
    Article
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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

4 authors at 2 institutions in 2 countries.

S K ServiceNeurogenetics Laboratory and Center for Neurobiology and Psychiatry, Department of Psychiatry, University of California, San Francisco, CA 94143, USA. service@ngl.ucsf.edu
D W Lang
N B Freimer
L A Sandkuijl
University of California, San Francisco · USLeiden University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Linkage disequilibrium (LD) mapping may be a powerful means for genome screening to identify susceptibility loci for common diseases. A new statistical approach for detection of LD around a disease gene is presented here. This method compares the distribution of haplotypes in affected individuals versus that expected for individuals descended from a common ancestor who carried a mutation of the disease gene. Simulations demonstrate that this method, which we term "ancestral haplotype reconstruction" (AHR), should be powerful for genome screening of phenotypes characterized by a high degree of etiologic heterogeneity, even with currently available marker maps. AHR is best suited to application in isolated populations where affected individuals are relatively recently descended (< approximately 25 generations) from a common disease mutation-bearing founder.

Indexed as

Founder EffectHaplotypesLinkage DisequilibriumHumans

Identifiers

PMID10330361
PMCPMC1377917
OpenAlexW1967980922

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.