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| 36747613 | A harmonized public resource of deeply sequenced diverse human genomes. | bioRxiv | 2024 |
| 38036779 | Improving fine-mapping by modeling infinitesimal effects. | Nat Genet | 2024 |
| 36747613 | A harmonized public resource of deeply sequenced diverse human genomes. | bioRxiv | 2024 |
| 38036779 | Improving fine-mapping by modeling infinitesimal effects. | Nat Genet | 2024 |
| 36350676 | FAVOR: functional annotation of variants online resource and annotator for variation across the human genome. | Nucleic Acids Res | 2023 |
| 36350676 | FAVOR: functional annotation of variants online resource and annotator for variation across the human genome. | Nucleic Acids Res | 2023 |
| 37601974 | Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries. | Cell Genom | 2023 |
| 37755714 | An Ethical Framework for Research Using Genetic Ancestry. | Perspect Biol Med | 2023 |
| 37587338 | Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. | Nature | 2023 |
| 38000370 | CHARR efficiently estimates contamination from DNA sequencing data. | Am J Hum Genet | 2023 |
| 37640881 | Extremely sparse models of linkage disequilibrium in ancestrally diverse association studies. | Nat Genet | 2023 |
| 37961173 | Decoding Genetics, Ancestry, and Geospatial Context for Precision Health. | medRxiv | 2023 |
| 36711677 | Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. | medRxiv | 2023 |
| 37461573 | Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank. | medRxiv | 2023 |
| 37078667 | Wrestling with Social and Behavioral Genomics: Risks, Potential Benefits, and Ethical Responsibility. | Hastings Cent Rep | 2023 |
| 36755575 | Ancestry: How researchers use it and what they mean by it. | Front Genet | 2023 |
| 36755099 | Polygenic architecture of rare coding variation across 394,783 exomes. | Nature | 2023 |
| 37386106 | Patterns of item nonresponse behaviour to survey questionnaires are systematic and associated with genetic loci. | Nat Hum Behav | 2023 |
| 37253541 | Discordant calls across genotype discovery approaches elucidate variants with systematic errors. | Genome Res | 2023 |
| 36993580 | Inferring compound heterozygosity from large-scale exome sequencing data. | bioRxiv | 2023 |
| 36865150 | Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries. | medRxiv | 2023 |
| 37045567 | Cohort profile: SUPER-Finland - the Finnish study for hereditary mechanisms of psychotic disorders. | BMJ Open | 2023 |
| 37425834 | CHARR efficiently estimates contamination from DNA sequencing data. | bioRxiv | 2023 |
| 37543680 | Multi-PGS enhances polygenic prediction by combining 937 polygenic scores. | Nat Commun | 2023 |
| 37755714 | An Ethical Framework for Research Using Genetic Ancestry. | Perspect Biol Med | 2023 |
| 37961173 | Decoding Genetics, Ancestry, and Geospatial Context for Precision Health. | medRxiv | 2023 |
| 37587338 | Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. | Nature | 2023 |
| 38000370 | CHARR efficiently estimates contamination from DNA sequencing data. | Am J Hum Genet | 2023 |
| 37543680 | Multi-PGS enhances polygenic prediction by combining 937 polygenic scores. | Nat Commun | 2023 |
| 37640881 | Extremely sparse models of linkage disequilibrium in ancestrally diverse association studies. | Nat Genet | 2023 |
| 37601974 | Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries. | Cell Genom | 2023 |
| 37425834 | CHARR efficiently estimates contamination from DNA sequencing data. | bioRxiv | 2023 |
| 36993580 | Inferring compound heterozygosity from large-scale exome sequencing data. | bioRxiv | 2023 |
| 37253541 | Discordant calls across genotype discovery approaches elucidate variants with systematic errors. | Genome Res | 2023 |
| 37386106 | Patterns of item nonresponse behaviour to survey questionnaires are systematic and associated with genetic loci. | Nat Hum Behav | 2023 |
| 37078667 | Wrestling with Social and Behavioral Genomics: Risks, Potential Benefits, and Ethical Responsibility. | Hastings Cent Rep | 2023 |
| 37045567 | Cohort profile: SUPER-Finland - the Finnish study for hereditary mechanisms of psychotic disorders. | BMJ Open | 2023 |
| 37461573 | Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank. | medRxiv | 2023 |
| 36711677 | Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. | medRxiv | 2023 |
| 36865150 | Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries. | medRxiv | 2023 |
| 36755575 | Ancestry: How researchers use it and what they mean by it. | Front Genet | 2023 |
| 36755099 | Polygenic architecture of rare coding variation across 394,783 exomes. | Nature | 2023 |
| 34508597 | A data harmonization pipeline to leverage external controls and boost power in GWAS. | Hum Mol Genet | 2022 |
| 35396580 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia. | Nature | 2022 |
| 35396579 | Rare coding variants in ten genes confer substantial risk for schizophrenia. | Nature | 2022 |
| 35591975 | Genome-wide risk prediction of common diseases across ancestries in one million people. | Cell Genom | 2022 |
| 36163277 | Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups. | Nat Genet | 2022 |
| 35760976 | The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia. | Nat Commun | 2022 |
| 36138231 | SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association tests. | Nat Genet | 2022 |
| 35935918 | Incorporating family history of disease improves polygenic risk scores in diverse populations. | Cell Genom | 2022 |