Evidence map›Paper›PMID 16451657›Full record

ArticleBMC genetics2005

Modeling the effect of an associated single-nucleotide polymorphism in linkage studies.

Jeanine J Houwing-Duistermaat, Hae-Won Uh, Jeremie J P Lebrec, Hein Putter, Li Hsu

Abstract read
In one paragraph

Article in BMC genetics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. 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

5 authors.

Jeanine J Houwing-DuistermaatDepartment of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, The Netherlands. j.j.houwing@lumc.nl
Hae-Won Uh
Jeremie J P Lebrec
Hein Putter
Li Hsu

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For linkage analysis in affected sibling pairs, we propose a regression model to incorporate information from a disease-associated single-nucleotide polymorphism located under the linkage peak. This model can be used to study if the associated single-nucleotide polymorphism marker partly explains the original linkage peak. Two sources of information are used for performing this task, namely the genotypes of the parents and the genotypes of the siblings. We applied the methods to three significantly disease-associated single-nucleotide polymorphisms and five microsatellite markers at the end of chromosome 3 of replicate 1 of Aipotu population. Two out of five of the microsatellite markers showed a LOD score higher than 3. The question to be answered was whether one of the single-nucleotide polymorphisms partly explains these high LOD scores. We did not have the answers when we analyzed the data.

Indexed as

Genetic LinkageGenetic Predisposition to DiseaseModels, GeneticChromosomes, Human, Pair 3HumansLod ScoreMicrosatellite RepeatsPolymorphism, Single Nucleotide

Identifiers

PMID16451657
PMCPMC1866738

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Registered trials

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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.