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J. Dupuis, P. Brown, D. Siegmund (1995)
Statistical methods for linkage analysis of complex traits from high-resolution maps of identity by descent.Genetics, 140 2
J. Blouin, B. Dombroski, S. Nath, V. Lasseter, P. Wolyniec, G. Nestadt, M. Thornquist, Gail Ullrich, J. Mcgrath, L. Kasch, M. Lamacz, M. Thomas, C. Gehrig, U. Radhakrishna, S. Snyder, Katherine Balk, K. Neufeld, K. Swartz, N. deMarchi, G. Papadimitriou, D. Dikeos, C. Stefanis, A. Chakravarti, B. Childs, D. Housman, H. Kazazian, S. Antonarakis, A. Pulver (1998)
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21Nature Genetics, 20
Y. Chiu, J. McGrath, M. Thornquist, P. Wolyniec, G. Nestadt, K. Swartz, V. Lasseter, K. Liang, A. Pulver (2002)
Genetic heterogeneity in schizophrenia II: conditional analyses of affected schizophrenia sibling pairs provide evidence for an interaction between markers on chromosome 8p and 14qMolecular Psychiatry, 7
Dupuis (1995)
843Genet, 140
E. Lander, D. Botstein (1986)
Strategies for studying heterogeneous genetic traits in humans by using a linkage map of restriction fragment length polymorphisms.Proceedings of the National Academy of Sciences of the United States of America, 83 19
L. Kruglyak, M. Daly, Mary Reeve-Daly, E. Lander (1996)
Parametric and nonparametric linkage analysis: a unified multipoint approach.American journal of human genetics, 58 6
Cordell (1995)
920Am J Hum Genet, 57
A. Kong, A. Kong, N. Cox (1997)
Allele-sharing models: LOD scores and accurate linkage tests.American journal of human genetics, 61 5
Shork (1993)
1127Am J Hum Genet, 53
H. Cordell, J. Todd, Stephen Bennett, Y. Kawaguchi, M. Farrall (1995)
Two-locus maximum lod score analysis of a multifactorial trait: joint consideration of IDDM2 and IDDM4 with IDDM1 in type 1 diabetes.American journal of human genetics, 57 4
Hsiu-Khuern Tang, D. Siegmund (2002)
Mapping multiple genes for quantitative or complex traitsGenetic Epidemiology, 22
K. Liang, Y. Chiu, T. Beaty, M. Wjst (2001)
Multipoint analysis using affected sib pairs: Incorporating linkage evidence from unlinked regionsGenetic Epidemiology, 21
N. Risch (1990)
Linkage strategies for genetically complex traits. I. Multilocus models.American journal of human genetics, 46 2
H. Cordell, Geoffrey Wedig, K. Jacobs, R. Elston (2000)
Multilocus linkage tests based on affected relative pairs.American journal of human genetics, 66 4
K. Liang, S. Zeger (1986)
Longitudinal data analysis using generalized linear modelsBiometrika, 73
N. Risch (1990)
Linkage strategies for genetically complex traits. II. The power of affected relative pairs.American journal of human genetics, 46 2
Risch (1990)
222Am J Hum Genet, 46
N. Cox, M. Frigge, D. Nicolae, P. Concannon, C. Hanis, G. Bell, A. Kong (1999)
Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican AmericansNature Genetics, 21
K. Liang, Y. Chiu, T. Beaty (2000)
A Robust Identity-by-Descent Procedure Using Affected Sib Pairs: Multipoint Mapping for Complex DiseasesHuman Heredity, 51
N. Schork, M. Boehnke, J. Terwilliger, J. Ott (1993)
Two-trait-locus linkage analysis: a powerful strategy for mapping complex genetic traits.American journal of human genetics, 53 5
M. Baron (2001)
Genetics of schizophrenia and the new millennium: progress and pitfalls.American journal of human genetics, 68 2
A. Pulver, Jennifer Mulle, G. Nestadt, Karen Swartz, Jean-Louis Blouin, Beth Dombroski, K. Liang, D. Housman, H. Kazazian, S. Antonarakis, V. Lasseter, P. Wolyniec, M. Thornquist, J. McGrath (2000)
Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypesMolecular Psychiatry, 5
Kruglyak (1996)
1347Am J Hum Genet, 58
M. Farrall (1997)
Affected sibpair linkage tests for multiple linked susceptibility genesGenetic Epidemiology, 14
Recently, Liang et al. ((2001b) Genet. Epidemiol. 21:105–122) proposed a conditional approach to assess linkage evidence on the target region by incorporating linkage information from an unlinked (reference) region using allele shared IBD (identity‐by‐decent) from affected sib pairs. This is carried out by conditioning on the IBD sharing value at the estimated trait locus of the reference region. Since markers considered are typically non‐fully informative, the IBD sharing at each marker needs to be estimated (or imputed). In this report, we propose an alternative approach to deal with the IBD sharing in the reference region. This new approach makes full use of the observed data without having to categorize the imputed IBD sharing as needed in Liang et al. ((2001b) Genet. Epidemiol. 21:105–122). We compare these two approaches by simulating data from a variety of two‐locus models including heterogeneity, additive and multiplicative with either fully informative markers or non‐fully informative markers. The performance of both approaches is quite comparable showing consistent estimates of the trait locus and key genetic parameters. Genet Epidemiol 26:108–115, 2004. © 2004 Wiley‐Liss, Inc.
Genetic Epidemiology – Wiley
Published: Feb 1, 2004
Keywords: identity by descent; two‐locus models; affected sib pairs; conditional analysis
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