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A Genome-Wide Association Study Identifies <i>IL23R</i> as an Inflammatory Bowel Disease Gene

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A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

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Genome-wide association study identifies novel breast cancer susceptibility loci

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Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes

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Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

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A Common Allele on Chromosome 9 Associated with Coronary Heart Disease

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Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

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Replicating genotype–phenotype associations

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Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

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A Large-Scale Genetic Association Study Confirms IL12B and Leads to the Identification of IL23R as Psoriasis-Risk Genes

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Multiple regions within 8q24 independently affect risk for prostate cancer

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A Spectrum of PCSK9 Alleles Contributes to Plasma Levels of Low-Density Lipoprotein Cholesterol

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A second generation human haplotype map of over 3.1 million SNPs

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Genome-wide association studies for complex traits: consensus, uncertainty and challenges

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Genetic Mapping in Human Disease

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Genetic architectures of psychiatric disorders: the emerging picture and its implications

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Human genetic variation and its contribution to complex traits

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Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease

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Consanguinity, human evolution, and complex diseases

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Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

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Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

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GATES: A Rapid and Powerful Gene-Based Association Test Using Extended Simes Procedure

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Common Variation in the FTO Gene Alters Diabetes-Related Metabolic Traits to the Extent Expected Given Its Effect on BMI

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Genetics of Type 1 Diabetes: What's Next?

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Leader of the pack: gene mapping in dogs and other model organisms

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The Psychiatric GWAS Consortium: Big Science Comes to Psychiatry

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Genome-wide association study of recurrent major depressive disorder in two European case–control cohorts

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Genome-wide Association Scan of Attention Deficit Hyperactivity Disorder

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The road to genome-wide association studies

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A framework for interpreting genome-wide association studies of psychiatric disorders

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Design and cohort description of the InterAct Project: an examination of the interaction of genetic and lifestyle factors on the incidence of type 2 diabetes in the EPIC Study

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Personalized Medicine in the Era of Genomics

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Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study

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Missing data imputation and haplotype phase inference for genome-wide association studies

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Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder

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Polymorphisms in E-cadherin ( CDH1 ) result in a mis-localised cytoplasmic protein that is associated with Crohn’s disease

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Genome-Wide Association Study of Suicide Attempts in Mood Disorder Patients

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What Can Genome-Wide Association Studies Tell Us about the Genetics of Common Disease?

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Genome-wide association studies: progress and potential for drug discovery and development

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Worldwide population differentiation at disease-associated SNPs

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Introduction: Race, Genetics, and Disease

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Learning From Molecular Genetics

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Endoplasmic reticulum stress in the intestinal epithelium and inflammatory bowel disease

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The major histocompatibility complex: a model for understanding graft-versus-host disease

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Genetic Tests:Clinical Validity and Clinical Utility

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

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Specific Glial Functions Contribute to Schizophrenia Susceptibility

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Immune-mediated disease genetics: the shared basis of pathogenesis

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A New Statistic to Evaluate Imputation Reliability

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Genetics of inflammatory bowel disease: implications for disease pathogenesis and natural history

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MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels

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Insulin signaling regulating genes: effect on T2DM and cardiovascular risk

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Is Obesity Our Genetic Legacy?

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Alcohol Addiction: A Molecular Biology Perspective

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A New Role for Endophenotypes in the GWAS Era: Functional Characterization of Risk Variants

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A diverse array of genetic factors contribute to the pathogenesis of Systemic Lupus Erythematosus

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Genome-wide SNP-Based Linkage Scan Identifies a Locus on 8q24 for an Age-Related Hearing Impairment Trait

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Association of human aryl hydrocarbon receptor gene polymorphisms with risk of lung cancer among cigarette smokers in a Chinese population

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A candidate gene study of tardive dyskinesia in the CATIE schizophrenia trial

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Genetic Variants Identified in a European Genome-Wide Association Study That Were Found to Predict Incident Coronary Heart Disease in the Atherosclerosis Risk in Communities Study

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Linking genes to diseases: it's all in the data

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Genome-Wide Association Studies for Atherosclerotic Vascular Disease and Its Risk Factors

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HapMap scanning of novel human minor histocompatibility antigens

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A Knowledge-Based Weighting Framework to Boost the Power of Genome-Wide Association Studies

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Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings.

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Defining the spectrum of alleles that contribute to blood lipid concentrations in humans

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Identification of new SLE-associated genes with a two-step Bayesian study design

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Male pattern baldness: current treatments, future prospects

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Genetic tests for common diseases: new insights, old concerns

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Linkage analysis without defined pedigrees

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An Overview of the Genetic Dissection of Complex Traits

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In situ oligonucleotide synthesis on carbon materials: stable substrates for microarray fabrication

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Between Candidate Genes and Whole Genomes: Time for Alternative Approaches in Blood Pressure Genetics

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Precision pharmacotherapy: psychiatry&amp;rsquo;s future direction in preventing, diagnosing, and treating mental disorders

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Update in endocrine autoimmunity.

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Meta-analysis of heterogeneous data sources for genome-scale identification of risk genes in complex phenotypes

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High Altitude Adaptation: Genetic Perspectives

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Direct-to-consumer genetic tests: beyond medical regulation?

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Crohn's Disease Loci Are Common Targets of Protozoa-Driven Selection

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Clinical Validity and Clinical Utility of Genetic Tests

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The association of MYO9B gene in Italian patients with inflammatory bowel diseases

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Chronic lymphocytic leukaemia genetics overview

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Genome-wide association study in RPGRIP1 −/− dogs identifies a modifier locus that determines the onset of retinal degeneration

Miyadera, K., Kato, K., Boursnell, M. E. G., Mellersh, C. S., & Sargan, D. R. (2011) · Mammalian Genome · doi:10.1007/s00335-011-9384-9 · Cited by 34 · see citing works

Human genetics offers an emerging picture of common pathways and mechanisms in autoimmunity

Voight, B. F., & Cotsapas, C. J. (2012) · Current Opinion in Immunology · doi:10.1016/j.coi.2012.07.013 · Cited by 33 · see citing works

Association of Genetic Variations in TCF7L2 , SLC30A8 , HHEX , LOC387761 , and EXT2 with Type 2 Diabetes Mellitus in Tunisia

Kifagi, C., Makni, K., Boudawara, M., Mnif, F., Hamza, N., Abid, M., Granier, C., & Ayadi, H. (2011) · Genetic Testing and Molecular Biomarkers · doi:10.1089/gtmb.2010.0199 · Cited by 32 · see citing works

A neurologist’s guide to genome-wide association studies

Mullen, S. A., Crompton, D. E., Carney, P. W., Helbig, I., & Berkovic, S. F. (2009) · Neurology · doi:10.1212/01.wnl.0000341942.29513.bd · Cited by 30 · see citing works

Genome-wide association studies of sleep disorders.

Raizen, D., & Wu, M. N. (2011) · Chest · doi:10.1378/chest.10-1313 · Cited by 25 · see citing works

Genome-Wide Association Study in Humans

Smith, J. G., & Newton‐Cheh, C. (2009) · Methods in molecular biology · doi:10.1007/978-1-60761-247-6_14 · Cited by 31 · see citing works

Genome-wide association in bipolar

Gershon, E. S., Liu, C., & Badner, J. A. (2007) · Molecular Psychiatry · doi:10.1038/sj.mp.4002117 · Cited by 27 · see citing works

The fat tail of obesity as told by the genome

Herbert, A. G. (2008) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e3283034990 · Cited by 26 · see citing works

Obesity Genes and Gene–Environment–Behavior Interactions: Recommendations for a Way Forward

Shuldiner, A. R. (2008) · Obesity · doi:10.1038/oby.2008.523 · Cited by 25 · see citing works

Common pathways in Crohn’s disease and other inflammatory diseases revealed by genomics: Table 1

Massey, D. C. O., & Parkes, M. (2007) · Gut · doi:10.1136/gut.2007.127928 · Cited by 25 · see citing works

On individual genome-wide association studies and their meta-analysis

Pei, Y., Zhang, L., Papasian, C. J., Wang, Y., & Deng, H. (2013) · Human Genetics · doi:10.1007/s00439-013-1366-4 · Cited by 24 · see citing works

The genomic landscape of human immune-mediated diseases

Wu, X., Chen, H., & Xu, H. (2015) · Journal of Human Genetics · doi:10.1038/jhg.2015.99 · Cited by 23 · see citing works

Gene Expression in Peripheral Blood Leukocytes in Monozygotic Twins Discordant for Chronic Fatigue: No Evidence of a Biomarker

Byrnes, A., Jacks, A., Dahlman‐Wright, K., Evengård, B., Wright, F. A., Pedersen, N. L., & Sullivan, P. F. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005805 · Cited by 24 · see citing works

Genetic Association Study of Endothelin-1 and Its Receptors EDNRA and EDNRB in Migraine with Aura

Tikka-Kleemola, P., Kaunisto, M. A., Hämäläinen, E., Todt, U., Göbel, H., Kaprio, J. A., Kubisch, C., Färkkilä, M. A., Palotie, A. V., Wessman, M., et al. (2009) · Cephalalgia · doi:10.1111/j.1468-2982.2009.01855.x · Cited by 23 · see citing works

Detecting new neurodegenerative disease genes: does phenotype accuracy limit the horizon?

Samuels, D. C., Burn, D. J., & Chinnery, P. F. (2009) · Trends in Genetics · doi:10.1016/j.tig.2009.09.008 · Cited by 23 · see citing works

Relationship of type 1 diabetes to ancestral proportions and HLA DR/DQ alleles in a sample of the admixed Cuban population

Díaz-Horta, O., Cintado, A., de Cossío, M. E. F., Nazábal, M., Ferrer, A., Roca, J. M., Camacho, H., Benı́tez, J., Ale, M., Villarreal, A., et al. (2010) · Annals of Human Biology · doi:10.3109/03014461003766984 · Cited by 21 · see citing works

Translational Genomics: Seeking a Shared Vision of Benefit

Burke, W., Kuszler, P. C., Starks, H. E., Holland, S., & Press, N. A. (2008) · The American Journal of Bioethics · doi:10.1080/15265160802109488 · Cited by 22 · see citing works

The era of genome-wide association studies: opportunities and challenges for asthma genetics

Zhang, G., Goldblatt, J., & Souëf, P. N. L. (2009) · Journal of Human Genetics · doi:10.1038/jhg.2009.97 · Cited by 21 · see citing works

Personalized Prognosis and Diagnosis of Type 2 Diabetes – Vision or Fiction?

Müller, G. A. (2010) · Pharmacology · doi:10.1159/000283780 · Cited by 20 · see citing works

Human Genetics: The Hidden Text of Genome-wide Associations

Gibson, G. C., & Goldstein, D. B. (2007) · Current Biology · doi:10.1016/j.cub.2007.08.044 · Cited by 19 · see citing works

Genetics of Bipolar Disorder

Lohoff, F. W., & Berrettini, W. H. (2010) · Wiley eBooks · doi:10.1002/9780470661277.ch12 · Cited by 19 · see citing works

The Use of Predictive or Prognostic Genetic Biomarkers in Endometrial and Other Hormone-Related Cancers: Justification for Extensive Candidate Gene Single Nucleotide Polymorphism Studies of the Matrix Metalloproteinase Family and their Inhibitors

O’Mara, T. A., Clements, J. A., & Spurdle, A. B. (2009) · Cancer Epidemiology Biomarkers & Prevention · doi:10.1158/1055-9965.epi-08-1184 · Cited by 18 · see citing works

High-Resolution Genetic Maps Identify Multiple Type 2 Diabetes Loci at Regulatory Hotspots in African Americans and Europeans

Lau, W., Andrew, T., & Maniatis, N. (2017) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2017.04.007 · Cited by 18 · see citing works

DTC genetic testing companies fail transparency prescriptions

Lewis, N. P., Treise, D. M., Hsu, S. I., Allen, W. L., & Kang, H. (2011) · New Genetics and Society · doi:10.1080/14636778.2011.600434 · Cited by 17 · see citing works

Chemical strategies for immobilization of oligonucleotides

Sethi, D., Gandhi, R., Kuma, P., & Gupta, K. C. (2009) · Biotechnology Journal · doi:10.1002/biot.200900162 · Cited by 14 · see citing works

Non‐random error in genotype calling procedures: Implications for family‐based and case–control genome‐wide association studies

Anney, R., Kenny, E. M., O'Dushlaine, C. T., Lasky-Su, J. A., Franke, B., Morris, D. W., Neale, B. M., Asherson, P. J., Faraone, S. V., & Gill, M. (2008) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30836 · Cited by 14 · see citing works

Genetic Predictors of Obesity

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Onwards and upwards for genome-wide association studies

Flintoft, L. (2007) · Nature Reviews Genetics · doi:10.1038/nrg2152

Guilt by association

Bowcock, A. M. (2007) · Nature · doi:10.1038/447645a · Cited by 39 · see citing works

Genome-wide association studies: the good, the bad and the ugly

Frayling, T. (2014) · Clinical Medicine · doi:10.7861/clinmedicine.14-4-428 · Cited by 30 · see citing works

Genomewide association studies--illuminating biologic pathways.

Hirschhorn, J. (2009) · New England Journal of Medicine · doi:10.1056/nejmp0808934 · Cited by 545 · see citing works

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

McCarthy, M. I., Abecasis, G. R., Cardon, L. R., Goldstein, D. B., Little, J., Ioannidis, J. P. A., & Hirschhorn, J. N. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2344 · Cited by 2,891 · see citing works