|
Raffield, Laura |
Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium
|
2023 |
bioRxiv |
|
de Vries, Paul |
Carriers of rare damaging CCR2 genetic variants are at lower risk of atherosclerotic disease
|
2023 |
medRxiv |
|
Huffman, Jennifer |
Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.
|
2023 |
medRxiv |
|
Justice, Anne |
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE
|
2023 |
medRxiv |
|
Wang, Yuxuan |
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study
|
2023 |
medRxiv |
|
Keener, Rebecca |
Validation of human telomere length trans-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as novel human telomere length regulation genes
|
2023 |
bioRxiv |
|
Yu, Zhi |
Human Plasma Proteomic Profile of Clonal Hematopoiesis
|
2023 |
medRxiv |
|
Hu, Xiaowei |
Multi-ancestry epigenome-wide analyses identify methylated sites associated with aortic augmentation index in TOPMed MESA
|
2023 |
Research Square |
|
Chen, Han |
StocSum: stochastic summary statistics for whole genome sequencing studies
|
2023 |
bioRxiv |
|
Xu, Weiling |
Mitochondrial DNA Copy Number Variation in Asthma Risk, Severity, and Exacerbations
|
2023 |
medRxiv |
