|
| 36824883 | Integrative multi-ancestry genetic analysis of gene regulation in coronary arteries prioritizes disease risk loci. | medRxiv | 2023 |
| 36444934 | Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease. | Hum Mol Genet | 2023 |
| 38028628 | Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci. | Front Genet | 2023 |
| 38014529 | Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis. | Circ Genom Precis Med | 2023 |
| 37904051 | Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing. | Nat Genet | 2023 |
| 37804200 | Association Between Whole Blood-Derived Mitochondrial DNA Copy Number, Low-Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk. | J Am Heart Assoc | 2023 |
| 37709864 | Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease. | Nat Genet | 2023 |
| 37961350 | A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies. | bioRxiv | 2023 |
| 37770635 | Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification. | Nat Genet | 2023 |
| 37034649 | Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. | medRxiv | 2023 |
| 36778386 | Structural variation across 138,134 samples in the TOPMed consortium. | Res Sq | 2023 |
| 36824883 | Integrative multi-ancestry genetic analysis of gene regulation in coronary arteries prioritizes disease risk loci. | medRxiv | 2023 |
| 37017084 | FHL5 Controls Vascular Disease-Associated Gene Programs in Smooth Muscle Cells. | Circ Res | 2023 |
| 36702996 | Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing. | Nat Genet | 2023 |
| 36747810 | Structural variation across 138,134 samples in the TOPMed consortium. | bioRxiv | 2023 |
| 37046083 | Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis. | Nature | 2023 |
| 37291111 | Author Correction: Genome-wide association study of serum liver enzymes implicates diverse metabolic and liver pathology. | Nat Commun | 2023 |
| 37096546 | Lowering of Circulating Sclerostin May Increase Risk of Atherosclerosis and Its Risk Factors: Evidence From a Genome-Wide Association Meta-Analysis Followed by Mendelian Randomization. | Arthritis Rheumatol | 2023 |
| 37804200 | Association Between Whole Blood-Derived Mitochondrial DNA Copy Number, Low-Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk. | J Am Heart Assoc | 2023 |
| 37961350 | A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies. | bioRxiv | 2023 |
| 38014529 | Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis. | Circ Genom Precis Med | 2023 |
| 37709864 | Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease. | Nat Genet | 2023 |
| 37904051 | Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing. | Nat Genet | 2023 |
| 37770635 | Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification. | Nat Genet | 2023 |
| 38028628 | Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci. | Front Genet | 2023 |
| 37291111 | Author Correction: Genome-wide association study of serum liver enzymes implicates diverse metabolic and liver pathology. | Nat Commun | 2023 |
| 37017084 | FHL5 Controls Vascular Disease-Associated Gene Programs in Smooth Muscle Cells. | Circ Res | 2023 |
| 37046083 | Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis. | Nature | 2023 |
| 37034649 | Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. | medRxiv | 2023 |
| 37096546 | Lowering of Circulating Sclerostin May Increase Risk of Atherosclerosis and Its Risk Factors: Evidence From a Genome-Wide Association Meta-Analysis Followed by Mendelian Randomization. | Arthritis Rheumatol | 2023 |
| 36444934 | Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease. | Hum Mol Genet | 2023 |
| 36747810 | Structural variation across 138,134 samples in the TOPMed consortium. | bioRxiv | 2023 |
| 36778386 | Structural variation across 138,134 samples in the TOPMed consortium. | Res Sq | 2023 |
| 36702996 | Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing. | Nat Genet | 2023 |
| 35179313 | Multivariate, region-based genetic analyses of facets of reproductive aging in White and Black women. | Mol Genet Genomic Med | 2022 |
| 35385311 | Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential. | Sci Adv | 2022 |
| 36220816 | Whole genome sequence analysis of blood lipid levels in >66,000 individuals. | Nat Commun | 2022 |
| 35551307 | Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. | Nat Genet | 2022 |
| 35927319 | Rare genetic variants explain missing heritability in smoking. | Nat Hum Behav | 2022 |
| 35534559 | Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. | Nat Genet | 2022 |
| 36568030 | Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. | HGG Adv | 2022 |
| 36477530 | Genetic diversity fuels gene discovery for tobacco and alcohol use. | Nature | 2022 |
| 35039093 | Epigenetics of single-site and multi-site atherosclerosis in African Americans from the Genetic Epidemiology Network of Arteriopathy (GENOA). | Clin Epigenetics | 2022 |
| 35179313 | Multivariate, region-based genetic analyses of facets of reproductive aging in White and Black women. | Mol Genet Genomic Med | 2022 |
| 35551307 | Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. | Nat Genet | 2022 |
| 35534559 | Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. | Nat Genet | 2022 |
| 35385311 | Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential. | Sci Adv | 2022 |
| 36477530 | Genetic diversity fuels gene discovery for tobacco and alcohol use. | Nature | 2022 |
| 36568030 | Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. | HGG Adv | 2022 |
| 35927319 | Rare genetic variants explain missing heritability in smoking. | Nat Hum Behav | 2022 |