| scholarly article | Q13442814 |
| P50 | author | Andrew Singleton | Q4758591 |
| John Anthony Hardy | Q6237755 | ||
| Stefania Bandinelli | Q28050064 | ||
| Bryan Traynor | Q28777952 | ||
| Sampath Arepalli | Q30089854 | ||
| Alan B. Zonderman | Q37368449 | ||
| Allissa Dillman | Q38637334 | ||
| Michael E. Weale | Q40357055 | ||
| Robert Walker | Q43080715 | ||
| Daniah Trabzuni | Q47816010 | ||
| Dena G. Hernandez | Q64856786 | ||
| Mina Ryten | Q66724661 | ||
| Mark R Cookson | Q67168137 | ||
| J Raphael Gibbs | Q114270383 | ||
| P2093 | author name string | Colin Smith | |
| Mike A Nalls | |||
| Matthew Moore | |||
| Juan Troncoso | |||
| Sean Chong | |||
| Richard O'Brien | |||
| P2860 | cites work | Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging | Q21092453 |
| Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain | Q21563315 | ||
| Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS | Q21563317 | ||
| Potential etiologic and functional implications of genome-wide association loci for human diseases and traits | Q22066284 | ||
| Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease | Q22251069 | ||
| Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls | Q24550675 | ||
| Genome-wide meta-analyses identify multiple loci associated with smoking behavior | Q24597886 | ||
| Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies | Q24606055 | ||
| Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci | Q24618592 | ||
| Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes | Q24632382 | ||
| Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease | Q24646902 | ||
| Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes | Q24652324 | ||
| Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium | Q24655591 | ||
| Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci | Q24658255 | ||
| Genome-wide association identifies multiple ulcerative colitis susceptibility loci | Q27865246 | ||
| A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study | Q28264836 | ||
| A genome-wide association study identifies novel risk loci for type 2 diabetes | Q28287727 | ||
| Mapping the genetic architecture of gene expression in human liver | Q28472693 | ||
| Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy | Q29417026 | ||
| Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes | Q29417138 | ||
| A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants | Q29547210 | ||
| Genetics of gene expression and its effect on disease | Q29614591 | ||
| A genome-wide association study of global gene expression | Q29614592 | ||
| A variant in CDKAL1 influences insulin response and risk of type 2 diabetes | Q29614878 | ||
| A whole-genome association study of major determinants for host control of HIV-1 | Q29614891 | ||
| Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma | Q29614903 | ||
| Population genomics of human gene expression | Q29614905 | ||
| Genetic analysis of genome-wide variation in human gene expression | Q29617852 | ||
| Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study | Q30439341 | ||
| Quality control parameters on a large dataset of regionally dissected human control brains for whole genome expression studies | Q30485119 | ||
| Tissue-specific genetic control of splicing: implications for the study of complex traits | Q33409947 | ||
| Digital quantification of human eye color highlights genetic association of three new loci | Q33576746 | ||
| Genome-wide association study of alcohol dependence implicates a region on chromosome 11. | Q33907650 | ||
| Multiple loci are associated with white blood cell phenotypes | Q33954440 | ||
| Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned | Q34147518 | ||
| Gene expression in skin and lymphoblastoid cells: Refined statistical method reveals extensive overlap in cis-eQTL signals | Q34381709 | ||
| Mapping determinants of human gene expression by regional and genome-wide association | Q34421244 | ||
| Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study | Q34450740 | ||
| Disentangling the role of the tau gene locus in sporadic tauopathies | Q34622443 | ||
| Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls | Q34758752 | ||
| Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes | Q34861754 | ||
| A survey of the genetics of stomach, liver, and adipose gene expression from a morbidly obese cohort | Q35085253 | ||
| Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association | Q35225238 | ||
| Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors | Q36020848 | ||
| Genetic control of human brain transcript expression in Alzheimer disease | Q37156046 | ||
| Expression quantitative trait loci detected in cell lines are often present in primary tissues | Q37397399 | ||
| Genetic variants influencing circulating lipid levels and risk of coronary artery disease | Q37477713 | ||
| Whole-genome association mapping of gene expression in the human prefrontal cortex. | Q42688558 | ||
| A survey of genetic human cortical gene expression | Q57272923 | ||
| P433 | issue | 1 | |
| P921 | main subject | genome-wide association study | Q1098876 |
| P304 | page(s) | 20-28 | |
| P577 | publication date | 2012-03-12 | |
| P1433 | published in | Neurobiology of Disease | Q15716606 |
| P1476 | title | Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain | |
| P478 | volume | 47 |
| Q36146002 | A Population-Based Study of Four Genes Associated with Heroin Addiction in Han Chinese |
| Q36089387 | A multiancestry study identifies novel genetic associations with CHRNA5 methylation in human brain and risk of nicotine dependence |
| Q92639275 | A practical view of fine-mapping and gene prioritization in the post-genome-wide association era |
| Q34775670 | A quantitative framework to evaluate modeling of cortical development by neural stem cells |
| Q91329623 | A regulatory variant of CHRM3 is associated with cannabis-induced hallucinations in European Americans |
| Q33631445 | A20 Inhibits β-Cell Apoptosis by Multiple Mechanisms and Predicts Residual β-Cell Function in Type 1 Diabetes |
| Q34487421 | Age-associated changes in gene expression in human brain and isolated neurons |
| Q37147054 | Aging Shapes the Population-Mean and -Dispersion of Gene Expression in Human Brains |
| Q48444509 | AlzBase: an Integrative Database for Gene Dysregulation in Alzheimer's Disease |
| Q89863903 | An atlas of genetic correlations between psychiatric disorders and human blood plasma proteome |
| Q92059765 | An epistasis between dopaminergic and oxytocinergic systems confers risk of post-traumatic stress disorder in a traumatized Chinese cohort |
| Q38089094 | Analytical strategies for large imaging genetic datasets: experiences from the IMAGEN study |
| Q38084740 | Application of genomics, proteomics and metabolomics in drug discovery, development and clinic. |
| Q28660129 | Bayesian test for colocalisation between pairs of genetic association studies using summary statistics |
| Q47874535 | Beyond genome-wide significance: integrative approaches to the interpretation and extension of GWAS findings for alcohol use disorder. |
| Q33685725 | Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome |
| Q38728036 | Blood gene expression studies in migraine: Potential and caveats |
| Q35058477 | Cis-regulatory variants affect CHRNA5 mRNA expression in populations of African and European ancestry |
| Q34458961 | Common genetic variants influence human subcortical brain structures |
| Q39036548 | Comprehensive Computational Analysis of GWAS Loci Identifies CCR2 as a Candidate Gene for Celiac Disease Pathogenesis |
| Q34478063 | Cross-tissue and tissue-specific eQTLs: partitioning the heritability of a complex trait |
| Q31126943 | Data sources for in vivo molecular profiling of human phenotypes |
| Q41645969 | Expression of asthma susceptibility genes in bronchial epithelial cells and bronchial alveolar lavage in the Severe Asthma Research Program (SARP) cohort |
| Q89747591 | Expression quantitative trait loci-derived scores and white matter microstructure in UK Biobank: a novel approach to integrating genetics and neuroimaging |
| Q35748666 | Fast eQTL Analysis for Twin Studies |
| Q30656680 | GLiMMPS: robust statistical model for regulatory variation of alternative splicing using RNA-seq data |
| Q38993873 | Gene-based association study of genes linked to hippocampal sclerosis of aging neuropathology: GRN, TMEM106B, ABCC9, and KCNMB2. |
| Q34336768 | Genetic analysis in neurology: the next 10 years |
| Q34781864 | Genetic evidence for a pathogenic role for the vitamin D3 metabolizing enzyme CYP24A1 in multiple sclerosis |
| Q34398489 | Genetic variability in the regulation of gene expression in ten regions of the human brain |
| Q52686362 | Genome-wide Association Study Identifies a Regulatory Variant of RGMA Associated With Opioid Dependence in European Americans. |
| Q37058626 | Genome-wide differential expression of synaptic long noncoding RNAs in autism spectrum disorder |
| Q33638413 | Genome-wide identification of expression quantitative trait loci (eQTLs) in human heart |
| Q45821536 | Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus |
| Q36084287 | Genomic approaches for understanding the genetics of complex disease |
| Q39213503 | Genomics and CSF analyses implicate thyroid hormone in hippocampal sclerosis of aging |
| Q52316078 | Human Genetics of Addiction: New Insights and Future Directions. |
| Q91763306 | Human gene expression variability and its dependence on methylation and aging |
| Q49190145 | Identification of expression quantitative trait loci of MTOR associated with the progression of glioma |
| Q38683029 | Inherited variation in circadian rhythm genes and risks of prostate cancer and three other cancer sites in combined cancer consortia |
| Q57104364 | Integrating GWAS and gene expression data for functional characterization of resistance to white mould in soya bean |
| Q36641588 | Integrative genomics in cardiovascular medicine |
| Q34499419 | Lung eQTLs to help reveal the molecular underpinnings of asthma |
| Q36190981 | MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies |
| Q37368024 | Mapping eQTLs in the Norfolk Island genetic isolate identifies candidate genes for CVD risk traits. |
| Q92153553 | Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits |
| Q41687462 | Neuregulin signaling pathway in smoking behavior |
| Q38731672 | NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases |
| Q41654368 | Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies |
| Q33789101 | Overlap of expression quantitative trait loci (eQTL) in human brain and blood |
| Q34481921 | Pathways to Parkinsonism Redux: convergent pathobiological mechanisms in genetics of Parkinson's disease |
| Q26786091 | Peripheral Biomarker Candidates of Posttraumatic Stress Disorder |
| Q27012892 | Peripheral biomarkers revisited: integrative profiling of peripheral samples for psychiatric research |
| Q35849067 | RNA sequencing of transcriptomes in human brain regions: protein-coding and non-coding RNAs, isoforms and alleles |
| Q36769422 | Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies |
| Q37619306 | Sex- and age-interacting eQTLs in human complex diseases |
| Q35786960 | Systematic noise degrades gene co-expression signals but can be corrected |
| Q63814903 | Transcriptomic metaanalyses of autistic brains reveals shared gene expression and biological pathway abnormalities with cancer |
| Q93194851 | Translating Alzheimer's disease-associated polymorphisms into functional candidates: a survey of IGAP genes and SNPs |
| Q91185200 | Variation among intact tissue samples reveals the core transcriptional features of human CNS cell classes |
| Q37403819 | Widespread sex differences in gene expression and splicing in the adult human brain |
| Q42211335 | brain-coX: investigating and visualising gene co-expression in seven human brain transcriptomic datasets |
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