|
| 37961373 | Frequency of Variants in Mendelian Alzheimer's Disease Genes within the Alzheimer's Disease Sequencing Project (ADSP). | medRxiv | 2024 |
| 36723951 | Association of Rare Protein-Truncating DNA Variants in APOB or PCSK9 With Low-density Lipoprotein Cholesterol Level and Risk of Coronary Heart Disease. | JAMA Cardiol | 2023 |
| 36111689 | Plasma metabolites associated with cognitive function across race/ethnicities affirming the importance of healthy nutrition. | Alzheimers Dement | 2023 |
| 35943854 | Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI. | Brain | 2023 |
| 36444934 | Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease. | Hum Mol Genet | 2023 |
| 38038215 | Chromosome 10q24.32 Variants Associate With Brain Arterial Diameters in Diverse Populations: A Genome-Wide Association Study. | | 2023 |
| 37756531 | Clonal Hematopoiesis of Indeterminate Potential (CHIP) and Incident Type 2 Diabetes Risk. | Diabetes Care | 2023 |
| 38028628 | Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci. | Front Genet | 2023 |
| 37745480 | Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium. | bioRxiv | 2023 |
| 37662265 | WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE. | medRxiv | 2023 |
| 38014529 | Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis. | Circ Genom Precis Med | 2023 |
| 37923804 | Identification of circulating proteins associated with general cognitive function among middle-aged and older adults. | Commun Biol | 2023 |
| 37649099 | A polygenic risk score for Alzheimer's disease constructed using APOE-region variants has stronger association than APOE alleles with mild cognitive impairment in Hispanic/Latino adults in the U.S. | Alzheimers Res Ther | 2023 |
| 37905118 | Determinants of mosaic chromosomal alteration fitness. | medRxiv | 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 |
| 37802043 | Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study. | Am J Hum Genet | 2023 |
| 37875120 | Estimating heritability explained by local ancestry and evaluating stratification bias in admixture mapping from summary statistics. | Am J Hum Genet | 2023 |
| 37961350 | A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies. | bioRxiv | 2023 |
| 37693521 | Association of Common and Rare Variants with Alzheimer's Disease in over 13,000 Diverse Individuals with Whole-Genome Sequencing from the Alzheimer's Disease Sequencing Project. | medRxiv | 2023 |
| 37693453 | Key variants via Alzheimer's Disease Sequencing Project whole genome sequence data. | medRxiv | 2023 |
| 37770635 | Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification. | Nat Genet | 2023 |
| 37609313 | Epigenome-wide association study of incident type 2 diabetes in Black and White participants from the Atherosclerosis Risk in Communities Study. | medRxiv | 2023 |
| 37348055 | Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants. | Genetics | 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 |
| 36778463 | Chromosome 10q24.32 Variants Associate with Brain Arterial Diameters in Diverse Populations: A Genome-Wide Association Study. | medRxiv | 2023 |
| 36719767 | Epigenome-Wide Association Study Reveals CpG Sites Associated with Thyroid Function and Regulatory Effects on KLF9. | Thyroid | 2023 |
| 36716967 | DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood. | J Thromb Haemost | 2023 |
| 37470492 | Investigating Associations of Omega-3 Fatty Acids, Lung Function Decline, and Airway Obstruction. | Am J Respir Crit Care Med | 2023 |
| 36778406 | Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants. | bioRxiv | 2023 |
| 36778386 | Structural variation across 138,134 samples in the TOPMed consortium. | Res Sq | 2023 |
| 37467317 | Proteomics analysis of plasma from middle-aged adults identifies protein markers of dementia risk in later life. | Sci Transl Med | 2023 |
| 36511390 | Alzheimer's Disease Genetic Risk, Cognition, and Brain Aging in Midlife. | Ann Neurol | 2023 |
| 36711663 | Investigating associations of omega-3 fatty acids, lung function decline, and airway obstruction. | medRxiv | 2023 |
| 37398003 | Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles. | medRxiv | 2023 |
| 37268629 | Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups. | Nat Commun | 2023 |
| 36493726 | Genetic associations between sleep traits and cognitive ageing outcomes in the Hispanic Community Health Study/Study of Latinos. | EBioMedicine | 2023 |
| 37391434 | A Mendelian randomization study of genetic liability to post-traumatic stress disorder and risk of ischemic stroke. | | 2023 |
| 37327218 | Coronary heart disease and ischemic stroke polygenic risk scores and atherosclerotic cardiovascular disease in a diverse, population-based cohort study. | PLoS One | 2023 |
| 37131817 | Estimating heritability explained by local ancestry and evaluating stratification bias in admixture mapping from summary statistics. | bioRxiv | 2023 |
| 37126548 | The genetic determinants of recurrent somatic mutations in 43,693 blood genomes. | Sci Adv | 2023 |
| 36941441 | Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals. | Nat Genet | 2023 |
| 36747810 | Structural variation across 138,134 samples in the TOPMed consortium. | bioRxiv | 2023 |
| 37186683 | Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease. | Circulation | 2023 |
| 37120436 | Genetic loci of beta-aminoisobutyric acid are associated with aging-related mild cognitive impairment. | Transl Psychiatry | 2023 |
| 37046083 | Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis. | Nature | 2023 |
| 36927883 | Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function: A Meta-analysis of Community-Based Cohorts. | Neurology | 2023 |
| 36991100 | Interaction analysis of ancestry-enriched variants with APOE-É¿4 on MCI in the Study of Latinos-Investigation of Neurocognitive Aging. | Sci Rep | 2023 |
| 37425772 | Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study. | medRxiv | 2023 |
| 35263625 | Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits. | Am J Hum Genet | 2022 |