We performed Haseman-Elston regression on a set of bipolar pedigrees using each of three dependent variables: a binary trait indicating disease concordance or discordance, a binary trait adjusted for age-of-onset, and the residuals from a survival analysis. The latter two methods, which both adjust
Modeling age of onset and residual familial correlations for the linkage analysis of bipolar disorder
โ Scribed by Audrey H. Schnell; P. Mahinda Karunaratne; John S. Witte; Deborah V. Dawson; Robert C. Elston
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 47 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0741-0395
No coin nor oath required. For personal study only.
โฆ Synopsis
We applied regressive modeling to the data described by Stine et al. [1995] and further explored the possible linkage of bipolar disorder to marker D18S41 on chromosome 18. We performed analyses to determine age-dependent penetrance functions that best fit the data and that allow for residual familial correlations. Specifically, we introduce here a simple method to allow for a sibling correlation that is not due to segregation at the linked locus, and then extend the results of Stine et al. [1995] by using the best fitting "regressive" model of this kind as input into a lod score linkage analysis. Although a formal segregation analysis was not attempted, a surprising finding was that, except for doubtful linkage to D18S41, there is little evidence for genetic transmission of bipolar disorder in these families.
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## Abstract A previously published modelโfree linkage analysis of chromosome 2q33โ35, highlighted by previous caseโcontrol studies and supported by withinโfamily analyses employing the transmission disequilibrium test, revealed evidence of sexโspecific linkage of the __CREB1__โcontaining region of