Linda M. Polfus, Ph.D.
Affiliations: | 2013 | Epidemiology & Disease Control | The University of Texas School of Public Health |
Area:
Epidemiology, Genetics, Biostatistics BiologyGoogle:
"Linda Polfus"Parents
Sign in to add mentor| James E. Hixson | grad student | 2013 | The University of Texas School of Public Health | |
| (Discovering the spectrum of genetic architecture influencing coronary artery calcification.) | ||||
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Publications
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| Jiang MZ, Gaynor SM, Li X, et al. (2023) Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium. Biorxiv : the Preprint Server For Biology |
| Polfus LM, Darst BF, Highland H, et al. (2021) Genetic discovery and risk characterization in type 2 diabetes across diverse populations. Hgg Advances. 2 |
| Mikhaylova AV, McHugh CP, Polfus LM, et al. (2021) Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. American Journal of Human Genetics |
| Streicher SA, Lim U, Park SL, et al. (2021) Genome-wide association study of pancreatic fat: The Multiethnic Cohort Adiposity Phenotype Study. Plos One. 16: e0249615 |
| Raffield LM, Iyengar AK, Wang B, et al. (2019) Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts. American Journal of Human Genetics |
| Polfus LM, Raffield LM, Wheeler MM, et al. (2018) Whole genome sequence association with E-selectin levels reveals Loss-of-function variant in African Americans. Human Molecular Genetics |
| Garg PK, Norby FL, Polfus LM, et al. (2017) Lipoprotein-associated phospholipase A2 and risk of incident peripheral arterial disease: Findings from The Atherosclerosis Risk in Communities study (ARIC). Atherosclerosis. 268: 12-18 |
| Gregson JM, Freitag DF, Surendran P, et al. (2016) Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles. European Journal of Preventive Cardiology |
| Polfus LM, Khajuria RK, Schick UM, et al. (2016) Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis. American Journal of Human Genetics. 99: 785 |
| Polfus LM, Khajuria RK, Schick UM, et al. (2016) Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis. American Journal of Human Genetics. 99: 481-488 |