Our Publications
NCBI Pubmed Link for Jessica L Fetterman, PhD
NCBI Pubmed Link for Deepa M. Gopal, MD, MS
iCAMP Research Articles:
Peer-reviewed Primary Articles
- Moreira, J. D., Gower, A. C., Xue, L., Alekseyev, Y., Smith, K. K., Choi, S. H., Ayalon, N., Farb, M. G., Tenan, K., LeClerc, A., Levy, D., Benjamin, E. J., Lenburg, M. E., Mitchell, R. N., Padera, R. F., Fetterman, J. L., & Gopal, D. M. (2023). Systematic dissection, preservation, and multiomics in whole human and bovine hearts. Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology, 63, 107495. https://doi.org/10.1016/j.carpath.2022.107495
- Li, Y., Gray, A., Xue, L., Farb, M. G., Ayalon, N., Andersson, C., Ko, D., Benjamin, E. J., Levy, D., Vasan, R. S., Larson, M. G., Rong, J., Xanthakis, V., Liu, C., Fetterman, J. L., & Gopal, D. M. (2023). Metabolomic Profiles, Ideal Cardiovascular Health, and Risk of Heart Failure and Atrial Fibrillation: Insights From the Framingham Heart Study. Journal of the American Heart Association, 12(12), e028022. https://doi.org/10.1161/JAHA.122.028022
Preprints:
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iCAMP Review Articles:
- Moreira, J. D., Gopal, D. M., Kotton, D. N., & Fetterman, J. L. (2021). Gaining Insight into Mitochondrial Genetic Variation and Downstream Pathophysiology: What Can i(PSCs) Do?. Genes, 12(11), 1668. https://doi.org/10.3390/genes12111668
- Schwartz, B., Gjini, P., Gopal, D. M., & Fetterman, J. L. (2022). Inefficient Batteries in Heart Failure: Metabolic Bottlenecks Disrupting the Mitochondrial Ecosystem. JACC. Basic to translational science, 7(11), 1161–1179. https://doi.org/10.1016/j.jacbts.2022.03.017
- Smith, K. K., Moreira, J. D., Wilson, C. R., Padera, J. O., Lamason, A. N., Xue, L., Gopal, D. M., Flynn, D. B., & Fetterman, J. L. (2024). A systematic review on the biochemical threshold of mitochondrial genetic variants. Genome research, 34(3), 341–365. https://doi.org/10.1101/gr.278200.123
Other:
- Moreira, J. D., Smith, K. K., Zilber, S., Woleben, K., & Fetterman, J. L. (2023). Teamwork makes the dream work: functional collaborations between families, scientists, and healthcare providers to drive progress in the treatment of Leigh Syndrome. Orphanet journal of rare diseases, 18(1), 355. https://doi.org/10.1186/s13023-023-02871-7