TOPMed
Publications
| Submitting Author | Title | Journal Name | Publication Date Sort ascending | PMID | Associated proposal ID(s) |
|---|---|---|---|---|---|
| Konigsberg, Iain | Gene Expression Associations with Body Mass Index in the Multi-Ethnic Study of Atherosclerosis | International Journal of Obesity | 36463326 | 14732 | |
| Zhu, Xiaofeng | Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea | Am J Respir Crit Care Med. | 35822943 | 7616 | |
| Carlson, Jenna | A stop-gain variant in BTNL9 is associated with atherogenic lipid profiles | HGG Advances | 36340932 | 7109 | |
| Hecker, Julian | FGF20 and PGM2 variants are associated with childhood asthma in family-based whole-genome sequencing studies | Human Molecular Genetics | 36255742 | 11217 | |
| Young, Kristin | Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants | HGG Advances | 36568030 | 4753 | |
| Lee, Sanghun | DDX58 is Associated with Susceptibility to Severe Influenza Virus Infection in Children and Adolescents | Journal of Infectious Diseases | 35986912 | 13457 | |
| Liu, Chunyu | Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of Diseases | Scientific Report | 36424512 | 6718 | |
| Uddin, Md Mesbah | Clonal hematopoiesis of indeterminate potential, DNA methylation, and risk for coronary artery disease | Nature Communications | 36097025 | 13907 | |
| Sofer, Tamar | Social and scientific motivations to move beyond groups in allele frequencies: the TOPMed experience | American Journal of Human Genetics | 36055210 | 13483 | |
| Hanks, Sarah | Extent to which array genotyping and imputation with large reference panels approximates deep whole genome sequencing | American Journal of Human Genetics | 35981533 | 7193 |
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