Laura J. Rasmussen-Torvik, Ph.D.
Affiliations: | 2007 | University of Minnesota, Twin Cities, Minneapolis, MN |
Area:
EpidemiologyGoogle:
"Laura Rasmussen-Torvik"Parents
Sign in to add mentor| James S. Pankow | grad student | 2007 | UMN | |
| (An epidemiologic and genetic examination of associations among waist, adiponectin and insulin sensitivity.) | ||||
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Publications
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| Suzuki K, Hatzikotoulas K, Southam L, et al. (2024) Genetic drivers of heterogeneity in type 2 diabetes pathophysiology. Nature |
| Suzuki K, Hatzikotoulas K, Southam L, et al. (2023) Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. Medrxiv : the Preprint Server For Health Sciences |
| Westerman KE, Walker ME, Gaynor SM, et al. (2023) Investigating gene-diet interactions impacting the association between macronutrient intake and glycemic traits. Diabetes |
| DiCorpo D, Gaynor SM, Russell EM, et al. (2022) Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program. Communications Biology. 5: 756 |
| Ge T, Irvin MR, Patki A, et al. (2022) Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations. Genome Medicine. 14: 70 |
| Mahajan A, Spracklen CN, Zhang W, et al. (2022) Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. Nature Genetics |
| Chen J, Spracklen CN, Marenne G, et al. (2021) The trans-ancestral genomic architecture of glycemic traits. Nature Genetics |
| Graff M, Justice AE, Young KL, et al. (2021) Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. American Journal of Human Genetics |
| Lagou V, Mägi R, Hottenga JJ, et al. (2021) Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. Nature Communications. 12: 995 |
| Rosenthal EA, Crosslin DR, Gordon AS, et al. (2021) Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort. Bmc Medical Genomics. 14: 11 |