Literature DB >> 9433562

Modeling age of onset and residual familial correlations for the linkage analysis of bipolar disorder.

A H Schnell1, P M Karunaratne, J S Witte, D V Dawson, R C Elston.   

Abstract

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 correlations. 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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Year:  1997        PMID: 9433562     DOI: 10.1002/(SICI)1098-2272(1997)14:6<675::AID-GEPI21>3.0.CO;2-M

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  1 in total

1.  A genome-wide association study in American Indians implicates DNER as a susceptibility locus for type 2 diabetes.

Authors:  Robert L Hanson; Yunhua L Muller; Sayuko Kobes; Tingwei Guo; Li Bian; Victoria Ossowski; Kim Wiedrich; Jeffrey Sutherland; Christopher Wiedrich; Darin Mahkee; Ke Huang; Maryam Abdussamad; Michael Traurig; E Jennifer Weil; Robert G Nelson; Peter H Bennett; William C Knowler; Clifton Bogardus; Leslie J Baier
Journal:  Diabetes       Date:  2013-10-07       Impact factor: 9.461

  1 in total

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