| Stuart Brown with John Hay and Harry Ostrer |
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| Emerging strategies and applications of pharmacogenomics |
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| Robustness of the inference of human population structure: A comparison of X-chromosomal and autosomal microsatellites |
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| Editorial |
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| Chromosomal phenotypes and submicroscopic abnormalities |
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| Genome-wide analysis of the human Alu Yb-lineage |
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| Characterisation of SNP haplotype structure in chemokine and chemokine receptor genes using CEPH pedigrees and statistical estimation |
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| Single nucleotide polymorphism genotyping by two colour melting curve analysis using the MGB Eclipse™ Probe System in challenging sequence environment |
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| Editorial |
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| A survey of current Bayesian gene mapping method |
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| Christoph W. Sensen (Editor) |
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| 'Frankenstein genes', or the Mad Magazineversion of the human pseudogenome |
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| Design and Analysis of DNA Microarray Investigations: R. M. Simon, E. L. Korn, L. M. McShane, M. D. Radmacher, G. W. Wright, Y. Zhao, Springer-Verlag, New York, NY, USA; 2004; |
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| Whole genome DNA copy number changes identified by high density oligonucleotide arrays |
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| Analysis of the glutathione S-transferase (GST) gene family |
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| Distribution of genome-wide linkage disequilibrium based on microsatellite loci in the Samoan population |
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| The genomic distribution of population substructure in four populations using 8,525 autosomal SNPs |
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| Cytochrome P450 humanised mice |
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| The truth about mouse, human, worms and yeast |
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| Human pharmacogenomics: The development of a science |
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| Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels |
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| Cyclophilin nomenclature problems, or, 'a visit from the sequence police' |
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| Pharmacogenetics of lipid diseases |
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| Development of an integrated genome informatics, data management and workflow infrastructure: A toolbox for the study of complex disease genetics |
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| A survey of current software for genetic power calculations |
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| Editorial |
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| The extent and importance of intragenic recombination |
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| Population genetic analysis of ascertained SNP data |
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| Demographic estimates from Y chromosome microsatellite polymorphisms: Analysis of a worldwide sample |
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| A survey of current software for haplotype phase inference |
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| A genome-wide survey of segmental duplications that mediate common human genetic variation of chromosomal architecture |
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| Comparison of regional gene expression differences in the brains of the domestic dog and human |
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| Editorial |
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| Computational Biology: Unix/Linux, Data Processing and Programming |
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| The impact of sample size and marker selection on the study of haplotype structures |
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| Editorial |
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| Haplotype structure and linkage disequilibrium in chemokine and chemokine receptor genes |
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| Update on genome completion and annotations: Protein Information Resource |
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| Expression profiling of cardiovascular disease |
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| Geographic stratification of linkage disequilibrium: a worldwide population study in a region of chromosome 22 |
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| A review of the 'Statistical Analysis for Genetic Epidemiology' (SAGE) software package |
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| Genomic and proteomic approaches for studying human cancer: Prospects for true patient-tailored therapy |
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| Further statistical analysis for genome-wide expression evolution in primate brain/liver/fibroblast tissue |
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