ArticleAmerican journal of human genetics1999
Further evidence for the increased power of LOD scores compared with nonparametric methods.
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 43 papers.
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Who cites it
43 citing papers in PubMed.
- A genome-wide scan points to a susceptibility locus for bipolar disorder on chromosome 12.Molecular psychiatry · 2005Trial
- A rare missense variant in RCL1 segregates with depression in extended families.Molecular psychiatry · 2018Article
- A Genome-Wide Linkage Study for Chronic Obstructive Pulmonary Disease in a Dutch Genetic Isolate Identifies Novel Rare Candidate Variants.Frontiers in genetics · 2018Article
- A genome-wide linkage study of individuals with high scores on NEO personality traits.Molecular psychiatry · 2012Article
- Computer simulation is an undervalued tool for genetic analysis: a historical view and presentation of SHIMSHON--a Web-based genetic simulation package.Human heredity · 2011Article
- Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results.Human genetics · 2009Article
- Genome-wide linkage screen in familial Parkinson disease identifies loci on chromosomes 3 and 18.American journal of human genetics · 2009Article
- Genome-wide parametric linkage analyses of 644 bipolar pedigrees suggest susceptibility loci at chromosomes 16 and 20.Psychiatric genetics · 2008Article
- Association of synapsin 2 with schizophrenia in families of Northern European ancestry.Schizophrenia research · 2007Article
- Performance comparison of two-point linkage methods using microsatellite markers flanking known disease locations.BMC genetics · 2005Article
- The importance of modelling heterogeneity in complex disease: application to NIMH Schizophrenia Genetics Initiative data.Human genetics · 2005Article
- A genome wide linkage study of obesity as secondary effect of antipsychotics in multigenerational families of eastern Quebec affected by psychoses.Molecular psychiatry · 2004Article
- Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.American journal of human genetics · 2004Article
- Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2.American journal of human genetics · 2004Article
- A major lung cancer susceptibility locus maps to chromosome 6q23-25.American journal of human genetics · 2004Article
- Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19.Molecular psychiatry · 2004Article
- Confirmation of chromosome 7q11 locus for predisposition to intracranial aneurysm.Human genetics · 2004Article
- Linkage of bipolar affective disorder on chromosome 8q24: follow-up and parametric analysis.Molecular psychiatry · 2004Article
- A genomewide scan for age-related macular degeneration provides evidence for linkage to several chromosomal regions.American journal of human genetics · 2003Article
- Linkage of schizophrenia with chromosome 1q loci in Taiwanese families.Molecular psychiatry · 2003Article
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3 authors.
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Abstract
In genetic analysis of diseases in which the underlying model is unknown, "model free" methods-such as affected sib pair (ASP) tests-are often preferred over LOD-score methods, although LOD-score methods under the correct or even approximately correct model are more powerful than ASP tests. However, there might be circumstances in which nonparametric methods will outperform LOD-score methods. Recently, Dizier et al. reported that, in some complex two-locus (2L) models, LOD-score methods with segregation analysis-derived parameters had less power to detect linkage than ASP tests. We investigated whether these particular models, in fact, represent a situation that ASP tests are more powerful than LOD scores. We simulated data according to the parameters specified by Dizier et al. and analyzed the data by using a (a) single locus (SL) LOD-score analysis performed twice, under a simple dominant and a recessive mode of inheritance (MOI), (b) ASP methods, and (c) nonparametric linkage (NPL) analysis. We show that SL analysis performed twice and corrected for the type I-error increase due to multiple testing yields almost as much linkage information as does an analysis under the correct 2L model and is more powerful than either the ASP method or the NPL method. We demonstrate that, even for complex genetic models, the most important condition for linkage analysis is that the assumed MOI at the disease locus being tested is approximately correct, not that the inheritance of the disease per se is correctly specified. In the analysis by Dizier et al., segregation analysis led to estimates of dominance parameters that were grossly misspecified for the locus tested in those models in which ASP tests appeared to be more powerful than LOD-score analyses.
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