|
Kim, Min Seo |
An Integrated Germline and Somatic Genomic Model Improves Risk Prediction for Coronary Artery Disease
|
2024 |
medRxiv |
|
Weinstock, Joshua |
The Genetic Determinants and Genomic Consequences of Non-Leukemogenic Somatic Point Mutations
|
2024 |
medRxiv |
|
Bing Yu |
Genetic Architecture and Analysis Practices of Circulating Metabolites in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program
|
2024 |
bioRxiv |
|
Peterson, Tess |
Proteomic Signature of HIV-Associated Subclinical Left Atrial Remodeling and Incident Heart Failure
|
2024 |
medRxiv |
|
Kechris, Katerina |
Proteomic Networks and Related Genetic Variants Associated with Smoking and Chronic Obstructive Pulmonary Disease
|
2024 |
medRxiv |
|
Liu, Chunyu |
Association analysis of mitochondrial DNA heteroplasmic variants: Methods and application
|
2024 |
medRxiv |
|
Sofer, Tamar |
Machine learning models for blood pressure phenotypes combining multiple polygenic risk scores
|
2023 |
medRxiv |
|
Li, Xihao |
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies
|
2023 |
bioRxiv |
|
Carlson, Jenna |
Improving imputation quality in Samoans through the integration of population-specific sequences into existing reference panels
|
2023 |
medRxiv |
|
Li, Zilin |
Whole Genome association testing in 333,100 individuals across three Biobanks identifies rare non-coding single variant and genomic aggregate associations with height
|
2023 |
bioRxiv |
