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 |
Benson, Mark |
Lac-Phe mediates the anti-obesity effect of metformin |
2023 |
bioRxiv |
de Vries, Paul |
Carriers of rare damaging CCR2 genetic variants are at lower risk of atherosclerotic disease |
2023 |
medRxiv |
Justice, Anne |
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE |
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 |
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 |
Ha, Edward |
The Relationship of Duffy Gene Polymorphism, High Sensitivity C-Reactive Protein, and Long-term Outcomes |
2023 |
medRxiv |
Sankaran, Vijay G. |
Genetic regulation of fetal hemoglobin across global populations |
2023 |
medRxiv |