| Genetic association studies in cancer: Good, bad or no longer ugly? |
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| Stepwise haplotype analysis: Are LD patterns repeatable? |
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| Genome-wide approaches to understanding human ageing |
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| Multifactor dimensionality reduction: An analysis strategy for modelling and detecting gene - gene interactions in human genetics and pharmacogenomics studies |
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| Testing groups of genomic locations for enrichment in disease loci using linkage scan data: A method for hypothesis testing |
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| Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population |
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Palestinian population |
| Editorial |
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| A survey of data mining methods for linkage disequilibrium mapping |
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| Letter to the Editor |
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| Detecting multiple associations in genome-wide studies |
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| Integrated analysis of genetic data with R |
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| Functional nsSNPs from carcinogenesis-related genes expressed in breast tissue: Potential breast cancer risk alleles and their distribution across human populations |
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| From DNA to RNA to disease and back: The 'central dogma' of regulatory disease variation |
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| Comparison of human (and other) genome browsers |
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| Human SNPs resulting in premature stop codons and protein truncation |
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| Editorial |
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| Inference of ancestry: constructing hierarchical reference populations and assigning unknown individuals |
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| FDA perspectives on potential microarray-based clinical diagnostics |
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| Immunogenomics: Molecular hide and seek |
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| Genome-wide association studies getting more complicated but help is on the way |
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| Genetic factors leading to chronic Epstein-Barr virus infection and nasopharyngeal carcinoma in South East China: Study design, methods and feasibility |
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| Functional single nucleotide polymorphism-based association studies |
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| Fabry disease: Identification of 50 novel α-galactosidase A mutations causing the classic phenotype and three-dimensional structural analysis of 29 missense mutations |
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| Update of the NAD(P)H:quinone oxidoreductase (NQO) gene family |
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| Strategies for the detection of copy number and other structural variants in the human genome |
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| Bioinformatics methods for identifying candidate disease genes |
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| Letter to the Editor |
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| A non-parametric approach to population structure inference using multilocus genotypes |
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