Personal genomes: The case of the missing heritability

Transposable elements: targets for early nutritional effects on epigenetic gene regulation

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Large recurrent microdeletions associated with schizophrenia.

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Rare chromosomal deletions and duplications increase risk of schizophrenia

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Genetic Dissection of Transcriptional Regulation in Budding Yeast

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Genome-wide association analysis identifies 20 loci that influence adult height

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Many sequence variants affecting diversity of adult human height

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The genetics of autistic disorders and its clinical relevance: a review of the literature

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Identification of ten loci associated with height highlights new biological pathways in human growth

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Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL

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Sizing up human height variation

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Forest tree genomics: 10 achievements from the past 10 years and future prospects

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Invited review: A perspective on the future of genomic selection in dairy cattle

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Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain

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Constitutional epimutation as a mechanism for cancer causality and heritability?

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Accounting for eXentricities: Analysis of the X Chromosome in GWAS Reveals X-Linked Genes Implicated in Autoimmune Diseases

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Child Development and Molecular Genetics: 14 Years Later

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Transgenerational epigenetic influences of paternal environmental exposures on brain function and predisposition to psychiatric disorders

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An overview of SNP interactions in genome-wide association studies

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Estimating Effects and Making Predictions from Genome-Wide Marker Data

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Genetic diagnosis and prognosis of Alzheimer’s disease: challenges and opportunities

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Meta-analysis of twin studies highlights the importance of genetic variation in primary school educational achievement

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Genome‐wide association analysis and genetic architecture of egg weight and egg uniformity in layer chickens

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Functional Gene Group Analysis Reveals a Role of Synaptic Heterotrimeric G Proteins in Cognitive Ability

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Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures

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Metagenomics of the Human Body

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Genetics of impulsive behaviour

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The discovery of human genetic variations and their use as disease markers: past, present and future

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Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene

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Revisiting Human Cholesterol Synthesis and Absorption: The Reciprocity Paradigm and its Key Regulators

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Specific Glial Functions Contribute to Schizophrenia Susceptibility

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Human genome diversity: frequently asked questions

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Predicting Sensation Seeking From Dopamine Genes: A Candidate-System Approach

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Genomics of elite sporting performance: what little we know and necessary advances

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A variational Bayes algorithm for fast and accurate multiple locus genome-wide association analysis

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Extending the reach of public health genomics: What should be the agenda for public health in an era of genome-based and “personalized” medicine?

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Comparison of Family History and SNPs for Predicting Risk of Complex Disease

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Human genetics and genomics a decade after the release of the draft sequence of the human genome

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Bridging the genotype–phenotype gap: what does it take?

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Genotyping by Sequencing and Genome–Environment Associations in Wild Common Bean Predict Widespread Divergent Adaptation to Drought

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Toxoplasmosis: A pathway to neuropsychiatric disorders

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Gene-by-environment experiments: a new approach to finding the missing heritability

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Ultrafast genome-wide scan for SNP–SNP interactions in common complex diseasePreprint

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A Risk Model for Lung Cancer Incidence

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Genome‐wide association study for egg production and quality in layer chickens

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Genetic Basis of Drug-Induced Liver Injury: Present and Future

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Twin studies of posttraumatic stress disorder: Differentiating vulnerability factors from sequelae

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The search for gene-gene interactions in genome-wide association studies: challenges in abundance of methods, practical considerations, and biological interpretation

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Lessons Learned From GWAS of Asthma

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The evolutionary paradox and the missing heritability of schizophrenia

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The Developmental Origins of Health and Disease (DOHaD) Concept

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Genetic studies of Crohn's disease: Past, present and future

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Statistical analysis for genome-wide association study

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DNA methylation profiles at birth and child ADHD symptoms.

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Avatars of information: towards an inclusive evolutionary synthesis

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DNA evidence for strong genetic stability and increasing heritability of intelligence from age 7 to 12

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Genome-Wide Association Mapping of Flowering and Ripening Periods in Apple

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Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans

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Genetics of Atopic Dermatitis: From DNA Sequence to Clinical Relevance

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Discovering genetic interactions bridging pathways in genome-wide association studies

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Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: the biology of a neglected disease

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Epigenetics of major psychosis: progress, problems and perspectives

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Understanding risk for psychopathology through imaging gene–environment interactions

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Beyond the genome—Towards an epigenetic understanding of handedness ontogenesis

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Environment-Sensitive Epigenetics and the Heritability of Complex Diseases

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AstRoMap European Astrobiology Roadmap

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Exploring and Harnessing Haplotype Diversity to Improve Yield Stability in Crops

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Epigenome-wide association study in whole blood on type 2 diabetes among sub-Saharan African individuals: findings from the RODAM study

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Statistical Methods for Pathway Analysis of Genome-Wide Data for Association with Complex Genetic Traits

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Genome-wide Association Studies and Human Disease

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A Dormant Microbial Component in the Development of Preeclampsia

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The Brisbane Systems Genetics Study: Genetical Genomics Meets Complex Trait Genetics

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Common genetic variation and performance on standardized cognitive tests

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What has GWAS done for HLA and disease associations?

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Identification of Type 2 Diabetes-associated combination of SNPs using Support Vector Machine

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Biomarkers in the Age of Omics: Time for a Systems Biology Approach

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Crohn’s Disease: an Immune Deficiency State

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The role of longitudinal cohort studies in epigenetic epidemiology: challenges and opportunities

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Advances and Promises of Epigenetics for Forest Trees

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Overview of techniques to account for confounding due to population stratification and cryptic relatedness in genomic data association analyses

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Gallstones, Body Mass Index, C‐Reactive Protein, and Gallbladder Cancer: Mendelian Randomization Analysis of Chilean and European Genotype Data

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The immunopathogenesis of Crohn's disease: a three-stage model

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Metabolic profiling in diabetes

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Primers on nutrigenetics and nutri(epi)genomics: Origins and development of precision nutrition

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Third Report on Chicken Genes and Chromosomes 2015

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The Effect of Chromosome 9p21 Variants on Cardiovascular Disease May Be Modified by Dietary Intake: Evidence from a Case/Control and a Prospective Study

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Estimation of heritability for nine common cancers using data from genome‐wide association studies in Chinese population

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Strong genetic overlap between executive functions and intelligence.

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Psoriasis and Other Complex Trait Dermatoses: From Loci to Functional Pathways

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Marker-assisted selection in plant breeding

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The unforeseen challenge: from genotype-to-phenotype in cell populations

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Incorporating genomics into breast and prostate cancer screening: assessing the implications

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The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease

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Genetic variation in IBD: progress, clues to pathogenesis and possible clinical utility

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One Hundred Years of Linkage Disequilibrium.

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Social-biological transitions: how does the social become biological?

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Attentional biases to emotional stimuli: Key components of the RDoC constructs of sustained threat and loss

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To Identify Associations with Rare Variants, Just WHaIT: Weighted Haplotype and Imputation-Based Tests

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