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Dive into the research topics where Surendra Dasari is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
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Frontiers in Congenital Disorders of Glycosylation
Morava-Kozicz, E., Dasari, S., Freeze, H. H., Kozicz, L. T. & Lam, C.
9/15/19 → 7/31/24
Project: Research project
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Amino acid sequence homology of monoclonal serum free light chain dimers and tissue deposited light chains in AL amyloidosis: a pilot study
Goldis, R., Kaplan, B., Arad, M., Dispenzieri, A., Dasari, S., Kukuy, O. L., Simon, A. J., Dori, A., Shavit-Stein, E., Ziv, T., Murray, D., Kourelis, T., Gertz, M. A., Dominissini, D., Magen, H. & Muchtar, E., Feb 1 2024, In: Clinical Chemistry and Laboratory Medicine. 62, 3, p. 464-471 8 p.Research output: Contribution to journal › Article › peer-review
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Anakinra-associated renal amyloidosis
Nasr, S. H., Alehashemi, S., Dasari, S., Waldman, M., Afzali, B., Chiu, A., Bolanos, J., Goldbach-Mansky, R. & McPhail, E. D., Feb 2024, In: Kidney international. 105, 2, p. 395-396 2 p.Research output: Contribution to journal › Article › peer-review
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Anakinra-Associated Systemic Amyloidosis
Alehashemi, S., Dasari, S., Metpally, A., Uss, K., Castelo-Soccio, L. A., Heller, T., Kellman, P., Chen, M. Y., Ahlman, M., Kim, J., Wargo, S., Kuhns, D. B., Fink, D., de Jesus, A., Martin, P. S., Chang, R., Bolanos, J., Lee, C. C. R., Nasr, S. H., Goldbach-Mansky, R., & 1 others , Jan 2024, In: Arthritis and Rheumatology. 76, 1, p. 100-106 7 p.Research output: Contribution to journal › Article › peer-review
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A proteomic atlas of kidney amyloidosis provides insights into disease pathogenesis
Charalampous, C., Dasari, S., McPhail, E., Theis, J. D., Vrana, J. A., Dispenzieri, A., Leung, N., Muchtar, E., Gertz, M., Ramirez-Alvarado, M. & Kourelis, T., Mar 2024, In: Kidney international. 105, 3, p. 484-495 12 p.Research output: Contribution to journal › Article › peer-review
Open Access -
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3
Undiagnosed Diseases Network, Jan 4 2024, In: American journal of human genetics. 111, 1, p. 96-118 23 p.Research output: Contribution to journal › Article › peer-review