Diane T. Smelser, Ph.D.
Affiliations: | 2006 | University of Cincinnati, Cincinnati, OH |
Area:
Public Health, Genetics, EpidemiologyGoogle:
"Diane Smelser"Cross-listing: ID Tree
Parents
Sign in to add mentor| Ranjan Deka | grad student | 2006 | University of Cincinnati | |
| (A comparison of obesity candidate genes in the anabolic neuropeptide pathway in the Samoan and American Samoan populations.) | ||||
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Publications
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| Dershem R, Gorvin CM, Metpally RPR, et al. (2020) Familial Hypocalciuric Hypercalcemia Type 1 and Autosomal-Dominant Hypocalcemia Type 1: Prevalence in a Large Healthcare Population. American Journal of Human Genetics |
| Shah S, Henry A, Roselli C, et al. (2020) Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure. Nature Communications. 11: 163 |
| Dershem R, Metpally RPR, Jeffreys K, et al. (2019) Rare-variant pathogenicity triage and inclusion of synonymous variants improves analysis of disease associations of orphan G protein-coupled receptors. The Journal of Biological Chemistry |
| Haggerty CM, Damrauer SM, Levin MG, et al. (2019) Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants. Circulation |
| Choi SH, Weng LC, Roselli C, et al. (2018) Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation. Jama. 320: 2354-2364 |
| Shan Y, Tromp G, Kuivaniemi H, et al. (2017) Genetic risk models: Influence of model size on risk estimates and precision. Genetic Epidemiology |
| Jones GT, Tromp G, Kuivaniemi H, et al. (2016) Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci. Circulation Research |
| Carey DJ, Fetterolf SN, Davis FD, et al. (2016) The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Agrawal V, Smelser DT, Carey DJ, et al. (2016) Effect of the CEP72 Genotype and CYP3A5-Mediated Metabolism in Predicting Vincristine-Associated Peripheral Neuropathy Blood. 128: 5963-5963 |
| Schrodi SJ, Mukherjee S, Shan Y, et al. (2014) Genetic-based prediction of disease traits: prediction is very difficult, especially about the future. Frontiers in Genetics. 5: 162 |