| Current software for genotype imputation |
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| Identifying positive selection candidate loci for high-altitude adaptation in Andean populations |
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| Editorial |
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| Protein-protein interaction databases: keeping up with growing interactomes |
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| Aldo-keto reductase (AKR) superfamily: Genomics and annotation |
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| Genomics software: The view from 10,000 feet |
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| Orientation, distance, regulation and function of neighbouring genes |
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| Exploring the relationship between polymorphic (TG/CA) n repeats in intron 1 regions and gene expression |
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| The mammalian aldehyde oxidase gene family |
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| Association of ADHIB and ALDH2gene polymorphisms with alcohol dependence: A pilot study from India |
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| The Cytochrome P450 Homepage |
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| The tiny world of microRNAs in the cross hairs of the mammalian eye |
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| LIPE C-60G influences the effects of physical activity on body fat and plasma lipid concentrations: the Quebec Family Study |
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| Editorial |
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| Collection of variation causing disease - The Human Variome Project |
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| Neuroscience of birdsong |
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| Given the complexity of the human genome, can 'personalised medicine' or 'individualised drug therapy' ever be achieved? |
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| Identification of a novel cytosolic aldehyde dehydrogenase allele, ALDHIAI*4 |
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| Novel variants of major drug-metabolising enzyme genes in diverse African populations and their predicted functional effects |
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| Analysis and update of the human solute carrier (SLC) gene superfamily |
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| R and Bioconductor solutions for alternative splicing detection |
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| Book Reviews |
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| Alleles of alcohol and acetaldehyde metabolism genes modulate susceptibility to oesophageal cancer from alcohol consumption |
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| Recommendations for using standardised phenotypes in genetic association studies |
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| Human genomic diversity, viral genomics and proteomics, as exemplified by human papillomaviruses and H5N1 influenza viruses |
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| Comparative transcriptome analyses of Pseudomonas aeruginosa |
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| Animal Models in Eye Research |
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| A general integrative genomic feature transcription factor binding site prediction method applied to analysis of USF1 binding in cardiovascular disease |
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| Comparative genomics of aldehyde dehydrogenase 5a1 (succinate semialdehyde dehydrogenase) and accumulation of gamma-hydroxybutyrate associated with its deficiency |
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| Whole-genome approach implicates CD44 in cellular resistance to carboplatin |
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| Association tests and software for copy number variant data |
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| Approaches to analyse dynamic microbial communities such as those seen in cystic fibrosis lung |
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| Effect of the allelic variants of aldehyde dehydrogenase ALDH2*2 and alcohol dehydrogenase ADH1B*2 on blood acetaldehyde concentrations |
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| The Human Gene Mutation Database: providing a comprehensive central mutation database for molecular diagnostics and personalised genomics |
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| Gene sharing and evolution |
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| The Aldehyde Dehydrogenase Gene Superfamily Resource Center |
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| Detecting genes contributing to longevity using twin data |
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| Editorial |
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| Use of pathway information in molecular epidemiology |
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| Cholinesterase inhibitors in Alzheimer's disease and Lewy body spectrum disorders: the emerging pharmacogenetic story |
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| Genetic association tests: a method for the joint analysis of family and case-control data |
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| Response to Stenson et al. in Human Genomics Vol. 4, No. 2, pp. 69-72: 'The Human Gene Mutation Database: Providing a comprehensive central mutation database for molecular diagnostics and personalised |
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| Evolutionary dynamics of olfactory receptor genes in chordates: interaction between environments and genomic contents |
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| Evolutionary divergence and functions of the ADAM and ADAMTS gene families |
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