|
| 37934784 | Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration. | Hum Mol Genet | 2024 |
| 37934784 | Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration. | Hum Mol Genet | 2024 |
| 36739617 | A fast linkage method for population GWAS cohorts with related individuals. | Genet Epidemiol | 2023 |
| 37804200 | Association Between Whole Blood-Derived Mitochondrial DNA Copy Number, Low-Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk. | J Am Heart Assoc | 2023 |
| 36778386 | Structural variation across 138,134 samples in the TOPMed consortium. | Res Sq | 2023 |
| 37126548 | The genetic determinants of recurrent somatic mutations in 43,693 blood genomes. | Sci Adv | 2023 |
| 36807635 | Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes. | Nature | 2023 |
| 36747810 | Structural variation across 138,134 samples in the TOPMed consortium. | bioRxiv | 2023 |
| 36739617 | A fast linkage method for population GWAS cohorts with related individuals. | Genet Epidemiol | 2023 |
| 37046083 | Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis. | Nature | 2023 |
| 37804200 | Association Between Whole Blood-Derived Mitochondrial DNA Copy Number, Low-Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk. | J Am Heart Assoc | 2023 |
| 37046083 | Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis. | Nature | 2023 |
| 37126548 | The genetic determinants of recurrent somatic mutations in 43,693 blood genomes. | Sci Adv | 2023 |
| 36747810 | Structural variation across 138,134 samples in the TOPMed consortium. | bioRxiv | 2023 |
| 36807635 | Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes. | Nature | 2023 |
| 36778386 | Structural variation across 138,134 samples in the TOPMed consortium. | Res Sq | 2023 |
| 34459872 | FIVEx: an interactive eQTL browser across public datasets. | Bioinformatics | 2022 |
| 35710628 | Genome-wide meta-analysis of iron status biomarkers and the effect of iron on all-cause mortality in HUNT. | Commun Biol | 2022 |
| 35652341 | Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension. | Hypertension | 2022 |
| 35508176 | Meta-imputation: An efficient method to combine genotype data after imputation with multiple reference panels. | Am J Hum Genet | 2022 |
| 35385311 | Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential. | Sci Adv | 2022 |
| 35999217 | Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes. | Nat Commun | 2022 |
| 35939579 | Germline Mutations in <i>CIDEB</i> and Protection against Liver Disease. | N Engl J Med | 2022 |
| 35551307 | Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. | Nat Genet | 2022 |
| 36192399 | Author Correction: Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology. | Nat Commun | 2022 |
| 36450978 | Common and rare variant associations with clonal haematopoiesis phenotypes. | Nature | 2022 |
| 36777998 | The HUNT study: A population-based cohort for genetic research. | Cell Genom | 2022 |
| 36481753 | Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program. | Nat Commun | 2022 |
| 34990411 | Clonal hematopoiesis in sickle cell disease. | J Clin Invest | 2022 |
| 34927100 | Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine-mapping in the MHC and genomewide. | HGG Adv | 2022 |
| 34459872 | FIVEx: an interactive eQTL browser across public datasets. | Bioinformatics | 2022 |
| 34553764 | Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative. | Hum Mol Genet | 2022 |
| 35149777 | UGT1A1 genetic variants are associated with increases in bilirubin levels in rheumatoid arthritis patients treated with sarilumab. | Pharmacogenomics J | 2022 |
| 35347136 | Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology. | Nat Commun | 2022 |
| 35710628 | Genome-wide meta-analysis of iron status biomarkers and the effect of iron on all-cause mortality in HUNT. | 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 |
| 35652341 | Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension. | Hypertension | 2022 |
| 35508176 | Meta-imputation: An efficient method to combine genotype data after imputation with multiple reference panels. | Am J Hum Genet | 2022 |
| 35347136 | Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology. | Nat Commun | 2022 |
| 35385311 | Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential. | Sci Adv | 2022 |
| 36777998 | The HUNT study: A population-based cohort for genetic research. | Cell Genom | 2022 |
| 36481753 | Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program. | Nat Commun | 2022 |
| 36450978 | Common and rare variant associations with clonal haematopoiesis phenotypes. | Nature | 2022 |
| 35939579 | Germline Mutations in <i>CIDEB</i> and Protection against Liver Disease. | N Engl J Med | 2022 |
| 35999217 | Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes. | Nat Commun | 2022 |
| 36192399 | Author Correction: Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology. | Nat Commun | 2022 |
| 35149777 | UGT1A1 genetic variants are associated with increases in bilirubin levels in rheumatoid arthritis patients treated with sarilumab. | Pharmacogenomics J | 2022 |
| 34990411 | Clonal hematopoiesis in sickle cell disease. | J Clin Invest | 2022 |
| 34927100 | Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine-mapping in the MHC and genomewide. | HGG Adv | 2022 |
| 34553764 | Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative. | Hum Mol Genet | 2022 |