Intracranial Aneurysms in Finnish Families: Confirmation of Linkage and Refinement of the Interval to Chromosome 19q13.3  Monique van der Voet, Jane M.

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Intracranial Aneurysms in Finnish Families: Confirmation of Linkage and Refinement of the Interval to Chromosome 19q13.3  Monique van der Voet, Jane M. Olson, Helena Kuivaniemi, Doreen M. Dudek, Magdalena Skunca, Antti Ronkainen, Mika Niemelä, Juha Jääskeläinen, Juha Hernesniemi, Katariina Helin, Eira Leinonen, Moumita Biswas, Gerard Tromp  The American Journal of Human Genetics  Volume 74, Issue 3, Pages 564-571 (March 2004) DOI: 10.1086/382285 Copyright © 2004 The American Society of Human Genetics Terms and Conditions

Figure 1 Multipoint LOD score analyses for chromosome 19. A, One-parameter baseline linkage analysis that allows for the inclusion of covariates. Note that the mode of inheritance is not optimal, which resulted in a decrease of LOD scores compared with the two-parameter baseline (table 2). B, One-parameter linkage analysis with Naff as a covariate. The covariate significantly increased the LOD scores, which reached maximum values at 70 cM (LOD score 5.70) and at 80 cM (LOD score 3.99). The horizontal bars below each plot indicate the GENEFINDER (Department of Biostatistics Web site, Johns Hopkins University) 95% CIs (table 5) for the recessive (R), dominant (D), and partial-penetrance (P) models, respectively. The American Journal of Human Genetics 2004 74, 564-571DOI: (10.1086/382285) Copyright © 2004 The American Society of Human Genetics Terms and Conditions

Figure 2 Model-based multipoint LOD score for chromosome 19. The plot shows the results from a recessive model, with disease allele frequency of 0.01, disease penetrance of 0.3, and a phenocopy penetrance of 0.01. Note that the solid line (all families) and the dashed line (families with more than two affected individuals) very nearly overlap; therefore, the dashed line is visible only in a few places. The American Journal of Human Genetics 2004 74, 564-571DOI: (10.1086/382285) Copyright © 2004 The American Society of Human Genetics Terms and Conditions