A genome-wide association study of global gene expression

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A genome-wide association study identifies novel risk loci for type 2 diabetes

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Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

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Genome-wide association study of blood pressure and hypertension

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Common variants near MC4R are associated with fat mass, weight and risk of obesity

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Genotype Imputation

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Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

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

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Mapping complex disease traits with global gene expression

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Protein networks in disease

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Mapping cis- and trans-regulatory effects across multiple tissues in twins

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Sex-specific genetic architecture of human disease

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Aberrant Mucin Assembly in Mice Causes Endoplasmic Reticulum Stress and Spontaneous Inflammation Resembling Ulcerative Colitis

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Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

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A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk

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Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

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Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

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Progress and promise of genome-wide association studies for human complex trait genetics

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Etiology of Type 1 Diabetes

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High-Resolution Mapping of Expression-QTLs Yields Insight into Human Gene Regulation

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Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles

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Polarization of the Effects of Autoimmune and Neurodegenerative Risk Alleles in Leukocytes

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The Ensembl Regulatory Build

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A genome-wide association study identifies protein quantitative trait loci (pQTLs)

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Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis

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Human whole genome genotype and transcriptome data for Alzheimer’s and other neurodegenerative diseases

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Genome-Wide Association Study of Plasma Polyunsaturated Fatty Acids in the InCHIANTI Study

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Global analysis of DNA methylation variation in adipose tissue from twins reveals links to disease-associated variants in distal regulatory elements

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Cytokine and cytokine receptor gene polymorphisms and their functionality

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Extensive Variation in Chromatin States Across Humans

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Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33

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A common variant on chromosome 11q13 is associated with atopic dermatitis

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Genetic Control of Human Brain Transcript Expression in Alzheimer Disease

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Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease

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Genetics and Pathogenesis of Inflammatory Bowel Disease

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CD39 deletion exacerbates experimental murine colitis and human polymorphisms increase susceptibility to inflammatory bowel disease

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Transcriptome analysis and molecular signature of human retinal pigment epithelium

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The study of eQTL variations by RNA-seq: from SNPs to phenotypes

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A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order

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Understanding type 1 diabetes through genetics: advances and prospects

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Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype

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Integrative Genomics Reveals Novel Molecular Pathways and Gene Networks for Coronary Artery Disease

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Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease

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Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis

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Gene expression in skin and lymphoblastoid cells: refined statistical method reveals extensive overlap in cis-eQTL signals

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Geographical genomics of human leukocyte gene expression variation in southern Morocco

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A Common Variation in Deiodinase 1 Gene DIO1 Is Associated with the Relative Levels of Free Thyroxine and Triiodothyronine

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RNA-sequence analysis of human B-cells

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Single-cell genomics meets human genetics

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The effects of EBV transformation on gene expression levels and methylation profiles

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RNA sequencing reveals the role of splicing polymorphisms in regulating human gene expression

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Pooled ChIP-Seq Links Variation in Transcription Factor Binding to Complex Disease Risk

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Statistical independence of the colocalized association signals for type 1 diabetes and RPS26 gene expression on chromosome 12q13

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Systems genetics analysis of gene-by-environment interactions in human cells

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Pathogenic implications for autoimmune mechanisms derived by comparative eQTL analysis of CD4+ versus CD8+ T cells

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First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children

Roeske, D., Ludwig, K. U., Neuhoff, N., Becker, J., Bartling, J., Bruder, J., Brockschmidt, F. F., Warnke, A., Remschmidt, H., Hoffmann, P., et al. (2011) · Molecular Psychiatry · doi:10.1038/mp.2009.102 · Cited by 106

Genetic control of the human brain proteome

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Genome-wide association reveals genetic effects on human Aβ 42 and τ protein levels in cerebrospinal fluids: a case control study

Han, M.-R., Schellenberg, G. D., Wang, L.-S., & Initiative, T. A. D. N. (2010) · BMC Neurology · doi:10.1186/1471-2377-10-90 · Cited by 93

Joint analysis of SNP and gene expression data in genetic association studies of complex diseases

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Identification of genetic variants influencing the human plasma proteome

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A meta-analysis of gene expression quantitative trait loci in brain

Kim, Y., Xia, K., Tao, R., Giusti-Rodriguez, P., Vladimirov, V, van den Oord, E., & Sullivan, P. F. (2014) · Translational Psychiatry · doi:10.1038/tp.2014.96 · Cited by 73

Antimicrobial effects of black soldier fly and yellow mealworm fats and their impact on gut microbiota of growing rabbits.

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Effects of Long-Term Averaging of Quantitative Blood Pressure Traits on the Detection of Genetic Associations

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Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders

Waltes, R., Duketis, E., Knapp, M., Anney, R. J. L., Huguet, G., Schlitt, S., Jarczok, T. A., Sachse, M., Kämpfer, L. M., Kleinböck, T., et al. (2014) · Human Genetics · doi:10.1007/s00439-013-1416-y · Cited by 71

Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis

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Effects of chronic interpersonal stress exposure on depressive symptoms are moderated by genetic variation at IL6 and IL1β in youth

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Whole-genome association mapping of gene expression in the human prefrontal cortex

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Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk

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CHIT1 at Diagnosis Reflects Long‐Term Multiple Sclerosis Disease Activity

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Cancer-associated variants and a common polymorphism of MUTYH exhibit reduced repair of oxidative DNA damage using a GFP-based assay in mammalian cells

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Adaptive variation regulates the expression of the human SGK1 gene in response to stress

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Mapping the Genetic Architecture of Gene Regulation in Whole Blood

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Identification of Quantitative Trait Loci Underlying Proteome Variation in Human Lymphoblastoid Cells

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Immune and genetic aspects of asthma, allergy and parasitic worm infections: evolutionary links

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Signatures of evolutionary adaptation in quantitative trait loci influencing trace element homeostasis in liver

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