Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types.
- Authors
- Finucane, Hilary K; Reshef, Yakir A; Anttila, Verneri; Slowikowski, Kamil; Gusev, Alexander; Byrnes, Andrea; Gazal, Steven; Loh, Po-Ru; Lareau, Caleb; Shoresh, Noam; Genovese, Giulio; Saunders, Arpiar; Macosko, Evan; Pollack, Samuela; Brainstorm Consortium; Perry, John R B; Buenrostro, Jason D; Bernstein, Bradley E; Raychaudhuri, Soumya; McCarroll, Steven; Neale, Benjamin M; Price, Alkes L
- Year
- 2018
- Journal
- Nature genetics
- PMID
- 29632380
- DOI
- 10.1038/s41588-018-0081-4
- PMCID
- PMC5896795
We introduce an approach to identify disease-relevant tissues and cell types by analyzing gene expression data together with genome-wide association study (GWAS) summary statistics. Our approach uses stratified linkage disequilibrium (LD) score regression to test whether disease heritability is enriched in regions surrounding genes with the highest specific expression in a given tissue. We applied our approach to gene expression data from several sources together with GWAS summary statistics for 48 diseases and traits (average Nβ=β169,331) and found significant tissue-specific enrichments (false discovery rate (FDR)β<β5%) for 34 traits. In our analysis of multiple tissues, we detected a broad range of enrichments that recapitulated known biology. In our brain-specific analysis, significant enrichments included an enrichment of inhibitory over excitatory neurons for bipolar disorder, and excitatory over inhibitory neurons for schizophrenia and body mass index. Our results demonstrate that our polygenic approach is a powerful way to leverage gene expression data for interpreting GWAS signals.
Overview of the approach. For each tissue in our gene expression data set, we compute t-statistics for differential expression for each gene. We then rank genes by t-statistic, take the top 10% of genes, and add a 100kb window to get a genome annotation. We use stratified LD score regression7 to test whether this annotation is significantly enriched for per-SNP heritability, conditional on the baseline model7 and the set of all genes.
Results of the multiple-tissue analysis for selected traits. Results for the remaining traits are displayed in Figure S1. Each point represents a tissue/cell type from either the GTEx data set or the Franke lab data set. Large points pass the FDR<5% cutoff, βlog10(P)=2.75. GWAS data is described in Table S4, gene expression data is described in the Online Methods and Tables S2-3, and the statistical method is described in the Overview of Methods and the Online Methods. Numerical results are reported in Table S6.
Validation of gene expression results with chromatin data. (A) Examples of validation using chromatin data (bottom) of results from gene expression data (top), for selected traits. Results using chromatin data for all traits are displayed in Figure S5, with numerical results in Table S7. For the chromatin results, each point represents a track of peaks for H3K4me3, H3K4me1, H3K9ac, H3K27ac, H3K36me3, or DHS in a single tissue/cell type. (B) Results using gene expression data (including GTEx), Roadmap, and EN-TEx, for migraine (all subtypes) and migraine without aura. For both subfigures, large points pass the FDR<5% cutoff, βlog10(P)=2.85 (chromatin) or βlog10(P)=2.75 (gene expression). GWAS data is described in Table S4; gene expression data and chromatin data are described in the Online Methods, Tables S2-3, and Table S7; and the statistical method is described in the Overview of Methods and the Online Methods.
Results of the brain analysis for selected traits. Numerical results for all traits are reported in Table S8. (A) Results from within-brain analysis of 13 brain regions in GTEx, classified into four groups, for seven of 12 brain-related traits. Large points passed the FDR<5% cutoff, βlog10(P)=2.34. (B) Results from the data of Cahoy et al. on three brain cell types for seven of 12 brain-related traits. Large points passed the FDR<5% cutoff, βlog10(P)=2.22. (C) Results from PyschENCODE data on two neuronal subtypes for three of five neuron-related traits. Large points passed the Bonferroni significance threshold in this analysis, βlog10(P)=2.06. GWAS data is described in Table S4, gene expression data is described in the Online Methods and Table S8, and the statistical method is described in the Overview of Methods and the Online Methods.
Results of the analysis of ImmGen gene expression data (top) and hematopoiesis ATAC-seq data (bottom) for selected traits. Results for the remaining traits are displayed in Figure S9. Large points passed the FDR<5% cutoff, βlog10(P)=3.03 (Gene expression) or βlog10(P)=2.32 (Chromatin). Numerical results are reported in Table S10. GWAS data is described in Table S4, gene expression and chromatin data is described in the Online Methods and Table S10, and the statistical method is described in the Overview of Methods and the Online Methods.
| Name | Type |
|---|---|
| 1000 Genomes Project | cohort |
| 13 traits local | phenotype |
| 30 phenotypes local | phenotype |
| 34 traits local | phenotype |
| 48 diseases and traits local | phenotype |
| ADHD | phenotype |
| adipose tissue | phenotype |
| age at menarche | phenotype |
| alpha beta T cells local | phenotype |
| Alzheimerβs disease | phenotype |
| anorexia nervosa | phenotype |
| antigen presentation local | phenotype |
| aorta local | anatomy |
| artery local | anatomy |
| asthma | phenotype |
| ATAC-seq | drug |
| B cells | cohort |
| B cells local | drug |
| bipolar disorder | phenotype |
| blood | drug |
| blood pressure | phenotype |
| BMI | phenotype |
| BMI-adjusted waist-hip ratio local | phenotype |
| brain | anatomy |
| brain-related phenotypes | phenotype |
| Brainstorm Consortium | cohort |
| brain tissue | anatomy |
| Cahoy data set local | cohort |
| Cahoy et al. local | cohort |
| cardiovascular disease | phenotype |
| cardiovascular phenotypes local | phenotype |
| celiac disease | phenotype |
| central nervous system | anatomy |
| cerebellum | anatomy |
| chromatin-based annotations local | drug |
| chromatin data local | drug |
| complement system | drug |
| coronary artery local | anatomy |
| cortex | anatomy |
| Crohnβs disease | phenotype |
| cytokine-mediated signaling local | phenotype |
| depressive symptoms | phenotype |
| DHS | drug |
| disease | phenotype |
| disease etiology local | phenotype |
| disease-relevant tissues local | phenotype |
| disease-relevant tissues and cell types local | phenotype |
| DNase hypersensitivity | drug |
| dorsolateral prefrontal cortex | anatomy |
| eczema | phenotype |
| ENCODE project | cohort |
| Ensembl | drug |
| EN-Tex local | cohort |
| EN-TEx local | cohort |
| EN-Tex data local | cohort |
| epigenetic marks local | drug |
| epilepsy | phenotype |
| eQTLGen Consortium | cohort |
| esophagus local | anatomy |
| fetal brain | anatomy |
| Franke lab data local | cohort |
| Franke lab data set local | cohort |
| Franke lab dataset | cohort |
| GABA | phenotype |
| gamma delta T cells local | phenotype |
| gene expression data local | cohort |
| gene expression data local | drug |
| gene g | gene |
| genetic variants | cohort |
| glutamatergic neurons | phenotype |
| GSE15907 local | cohort |
| GSE37448 local | cohort |
| GTEx | cohort |
| GTEx brain regions | anatomy |
| GTEx data set local | cohort |
| GTEx project | cohort |
| GWAS | cohort |
| H3K27ac | drug |
| H3K36me3 | drug |
| H3K36me3 peaks local | drug |
| H3K4me1 | drug |
| H3K4me3 | drug |
| H3K9ac | drug |
| HDL cholesterol | phenotype |
| height | phenotype |
| hematopoiesis data set local | cohort |
| hematopoietic data set local | cohort |
| histone marks | drug |
| HLA | gene |
| hypertension | phenotype |
| ImmGen | cohort |
| ImmGen analysis local | cohort |
| ImmGen Consortium local | cohort |
| ImmGen data set local | cohort |
| ImmGen project local | cohort |
| immune activation local | drug |
| immune activity local | phenotype |
| immune category local | phenotype |
| immune cells local | drug |
| immune cell types local | cohort |
| immune-related phenotypes local | phenotype |
| immune response | phenotype |
| immunological disease local | phenotype |
| immunological diseases local | phenotype |
| Immunological diseases local | phenotype |
| immunological traits local | phenotype |
| inflammatory bowel disease | phenotype |
| innate lymphocytes local | phenotype |
| joint local | anatomy |
| joint capsule local | anatomy |
| LDL cholesterol | phenotype |
| liver | anatomy |
| lung | anatomy |
| metabolic traits | phenotype |
| MHC region | gene |
| mice | cohort |
| migraine | phenotype |
| migraine (all subtypes) local | phenotype |
| migraine with aura local | phenotype |
| migraine without aura local | phenotype |
| Migraine without aura local | phenotype |
| monocytes | cohort |
| mouse forebrain local | anatomy |
| multiple sclerosis | phenotype |
| musculoskeletal/connective phenotypes local | phenotype |
| myeloid cells | phenotype |
| nasal mucosa local | anatomy |
| neurological | phenotype |
| neurological disorders | phenotype |
| neurons | phenotype |
| neurospheres local | anatomy |
| neuroticism | phenotype |
| neurotypical human donors local | cohort |
| NK cells | cohort |
| NK cells local | drug |
| NKT cells local | phenotype |
| non-brain tissues | anatomy |
| nose | anatomy |
| Other | phenotype |
| other brain regions | anatomy |
| other cells local | cohort |
| pancreas | anatomy |
| Parkinsonβs disease | phenotype |
| phenotype | phenotype |
| phenotypes studied here local | phenotype |
| phenotype Y local | phenotype |
| plasma | anatomy |
| plasma cells local | anatomy |
| primary biliary cirrhosis | phenotype |
| PsychENCODE | cohort |
| PsychENCODE20 local | cohort |
| PsychENCODE data set local | cohort |
| psychiatric disorders | phenotype |
| psychiatric traits | phenotype |
| quadriceps muscle local | anatomy |
| reference panel | cohort |
| Reproductive local | cohort |
| rheumatoid arthritis | phenotype |
| RNA-seq | drug |
| Roadmap local | cohort |
| Roadmap data local | cohort |
| Roadmap dataset local | cohort |
| Roadmap Epigenomics | cohort |
| Roadmap Epigenomics consortium | cohort |
| schizophrenia | phenotype |
| serous membrane local | phenotype |
| Skeletal muscle | cohort |
| SLE | phenotype |
| smoking status | phenotype |
| SNP | cohort |
| SNP i local | variant |
| specifically expressed genes local | gene |
| stem cells local | phenotype |
| striatum | anatomy |
| stromal cells | phenotype |
| Stromal cells local | drug |
| T cell activation local | phenotype |
| T cells local | drug |
| T cells | phenotype |
| tibial artery local | anatomy |
| tissue/cell type local | anatomy |
| Tourette syndrome | phenotype |
| trait | phenotype |
| triglycerides | phenotype |
| type 1 diabetes | phenotype |
| type 2 diabetes | phenotype |
| UK Biobank | cohort |
| ulcerative colitis | phenotype |
| uterus local | anatomy |
| years of education | phenotype |
No uploaded files.
In this knowledge base
External
| Title | Authors | Journal | Year | Link |
|---|---|---|---|---|
| Cardiovascular measures from abdominal MRI provide insights into abdominal vessel genetic architecture. | Basty N et al. | β | 2026 | β |
| Construction of a Multitissue Cell Atlas Reveals Cell-Type-Specific Regulation of Molecular and Complex Phenotypes in Pigs. | Chen L et al. | β | 2026 | β |
| Cross-Trait Genome-Wide Association Studies Identify Shared Genetic Risk Loci Between Psoriasis and Metabolic Syndrome and Their Associated Traits. | Jiang X et al. | β | 2026 | β |
| Cross-trait genomic modeling reveals the polygenic architecture and systemic impact of MASLD. | Du M et al. | β | 2026 | β |
| Discovery of disease-associated cellular states using ResidPCA in single-cell RNA and ATAC sequencing data. | Carver S et al. | β | 2026 | β |
| Dissecting PGE<sub>2</sub>-driven inhibition of T cell activation using single-cell multi-omic and inflammatory bowel disease genetic association analysis. | Xu Z et al. | β | 2026 | β |
| Dissecting pleiotropy to gain mechanistic insights into human disease. | Jee YH et al. | β | 2026 | β |
| Dissecting the shared genetic architecture between anxiety and cognitive function. | Yang M et al. | β | 2026 | β |
| Estrogen signaling in PDGFRΞ±+ cells positively regulates cortical bone metabolism via IGFBP5 in female mice. | Ikedo A et al. | β | 2026 | β |
| Exploring the genetic overlap between substance use disorder and educational attainment. | Cabana-DomΓnguez J et al. | β | 2026 | β |
| Fine-mapping a genome-wide meta-analysis of 98,374 migraine cases identifies 181 sets of candidate causal variants. | Hautakangas H et al. | β | 2026 | β |
| Functional implications of polygenic risk for schizophrenia in human neurons. | Michael Deans PJ et al. | β | 2026 | β |
| Genetic architecture of primary sclerosing cholangitis: shared pathways with inflammatory bowel disease and gut-liver axis mediation. | Chen Y et al. | β | 2026 | β |
| Genetic Evidence for a Neuroimmune Model of Schizophrenia. | van der Walt K et al. | β | 2026 | β |
| Genome-wide association study of major anxiety disorders in 122,341 European-ancestry cases identifies 58 loci and highlights GABAergic signaling. | Strom NI et al. | β | 2026 | β |
| Human and bacterial genetic variation shape oral microbiomes and health. | Kamitaki N et al. | β | 2026 | β |
| Independent association of leg-height ratio with 15 cardiometabolic diseases. | Zhao R et al. | β | 2026 | β |
| Integrating polygenic signals and single-cell multiomics identifies cell-type-specific regulomes critical for immune- and aging-related diseases. | Ma Y et al. | β | 2026 | β |
| Investigating the Shared Genetic Architecture of 3 Age-Related Ocular Disorders. | Bai ZP et al. | β | 2026 | β |
| Organism-wide cellular dynamics and epigenomic remodeling in mammalian aging. | Lu Z et al. | β | 2026 | β |
| Spatially resolved molecular sex differences at single-cell resolution in the adult human ventromedial and arcuate hypothalamus. | Mulvey B et al. | β | 2026 | β |
| The gene expression landscape of disease genes. | GarcΓa-GonzΓ‘lez J et al. | β | 2026 | β |
| The genetic basis of dermatophytosis skin infection susceptibility. | Haapaniemi H et al. | β | 2026 | β |
| The genetic relationships between post-traumatic stress disorder and its corresponding neural circuit structures. | Gong Q et al. | β | 2026 | β |
| The High-Altitude Adaptation Characteristics of Microbiota-Host Cross-Talk in Yak Gastrointestinal Track. | Huang C et al. | β | 2026 | β |
| The polygenic, omnigenic and stratagenic models of complex disease risk. | GarcΓa-GonzΓ‘lez J et al. | β | 2026 | β |
| The shared genetic architecture underlying the autoimmune and cardiovascular disease: a multivariate genome-wide analysis. | Zhang J et al. | β | 2026 | β |
| Unravelling genetic susceptibility and causal factors in liver health using MRI quantification of inflammation, fat and iron in the liver. | Meena D et al. | β | 2026 | β |
| A Developmental Gene Expression Atlas Reveals Novel Biological Basis of Complex Phenotypes in Sheep. | Zhao B et al. | β | 2025 | β |
| A genetic common factor underlying self-reported math ability and highest math class taken. | Giannelis A et al. | β | 2025 | β |
| A genome-wide association study integrated with single-cell and bulk profiles uncovers susceptibility genes for nasopharyngeal carcinoma involved in tumorigenesis via regulation of T cells. | Wang TM et al. | β | 2025 | β |
| A genome-wide meta-analysis reveals shared and population-specific variants for allergic sensitization. | Noguchi E et al. | β | 2025 | β |
| An Integrated Large-Scale Atlas of Protein Quantitative Trait Loci across Olink and SomaScan platforms | Khunsriraksakul C et al. | β | 2025 | β |
| An integrated single-nucleus and spatial transcriptomics atlas reveals the molecular landscape of the human hippocampus. | Thompson JR et al. | β | 2025 | β |
| An mRNA expression atlas for the duck with public RNA-seq datasets. | Tao Q et al. | β | 2025 | β |
| An Ocular Gene-Set Expression Library for Heritability Partition and Cell Line Enrichment Analyses. | Hysi PG et al. | β | 2025 | β |
| Association between genetically predicted leisure and social activities and cardiovascular disease and other health outcomes. | Kim S et al. | β | 2025 | β |
| Associations between common genetic variants and income provide insights about the socio-economic health gradient. | Kweon H et al. | β | 2025 | β |
| A unified framework for identification of cell-type-specific spatially variable genes in spatial transcriptomic studies. | Wang Z et al. | β | 2025 | β |
| Behavioural, immunological and transcriptomic consequences of post-weaning social isolation and chronic celecoxib administration in mouse. | Laighneach A et al. | β | 2025 | β |
| Canine genome-wide association study identifies <i>DENND1B</i> as an obesity gene in dogs and humans. | Wallis NJ et al. | β | 2025 | β |
| Cell-weighted polygenic risk scores are associated with Ξ²-amyloid and tau biomarkers in Alzheimer's disease. | Kumar A et al. | β | 2025 | β |
| Chromatin accessibility during human first-trimester neurodevelopment. | Mannens CCA et al. | β | 2025 | β |
| Combining phenomics with transcriptomics reveals cell-type-specific morphological and molecular signatures of the 22q11.2 deletion. | Tegtmeyer M et al. | β | 2025 | β |
| Common genetic basis and causality between central nervous system disease and cancer. | Tan S et al. | β | 2025 | β |
| Common genetic variation influencing the human lung imaging phenotypes. | Zhu M et al. | β | 2025 | β |
| Comparative single-cell multiome identifies evolutionary changes in neural progenitor cells during primate brain development. | Liu Y et al. | β | 2025 | β |
| Comprehensive analysis of 1,771 transcriptomes from 7 tissues enhance genetic and biological interpretations of maize complex traits. | Lei M et al. | β | 2025 | β |
| Contribution of leukocyte telomere length to cardiovascular disease onset from genome-wide cross-trait analysis. | Qiao J et al. | β | 2025 | β |
| Cross-tissue transcriptome-wide association identify novel T1D susceptibility genes and drug candidates. | Liu Y et al. | β | 2025 | β |
| Deciphering the shared genetic architecture between bipolar disorder and body mass index. | Ma H et al. | β | 2025 | β |
| Deciphering the shared genetic structure between hip osteoarthritis and femoral neck bone mineral density. | Zhou J et al. | β | 2025 | β |
| Decoding DNA sequence-driven evolution of the human brain epigenome at cellular resolution. | Caglayan E et al. | β | 2025 | β |
| Decoding the germline genetic architecture of prostate cancer at a single cell resolution. | Wang C et al. | β | 2025 | β |
| DEDUCE: statistical inference on disease-associated genes uncovers tissue-disease associations. | Wang B et al. | β | 2025 | β |
| Disease-linked regulatory DNA variants and homeostatic transcription factors in epidermis. | Porter DF et al. | β | 2025 | β |
| Disentangling associations between complex traits and cell types with seismic. | Lai Q et al. | β | 2025 | β |
| Effects of Shared and Nonshared Schizophrenia and Bipolar Disorder Alleles on Cognition and Educational Attainment in the UK Biobank. | Richards AL et al. | β | 2025 | β |
| Elucidating shared genetic association between female body mass index and preeclampsia. | Yang F et al. | β | 2025 | β |
| European and African ancestry-specific plasma protein-QTL and metabolite-QTL analyses identify ancestry-specific T2D effector proteins and metabolites. | Yang C et al. | β | 2025 | β |
| Evaluating the nonlinear effects of sleep duration on biological aging across phenotypic, genomic, and epigenomic data. | Wu X et al. | β | 2025 | β |
| Exploring genetic loci linked to COVID-19 severity and immune response through multi-trait GWAS analyses. | Meng Z et al. | β | 2025 | β |
| Exploring the shared genetic architecture between leukocyte telomere length and renal cell carcinoma: a cross-trait analysis. | Wang L et al. | β | 2025 | β |
| Fine-mapping causal tissues and genes at disease-associated loci. | Strober BJ et al. | β | 2025 | β |
| From variants to mechanisms: Neurogenomics in the post-GWAS era. | Margolis MP et al. | β | 2025 | β |
| Functional genomics implicates natural killer cells in the pathogenesis of ankylosing spondylitis. | ChiΓ±as M et al. | β | 2025 | β |
| Functional genomics of human skeletal development and the patterning of height heritability. | Richard D et al. | β | 2025 | β |
| Genetic and epigenetic screens in primary human Tβcells link candidate causal autoimmune variants to Tβcell networks. | Ho CH et al. | β | 2025 | β |
| Genetic association between gene expression profiles in oligodendrocyte precursor cells and psychiatric disorders. | Kondo R et al. | β | 2025 | β |
| Genetic determinants of proteomic aging. | MΓΆrseburg A et al. | β | 2025 | β |
| Genetic insights into modifiable risk factors of stroke and their joint effects: A genome-wide pleiotropic analysis. | Yang Z et al. | β | 2025 | β |
| Genetic insights into the association between inflammatory bowel disease and Alzheimer's disease. | Zeng L et al. | β | 2025 | β |
| Genetic overlap between schizophrenia and constipation: insights from a genome-wide association study in a European population. | Luo Q et al. | β | 2025 | β |
| Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum. | Venkatesh SS et al. | β | 2025 | β |
| Genome-wide association meta-analysis of age at onset of walking in over 70,000 infants of European ancestry. | Gui A et al. | β | 2025 | β |
| Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes. | Henry A et al. | β | 2025 | β |
| Genome-wide association study provides insights into the genetic basis of Lewy body dementia. | Zhu P et al. | β | 2025 | β |
| Genomic Correlations, Shared Loci, and Drug Targets Between Polycystic Ovary Syndrome and Asthma: Insights From Genome-wide Association Analysis. | Ji E et al. | β | 2025 | β |
| Genomics of schizophrenia, bipolar disorder and major depressive disorder. | Owen MJ et al. | β | 2025 | β |
| Identification of potential therapeutic targets for problematic alcohol use using multi-omics data. | Lee DJ et al. | β | 2025 | β |
| Integrating genetics and transcriptomics to characterize shared mechanisms in digestive diseases and psychiatric disorders. | Ding H et al. | β | 2025 | β |
| Integrating microbial GWAS and single-cell transcriptomics reveals associations between host cell populations and the gut microbiome. | Li J et al. | β | 2025 | β |
| Integrating Proteomics and GWAS to Identify Key Tissues and Genes Underlying Human Complex Diseases. | Xue C et al. | β | 2025 | β |
| Integrative genome-wide analysis unveils the genetic landscape of gallstone disease and highlights novel loci with therapeutic potential. | Chen H et al. | β | 2025 | β |
| Integrative Genome-wide Association Meta-analysis of Aortic Aneurysm and Dissection Identifies Five Novel Genes. | Du Y et al. | β | 2025 | β |
| Integrative multi-omics data from early development to identify the genes and cell types underlying attention-deficit/hyperactivity disorder. | Jiao S et al. | β | 2025 | β |
| Investigating the Shared Genetic Architecture Between Leukocyte Telomere Length and Prostate Cancer. | Li Z et al. | β | 2025 | β |
| Investigating the shared genetic information between serum concentration levels of liver enzymes and cholelithiasis. | Tian W et al. | β | 2025 | β |
| IPGCA: A Comprehensive Single Cell Atlas of 1Β 074Β 127 Porcine Intestinal Cells Revealing Cellular Dynamics, Genetic Regulation, and Cross-Species Conservation. | Yu P et al. | β | 2025 | β |
| Joint profiling of cell morphology and gene expression during in vitro neurodevelopment. | Sundaresh A et al. | β | 2025 | β |
| Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants. | Liu H et al. | β | 2025 | β |
| Large-scale genome-wide analyses of stuttering. | Polikowsky HG et al. | β | 2025 | β |
| Local Climate Adaptation in Chinese Indigenous Pig Genomes. | Liu Y et al. | β | 2025 | β |
| Mammary gland multi-omics data reveals new genetic insights into milk production traits in dairy cattle. | Cai W et al. | β | 2025 | β |
| Mapping the cellular etiology of schizophrenia and complex brain phenotypes. | Duncan LE et al. | β | 2025 | β |
| Molecular and genetic landscapes of retina and brain microglia in neurodegenerative diseases. | Ma K et al. | β | 2025 | β |
| Multi-INTACT: integrative analysis of the genome, transcriptome, and proteome identifies causal mechanisms of complex traits. | Okamoto J et al. | β | 2025 | β |
| Multivariate genome-wide analysis reveals shared genetic architecture and brain structural correlates of human cognitive abilities. | Chen H et al. | β | 2025 | β |
| New insights into genetic comorbidity mechanisms: type 2 diabetes and primary open-angle glaucoma. | Wang Y et al. | β | 2025 | β |
| Regional and aging-specific cellular architecture of non-human primate brains. | Wang YM et al. | β | 2025 | β |
| Sex-specific genetics underlie increased chronic pain risk in women: genome-wide association studies from the UK Biobank. | Parisien M et al. | β | 2025 | β |
| Shared genetic architecture contributes to risk of major cardiovascular diseases. | Qiao J et al. | β | 2025 | β |
| Shared genetics of lung cancer and type 2 diabetes: a large-scale genome-wide cross-trait analysis. | Wang Z et al. | β | 2025 | β |
| Simple scaling laws control the genetic architectures of human complex traits. | Simons YB et al. | β | 2025 | β |
| Single-cell multi-omics analysis reveals cancer regulatory elements of transcriptional programs and clinical implications. | Tang X et al. | β | 2025 | β |
| Single-Cell Profiling Identifies Reward Behavior-Related Neurons and Alterations in the Ventral Tegmental Area Based on <i>Arvcf</i>-Knockout Mouse Model. | Zhang M et al. | β | 2025 | β |
| Single-cell ultra-high-throughput multiplexed chromatin and RNA profiling reveals gene regulatory dynamics. | Lobato-Moreno S et al. | β | 2025 | β |
| Sparse matrix factorization robust to sample sharing across GWASs reveals interpretable genetic components. | Omdahl AR et al. | β | 2025 | β |
| Sparse modeling of interactions enables fast detection of genome-wide epistasis in biobank-scale studies. | Stamp J et al. | β | 2025 | β |
| Spatially resolved mapping of cells associated with human complex traits. | Song L et al. | β | 2025 | β |
| Systematic dissection of pleiotropic loci and critical regulons in excitatory neurons and microglia relevant to neuropsychiatric and ocular diseases. | Ma Y et al. | β | 2025 | β |
| The cell-type-specific genetic architecture of chronic pain in brain and dorsal root ganglia. | Toikumo S et al. | β | 2025 | β |
| The Eating Disorders Genetics Initiative 2 (EDGI2): study protocol. | Berthold N et al. | β | 2025 | β |
| The Genetic Architecture of the Human Corpus Callosum and its Subregions. | Bhatt RR et al. | β | 2025 | β |
| The impact of common and rare genetic variants on bradyarrhythmia development. | Weng LC et al. | β | 2025 | β |
| The relationship between vitamin D levels and depression: a genetically informed study. | Lyu H et al. | β | 2025 | β |
| Towards improved fine-mapping of candidate causal variants. | Li Z et al. | β | 2025 | β |
| Transcriptome-wide root causal inference. | Strobl EV et al. | β | 2025 | β |
| Transcriptomic diversity of amygdalar subdivisions across humans and nonhuman primates. | Totty MS et al. | β | 2025 | β |
| Uncovering pleiotropic loci in allergic rhinitis and leukocyte traits through multi-trait GWAS. | Yang L et al. | β | 2025 | β |
| Uncovering shared genetic features between inflammatory bowel disease and systemic lupus erythematosus. | Shaw VR et al. | β | 2025 | β |
| Unveiling migraine subtype heterogeneity and risk loci: integrated genome-wide association study and single-cell transcriptomics discovery. | Wei S et al. | β | 2025 | β |
| Abdominal aortic aneurysm and cardiometabolic traits share strong genetic susceptibility to lipid metabolism and inflammation. | Zheng S et al. | β | 2024 | β |
| A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disorders. | Lee AS et al. | β | 2024 | β |
| A comprehensive genome-wide cross-trait analysis of sexual factors and uterine leiomyoma. | Wu X et al. | β | 2024 | β |
| A concerted neuron-astrocyte program declines in ageing and schizophrenia. | Ling E et al. | β | 2024 | β |
| A holistic approach to understanding immune-mediated inflammatory diseases: bioinformatic tools to integrate omics data. | Borrego-Yaniz G et al. | β | 2024 | β |
| A multi-ancestry genetic study of pain intensity in 598,339 veterans. | Toikumo S et al. | β | 2024 | β |
| An integrative framework to prioritize genes in more than 500 loci associated with body mass index. | Hemerich D et al. | β | 2024 | β |
| An integrative multi-context Mendelian randomization method for identifying risk genes across human tissues. | Lu Y et al. | β | 2024 | β |
| An RNA-seq atlas of mouse brain areas during fasting and diet-induced obesity. | Todorov PV et al. | β | 2024 | β |
| Antipsychotic-induced epigenomic reorganization in frontal cortex of individuals with schizophrenia. | Zhu B et al. | β | 2024 | β |
| A scalable and robust variance components method reveals insights into the architecture of gene-environment interactions underlying complex traits. | Pazokitoroudi A et al. | β | 2024 | β |
| A time-resolved multi-omics atlas of transcriptional regulation in response to high-altitude hypoxia across whole-body tissues. | Yan Z et al. | β | 2024 | β |
| Bayesian estimation of gene constraint from an evolutionary model with gene features. | Zeng T et al. | β | 2024 | β |
| Chromatin profiling and state predictions reveal insights into epigenetic regulation during early porcine development. | Innis SM et al. | β | 2024 | β |
| Comparative transcriptome analysis of T lymphocyte subpopulations and identification of critical regulators defining porcine thymocyte identity. | Han P et al. | β | 2024 | β |
| Comprehensive Evaluation of the Genetic Basis of Keratoconus: New Perspectives for Clinical Translation. | CervΓ‘n-MartΓn M et al. | β | 2024 | β |
| Convergence of coronary artery disease genes onto endothelial cell programs. | Schnitzler GR et al. | β | 2024 | β |
| Cross-ancestry analysis of brain QTLs enhances interpretation of schizophrenia genome-wide association studies. | Chen Y et al. | β | 2024 | β |
| Current genomic deep learning models display decreased performance in cell type-specific accessible regions. | Kathail P et al. | β | 2024 | β |
| Deciphering the impact of genomic variation on function. | IGVF Consortium | β | 2024 | β |
| Discovery and prioritization of genetic determinants of kidney function in 297,355 individuals from Taiwan and Japan. | Chen HL et al. | β | 2024 | β |
| Disentangling the genetic overlap between ischemic stroke and obesity. | Yang R et al. | β | 2024 | β |
| Dissecting shared genetic architecture between depression and body mass index. | Zhang H et al. | β | 2024 | β |
| Dissecting the polygenic contribution of attention-deficit/hyperactivity disorder and autism spectrum disorder on school performance by their relationship with educational attainment. | Cabana-DomΓnguez J et al. | β | 2024 | β |
| Dissecting the shared genetic architecture between endometriosis and polycystic ovary syndrome. | Tan H et al. | β | 2024 | β |
| Epidemiologic and genetic associations between primary biliary cholangitis and extrahepatic rheumatic diseases. | Qian Q et al. | β | 2024 | β |
| Evaluating methods for integrating single-cell data and genetics to understand inflammatory disease complexity. | Townsend HA et al. | β | 2024 | β |
| Evidence for the gut-skin axis: Common genetic structures in inflammatory bowel disease and psoriasis. | Guo J et al. | β | 2024 | β |
| Examination of a novel expression-based gene-SNP annotation strategy to identify tissue-specific contributions to heritability in multiple traits. | Mize TJ et al. | β | 2024 | β |
| Exploring the shared genetic basis of major depressive disorder and frailty. | Fu W et al. | β | 2024 | β |
| Expression patterns of housekeeping genes and tissue-specific genes in black goats across multiple tissues. | Qin C et al. | β | 2024 | β |
| Gene-environment pathways to cognitive intelligence and psychotic-like experiences in children. | Park J et al. | β | 2024 | β |
| Genes with differential expression across ancestries are enriched in ancestry-specific disease effects likely due to gene-by-environment interactions. | Wang J et al. | β | 2024 | β |
| Genetic analyses of 104 phenotypes in 20,900 Chinese pregnant women reveal pregnancy-specific discoveries. | Xiao H et al. | β | 2024 | β |
| Genetic analysis of key agronomic traits of local sheep breeds in Xinjiang, China. | Zhang J et al. | β | 2024 | β |
| Genetic and molecular architecture of complex traits. | Lappalainen T et al. | β | 2024 | β |
| Genetic architecture distinguishes tinnitus from hearing loss. | Clifford RE et al. | β | 2024 | β |
| Genetic correlation between smoking behavior and gastroesophageal reflux disease: insights from integrative multi-omics data. | Yan Z et al. | β | 2024 | β |
| Genetic drivers and cellular selection of female mosaic X chromosome loss. | Liu A et al. | β | 2024 | β |
| Genetic Implication of Prenatal GABAergic and Cholinergic Neuron Development in Susceptibility to Schizophrenia. | Cameron D et al. | β | 2024 | β |
| Genetic Implication of Specific Glutamatergic Neurons of the Prefrontal Cortex in the Pathophysiology of Schizophrenia. | Tume CE et al. | β | 2024 | β |
| Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy. | Zheng SL et al. | β | 2024 | β |
| Genome-wide association studies and Mendelian randomization analyses provide insights into the causes of early-onset colorectal cancer. | Laskar RS et al. | β | 2024 | β |
| Genome-wide association study and fine-mapping on Korean biobank to discover renal trait-associated variants. | Lee DJ et al. | β | 2024 | β |
| Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience. | Jurgens SJ et al. | β | 2024 | β |
| Genome-wide classification of epigenetic activity reveals regions of enriched heritability in immune-related traits. | Stricker M et al. | β | 2024 | β |
| GWAS shows the genetics behind cell-free DNA and highlights the importance of p.Arg206Cys in DNASE1L3 for non-invasive testing. | Linthorst J et al. | β | 2024 | β |
| Haplotype function score improves biological interpretation and cross-ancestry polygenic prediction of human complex traits. | Song W et al. | β | 2024 | β |
| Hemochromatosis neural archetype reveals iron disruption in motor circuits. | Loughnan R et al. | β | 2024 | β |
| High-dimensional phenotyping to define the genetic basis of cellular morphology. | Tegtmeyer M et al. | β | 2024 | β |
| Identifying risk loci for obsessive-compulsive disorder and shared genetic component with schizophrenia: A large-scale multi-trait association analysis with summary statistics. | Dai J et al. | β | 2024 | β |
| Inflammatory bowel disease and rheumatoid arthritis share a common genetic structure. | Cao G et al. | β | 2024 | β |
| Integrating genetic regulation and single-cell expression with GWAS prioritizes causal genes and cell types for glaucoma. | Hamel AR et al. | β | 2024 | β |
| Integrating Multiple Database Resources to Elucidate the Gene Flow in Southeast Asian Pig Populations. | Li G et al. | β | 2024 | β |
| Integrating single-cell RNA sequencing data to genome-wide association analysis data identifies significant cell types in influenza A virus infection and COVID-19. | Zou Y et al. | β | 2024 | β |
| Integration of human organoids single-cell transcriptomic profiles and human genetics repurposes critical cell type-specific drug targets for severe COVID-19. | Ma Y et al. | β | 2024 | β |
| Integrative annotation scores of variants for impact on RNA binding protein activities. | Duan J et al. | β | 2024 | β |
| Integrative cross-omics and cross-context analysis elucidates molecular links underlying genetic effects on complex traits. | Lu Y et al. | β | 2024 | β |
| Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects. | Kasela S et al. | β | 2024 | β |
| Investigating shared genetic architecture between inflammatory bowel diseases and primary biliary cholangitis. | Huang W et al. | β | 2024 | β |
| Investigating the shared genetic basis of inflammatory bowel disease and systemic lupus erythematosus using genetic overlap analysis. | Yuan W et al. | β | 2024 | β |
| Large-scale integrative analysis of juvenile idiopathic arthritis for new insight into its pathogenesis. | Kim D et al. | β | 2024 | β |
| Leveraging single-cell ATAC-seq and RNA-seq to identify disease-critical fetal and adult brain cell types. | Kim SS et al. | β | 2024 | β |
| Mapping the functional impact of non-coding regulatory elements in primary T cells through single-cell CRISPR screens. | Alda-Catalinas C et al. | β | 2024 | β |
| MPH: fast REML for large-scale genome partitioning of quantitative genetic variation. | Jiang J | β | 2024 | β |
| Multi-ancestry meta-analysis of tobacco use disorder identifies 461 potential risk genes and reveals associations with multiple health outcomes. | Toikumo S et al. | β | 2024 | β |
| Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications. | Sterenborg RBTM et al. | β | 2024 | β |
| Multivariate genomic analysis of 5βmillion people elucidates the genetic architecture of shared components of the metabolic syndrome. | Park S et al. | β | 2024 | β |
| Neurogenetic and multi-omic sources of overlap among sensation seeking, alcohol consumption, and alcohol use disorder. | Miller AP et al. | β | 2024 | β |
| Non-coding autoimmune risk variant defines role for ICOS in T peripheral helper cell development. | Kim T et al. | β | 2024 | β |
| Novel insight into the etiology of ischemic stroke gained by integrative multiome-wide association study. | Jung J et al. | β | 2024 | β |
| Omics Approaches to Investigate the Pathogenesis of Suicide. | Boldrini M et al. | β | 2024 | β |
| PigBiobank: a valuable resource for understanding genetic and biological mechanisms of diverse complex traits in pigs. | Zeng H et al. | β | 2024 | β |
| Polygenic profiles define aspects of clinical heterogeneity in attention deficit hyperactivity disorder. | LaBianca S et al. | β | 2024 | β |
| Principled distillation of UK Biobank phenotype data reveals underlying structure in human variation. | Carey CE et al. | β | 2024 | β |
| Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study. | Choi E et al. | β | 2024 | β |
| Protein interaction networks in the vasculature prioritize genes and pathways underlying coronary artery disease. | Zhu QM et al. | β | 2024 | β |
| Regression convolutional neural network models implicate peripheral immune regulatory variants in the predisposition to Alzheimer's disease. | Ramamurthy E et al. | β | 2024 | β |
| Regulatory landscape enrichment analysis (RLEA): a computational toolkit for non-coding variant enrichment and cell type prioritization. | Rosean S et al. | β | 2024 | β |
| Revealing brain cell-stratified causality through dissecting causal variants according to their cell-type-specific effects on gene expression. | Hao RH et al. | β | 2024 | β |
| Rhinovirus infection of airway epithelial cells uncovers the non-ciliated subset as a likely driver of genetic risk to childhood-onset asthma. | Djeddi S et al. | β | 2024 | β |
| Schizophrenia genomics: genetic complexity and functional insights. | Sullivan PF et al. | β | 2024 | β |
| Shared genetic architectures of educational attainment in East Asian and European populations. | Chen TT et al. | β | 2024 | β |
| Single-cell spatial transcriptomic and translatomic profiling of dopaminergic neurons in health, aging, and disease. | Kilfeather P et al. | β | 2024 | β |
| Spatial multiomic landscape of the human placenta at molecular resolution. | Ounadjela JR et al. | β | 2024 | β |
| Systems biology dissection of PTSD and MDD across brain regions, cell types, and blood. | Daskalakis NP et al. | β | 2024 | β |
| Temporally distinct 3D multi-omic dynamics in the developing human brain. | Heffel MG et al. | β | 2024 | β |
| The cells of the sensory epithelium, and not the stria vascularis, are the main cochlear cells related to the genetic pathogenesis of age-related hearing loss. | Eshel M et al. | β | 2024 | β |
| The impact of exercise on gene regulation in association with complex trait genetics. | Vetr NG et al. | β | 2024 | β |
| The shared genetic landscape of polycystic ovary syndrome and breast cancer: convergence on ERβ+βbreast cancer but not ER- breast cancer. | Bi K et al. | β | 2024 | β |
| Transcriptomic dysregulation and autistic-like behaviors in Kmt2c haploinsufficient mice rescued by an LSD1 inhibitor. | Nakamura T et al. | β | 2024 | β |
| TWAS facilitates gene-scale trait genetic dissection through gene expression, structural variations, and alternative splicing in soybean. | Li D et al. | β | 2024 | β |
| Two genome-wide interaction loci modify the association of nonsteroidal anti-inflammatory drugs with colorectal cancer. | Drew DA et al. | β | 2024 | β |
| Uncovering cell-type-specific immunomodulatory variants and molecular phenotypes in COVID-19 using structurally resolved protein networks. | Chhibbar P et al. | β | 2024 | β |
| Understanding the genetic complexity of puberty timing across the allele frequency spectrum. | Kentistou KA et al. | β | 2024 | β |
| Unveiling the Genetic Mechanism of Meat Color in Pigs through GWAS, Multi-Tissue, and Single-Cell Transcriptome Signatures Exploration. | Liu C et al. | β | 2024 | β |
| Utilizing multimodal approach to identify candidate pathways and biomarkers and predicting frailty syndrome in individuals from UK Biobank. | Tseng WH et al. | β | 2024 | β |
| Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes. | Keener R et al. | β | 2024 | β |
| 150 risk variants for diverticular disease of intestine prioritize cell types and enable polygenic prediction of disease susceptibility. | Wu Y et al. | β | 2023 | β |
| A Bayesian method for estimating gene-level polygenicity under the framework of transcriptome-wide association study. | Majumdar A et al. | β | 2023 | β |
| A Common Genetic Factor Underlies Genetic Risk for Gynaecological and Reproductive Disorders and Is Correlated with Risk to Depression. | Kiewa J et al. | β | 2023 | β |
| A flexible empirical Bayes approach to multivariate multiple regression, and its improved accuracy in predicting multi-tissue gene expression from genotypes. | Morgante F et al. | β | 2023 | β |
| Analysis of genetic dominance in the UK Biobank. | Palmer DS et al. | β | 2023 | β |
| Analyzing histone ChIP-seq data with a bin-based probability of being signal. | Hecht V et al. | β | 2023 | β |
| An analytical framework for decoding cell type-specific genetic variation of gene regulation. | Xiao Y et al. | β | 2023 | β |
| An integrated cell atlas of the lung in health and disease. | Sikkema L et al. | β | 2023 | β |
| A prognostic risk score for development and spread of chronic pain. | Tanguay-Sabourin C et al. | β | 2023 | β |
| A scalable approach to characterize pleiotropy across thousands of human diseases and complex traits using GWAS summary statistics. | Zhang Z et al. | β | 2023 | β |
| A statistical framework to identify cell types whose genetically regulated proportions are associated with complex diseases. | Liu W et al. | β | 2023 | β |
| A Transcriptome-Wide Analysis of Psoriasis: Identifying the Potential Causal Genes and Drug Candidates. | Jeong Y et al. | β | 2023 | β |
| Causal associations between cardiorespiratory fitness and type 2 diabetes. | Cai L et al. | β | 2023 | β |
| Cell-type-specific Alzheimer's disease polygenic risk scores are associated with distinct disease processes in Alzheimer's disease. | Yang HS et al. | β | 2023 | β |
| Characterization of altered molecular mechanisms in Parkinson's disease through cell type-resolved multiomics analyses. | Lee AJ et al. | β | 2023 | β |
| Cluster Headache Genomewide Association Study and Meta-Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor. | Winsvold BS et al. | β | 2023 | β |
| Common genetic factors among autoimmune diseases. | Harroud A et al. | β | 2023 | β |
| Decoding the genetic and epigenetic basis of asthma. | Stikker BS et al. | β | 2023 | β |
| Dissecting shared genetic architecture between obesity and multiple sclerosis. | Zeng R et al. | β | 2023 | β |
| Dynamic regulatory elements in single-cell multimodal data implicate key immune cell states enriched for autoimmune disease heritability. | Gupta A et al. | β | 2023 | β |
| East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease. | He Y et al. | β | 2023 | β |
| Examining the shared etiology of psychopathology with genome-wide association studies. | Mallard TT et al. | β | 2023 | β |
| Factorizing polygenic epistasis improves prediction and uncovers biological pathways in complex traits. | Tang D et al. | β | 2023 | β |
| Gene, cell type, and drug prioritization analysis suggest genetic basis for the utility of diuretics in treating Alzheimer disease. | Pinakhina D et al. | β | 2023 | β |
| Genetic and neural bases of the neuroticism general factor. | Kim Y et al. | β | 2023 | β |
| Genetic Associations Between Stress-Related Disorders and Autoimmune Disease. | Zeng Y et al. | β | 2023 | β |
| Genetic correlation, causal relationship, and shared loci between vitamin D and COVID-19: A genome-wide cross-trait analysis. | Qiu S et al. | β | 2023 | β |
| Genetic effects on the timing of parturition and links to fetal birth weight. | SolΓ©-Navais P et al. | β | 2023 | β |
| Genetic insights into human cortical organization and development through genome-wide analyses of 2,347 neuroimaging phenotypes. | Warrier V et al. | β | 2023 | β |
| Genetics and epigenetics in the obesity phenotyping scenario. | Trang K et al. | β | 2023 | β |
| Genetics implicates overactive osteogenesis in the development of diffuse idiopathic skeletal hyperostosis. | Sethi A et al. | β | 2023 | β |
| Genetics of migraine: Delineation of contemporary understanding of the genetic underpinning of migraine. | de Boer I et al. | β | 2023 | β |
| Genetics of migraine: where are we now? | Grangeon L et al. | β | 2023 | β |
| Genetics of sexually dimorphic adipose distribution in humans. | Hansen GT et al. | β | 2023 | β |
| Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains. | Demontis D et al. | β | 2023 | β |
| Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. | Mathieson I et al. | β | 2023 | β |
| Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target. | Roychowdhury T et al. | β | 2023 | β |
| Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. | Williamson A et al. | β | 2023 | β |
| Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population. | Shi J et al. | β | 2023 | β |
| Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program. | Klarin D et al. | β | 2023 | β |
| Genome-wide meta-analysis and fine-mapping prioritize potential causal variants and genes related to leprosy. | Wang Z et al. | β | 2023 | β |
| Germline mechanisms of immunotherapy toxicities in the era of genome-wide association studies. | Gusev A | β | 2023 | β |
| GRaNIE and GRaNPA: inference and evaluation of enhancer-mediated gene regulatory networks. | Kamal A et al. | β | 2023 | β |
| graph-GPA 2.0: improving multi-disease genetic analysis with integration of functional annotation data. | Deng Q et al. | β | 2023 | β |
| GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. | International League Against Epilepsy Consortium on Complex Epilepsies | β | 2023 | β |
| GWAS on retinal vasculometry phenotypes. | Jiang X et al. | β | 2023 | β |
| Human height: a model common complex trait. | Conery M et al. | β | 2023 | β |
| Identification of brain cell types underlying genetic association with word reading and correlated traits. | Price KM et al. | β | 2023 | β |
| Identification of the shared genetic architecture underlying seven autoimmune diseases with GWAS summary statistics. | Wang Y et al. | β | 2023 | β |
| Identifying critical cell types and gene regulatory pathways for hair and skin disease. | β | β | 2023 | β |
| Independent Associated SNPs at SORCS3 and Its Protein Interactors for Multiple Brain-Related Disorders and Traits. | Kamran M et al. | β | 2023 | β |
| Induction of dopaminergic neurons for neuronal subtype-specific modeling of psychiatric disease risk. | Powell SK et al. | β | 2023 | β |
| Inferring disease architecture and predictive ability with LDpred2-auto. | PrivΓ© F et al. | β | 2023 | β |
| Integrated single-cell chromatin and transcriptomic analyses of human scalp identify gene-regulatory programs and critical cell types for hair and skin diseases. | Ober-Reynolds B et al. | β | 2023 | β |
| Integrating eQTL and GWAS data characterises established and identifies novel migraine risk loci. | Ghaffar A et al. | β | 2023 | β |
| Integration of genetic data with dynamic gene regulatory elements identifies autoimmune effector cell states. | β | β | 2023 | β |
| Integration of transcriptome-wide association study with neuronal dysfunction assays provides functional genomics evidence for Parkinson's disease genes. | Li J et al. | β | 2023 | β |
| Integrative analyses highlight functional regulatory variants associated with neuropsychiatric diseases. | Guo MG et al. | β | 2023 | β |
| Integrative genetic analysis illuminates ALS heritability and identifies risk genes. | Megat S et al. | β | 2023 | β |
| Integrative genome-wide analyses identify novel loci associated with kidney stones and provide insights into its genetic architecture. | Hao X et al. | β | 2023 | β |
| Integrative single-cell meta-analysis reveals disease-relevant vascular cell states and markers in human atherosclerosis. | Mosquera JV et al. | β | 2023 | β |
| Investigating the shared genetic architecture between schizophrenia and body mass index. | Yu Y et al. | β | 2023 | β |
| Investigating the shared genetic architecture of post-traumatic stress disorder and gastrointestinal tract disorders: a genome-wide cross-trait analysis. | Zhou S et al. | β | 2023 | β |
| Investigation of convergent and divergent genetic influences underlying schizophrenia and alcohol use disorder. | Johnson EC et al. | β | 2023 | β |
| Landscape genomics reveals adaptive divergence of indigenous sheep in different ecological environments of Xinjiang, China. | Zhang CL et al. | β | 2023 | β |
| Large scale phenotype imputation and in vivo functional validation implicate ADAMTS14 as an adiposity gene. | Kentistou KA et al. | β | 2023 | β |
| Leveraging genetic overlap between irritability and psychiatric disorders to identify genetic variants of major psychiatric disorders. | Jung K et al. | β | 2023 | β |
| Locus for severity implicates CNS resilience in progression of multiple sclerosis. | International Multiple Sclerosis Genetics Consortium et al. | β | 2023 | β |
| Massively parallel functional dissection of schizophrenia-associated noncoding genetic variants. | Rummel CK et al. | β | 2023 | β |
| Modeling of horizontal pleiotropy identifies possible causal gene expression in systemic lupus erythematosus. | Chepelev I et al. | β | 2023 | β |
| Modeling tissue co-regulation estimates tissue-specific contributions to disease. | Amariuta T et al. | β | 2023 | β |
| Multitissue H3K27ac profiling of GTEx samples links epigenomic variation to disease. | Hou L et al. | β | 2023 | β |
| Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. | Gupta R et al. | β | 2023 | β |
| Patterns of item nonresponse behaviour to survey questionnaires are systematic and associated with genetic loci. | Mignogna G et al. | β | 2023 | β |
| Polygenic architecture of rare coding variation across 394,783 exomes. | Weiner DJ et al. | β | 2023 | β |
| Polygenic regression uncovers trait-relevant cellular contexts through pathway activation transformation of single-cell RNA sequencing data. | Ma Y et al. | β | 2023 | β |
| Polygenic risk score association with multiple sclerosis susceptibility and phenotype in Europeans. | Shams H et al. | β | 2023 | β |
| Prediction of the cell-type-specific transcription of non-coding RNAs from genome sequences via machine learning. | Koido M et al. | β | 2023 | β |
| Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms. | Pividori M et al. | β | 2023 | β |
| Protein interaction studies in human induced neurons indicate convergent biology underlying autism spectrum disorders. | Pintacuda G et al. | β | 2023 | β |
| Recent natural selection conferred protection against schizophrenia by non-antagonistic pleiotropy. | GonzΓ‘lez-PeΓ±as J et al. | β | 2023 | β |
| scLiverDB: a Database of Human and Mouse Liver Transcriptome Landscapes at Single-Cell Resolution. | Pan Q et al. | β | 2023 | β |
| Single-Nuclei RNA Sequencing of 5 Regions of the Human Prenatal Brain Implicates Developing Neuron Populations in Genetic Risk for Schizophrenia. | Cameron D et al. | β | 2023 | β |
| Social isolation-induced transcriptomic changes in mouse hippocampus impact the synapse and show convergence with human genetic risk for neurodevelopmental phenotypes. | Laighneach A et al. | β | 2023 | β |
| SparsePro: An efficient fine-mapping method integrating summary statistics and functional annotations. | Zhang W et al. | β | 2023 | β |
| The molecular cytoarchitecture of the adult mouse brain. | Langlieb J et al. | β | 2023 | β |
| The Physiological Regulation of Body Fat Mass. | Sumithran P | β | 2023 | β |
| The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits. | Costanzo MC et al. | β | 2023 | β |
| Tissue-specific and tissue-agnostic effects of genome sequence variation modulating blood pressure. | Lee D et al. | β | 2023 | β |
| Topic modeling identifies novel genetic loci associated with multimorbidities in UK Biobank. | Zhang Y et al. | β | 2023 | β |
| Transcriptome-wide association study identifies novel candidate susceptibility genes for migraine. | Meyers TJ et al. | β | 2023 | β |
| Transcriptome-wide gene-gene interaction associations elucidate pathways and functional enrichment of complex traits. | Evans LM et al. | β | 2023 | β |
| Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia. | Hsu YH et al. | β | 2023 | β |
| A joint transcriptional regulatory network and protein activity inference analysis identifies clinically associated master regulators for biliary atresia. | Sun P et al. | β | 2022 | β |
| A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation. | Vujkovic M et al. | β | 2022 | β |
| A multiethnic whole genome sequencing study to identify novel loci for bone mineral density. | Greenbaum J et al. | β | 2022 | β |
| Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis. | Choquet H et al. | β | 2022 | β |
| Aortic Cellular Diversity and Quantitative Genome-Wide Association Study Trait Prioritization Through Single-Nuclear RNA Sequencing of the Aneurysmal Human Aorta. | Chou EL et al. | β | 2022 | β |
| A quantile integral linear model to quantify genetic effects on phenotypic variability. | Miao J et al. | β | 2022 | β |
| A sequence-based global map of regulatory activity for deciphering human genetics. | Chen KM et al. | β | 2022 | β |
| Beyond GWAS: from simple associations to functional insights. | Ishigaki K | β | 2022 | β |
| Cell type-specific histone acetylation profiling of Alzheimer's disease subjects and integration with genetics. | Ramamurthy E et al. | β | 2022 | β |
| Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity. | Gazal S et al. | β | 2022 | β |
| Comparative immune-relevant transcriptome reveals the evolutionary basis of complex traits. | Yang W et al. | β | 2022 | β |
| Complement C1q-dependent excitatory and inhibitory synapse elimination by astrocytes and microglia in Alzheimer's disease mouse models. | Dejanovic B et al. | β | 2022 | β |
| Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction. | Kember RL et al. | β | 2022 | β |
| Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease. | Uellendahl-Werth F et al. | β | 2022 | β |
| Deciphering the distinct transcriptomic and gene regulatory map in adult macaque basal ganglia cells. | Li Z et al. | β | 2022 | β |
| Deep learning enables genetic analysis of the human thoracic aorta. | Pirruccello JP et al. | β | 2022 | β |
| Discovery of 42 genome-wide significant loci associated with dyslexia. | Doust C et al. | β | 2022 | β |
| Dissection of multiple sclerosis genetics identifies B and CD4+ T cells as driver cell subsets. | Guo MH et al. | β | 2022 | β |
| Distinct transcriptome architectures underlying lupus establishment and exacerbation. | Nakano M et al. | β | 2022 | β |
| Enhancer promoter interactome and Mendelian randomization identify network of druggable vascular genes in coronary artery disease. | Chignon A et al. | β | 2022 | β |
| EPIC: Inferring relevant cell types for complex traits by integrating genome-wide association studies and single-cell RNA sequencing. | Wang R et al. | β | 2022 | β |
| Epigenetics of neural differentiation: Spotlight on enhancers. | Giacoman-Lozano M et al. | β | 2022 | β |
| Epigenomic priming of immune genes implicates oligodendroglia in multiple sclerosis susceptibility. | Meijer M et al. | β | 2022 | β |
| Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia. | Palmer DS et al. | β | 2022 | β |
| Functional annotation of breast cancer risk loci: current progress and future directions. | Romualdo Cardoso S et al. | β | 2022 | β |
| Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1. | Restuadi R et al. | β | 2022 | β |
| Functional Implications of Intergenic GWAS SNPs in Immune-Related LncRNAs. | Castellanos-Rubio A et al. | β | 2022 | β |
| Gene-lifestyle interactions in the genomics of human complex traits. | Laville V et al. | β | 2022 | β |
| Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate. | Mishra A et al. | β | 2022 | β |
| Genetic analysis of right heart structure and function in 40,000 people. | Pirruccello JP et al. | β | 2022 | β |
| Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis. | Grotzinger AD et al. | β | 2022 | β |
| Genetic identification of tissues and cell types underlying attention-deficit/hyperactivity disorder. | Wei WQ et al. | β | 2022 | β |
| Genetic variants associated with psychiatric disorders are enriched at epigenetically active sites in lymphoid cells. | Lynall ME et al. | β | 2022 | β |
| Genome-wide analyses of 200,453 individuals yield new insights into the causes and consequences of clonal hematopoiesis. | Kar SP et al. | β | 2022 | β |
| Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. | Eising E et al. | β | 2022 | β |
| Genome-wide analysis identifies impaired axonogenesis in chronic overlapping pain conditions. | Khoury S et al. | β | 2022 | β |
| Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles. | Hautakangas H et al. | β | 2022 | β |
| Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. | Barc J et al. | β | 2022 | β |
| Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure. | Levin MG et al. | β | 2022 | β |
| Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. | Qi G et al. | β | 2022 | β |
| Genome-wide association study of musical beat synchronization demonstrates high polygenicity. | Niarchou M et al. | β | 2022 | β |
| Genome-wide association study of occupational attainment as a proxy for cognitive reserve. | Ko H et al. | β | 2022 | β |
| Genome-wide imputed differential expression enrichment analysis identifies trait-relevant tissues. | Ghaffar A et al. | β | 2022 | β |
| Genomic correlation, shared loci, and causal relationship between obesity and polycystic ovary syndrome: a large-scale genome-wide cross-trait analysis. | Liu Q et al. | β | 2022 | β |
| GWAS and autoimmunity: What have we learned and what next. | Gerussi A et al. | β | 2022 | β |
| Heritability enrichment in context-specific regulatory networks improves phenotype-relevant tissue identification. | Feng Z et al. | β | 2022 | β |
| Identifying disease-critical cell types and cellular processes by integrating single-cell RNA-sequencing and human genetics. | Jagadeesh KA et al. | β | 2022 | β |
| Identifying enhancer properties associated with genetic risk for complex traits using regulome-wide association studies. | Casella AM et al. | β | 2022 | β |
| Immune cell multiomics analysis reveals contribution of oxidative phosphorylation to B-cell functions and organ damage of lupus. | Takeshima Y et al. | β | 2022 | β |
| Incorporating regulatory interactions into gene-set analyses for GWAS data: A controlled analysis with the MAGMA tool. | Groenewoud D et al. | β | 2022 | β |
| Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. | Agrawal S et al. | β | 2022 | β |
| Integrated bioinformatics-based identification of diagnostic markers in Alzheimer disease. | Chen D et al. | β | 2022 | β |
| Integrating single-cell sequencing data with GWAS summary statistics reveals CD16+monocytes and memory CD8+T cells involved in severe COVID-19. | Ma Y et al. | β | 2022 | β |
| Integration of Distinct Analysis Strategies Improves Tissue-Trait Association Identification. | Yang Z et al. | β | 2022 | β |
| Integrative transcriptome-wide analysis of atopic dermatitis for drug repositioning. | Song J et al. | β | 2022 | β |
| Investigating the shared genetic architecture of uterine leiomyoma and breast cancer: A genome-wide cross-trait analysis. | Wu X et al. | β | 2022 | β |
| Leveraging gene co-regulation to identify gene sets enriched for disease heritability. | Siewert-Rocks KM et al. | β | 2022 | β |
| Leveraging the Genetic Diversity of Human Stem Cells in Therapeutic Approaches. | Tegtmeyer M et al. | β | 2022 | β |
| Leveraging the local genetic structure for trans-ancestry association mapping. | Xiao J et al. | β | 2022 | β |
| Locus-level antagonistic selection shaped the polygenic architecture of human complex diseases. | Song W et al. | β | 2022 | β |
| Long-Read Genome Sequencing Provides Molecular Insights into Scavenging and Societal Complexity in Spotted Hyena Crocuta crocuta. | Shao Y et al. | β | 2022 | β |
| Mapping cis-regulatory elements in human neurons links psychiatric disease heritability and activity-regulated transcriptional programs. | Sanchez-Priego C et al. | β | 2022 | β |
| Mapping genomic loci implicates genes and synaptic biology in schizophrenia. | Trubetskoy V et al. | β | 2022 | β |
| Mediators of Capillary-to-Venule Conversion in the Chronic Inflammatory Skin Disease Psoriasis. | He Y et al. | β | 2022 | β |
| Model Comparison of Heritability Enrichment Analysis in Livestock Population. | Cai X et al. | β | 2022 | β |
| Molecular rhythm alterations in prefrontal cortex and nucleus accumbens associated with opioid use disorder. | Xue X et al. | β | 2022 | β |
| Multi-ancestry eQTL meta-analysis of human brain identifies candidate causal variants for brain-related traits. | Zeng B et al. | β | 2022 | β |
| Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis. | Ishigaki K et al. | β | 2022 | β |
| Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversity. | Tsuo K et al. | β | 2022 | β |
| Multiplexed functional genomic assays to decipher the noncoding genome. | Cooper YA et al. | β | 2022 | β |
| Multi-trait and cross-population genome-wide association studies across autoimmune and allergic diseases identify shared and distinct genetic component. | Shirai Y et al. | β | 2022 | β |
| Multivariate genome-wide association study on tissue-sensitive diffusion metrics highlights pathways that shape the human brain. | Fan CC et al. | β | 2022 | β |
| Omics approaches to discover pathophysiological pathways contributing to human pain. | Diatchenko L et al. | β | 2022 | β |
| Partitioning gene-mediated disease heritability without eQTLs. | Weiner DJ et al. | β | 2022 | β |
| Plasma IL-12/IFN-Ξ³ axis predicts cognitive trajectories in cognitively unimpaired older adults. | Yang HS et al. | β | 2022 | β |
| Polygenic contribution to the relationship of loneliness and social isolation with schizophrenia. | Andreu-Bernabeu Γ et al. | β | 2022 | β |
| Polygenic enrichment distinguishes disease associations of individual cells in single-cell RNA-seq data. | Zhang MJ et al. | β | 2022 | β |
| Powerful and robust inference of complex phenotypes' causal genes with dependent expression quantitative loci by a median-based Mendelian randomization. | Jiang L et al. | β | 2022 | β |
| Predicting causal genes from psychiatric genome-wide association studies using high-level etiological knowledge. | Wainberg M et al. | β | 2022 | β |
| Rare coding variants in ten genes confer substantial risk for schizophrenia. | Singh T et al. | β | 2022 | β |
| Redefining tissue specificity of genetic regulation of gene expression in the presence of allelic heterogeneity. | Arvanitis M et al. | β | 2022 | β |
| scGWAS: landscape of trait-cell type associations by integrating single-cell transcriptomics-wide and genome-wide association studies. | Jia P et al. | β | 2022 | β |
| Sex-specific epigenetic development in the mouse hypothalamic arcuate nucleus pinpoints human genomic regions associated with body mass index. | MacKay H et al. | β | 2022 | β |
| Shared components of heritability across genetically correlated traits. | Ballard JL et al. | β | 2022 | β |
| Shared genetics and causality underlying epilepsy and attention-deficit hyperactivity disorder. | Wu Y et al. | β | 2022 | β |
| Single-cell genomic profiling of human dopamine neurons identifies a population that selectively degenerates in Parkinson's disease. | Kamath T et al. | β | 2022 | β |
| Single-cell RNA-seq reveals cell type-specific molecular and genetic associations to lupus. | Perez RK et al. | β | 2022 | β |
| Single-cell RNA sequencing reveals time- and sex-specific responses of mouse spinal cord microglia to peripheral nerve injury and links ApoE to chronic pain. | Tansley S et al. | β | 2022 | β |
| SNP-to-gene linking strategies reveal contributions of enhancer-related and candidate master-regulator genes to autoimmune disease. | Dey KK et al. | β | 2022 | β |
| Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p. | Weiner DJ et al. | β | 2022 | β |
| Super interactive promoters provide insight into cell type-specific regulatory networks in blood lineage cell types. | Wen J et al. | β | 2022 | β |
| Systematic discovery and perturbation of regulatory genes in human T cells reveals the architecture of immune networks. | Freimer JW et al. | β | 2022 | β |
| Systematic Heritability and Heritability Enrichment Analysis for Diabetes Complications in UK Biobank and ACCORD Studies. | Kim J et al. | β | 2022 | β |
| The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia. | Nehme R et al. | β | 2022 | β |
| The energy balance model of obesity: beyond calories in, calories out. | Hall KD et al. | β | 2022 | β |
| The genetics of obesity: from discovery to biology. | Loos RJF et al. | β | 2022 | β |
| The nuclear receptor THRB facilitates differentiation of human PSCs into more mature hepatocytes. | Ma H et al. | β | 2022 | β |
| Transcriptional atlas analysis from multiple tissues reveals the expression specificity patterns in beef cattle. | Zhang T et al. | β | 2022 | β |
| TSABL: Trait Specific Annotation Based Locus predictor. | Lorenz K et al. | β | 2022 | β |
| Uncovering mechanisms of brain inflammation in Alzheimer's disease with APOE4: Application of single cell-type lipidomics. | Asante I et al. | β | 2022 | β |
| Unfolding the genotype-to-phenotype black box of cardiovascular diseases through cross-scale modeling. | Xi X et al. | β | 2022 | β |
| webTWAS: a resource for disease candidate susceptibility genes identified by transcriptome-wide association study. | Cao C et al. | β | 2022 | β |
| 3D promoter architecture re-organization during iPSC-derived neuronal cell differentiation implicates target genes for neurodevelopmental disorders. | Su C et al. | β | 2021 | β |
| Addiction-Associated Genetic Variants Implicate Brain Cell Type- and Region-Specific Cis-Regulatory Elements in Addiction Neurobiology. | Srinivasan C et al. | β | 2021 | β |
| A genome-wide association study of the frailty index highlights brain pathways in ageing. | Atkins JL et al. | β | 2021 | β |
| A model and test for coordinated polygenic epistasis in complex traits. | Sheppard B et al. | β | 2021 | β |
| A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus. | Hardcastle AJ et al. | β | 2021 | β |
| An integrated approach to identify environmental modulators of genetic risk factors for complex traits. | Balliu B et al. | β | 2021 | β |
| A regulatory variant at 3q21.1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density. | Sinnott-Armstrong N et al. | β | 2021 | β |
| A transcriptome-wide association study of Alzheimer's disease using prediction models of relevant tissues identifies novel candidate susceptibility genes. | Sun Y et al. | β | 2021 | β |
| A transcriptome-wide association study to detect novel genes for volumetric bone mineral density. | Liu A et al. | β | 2021 | β |
| Bench Research Informed by GWAS Results. | Kondratyev NV et al. | β | 2021 | β |
| Beyond association: successes and challenges in linking non-coding genetic variation to functional consequences that modulate Alzheimer's disease risk. | Novikova G et al. | β | 2021 | β |
| Brain gene co-expression networks link complement signaling with convergent synaptic pathology in schizophrenia. | Kim M et al. | β | 2021 | β |
| Causal Inference Methods to Integrate Omics and Complex Traits. | Porcu E et al. | β | 2021 | β |
| Cellular Models and High-Throughput Screening for Genetic Causality of Intellectual Disability. | Fell CW et al. | β | 2021 | β |
| Chromatin accessibility and gene expression during adipocyte differentiation identify context-dependent effects at cardiometabolic GWAS loci. | Perrin HJ et al. | β | 2021 | β |
| Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep. | Zhao B et al. | β | 2021 | β |
| Convergence and Divergence in the Genetics of Psychiatric Disorders From Pathways to Developmental Stages. | Shohat S et al. | β | 2021 | β |
| Cortical cellular diversity and development in schizophrenia. | Price AJ et al. | β | 2021 | β |
| Cross-platform transcriptional profiling identifies common and distinct molecular pathologies in Lewy body diseases. | Feleke R et al. | β | 2021 | β |
| CSEA-DB: an omnibus for human complex trait and cell type associations. | Dai Y et al. | β | 2021 | β |
| Delineating the Genetic Component of Gene Expression in Major Depression. | Dall'Aglio L et al. | β | 2021 | β |
| Dendritic Cells: Neglected Modulators of Peripheral Immune Responses and Neuroinflammation in Mood Disorders? | Leite Dantas R et al. | β | 2021 | β |
| Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals. | Stanzick KJ et al. | β | 2021 | β |
| Dissecting polygenic signals from genome-wide association studies on human behaviour. | Abdellaoui A et al. | β | 2021 | β |
| Editing GWAS: experimental approaches to dissect and exploit disease-associated genetic variation. | Rao S et al. | β | 2021 | β |
| Estimating heritability and its enrichment in tissue-specific gene sets in admixed populations. | Luo Y et al. | β | 2021 | β |
| Estimating the effective sample size in association studies of quantitative traits. | Ziyatdinov A et al. | β | 2021 | β |
| Evolution of DNA methylation in the human brain. | Jeong H et al. | β | 2021 | β |
| From GWAS to Gene: Transcriptome-Wide Association Studies and Other Methods to Functionally Understand GWAS Discoveries. | Li B et al. | β | 2021 | β |
| From serendipity to rational drug design in brain disorders: in silico, inΒ vitro, and inΒ vivo approaches. | Oh H et al. | β | 2021 | β |
| Gaining insight into metabolic diseases from human genetic discoveries. | Claussnitzer M et al. | β | 2021 | β |
| Gene-environment correlations and causal effects of childhood maltreatment on physical and mental health: a genetically informed approach. | Warrier V et al. | β | 2021 | β |
| Gene expression imputation and cell-type deconvolution in human brain with spatiotemporal precision and its implications for brain-related disorders. | Pei G et al. | β | 2021 | β |
| Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health. | Strausz S et al. | β | 2021 | β |
| Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning. | Liu Y et al. | β | 2021 | β |
| Genetic architecture of four smoking behaviors using partitioned SNP heritability. | Evans LM et al. | β | 2021 | β |
| Genetic Epidemiology of Complex Phenotypes. | O'Rielly DD et al. | β | 2021 | β |
| Genetic insights into biological mechanisms governing human ovarian ageing. | Ruth KS et al. | β | 2021 | β |
| Genetic mapping of developmental trajectories for complex traits and diseases. | Shulman ED et al. | β | 2021 | β |
| Genetics of migraine. | Ducros A | β | 2021 | β |
| GenNet framework: interpretable deep learning for predicting phenotypes from genetic data. | van Hilten A et al. | β | 2021 | β |
| Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders. | Eijsbouts C et al. | β | 2021 | β |
| Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. | Gialluisi A et al. | β | 2021 | β |
| Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women. | Jones G et al. | β | 2021 | β |
| Genomic analysis of diet composition finds novel loci and associations with health and lifestyle. | Meddens SFW et al. | β | 2021 | β |
| Genoppi is an open-source software for robust and standardized integration of proteomic and genetic data. | Pintacuda G et al. | β | 2021 | β |
| GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression. | Wu Y et al. | β | 2021 | β |
| H3K27ac HiChIP in prostate cell lines identifies risk genes for prostate cancer susceptibility. | Giambartolomei C et al. | β | 2021 | β |
| Heritability Enrichment Implicates Microglia in Parkinson's Disease Pathogenesis. | Andersen MS et al. | β | 2021 | β |
| Heritability Enrichment of Immunoglobulin G N-Glycosylation in Specific Tissues. | Li X et al. | β | 2021 | β |
| Human genetic analyses of organelles highlight the nucleus in age-related trait heritability. | Gupta R et al. | β | 2021 | β |
| Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder. | Bonelli R et al. | β | 2021 | β |
| Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets. | MΓ‘rquez-Luna C et al. | β | 2021 | β |
| Inflammation and JNK's Role in Niacin-GPR109A Diminished Flushed Effect in Microglial and Neuronal Cells With Relevance to Schizophrenia. | Ansarey SH | β | 2021 | β |
| InTACT: An adaptive and powerful framework for joint-tissue transcriptome-wide association studies. | Bae YE et al. | β | 2021 | β |
| Integration of Alzheimer's disease genetics and myeloid genomics identifies disease risk regulatory elements and genes. | Novikova G et al. | β | 2021 | β |
| Integration of a single-step genome-wide association study with a multi-tissue transcriptome analysis provides novel insights into the genetic basis of wool and weight traits in sheep. | Zhao B et al. | β | 2021 | β |
| Investigating asthma heterogeneity through shared and distinct genetics: Insights from genome-wide cross-trait analysis. | Zhu Z et al. | β | 2021 | β |
| Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction. | Demange PA et al. | β | 2021 | β |
| Investigating the shared genetic architecture between multiple sclerosis and inflammatory bowel diseases. | Yang Y et al. | β | 2021 | β |
| Leveraging eQTLs to identify individual-level tissue of interest for a complex trait. | Majumdar A et al. | β | 2021 | β |
| Leveraging expression from multiple tissues using sparse canonical correlation analysis and aggregate tests improves the power of transcriptome-wide association studies. | Feng H et al. | β | 2021 | β |
| Leveraging phenotypic variability to identify genetic interactions in human phenotypes. | Marderstein AR et al. | β | 2021 | β |
| Leveraging Single-Cell RNA-seq Data to Uncover the Association Between Cell Type and Chronic Liver Diseases. | Ye X et al. | β | 2021 | β |
| Machine Learning Identifies Six Genetic Variants and Alterations in the Heart Atrial Appendage as Key Contributors to PD Risk Predictivity. | Ho D et al. | β | 2021 | β |
| Mapping the genetic architecture of human traits to cell types in the kidney identifies mechanisms of disease and potential treatments. | Sheng X et al. | β | 2021 | β |
| Mapping the human genetic architecture of COVID-19. | COVID-19 Host Genetics Initiative | β | 2021 | β |
| Meta-Analyses of Splicing and Expression Quantitative Trait Loci Identified Susceptibility Genes of Glioma. | Patro CPK et al. | β | 2021 | β |
| Migraine: disease characterisation, biomarkers, and precision medicine. | Ashina M et al. | β | 2021 | β |
| Modeling regulatory network topology improves genome-wide analyses of complex human traits. | Zhu X et al. | β | 2021 | β |
| Multi-omics study for interpretation of genome-wide association study. | Akiyama M | β | 2021 | β |
| Mutations in DISC1 alter IP<sub>3</sub>R and voltage-gated Ca<sup>2+</sup> channel functioning, implications for major mental illness. | Rittenhouse AR et al. | β | 2021 | β |
| Novel characterization of the multivariate genetic architecture of internalizing psychopathology and alcohol use. | Colbert SMC et al. | β | 2021 | β |
| One size does not fit all. Genomics differentiates among anorexia nervosa, bulimia nervosa, and binge-eating disorder. | HΓΌbel C et al. | β | 2021 | β |
| Overlapping Genetic Architecture Between Schizophrenia and Neurodegenerative Disorders. | Li C et al. | β | 2021 | β |
| Partitioned glioma heritability shows subtype-specific enrichment in immune cells. | Ostrom QT et al. | β | 2021 | β |
| Pig genome functional annotation enhances the biological interpretation of complex traits and human disease. | Pan Z et al. | β | 2021 | β |
| Polygenic risk modeling with latent trait-related genetic components. | Aguirre M et al. | β | 2021 | β |
| Population-specific causal disease effect sizes in functionally important regions impacted by selection. | Shi H et al. | β | 2021 | β |
| Predicting regulatory variants using a dense epigenomic mapped CNN model elucidated the molecular basis of trait-tissue associations. | Pei G et al. | β | 2021 | β |
| Rare genetic variants affecting urine metabolite levels link population variation to inborn errors of metabolism. | Cheng Y et al. | β | 2021 | β |
| Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease. | Shadrin AA et al. | β | 2021 | β |
| Single-cell epigenomics reveals mechanisms of human cortical development. | Ziffra RS et al. | β | 2021 | β |
| Single-Cell RNA Sequencing in Parkinson's Disease. | Ma SX et al. | β | 2021 | β |
| Single cell transcriptomics of primate sensory neurons identifies cell types associated with chronic pain. | Kupari J et al. | β | 2021 | β |
| Single-nucleus chromatin accessibility and transcriptomic characterization of Alzheimer's disease. | Morabito S et al. | β | 2021 | β |
| Step-by-Step Construction of Gene Co-Expression Network Analysis for Identifying Novel Biomarkers of Sepsis Occurrence and Progression. | Yu X et al. | β | 2021 | β |
| Strategies to Understand the Weight-Reduced State: Genetics and Brain Imaging. | Loos RJF et al. | β | 2021 | β |
| System Genetics Including Causal Inference Identify Immune Targets for Coronary Artery Disease and the Lifespan. | Bon-Baret V et al. | β | 2021 | β |
| The distribution of common-variant effect sizes. | O'Connor LJ | β | 2021 | β |
| The dynamic, combinatorial cis-regulatory lexicon of epidermal differentiation. | Kim DS et al. | β | 2021 | β |
| The familiar dialectic between overclaiming and moral outrage over brain biology: disconnected from what matters. | Hyman SE | β | 2021 | β |
| The genetic architecture of the human thalamus and its overlap with ten common brain disorders. | ElvsΓ₯shagen T et al. | β | 2021 | β |
| The Landscape of the Heritable Cancer Genome. | Fanfani V et al. | β | 2021 | β |
| The Relationship Between Inflammation and Post-traumatic Stress Disorder. | Sun Y et al. | β | 2021 | β |
| Three decades of ASD genetics: building a foundation for neurobiological understanding and treatment. | Eyring KW et al. | β | 2021 | β |
| Transcriptional Alterations in Dorsolateral Prefrontal Cortex and Nucleus Accumbens Implicate Neuroinflammation and Synaptic Remodeling in Opioid Use Disorder. | Seney ML et al. | β | 2021 | β |
| Transcriptional mediators of treatment resistance in lethal prostate cancer. | He MX et al. | β | 2021 | β |
| Transcriptomic Insight Into the Polygenic Mechanisms Underlying Psychiatric Disorders. | Hernandez LM et al. | β | 2021 | β |
| Using Collaborative Mixed Models to Account for Imputation Uncertainty in Transcriptome-Wide Association Studies. | Shi X et al. | β | 2021 | β |
| Wringing Biological Insight From Polygenic Signals. | Hyman SE | β | 2021 | β |
| X-chromosome influences on neuroanatomical variation in humans. | Mallard TT et al. | β | 2021 | β |
| A brief history of human disease genetics. | Claussnitzer M et al. | β | 2020 | β |
| A chromosomal connectome for psychiatric and metabolic risk variants in adult dopaminergic neurons. | Espeso-Gil S et al. | β | 2020 | β |
| Advances in genetics toward identifying pathogenic cell states of rheumatoid arthritis. | Amariuta T et al. | β | 2020 | β |
| An Activity-Mediated Transition in Transcription in Early Postnatal Neurons. | Stroud H et al. | β | 2020 | β |
| Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy. | Pirruccello JP et al. | β | 2020 | β |
| Annotations capturing cell type-specific TF binding explain a large fraction of disease heritability. | van de Geijn B et al. | β | 2020 | β |
| A Review of Statistical Methods for Identifying Trait-Relevant Tissues and Cell Types. | Zhu H et al. | β | 2020 | β |
| A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disorders. | Agarwal D et al. | β | 2020 | β |
| A tissue-specific collaborative mixed model for jointly analyzing multiple tissues in transcriptome-wide association studies. | Shi X et al. | β | 2020 | β |
| Bayesian reassessment of the epigenetic architecture of complex traits. | Trejo Banos D et al. | β | 2020 | β |
| Comprehensive analyses of 723 transcriptomes enhance genetic and biological interpretations for complex traits in cattle. | Fang L et al. | β | 2020 | β |
| Convergent Evidence for Predispositional Effects of Brain Gray Matter Volume on Alcohol Consumption. | Baranger DAA et al. | β | 2020 | β |
| Convergent molecular, cellular, and cortical neuroimaging signatures of major depressive disorder. | Anderson KM et al. | β | 2020 | β |
| Cross-disorder genetic analyses implicate dopaminergic signaling as a biological link between Attention-Deficit/Hyperactivity Disorder and obesity measures. | Mota NR et al. | β | 2020 | β |
| Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache. | Siewert KM et al. | β | 2020 | β |
| Deriving stratified effects from joint models investigating gene-environment interactions. | Laville V et al. | β | 2020 | β |
| Developmental Gene Expression Differences between Humans and Mammalian Models. | Cardoso-Moreira M et al. | β | 2020 | β |
| Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis. | Vujkovic M et al. | β | 2020 | β |
| Dosage-sensitive molecular mechanisms are associated with the tissue-specificity of traits and diseases. | Jubran J et al. | β | 2020 | β |
| Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders. | Mencacci NE et al. | β | 2020 | β |
| Epigenomics and genotype-phenotype association analyses reveal conserved genetic architecture of complex traits in cattle and human. | Liu S et al. | β | 2020 | β |
| Evolutionary perspectives on polygenic selection, missing heritability, and GWAS. | Uricchio LH | β | 2020 | β |
| Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits. | Quach BC et al. | β | 2020 | β |
| From GWAS to Function: Using Functional Genomics to Identify the Mechanisms Underlying Complex Diseases. | Cano-Gamez E et al. | β | 2020 | β |
| Genetic basis of falling risk susceptibility in the UK Biobank Study. | Trajanoska K et al. | β | 2020 | β |
| Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease. | Bryois J et al. | β | 2020 | β |
| Genetic mapping of etiologic brain cell types for obesity. | Timshel PN et al. | β | 2020 | β |
| Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans. | Schlosser P et al. | β | 2020 | β |
| Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. | Landi MT et al. | β | 2020 | β |
| Genome-wide Association Study for Vitamin D Levels Reveals 69 Independent Loci. | Manousaki D et al. | β | 2020 | β |
| Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. | Revez JA et al. | β | 2020 | β |
| Genome wide association study of incomplete hippocampal inversion in adolescents. | Cury C et al. | β | 2020 | β |
| Genome-wide association study of MRI markers of cerebral small vessel disease in 42,310 participants. | Persyn E et al. | β | 2020 | β |
| Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. | Zhou H et al. | β | 2020 | β |
| Genomic dissection of 43 serum urate-associated loci provides multiple insights into molecular mechanisms of urate control. | Boocock J et al. | β | 2020 | β |
| Genomics at cellular resolution: insights into cognitive disorders and their evolution. | Berto S et al. | β | 2020 | β |
| Global Analysis of Transcription Start Sites in the New Ovine Reference Genome (<i>Oar rambouillet v1.0</i>). | Salavati M et al. | β | 2020 | β |
| GWAS and fine-mapping of livability and six disease traits in Holstein cattle. | Freebern E et al. | β | 2020 | β |
| Identification of relevant hub genes for early intervention at gene coexpression modules with altered predicted expression in schizophrenia. | Rodriguez-LΓ³pez J et al. | β | 2020 | β |
| Improving the informativeness of Mendelian disease-derived pathogenicity scores for common disease. | Kim SS et al. | β | 2020 | β |
| Improving the trans-ancestry portability of polygenic risk scores by prioritizing variants in predicted cell-type-specific regulatory elements. | Amariuta T et al. | β | 2020 | β |
| Incomplete annotation has a disproportionate impact on our understanding of Mendelian and complex neurogenetic disorders. | Zhang D et al. | β | 2020 | β |
| Index and biological spectrum of human DNase I hypersensitive sites. | Meuleman W et al. | β | 2020 | β |
| Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells. | Bao EL et al. | β | 2020 | β |
| Integrating RNA-Seq with GWAS reveals novel insights into the molecular mechanism underpinning ketosis in cattle. | Yan Z et al. | β | 2020 | β |
| Integration of GWAS Summary Statistics and Gene Expression Reveals Target Cell Types Underlying Kidney Function Traits. | Li Y et al. | β | 2020 | β |
| Integrative analysis of scRNA-seq and GWAS data pinpoints periportal hepatocytes as the relevant liver cell types for blood lipids. | Hao X et al. | β | 2020 | β |
| In The Blood: Connecting Variant to Function In Human Hematopoiesis. | Nandakumar SK et al. | β | 2020 | β |
| Investigation of Schizophrenia with Human Induced Pluripotent Stem Cells. | Powell SK et al. | β | 2020 | β |
| Leveraging gene co-expression patterns to infer trait-relevant tissues in genome-wide association studies. | Shang L et al. | β | 2020 | β |
| Leveraging mouse chromatin data for heritability enrichment informs common disease architecture and reveals cortical layer contributions to schizophrenia. | Hook PW et al. | β | 2020 | β |
| Localizing Components of Shared Transethnic Genetic Architecture of Complex Traits from GWAS Summary Data. | Shi H et al. | β | 2020 | β |
| Massively parallel techniques for cataloguing the regulome of the human brain. | Townsley KG et al. | β | 2020 | β |
| Maternal antioxidant treatment prevents the adverse effects of prenatal stress on the offspring's brain and behavior. | Scott H et al. | β | 2020 | β |
| Mechanisms of tissue and cell-type specificity in heritable traits andΒ diseases. | Hekselman I et al. | β | 2020 | β |
| Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia. | Hysi PG et al. | β | 2020 | β |
| Migraine. | Ashina M | β | 2020 | β |
| Minimal phenotyping yields genome-wide association signals of low specificity for major depression. | Cai N et al. | β | 2020 | β |
| Modeling the complex genetic architectures of brain disease. | Fernando MB et al. | β | 2020 | β |
| Multiple-Tissue Integrative Transcriptome-Wide Association Studies Discovered New Genes Associated With Amyotrophic Lateral Sclerosis. | Xiao L et al. | β | 2020 | β |
| Novel Approaches for Identifying the Molecular Background of Schizophrenia. | Golov AK et al. | β | 2020 | β |
| Partitioning gene-based variance of complex traits by gene score regression. | Zhang W et al. | β | 2020 | β |
| Pathway paradigms revealed from the genetics of inflammatory bowel disease. | Graham DB et al. | β | 2020 | β |
| Prioritizing disease and trait causal variants at the TNFAIP3 locus using functional and genomic features. | Ray JP et al. | β | 2020 | β |
| QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes. | Zheng Z et al. | β | 2020 | β |
| Quantifying genetic effects on disease mediated by assayed gene expression levels. | Yao DW et al. | β | 2020 | β |
| Regulatory landscape in brain development and disease. | Spiess K et al. | β | 2020 | β |
| S100B has pleiotropic effects on vaso-occlusive manifestations in sickle cell disease. | Zhang X et al. | β | 2020 | β |
| Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer's and Parkinson's diseases. | Corces MR et al. | β | 2020 | β |
| sn-spMF: matrix factorization informs tissue-specific genetic regulation of gene expression. | He Y et al. | β | 2020 | β |
| The emergence and promise of single-cell temporal-omics approaches. | Lederer AR et al. | β | 2020 | β |
| The genetic architecture of appendicular lean mass characterized by association analysis in the UK Biobank study. | Pei YF et al. | β | 2020 | β |
| The genetic architecture of the human cerebral cortex. | Grasby KL et al. | β | 2020 | β |
| The Genetic Relevance of Human Induced Pluripotent Stem Cell-Derived Microglia to Alzheimer's Disease and Major Neuropsychiatric Disorders. | Butler Iii RR et al. | β | 2020 | β |
| The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls. | Coleman JRI et al. | β | 2020 | β |
| The polygenic architecture of schizophrenia - rethinking pathogenesis and nosology. | Smeland OB et al. | β | 2020 | β |
| Tissue-specific genetic features inform prediction of drug side effects in clinical trials. | Duffy Γ et al. | β | 2020 | β |
| Tissue specific regulation of transcription in endometrium and association with disease. | Mortlock S et al. | β | 2020 | β |
| Transcriptional and Cellular Diversity of the Human Heart. | Tucker NR et al. | β | 2020 | β |
| TSEA-DB: a trait-tissue association map for human complex traits and diseases. | Jia P et al. | β | 2020 | β |
| Using human genetics to understand the disease impacts of testosterone in men and women. | Ruth KS et al. | β | 2020 | β |
| 2018 William Allan Award: Discovering the Genes for Common Disease: From Families to Populations. | Lander ES | β | 2019 | β |
| A genome-wide association analysis identifies 16 novel susceptibility loci for carpal tunnel syndrome. | Wiberg A et al. | β | 2019 | β |
| A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment. | Schork AJ et al. | β | 2019 | β |
| A Longitudinal Model of Human Neuronal Differentiation for Functional Investigation of Schizophrenia Polygenic Risk. | Ori APS et al. | β | 2019 | β |
| A statistical framework for cross-tissue transcriptome-wide association analysis. | Hu Y et al. | β | 2019 | β |
| Benchmarker: An Unbiased, Association-Data-Driven Strategy to Evaluate Gene Prioritization Algorithms. | Fine RS et al. | β | 2019 | β |
| Characterising the genetic basis of immune response variation to identify causal mechanisms underlying disease susceptibility. | Rotival M | β | 2019 | β |
| Chromatin activity at GWAS loci identifies T cell states driving complex immune diseases. | Soskic B et al. | β | 2019 | β |
| Colonic epithelial cell diversity in health and inflammatory bowel disease. | Parikh K et al. | β | 2019 | β |
| Deconvolution of transcriptional networks identifies TCF4 as a master regulator in schizophrenia. | Doostparast Torshizi A et al. | β | 2019 | β |
| Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders. | Sullivan PF et al. | β | 2019 | β |
| DESE: estimating driver tissues by selective expression of genes associated with complex diseases or traits. | Jiang L et al. | β | 2019 | β |
| deTS: tissue-specific enrichment analysis to decode tissue specificity. | Pei G et al. | β | 2019 | β |
| Dyslexia associated functional variants in Europeans are not associated with dyslexia in Chinese. | Liu L et al. | β | 2019 | β |
| Genes with High Network Connectivity Are Enriched for Disease Heritability. | Kim SS et al. | β | 2019 | β |
| Genetic analyses of human fetal retinal pigment epithelium gene expression suggest ocular disease mechanisms. | Liu B et al. | β | 2019 | β |
| Genetic correlations of psychiatric traits with body composition and glycemic traits are sex- and age-dependent. | HΓΌbel C et al. | β | 2019 | β |
| Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. | Sakornsakolpat P et al. | β | 2019 | β |
| Genetic mapping of cell type specificity for complex traits. | Watanabe K et al. | β | 2019 | β |
| Genetic predisposition to mosaic Y chromosome loss in blood. | Thompson DJ et al. | β | 2019 | β |
| Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income. | Hill WD et al. | β | 2019 | β |
| Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. | Shungin D et al. | β | 2019 | β |
| Genome-wide association analysis of 19,629 individuals identifies variants influencing regional brain volumes and refines their genetic co-architecture with cognitive and mental health traits. | Zhao B et al. | β | 2019 | β |
| Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. | Kranzler HR et al. | β | 2019 | β |
| Genome-wide association study of medication-use and associated disease in the UK Biobank. | Wu Y et al. | β | 2019 | β |
| Genome-wide association study of post-traumatic stress disorder reexperiencing symptoms in >165,000 US veterans. | Gelernter J et al. | β | 2019 | β |
| Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. | Helgeland Γ et al. | β | 2019 | β |
| Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions. | Howard DM et al. | β | 2019 | β |
| Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. | HΓΌbel C et al. | β | 2019 | β |
| Genomic updates in understanding PTSD. | Sharma S et al. | β | 2019 | β |
| GREP: genome for REPositioning drugs. | Sakaue S et al. | β | 2019 | β |
| GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation. | Terao C et al. | β | 2019 | β |
| IMPACT: Genomic Annotation of Cell-State-Specific Regulatory Elements Inferred from the Epigenome of Bound Transcription Factors. | Amariuta T et al. | β | 2019 | β |
| Informing disease modelling with brain-relevant functional genomic annotations. | Reynolds RH et al. | β | 2019 | β |
| Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMI. | Major M et al. | β | 2019 | β |
| Leveraging brain cortex-derived molecular data to elucidate epigenetic and transcriptomic drivers of complex traits and disease. | Hatcher C et al. | β | 2019 | β |
| Leveraging Polygenic Functional Enrichment to Improve GWAS Power. | Kichaev G et al. | β | 2019 | β |
| Low-frequency variation in TP53 has large effects on head circumference and intracranial volume. | Haworth S et al. | β | 2019 | β |
| Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. | Warrington NM et al. | β | 2019 | β |
| Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson's disease heritability. | Reynolds RH et al. | β | 2019 | β |
| Multivariate genome-wide analyses of the well-being spectrum. | Baselmans BML et al. | β | 2019 | β |
| New considerations for hiPSC-based models of neuropsychiatric disorders. | Hoffman GE et al. | β | 2019 | β |
| Novel hypotheses emerging from GWAS in migraine? | van den Maagdenberg AMJM et al. | β | 2019 | β |
| Opportunities and challenges for transcriptome-wide association studies. | Wainberg M et al. | β | 2019 | β |
| Prioritizing Parkinson's disease genes using population-scale transcriptomic data. | Li YI et al. | β | 2019 | β |
| Research Domain Criteria: Strengths, Weaknesses, and Potential Alternatives for Future Psychiatric Research. | Ross CA et al. | β | 2019 | β |
| Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration. | Ratnapriya R et al. | β | 2019 | β |
| Reverse GWAS: Using genetics to identify and model phenotypic subtypes. | Dahl A et al. | β | 2019 | β |
| Selective vulnerability in Ξ±-synucleinopathies. | Alegre-Abarrategui J et al. | β | 2019 | β |
| Single-cell transcriptomic atlas of the human retina identifies cell types associated with age-related macular degeneration. | Menon M et al. | β | 2019 | β |
| Synergistic effects of common schizophrenia risk variants. | Schrode N et al. | β | 2019 | β |
| Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes. | Zhang T et al. | β | 2018 | β |
| Characterizing the Relation Between Expression QTLs and Complex Traits: Exploring the Role of Tissue Specificity. | Ip HF et al. | β | 2018 | β |
| Cross-tissue eQTL enrichment of associations in schizophrenia. | Bettella F et al. | β | 2018 | β |
| Elucidating the genetic architecture of reproductive ageing in the Japanese population. | Horikoshi M et al. | β | 2018 | β |
| Elucidating the genetic basis of social interaction and isolation. | Day FR et al. | β | 2018 | β |
| Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes. | Westra HJ et al. | β | 2018 | β |
| Functional architecture of low-frequency variants highlights strength of negative selection across coding and non-coding annotations. | Gazal S et al. | β | 2018 | β |
| Genetic identification of brain cell types underlying schizophrenia. | Skene NG et al. | β | 2018 | β |
| Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. | Wray NR et al. | β | 2018 | β |
| Genome-wide association study for risk taking propensity indicates shared pathways with body mass index. | Clifton EAD et al. | β | 2018 | β |
| Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. | International League Against Epilepsy Consortium on Complex Epilepsies | β | 2018 | β |
| Identifying and exploiting trait-relevant tissues with multiple functional annotations in genome-wide association studies. | Hao X et al. | β | 2018 | β |
| Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood. | Qi T et al. | β | 2018 | β |
| Integration of genetics and miRNA-target gene network identified disease biology implicated in tissue specificity. | Sakaue S et al. | β | 2018 | β |
| Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits. | Hormozdiari F et al. | β | 2018 | β |
| Linking tissues to disease. | Cloney R | β | 2018 | β |
| Theme 1 Genetics and genomics. | β | β | 2018 | β |
| Tracing Early Neurodevelopment in Schizophrenia with Induced Pluripotent Stem Cells. | Ahmad R et al. | β | 2018 | β |
| Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation. | Gamazon ER et al. | β | 2018 | β |
| Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk. | Day FR et al. | β | 2017 | β |
| Inferring Relevant Cell Types for Complex Traits by Using Single-Cell Gene Expression. | Calderon D et al. | β | 2017 | β |
| Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets. | Lam M et al. | β | 2017 | β |
| Systematic tissue-specific functional annotation of the human genome highlights immune-related DNA elements for late-onset Alzheimer's disease. | Lu Q et al. | β | 2017 | β |