|
| 36747613 | A harmonized public resource of deeply sequenced diverse human genomes. | bioRxiv | 2024 |
| 38036779 | Improving fine-mapping by modeling infinitesimal effects. | Nat Genet | 2024 |
| 38057664 | A genomic mutational constraint map using variation in 76,156 human genomes. | Nature | 2024 |
| 38057443 | Inferring compound heterozygosity from large-scale exome sequencing data. | Nat Genet | 2024 |
| 36747613 | A harmonized public resource of deeply sequenced diverse human genomes. | bioRxiv | 2024 |
| 38057664 | A genomic mutational constraint map using variation in 76,156 human genomes. | Nature | 2024 |
| 38057443 | Inferring compound heterozygosity from large-scale exome sequencing data. | Nat Genet | 2024 |
| 38036779 | Improving fine-mapping by modeling infinitesimal effects. | Nat Genet | 2024 |
| 36929174 | GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer. | Hum Mol 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 |
| 37841595 | Profiling the inflammatory bowel diseases using genetics, serum biomarkers, and smoking information. | iScience | 2023 |
| 37988105 | Association of APOE Haplotypes With Common Age-Related Ocular Diseases in 412,171 Individuals. | Invest Ophthalmol Vis Sci | 2023 |
| 38076931 | Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events. | medRxiv | 2023 |
| 37878672 | Genetic vulnerability to Crohn's disease reveals a spatially resolved epithelial restitution program. | Sci Transl Med | 2023 |
| 37961173 | Decoding Genetics, Ancestry, and Geospatial Context for Precision Health. | medRxiv | 2023 |
| 36653562 | FinnGen provides genetic insights from a well-phenotyped isolated population. | Nature | 2023 |
| 36908397 | LAVAA: a lightweight association viewer across ailments. | Bioinform Adv | 2023 |
| 36829046 | Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population. | Nature | 2023 |
| 36653560 | Mono- and biallelic variant effects on disease at biobank scale. | Nature | 2023 |
| 36653479 | Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. | Nat Med | 2023 |
| 36653354 | Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. | Nat Commun | 2023 |
| 36653343 | Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure. | Nat Commun | 2023 |
| 37464041 | Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses. | Nat Med | 2023 |
| 37400429 | Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. | Nat Commun | 2023 |
| 37080976 | Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients. | Nat Commun | 2023 |
| 37079300 | Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration. | JAMA Ophthalmol | 2023 |
| 37453564 | Genome-Wide Association Study Identifies 4 Novel Risk Loci for Small Intestinal Neuroendocrine Tumors Including a Missense Mutation in LGR5. | Gastroenterology | 2023 |
| 37253541 | Discordant calls across genotype discovery approaches elucidate variants with systematic errors. | Genome Res | 2023 |
| 36865330 | Distinct and shared genetic architectures of Gestational diabetes mellitus and Type 2 Diabetes Mellitus. | medRxiv | 2023 |
| 36993580 | Inferring compound heterozygosity from large-scale exome sequencing data. | bioRxiv | 2023 |
| 37301908 | Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. | Nat Commun | 2023 |
| 36993194 | Mapping the dynamic genetic regulatory architecture of <i>HLA</i> genes at single-cell resolution. | medRxiv | 2023 |
| 36929174 | GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer. | Hum Mol Genet | 2023 |
| 37045567 | Cohort profile: SUPER-Finland - the Finnish study for hereditary mechanisms of psychotic disorders. | BMJ Open | 2023 |
| 37425837 | Metabolome-wide Mendelian randomization characterizes heterogeneous and shared causal effects of metabolites on human health. | medRxiv | 2023 |
| 37425834 | CHARR efficiently estimates contamination from DNA sequencing data. | bioRxiv | 2023 |
| 38076931 | Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events. | medRxiv | 2023 |
| 37961173 | Decoding Genetics, Ancestry, and Geospatial Context for Precision Health. | medRxiv | 2023 |
| 37841595 | Profiling the inflammatory bowel diseases using genetics, serum biomarkers, and smoking information. | iScience | 2023 |
| 37988105 | Association of APOE Haplotypes With Common Age-Related Ocular Diseases in 412,171 Individuals. | Invest Ophthalmol Vis Sci | 2023 |
| 37878672 | Genetic vulnerability to Crohn's disease reveals a spatially resolved epithelial restitution program. | Sci Transl Med | 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 |
| 37425837 | Metabolome-wide Mendelian randomization characterizes heterogeneous and shared causal effects of metabolites on human health. | medRxiv | 2023 |
| 37425834 | CHARR efficiently estimates contamination from DNA sequencing data. | bioRxiv | 2023 |
| 36993580 | Inferring compound heterozygosity from large-scale exome sequencing data. | bioRxiv | 2023 |
| 36993194 | Mapping the dynamic genetic regulatory architecture of <i>HLA</i> genes at single-cell resolution. | medRxiv | 2023 |
| 37453564 | Genome-Wide Association Study Identifies 4 Novel Risk Loci for Small Intestinal Neuroendocrine Tumors Including a Missense Mutation in LGR5. | Gastroenterology | 2023 |
| 37253541 | Discordant calls across genotype discovery approaches elucidate variants with systematic errors. | Genome Res | 2023 |
| 37080976 | Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients. | Nat Commun | 2023 |
| 37079300 | Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration. | JAMA Ophthalmol | 2023 |