Evidence map›Paper›PMID 17898537›Full record

ArticleHuman heredity2008

Haseman-Elston regression in ascertained samples: importance of dependent variable and mean correction factor selection.

Ritwik Sinha, Courtney Gray-McGuire

Abstract read
In one paragraph

Article in Human heredity, 2008. 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

2 authors.

Ritwik SinhaCase Western Reserve University, Cleveland, Ohio 44106-7281, USA.
Courtney Gray-McGuire

Funding

X-LINKED EXTENSION OF THE REVISED HASEMAN-ELSTON ALGORITHM FOR LINKAGE ANALYSISP41RR003655 · NCRR · LOUISIANA STATE UNIV HSC NEW ORLEANS · PI ELSTON, ROBERT C. · 1987 to 2011
$11.5M
NCRR NIH HHS P41 RR003655NCRR NIH HHS RR03655
6 · The paper itself

Abstract

objectiveOne of the first tools for performing linkage analysis, Haseman-Elston regression (HE), has been successfully used to identify linkages to several disease traits. A recent explosion in extensions of HE leaves one faced with the task of choosing a flavor of HE best suited for a given situation. This paper puts this dilemma into perspective and proposes a modification to HE for highly ascertained samples (BLUP-PM).

methodsUsing data simulated for a range of models, we evaluated type I error and power of several dependent variables in HE, including the novel BLUP-PM.

resultsWhen analyzing a continuous trait, even in highly ascertained samples, type I error is stable and approximately nominal across dependent variables. When analyzing binary traits in highly ascertained samples, type I error is elevated and unstable for all except BLUP-PM. Regardless of trait type, the optimally weighted HE regression and BLUP-PM have the greatest power.

conclusionsAscertained samples do not always reflect the population from which they are drawn and therefore choice of dependent variable in HE becomes increasingly important. Our results do not reveal a single, universal choice, but offer criteria by which to choose and demonstrate BLUP-PM performs well in most situations.

Indexed as

Models, GeneticFamilyFemaleHumansMaleRegression AnalysisReproducibility of ResultsSelection, GeneticSiblings

Identifiers

PMID17898537
PMCPMC2857627

What OpenQuestion holds

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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.