Evidence map›Paper›PMID 12644967›Full record

ArticleAmerican journal of human genetics2003

Genetic linkage analysis of a dichotomous trait incorporating a tightly linked quantitative trait in affected sib pairs.

Jian Huang, Yanming Jiang

2 registry-linked trialsAbstract read
In one paragraph

Article in American journal of human genetics, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this 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.

NCT00005387 completednot on this map

Genetics of Hypertension in Blacks

TypeobservationalSponsorNational Heart, Lung, and Blood Institute (NHLBI)Ran1995 to 2008ConditionsCardiovascular Diseases, Heart Diseases, Hypertension
NCT00037271 completednot on this map

Genome Scan for Obesity in a Multi-Ethnic Sample

TypeobservationalSponsorNational Heart, Lung, and Blood Institute (NHLBI)Ran2001 to 2003ConditionsCardiovascular Diseases, Heart Diseases, Obesity
3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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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.

Jian HuangDepartment of Statistics and Actuarial Science, Division of Statistical Genetics, University of Iowa, Iowa City, IA 52242, USA. jian-huang@uiowa.edu
Yanming Jiang

Funding

GENETICS OF HYPERTENSION IN BLACKSR01HL053353 · NHLBI · LOYOLA UNIVERSITY CHICAGO · PI COOPER, RICHARD STANLEY · 1995 to 2013
$8.3M
STATISTICAL MODELS OF GENETIC ANTICIPATION IN PSYCHIATRYK01MH001541 · NIMH · UNIVERSITY OF IOWA · PI HUANG, JIAN · 1998 to 2002
$350k
Genome Scan for Obesity in a Multi-Ethnic SampleR03HL065702 · NHLBI · LOYOLA UNIVERSITY CHICAGO · PI ZHU, XIAOFENG · 2001 to 2002
$148k
NHLBI NIH HHS HL53353NHLBI NIH HHS HL65702NHLBI NIH HHS R01 HL053353NIMH NIH HHS K01-MH01541NIMH NIH HHS R01-MH52481
6 · The paper itself

Abstract

Many complex diseases are usually considered as dichotomous traits but are also associated with quantitative biological markers or quantitative risk factors. For such dichotomous traits, although their associated quantitative traits may not directly underly the diagnosis of the disease status, if the associated quantitative trait is also linked to the chromosomal regions linked to the dichotomous trait, then joint analysis of dichotomous and quantitative traits should be more efficient than consideration of them separately. Previous studies have focused on the situation when a dichotomous trait can be modeled by a threshold process acting on a single underlying normal liability distribution. However, for many complex disorders, including most psychiatric disorders, diagnosis is generally based on a set of binary or discrete criteria. These traits cannot be modeled on the basis of a threshold process acting on an underlying continuous trait. We propose a likelihood-based method that efficiently combines such a discrete trait and an associated quantitative trait in the analysis, using affected-sib-pair data. Our simulation studies suggest that joint analysis increases the power to detect linkage of dichotomous traits. We also apply the proposed new method to an asthma genome-scan data set and incorporate the total serum immunoglobulin E level in the analysis.

Indexed as

Models, GeneticQuantitative Trait LociAsthmaChromosome MappingChromosomes, HumanHumansImmunoglobulin ELikelihood FunctionsModels, StatisticalReproducibility of ResultsSiblingsImmunoglobulin E

Identifiers

PMID12644967
PMCPMC1180357

What OpenQuestion holds

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Registered trials

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.