|
| 37034649 | Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. | medRxiv | 2023 |
| 37647564 | Cell-Type Composition Affects Adipose Gene Expression Associations With Cardiometabolic Traits. | Diabetes | 2023 |
| 37777856 | GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors. | Am J Psychiatry | 2023 |
| 37961277 | Adipose tissue eQTL meta-analysis reveals the contribution of allelic heterogeneity to gene expression regulation and cardiometabolic traits. | bioRxiv | 2023 |
| 37280435 | Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion, after accounting for BMI in adulthood. | Diabetologia | 2023 |
| 36821788 | Evaluation of polygenic risk scores to differentiate between type 1 and type 2 diabetes. | | 2023 |
| 36693378 | Loci for insulin processing and secretion provide insight into type 2 diabetes risk. | Am J Hum Genet | 2023 |
| 36798216 | Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion. | medRxiv | 2023 |
| 37425837 | Metabolome-wide Mendelian randomization characterizes heterogeneous and shared causal effects of metabolites on human health. | medRxiv | 2023 |
| 34995504 | Subcutaneous adipose tissue splice quantitative trait loci reveal differences in isoform usage associated with cardiometabolic traits. | Am J Hum Genet | 2022 |
| 35396579 | Rare coding variants in ten genes confer substantial risk for schizophrenia. | Nature | 2022 |
| 35589964 | ACE2 expression in adipose tissue is associated with cardio-metabolic risk factors and cell type composition-implications for COVID-19. | Int J Obes (Lond) | 2022 |
| 35393509 | Identification of genetic effects underlying type 2 diabetes in South Asian and European populations. | Commun Biol | 2022 |
| 35513483 | Author Correction: Identification of genetic effects underlying type 2 diabetes in South Asian and European populations. | Commun Biol | 2022 |
| 35697829 | Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals. | Commun Biol | 2022 |
| 35551307 | Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. | Nat Genet | 2022 |
| 36055244 | Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk. | Am J Hum Genet | 2022 |
| 35981533 | Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing. | Am J Hum Genet | 2022 |
| 36777998 | The HUNT study: A population-based cohort for genetic research. | Cell Genom | 2022 |
| 34459872 | FIVEx: an interactive eQTL browser across public datasets. | Bioinformatics | 2022 |
| 34378841 | A survey of functional dyspepsia in 361,360 individuals: Phenotypic and genetic cross-disease analyses. | Neurogastroenterol Motil | 2022 |
| 34916535 | Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer. | Nat Commun | 2021 |
| 31883325 | Trans-ethnic meta-analysis of rare variants in sequencing association studies. | Biostatistics | 2021 |
| 33798444 | Association of structural variation with cardiometabolic traits in Finns. | Am J Hum Genet | 2021 |
| 33585870 | Revisiting the genome-wide significance threshold for common variant GWAS. | G3: Genes, Genomes, Genetics | 2021 |
| 34108472 | Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes. | Nat Commun | 2021 |
| 34002096 | Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. | Nat Genet | 2021 |
| 33734315 | LocusZoom.js: interactive and embeddable visualization of genetic association study results. | Bioinformatics | 2021 |
| 33674754 | Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. | Mol Psychiatry | 2021 |
| 33730541 | A powerful subset-based method identifies gene set associations and improves interpretation in UK Biobank. | Am J Hum Genet | 2021 |
| 33462485 | Large-scale association analyses identify host factors influencing human gut microbiome composition. | Nat Genet | 2021 |
| 33727701 | Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. | Nat Genet | 2021 |
| 34099068 | Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences. | Hum Genomics | 2021 |
| 33720349 | Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries. | Genetics | 2021 |
| 33558525 | Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. | Nat Commun | 2021 |
| 33402679 | Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. | Nat Commun | 2021 |
| 33385400 | Causal Relationship and Shared Genetic Loci between Psoriasis and Type 2 Diabetes through Trans-Disease Meta-Analysis. | | 2021 |
| 31520493 | Combining sequence data from multiple studies: Impact of analysis strategies on rare variant calling and association results. | Genetic Epidemiology | 2020 |
| 31980570 | Ancestry-agnostic estimation of DNA sample contamination from sequence reads. | Genome Res | 2020 |
| 32466134 | Association Analysis and Meta-Analysis of Multi-Allelic Variants for Large-Scale Sequence Data. | Genes (Basel) | 2020 |
| 32769997 | GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer. | Nat Commun | 2020 |
| 32817962 | ACE2 expression in adipose tissue is associated with COVID-19 cardio-metabolic risk factors and cell type composition. | medRxiv | 2020 |
| 32915782 | Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences. | PLoS Genet | 2020 |
| 32519380 | Sequencing and imputation in GWAS: Cost-effective strategies to increase power and genomic coverage across diverse populations. | Genet Epidemiol | 2020 |
| 32511788 | Power loss due to testing association between covariate-adjusted traits and genetic variants. | Genetic Epidemiology | 2020 |
| 33339817 | Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. | Nat Commun | 2020 |
| 33230300 | Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. | Nat Genet | 2020 |
| 32504056 | Exploring and visualizing large-scale genetic associations by using PheWeb. | Nat Genet | 2020 |
| 32999275 | Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D. | Nat Commun | 2020 |
| 33320851 | Integrating comprehensive functional annotations to boost power and accuracy in gene-based association analysis. | PLoS Genet | 2020 |