TOPMed
Publications
| Submitting Author | Title | Journal Name | Publication Date Sort ascending | PMID |
|---|---|---|---|---|
| Patel, Roshni | Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits | American Journal of Human Genetics | 35716666 | |
| Battle, Stephanie | A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data | NAR Genom Bioinform | 35591888 | |
| Sofer, Tamar | A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood | Nat Commun. | 35729114 | |
| Wheeler, Marsha | Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program | Nat Commun. | 36481753 | |
| Manichaikul, Ani | Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program | American Journal of Human Genetics | 35385699 | |
| Kim, Wonji | Assessing the Contribution of Rare Genetic Variants to Phenotypes of Chronic Obstructive Pulmonary Disease Using Whole-Genome Sequencing Data | Hum Mol Genet. | 35766891 | |
| Shabani, Mahsima | Rare Genetic Variants Associated with Myocardial Fibrosis; Multi-Ethnic Study of Atherosclerosis (MESA) | Frontiers in Cardiovascular Medicine | 35265679 | |
| Page, Grier | GAWMerge expands GWAS sample size and diversity by combining array-based genotyping and whole-genome sequencing | Commun Biol | 35953715 | |
| Li, Zilin | A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies | Nat Methods | 36303018 | |
| Kelly, Tanika | Whole-Exome Sequencing Study Identifies Four Novel Gene Loci Associated with Diabetic Kidney Disease | Hum Mol Genet. | 36444934 |
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