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| 37961373 | Frequency of Variants in Mendelian Alzheimer's Disease Genes within the Alzheimer's Disease Sequencing Project (ADSP). | medRxiv | 2024 |
| 37498674 | Genetic modification of inflammation- and clonal hematopoiesis-associated cardiovascular risk. | J Clin Invest | 2023 |
| 38014529 | Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis. | Circ Genom Precis Med | 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 |
| 37891690 | Multi-tissue epigenetic analysis identifies distinct associations underlying insulin resistance and Alzheimer's disease at CPT1A locus. | Clin Epigenetics | 2023 |
| 37777527 | Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality. | Nat Commun | 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 |
| 37186683 | Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease. | Circulation | 2023 |
| 36791419 | Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits. | Diabetes | 2023 |
| 37425772 | Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study. | medRxiv | 2023 |
| 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 |
| 34553764 | Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative. | Hum Mol Genet | 2022 |
| 36220816 | Whole genome sequence analysis of blood lipid levels in >66,000 individuals. | Nat Commun | 2022 |
| 35547845 | Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of Diseases. | medRxiv | 2022 |
| 35664994 | Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of Diseases. | Res Sq | 2022 |
| 36424512 | Whole genome DNA and RNA sequencing of whole blood elucidates the genetic architecture of gene expression underlying a wide range of diseases. | Sci Rep | 2022 |
| 36380121 | Elucidating the genetic architecture of DNA methylation to identify promising molecular mechanisms of disease. | Sci Rep | 2022 |
| 36513073 | Correlations between complex human phenotypes vary by genetic background, gender, and environment. | Cell Rep Med | 2022 |
| 34727735 | Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. | Stroke | 2022 |
| 34582791 | Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. | Am J Hum Genet | 2021 |
| 34108472 | Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes. | Nat Commun | 2021 |
| 33887194 | Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. | Am J Hum Genet | 2021 |
| 34087167 | Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. | Am J Hum Genet | 2021 |
| 34440402 | Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability. | Genes (Basel) | 2021 |
| 31964835 | De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population. | Proc Natl Acad Sci U S A | 2020 |
| 31118516 | Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. | Nature | 2019 |
| 31645637 | Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment. | Sci Rep | 2019 |
| 30474203 | Association of Maternal Prepregnancy Weight with Offspring Adiposity Throughout Adulthood over 37 Years of Follow-up. | Obesity (Silver Spring) | 2019 |
| 30232418 | Integrating genetic, transcriptional, and biological information provides insights into obesity. | Int J Obes (Lond) | 2019 |
| 30755687 | Revisit Population-based and Family-based Genotype Imputation. | Scientific Reports | 2019 |
| 31160809 | Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2019 |
| 29273807 | Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2018 |
| 29549330 | Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2018 |
| 29549329 | Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. | Nat Genet | 2018 |
| 28122634 | Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies. | Genome Biol | 2017 |
| 28448500 | Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. | PLoS Genet | 2017 |
| 28443625 | Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. | Nat Commun | 2017 |
| 28832619 | Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. | PLoS Genet | 2017 |
| 27918534 | Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. | Nat Genet | 2017 |
| 28146470 | Rare and low-frequency coding variants alter human adult height. | Nature | 2017 |
| 27876822 | A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. | Nat Commun | 2016 |
| 26757982 | Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project. | Eur J Hum Genet | 2016 |
| 27355579 | Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. | PLoS Genet | 2016 |
| 26577045 | Evaluation of power of the Illumina HumanOmni5M-4v1 BeadChip to detect risk variants for human complex diseases. | Eur J Hum Genet | 2016 |
| 26426971 | The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. | PLoS Genet | 2015 |
| 25673413 | Genetic studies of body mass index yield new insights for obesity biology. | Nature | 2015 |
| 25673412 | New genetic loci link adipose and insulin biology to body fat distribution. | Nature | 2015 |
| 26131930 | Directional dominance on stature and cognition in diverse human populations. | Nature | 2015 |