Population History and Natural Selection Shape Patterns of Genetic Variation in 132 Genes

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A Direct Approach to False Discovery Rates

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Statistical tests of neutrality of mutations.

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Human non-synonymous SNPs: server and survey

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Statistical tests of selective neutrality in the age of genomics

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Angiotensin-converting enzyme 2 is an essential regulator of heart function

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Genetic Signatures of Strong Recent Positive Selection at the Lactase Gene

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The Fine-Scale Structure of Recombination Rate Variation in the Human Genome

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Interrogating a High-Density SNP Map for Signatures of Natural Selection

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Properties of a neutral allele model with intragenic recombination

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Estimating African American Admixture Proportions by Use of Population-Specific Alleles

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The Ubiquitous Nature of Epistasis in Determining Susceptibility to Common Human Diseases

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Properties of statistical tests of neutrality for DNA polymorphism data.

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Inferring Nonneutral Evolution from Human-Chimp-Mouse Orthologous Gene Trios

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PANTHER: a browsable database of gene products organized by biological function, using curated protein family and subfamily classification

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Haplotype Diversity and Linkage Disequilibrium at Human G6PD : Recent Origin of Alleles That Confer Malarial Resistance

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Epidemiology of prostate cancer

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Dating the Origin of the CCR5-Δ32 AIDS-Resistance Allele by the Coalescence of Haplotypes

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The Signature of Positive Selection at Randomly Chosen Loci

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Norwalk Virus Infection and Disease Is Associated with ABO Histo–Blood Group Type

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Methods to Detect Selection in Populations with Applications to the Human

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Patterns of Human Genetic Diversity: Implications for Human Evolutionary History and Disease

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The Inherited Basis of Diabetes Mellitus: Implications for the Genetic Analysis of Complex Traits

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High Polymorphism at the Human Melanocortin 1 Receptor Locus

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Complex Signatures of Natural Selection at the Duffy Blood Group Locus

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Functional expression of the epithelial Ca2+ channels (TRPV5 and TRPV6) requires association of the S100A10-annexin 2 complex

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Comparison of human genetic and sequence-based physical maps

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Expression of CaT-like, a Novel Calcium-selective Channel, Correlates with the Malignancy of Prostate Cancer

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Adjusting the focus on human variation

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Phylogenetic Analysis of the Evolution of Lactose Digestion in Adults

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Demography and Natural Selection Have Shaped Genetic Variation in Drosophila melanogaster: A Multi-locus Approach

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Lactase Haplotype Diversity in the Old World

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Recombination and the power of statistical tests of neutrality

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Joint Effects of Genetic Hitchhiking and Background Selection on Neutral Variation

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Adaptive hitchhiking effects on genome variability

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LACTOSE NUTRITION AND NATURAL SELECTION

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Positive Selection on a Human-Specific Transcription Factor Binding Site Regulating IL4 Expression

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Population genomics: a bridge from evolutionary history to genetic medicine

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Geographic and Haplotype Structure of Candidate Type 2 Diabetes-Susceptibility Variants at the Calpain-10 Locus

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Molecular Analysis of the β-Globin Gene Cluster in the Niokholo Mandenka Population Reveals a Recent Origin of the βS Senegal Mutation

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DNA Variation at therp49Gene Region ofDrosophila simulans: Evolutionary Inferences From an Unusual Haplotype Structure

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Evidence for positive selection and population structure at the human MAO-A gene

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Inferences About Human Demography Based on Multilocus Analyses of Noncoding Sequences

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Detecting the form of selection from DNA sequence data

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(Patho)physiological implications of the novel epithelial Ca2+ channels TRPV5 and TRPV6

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Association of IL1A gene polymorphisms with susceptibility to and severity of systemic sclerosis in the Japanese population

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The Effect of Single Nucleotide Polymorphism Identification Strategies on Estimates of Linkage Disequilibrium

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Mathematical evolutionary theory

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Linkage of aggressive prostate cancer to chromosome 7q31-33 in German prostate cancer families

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Gene dose-dependent association of interleukin-1A [-889] allele 2 polymorphism with Alzheimer's disease

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The IL1A genotype is associated with nasal polyposis in asthmatic adults

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The IL1A genotype associates with atopy in nonasthmatic adults

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ABO/Secretor genetic complex and susceptibility to asthma in childhood

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The Decorin Gene 179 Allelic Variant Is Associated with a Slower Progression of Renal Disease in Patients with Type 1 Diabetes

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