Entropy-based SNP selection for genetic association studies

[1]  R. Trembath,et al.  Family-based analysis using a dense single-nucleotide polymorphism-based map defines genetic variation at PSORS1, the major psoriasis-susceptibility locus. , 2002, American journal of human genetics.

[2]  M. Waterman,et al.  A dynamic programming algorithm for haplotype block partitioning , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[3]  Fengzhu Sun,et al.  Haplotype block structure and its applications to association studies: power and study designs. , 2002, American journal of human genetics.

[4]  S. P. Fodor,et al.  Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21 , 2001, Science.

[5]  K. Huse,et al.  Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations , 2003, European Journal of Human Genetics.

[6]  L Kruglyak,et al.  Parametric and nonparametric linkage analysis: a unified multipoint approach. , 1996, American journal of human genetics.

[7]  S. Gabriel,et al.  The Structure of Haplotype Blocks in the Human Genome , 2002, Science.

[8]  J. Schmidtke,et al.  Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families , 1988, Human Genetics.

[9]  M. Boehnke,et al.  Experimentally-derived haplotypes substantially increase the efficiency of linkage disequilibrium studies , 2001, Nature Genetics.

[10]  Daniel J Schaid,et al.  Relative efficiency of ambiguous vs. directly measured haplotype frequencies , 2002, Genetic epidemiology.

[11]  J. Pritchard,et al.  The allelic architecture of human disease genes: common disease-common variant...or not? , 2002, Human molecular genetics.

[12]  J. Nurnberger,et al.  A non-organic and non-enzymatic extraction method gives higher yields of genomic DNA from whole-blood samples than do nine other methods tested. , 1992, Journal of biochemical and biophysical methods.

[13]  M. Daly,et al.  High-resolution haplotype structure in the human genome , 2001, Nature Genetics.

[14]  Pardis C Sabeti,et al.  Detecting recent positive selection in the human genome from haplotype structure , 2002, Nature.

[15]  Frank Dudbridge,et al.  Haplotype tagging for the identification of common disease genes , 2001, Nature Genetics.

[16]  Charles F. Hockett,et al.  A mathematical theory of communication , 1948, MOCO.

[17]  Michael Knapp,et al.  Efficiency of Haplotype Frequency Estimation when Nuclear Familiy Information Is Included , 2002, Human Heredity.

[18]  N. Katsanis,et al.  Human genetics and disease: Beyond Mendel: an evolving view of human genetic disease transmission , 2002, Nature Reviews Genetics.

[19]  P. McKeigue.  Efficiency of estimation of haplotype frequencies: use of marker phenotypes of unrelated individuals versus counting of phase-known gametes. , 2000, American journal of human genetics.

[20]  N Risch,et al.  The Future of Genetic Studies of Complex Human Diseases , 1996, Science.

[21]  Sinead B. O'Leary,et al.  Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease , 2001, Nature Genetics.

[22]  N. Morton,et al.  The optimal measure of allelic association , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[23]  E. Génin.  Selection of Single Nucleotide Polymorphisms for Association Studies in Candidate Genes , 2001, Genetic epidemiology.