TOPMed
Publications
| Submitting Author | Title | Journal Name | Publication Date Sort ascending | PMID |
|---|---|---|---|---|
| Li, Yun | Use of >100,000 Deep Coverage Whole Genome Sequences from the NHLBI Trans-Omics for Precision Medicine (TOPMed) Project Results in Improved Imputation Quality and Detection of Rare Variant Associations in Admixed African and Hispanic/Latino Populations | PLOS Genetics | 31869403 | |
| Sarnowski, Chloé | Impact of rare and common genetic variants on type 2 diabetes diagnosis by hemoglobin A1c in multi-ancestry populations from the Trans-Omics for Precision Medicine (TOPMed) Program | American Journal of Human Genetics | 31564435 | |
| Gogarten, Stephanie | Genetic association testing using the GENESIS R/Bioconductor package | Bioinformatics | 31329242 | |
| Weiss, Scott | Whole Genome Sequencing Identifies CRISPLD2 as a Lung Function Gene in Children with Airway Hyperresponsive Asthma | Chest | 31557467 | |
| Szpiech, Zachary | Ancestry-dependent Enrichment of Deleterious Homozygotes in Runs of Homozygosity | American Journal of Human Genetics | 31543216 | |
| Zhu, Xiaofeng | Leveraging linkage evidence to identify low frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data | Human Genetics | 30671673 | |
| Zhu, Xiaofeng | Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level. | American Journal of Human Genetics | 31668705 | |
| Auer, Paul | Whole genome sequences association with E-selectin levels reveals Loss-of-function variant in African Americans | Human Molecular Genetics | 30307499 | |
| Chen, Han | Efficient variant set mixed model association tests for continuous and binary traits in large-scale whole genome sequencing studies | American Journal of Human Genetics | 30639324 | |
| Sofer, Tamar | A Fully-Adjusted Two-Stage Procedure for Rank Normalization in Genetic Association Studies | Genetic Epidemiology | 30653739 |
Back to top
