Projects per year
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Dive into the research topics where Fernando Custodio Fervenza is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
Projects
- 2 Finished
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Nephrotic Syndrome Rare Disease Clinical Research Network III
Cattran, D. C. (CoPI), Fervenza, F. C. (CoPI), Holzman, L. B. (CoPI), Kretzler, M. (CoPI) & Gipson, D. S. (CoPI)
9/8/09 → 6/30/24
Project: Research project
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Membranous Nephropathy Observational Cohort Study
Fervenza, F. C. (PI)
National Institute of Diabetes and Digestive and Kidney Diseases
9/8/09 → 6/30/14
Project: Research project
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Alveolar Hemorrhage in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis Results of an International Randomized Controlled Trial (PEXIVAS)
the PEXIVAS Investigators, May 1 2024, In: American journal of respiratory and critical care medicine. 209, 9, p. 1141-1151 11 p.Research output: Contribution to journal › Article › peer-review
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Apolipoprotein E is enriched in dense deposits and is a marker for dense deposit disease in C3 glomerulopathy
Madden, B., Singh, R. D., Haas, M., Palma, L. M. P., Sharma, A., Vargas, M. J., Gross, L. A., Negron, V., Nate, T., Charlesworth, M. C., Theis, J. D., Nasr, S. H., Nath, K. A., Fervenza, F. C. & Sethi, S., May 2024, In: Kidney international. 105, 5, p. 1077-1087 11 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Association of COVID-19 Versus COVID-19 Vaccination With Kidney Function and Disease Activity in Primary Glomerular Disease: A Report of the Cure Glomerulonephropathy Study
Cure Glomerulonephropathy (CureGN) Study Consortium, Jan 2024, In: American Journal of Kidney Diseases. 83, 1, p. 37-46 10 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Correction to: Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD) (Journal of Translational Medicine, (2023), 21, 1, (410), 10.1186/s12967-023-04183-7)
Pinto e Vairo, F., Kemppainen, J. L., Vitek, C. R. R., Whalen, D. A., Kolbert, K. J., Sikkink, K. J., Kroc, S. A., Kruisselbrink, T., Shupe, G. F., Knudson, A. K., Burke, E. M., Loftus, E. C., Bandel, L. A., Prochnow, C. A., Mulvihill, L. A., Thomas, B., Gable, D. M., Graddy, C. B., Garzon, G. G. M. & Ekpoh, I. U. & 43 others, , Dec 2024, In: Journal of Translational Medicine. 22, 1, 400.Research output: Contribution to journal › Comment/debate › peer-review
Open Access -
Diagnostic yield of exome and genome sequencing after non-diagnostic multi-gene panels in patients with single-system diseases
Wilke, M. V. M. B., Klee, E. W., Dhamija, R., Fervenza, F. C., Thomas, B., Leung, N., Hogan, M. C., Hager, M. M., Kolbert, K. J., Kemppainen, J. L., Loftus, E. C., Leitzen, K. M., Vitek, C. R., McAllister, T., Lazaridis, K. N. & Pinto e Vairo, F., Dec 2024, In: Orphanet Journal of Rare Diseases. 19, 1, 216.Research output: Contribution to journal › Article › peer-review
Open Access