Andrew A. Hicks

A susceptibility gene for late-onset idiopathic Parkinson's disease.

PARK10 candidate RNF11 is expressed by vulnerable neurons and localizes to Lewy bodies in Parkinson disease brain.

Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis.

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.

Common variants at ten loci modulate the QT interval duration in the QTSCD Study.

Genome-wide linkage analysis of serum creatinine in three isolated European populations.

Parkin gene modifies the effect of RLS4 on the age at onset of restless legs syndrome (RLS).

Genetic determinants of circulating sphingolipid concentrations in European populations.

Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.

A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.

Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels.

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.

A global in vivo Drosophila RNAi screen identifies NOT3 as a conserved regulator of heart function.

Genes predict village of origin in rural Europe.

Copy number variation and association over T-cell receptor genes--influence of DNA source.

Variation in the uric acid transporter gene SLC2A9 and its association with AAO of Parkinson's disease.

Genome-wide association analysis identifies multiple loci related to resting heart rate.

Biological, clinical and population relevance of 95 loci for blood lipids.

Hundreds of variants clustered in genomic loci and biological pathways affect human height.

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

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.

Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.

Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.

Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster.

Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.

Genetic architecture of circulating lipid levels.

Linkage and association analysis of hyperthyrotropinaemia in an Alpine population reveal two novel loci on chromosomes 3q28-29 and 6q26-27.

Variants in STAT5B associate with serum TC and LDL-C levels.

Copy number variation across European populations.

Characterisation of genome-wide association epistasis signals for serum uric acid in human population isolates.

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.

New gene functions in megakaryopoiesis and platelet formation.

A genome-wide association search for type 2 diabetes genes in African Americans.

Genome-wide analysis of epistasis in body mass index using multiple human populations.

Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.

Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts.

Genetic adaptation of fatty-acid metabolism: a human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acids.

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.

Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.

Large-scale replication and heterogeneity in Parkinson disease genetic loci.

Evidence of inbreeding depression on human height.

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.

FTO genotype is associated with phenotypic variability of body mass index.

Discovery and fine mapping of serum protein loci through transethnic meta-analysis.

Fine-mapping of restless legs locus 4 (RLS4) identifies a haplotype over the SPATS2L and KCTD18 genes.

Localising loci underlying complex trait variation using Regional Genomic Relationship Mapping.

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants.

Seventy-five genetic loci influencing the human red blood cell.

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.

SNP prioritization using a Bayesian probability of association.

Importance of different types of prior knowledge in selecting genome-wide findings for follow-up.

A meta-analysis of thyroid-related traits reveals novel Loci and gender-specific differences in the regulation of thyroid function.

Involvement of proprotein convertase PCSK7 in the regulation of systemic iron homeostasis.

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

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.

Update on the management of restless legs syndrome: existing and emerging treatment options.

Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study.

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.

Common variants associated with plasma triglycerides and risk for coronary artery disease.

Discovery and refinement of loci associated with lipid levels.

Profiling of Parkin-binding partners using tandem affinity purification.

Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium.

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.

Meta-analysis of genome-wide association studies identifies two loci associated with circulating osteoprotegerin levels.

Defining the role of common variation in the genomic and biological architecture of adult human height.

Identification of a set of endogenous reference genes for miRNA expression studies in Parkinson's disease blood samples.

Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.

The arachidonic acid metabolome serves as a conserved regulator of cholesterol metabolism.

Overexpression of blood microRNAs 103a, 30b, and 29a in L-dopa-treated patients with PD.

New genetic loci link adipose and insulin biology to body fat distribution.

Genetic studies of body mass index yield new insights for obesity biology.

Modulation of genetic associations with serum urate levels by body-mass-index in humans.

Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.