Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix

[1]  David B Allison,et al.  "Are we there yet?": Deciding when one has demonstrated specific genetic causation in complex diseases and quantitative traits. , 2003, American journal of human genetics.

[2]  Y. Benjamini,et al.  THE CONTROL OF THE FALSE DISCOVERY RATE IN MULTIPLE TESTING UNDER DEPENDENCY , 2001 .

[3]  J. Ott,et al.  Mathematical multi-locus approaches to localizing complex human trait genes , 2003, Nature Reviews Genetics.

[4]  W. G. Hill,et al.  Linkage disequilibrium in finite populations , 1968, Theoretical and Applied Genetics.

[5]  Yanbin Jia,et al.  Association study of an SNP combination pattern in the dopaminergic pathway in paranoid schizophrenia: a novel strategy for complex disorders , 2004, Molecular Psychiatry.

[6]  Y. Benjamini,et al.  A step-down multiple hypotheses testing procedure that controls the false discovery rate under independence , 1999 .

[7]  C. Sing,et al.  A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variation. , 2001, Genome research.

[8]  V M Chinchilli,et al.  A generalized concordance correlation coefficient for continuous and categorical data , 2001, Statistics in medicine.

[9]  Z. Šidák.  Rectangular Confidence Regions for the Means of Multivariate Normal Distributions , 1967 .

[10]  M Farrall,et al.  Measured haplotype analysis of the angiotensin-I converting enzyme gene. , 1998, Human molecular genetics.

[11]  D. Nyholt.  A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other. , 2004, American journal of human genetics.

[12]  Harry Joe,et al.  A remark on algorithm 643: FEXACT: an algorithm for performing Fisher's exact test in r x c contingency tables , 1993, TOMS.

[13]  Thomas M. Cover,et al.  Elements of Information Theory , 2005 .

[14]  John D. Storey.  A direct approach to false discovery rates , 2002 .

[15]  J. Cheverud,et al.  A simple correction for multiple comparisons in interval mapping genome scans , 2001, Heredity.

[16]  E. Lander,et al.  Mapping mendelian factors underlying quantitative traits using RFLP linkage maps. , 1989, Genetics.

[17]  H. Piepho.  A quick method for computing approximate thresholds for quantitative trait loci detection. , 2001, Genetics.

[18]  Jason H. Moore,et al.  Power of multifactor dimensionality reduction for detecting gene‐gene interactions in the presence of genotyping error, missing data, phenocopy, and genetic heterogeneity , 2003, Genetic epidemiology.

[19]  E. Lander,et al.  Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results , 1995, Nature Genetics.

[20]  J. Cheverud,et al.  Genetic architecture of adiposity in the cross of LG/J and SM/J inbred mice , 2001, Mammalian Genome.

[21]  J. H. Moore,et al.  Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer. , 2001, American journal of human genetics.

[22]  R. Doerge,et al.  Empirical threshold values for quantitative trait mapping. , 1994, Genetics.

[23]  W. G. Cochran.  Some Methods for Strengthening the Common χ 2 Tests , 1954 .

[24]  D. Clayton,et al.  A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes. , 2002, American journal of human genetics.

[25]  J. Ott,et al.  Trimming, weighting, and grouping SNPs in human case-control association studies. , 2001, Genome research.

[26]  John D. Storey,et al.  Statistical significance for genomewide studies , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[27]  Heping Zhang,et al.  Use of classification trees for association studies , 2000, Genetic epidemiology.

[28]  Y. Benjamini,et al.  Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .