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Serrano, I., Luque, A., Ruiz-Cerulla, A., Navas, S., Blom, A.M., Rodríguez de Córdoba, S., Fernández, F.J., Cristina Vega, M., Rodríguez-Moranta, F., Guardiola, J., Aran, J.M. [2023]. C4BP(β-)-mediated immunomodulation attenuates inflammation in DSS-induced murine colitis and in myeloid cells from IBD patients. Pharmacological Research. 197:doi: /10.1016/j.phrs.2023.106948..

Huerta, A., Arjona, E., Portoles, J., Lopez-Sanchez, P., Cavero, T., Fernandez-Cusicanqui, J., Blasco, M., Cabello, V., Calvo, N., Diaz, M., Herrero-Goñi, M., Aguirre, M., Elías, S., Alcaide, M.P., Ramos, N., Sellares, J., Rodríguez de Córdoba, S. [2023]. On the relevance of thrombomodulin variants in atypical hemolytic uremic syndrome. Kidney International. 104:851-855.

Navas-Yuste, S., de la Paz, K., Querol-García, J., Gómez-Quevedo, S., Rodríguez de Córdoba, S., Fernández, F.J., Vega, M.C. [2023]. The structure of Leptospira interrogans GAPDH sheds light into an immunoevasion factor that can target the anaphylatoxin C5a of innate immunity. Frontiers in Immunology. 14:1190943. doi: 10.3389/fimmu.2023.1190943.

Caravaca-Fontán, F., Cavero, T., Díaz-Encarnación, M., Cabello, V., Ariceta, G., Quintana, L.F., Marco, H., Barros, X., Ramos, N., Rodríguez-Mendiola, N., Cruz, S., Fernández-Juárez, G., Rodríguez, A., Pérez De José, A., Rabasco, C., Rodado, R., Fernández, L., Pérez-Gómez, V., Ávila, A., Bravo, L., Espinosa, N., Allende, N., Sanchez De La Nieta, M.D., Rodríguez, E., Rivas, B., Melgosa, M., Huerta, A., Miquel, R., Mon, C., Fraga, G., De Lorenzo, A., Draibe, J., González, F., Shabaka, A., López-Rubio, M.E., Fenollosa, M.Á., Martín-Penagos, L., Da Silva, I., Titos, J.A., Rodríguez De Córdoba, S., Goicoechea De Jorge, E., Praga, M. [2023]. Clinical Profiles and Patterns of Kidney Disease Progression in C3 Glomerulopathy. Kidney360. 4:659-672.

Giang, J., van Doorn, M.B.A., Diercks, G.F.H., de Cordoba, S.R., van den Bosch, T.P.P., Schreurs, M.W.J., Poppelaars, F., Damman, J. [2023]. Successful pharmacological intervention at different levels of the complement system in an in vitro complement fixation model for bullous pemphigoid. Experimental Dermatology. 32:632-640.

Okrój, M., Rodriguez de Córdoba, S. [2023]. Will a hyperactive classical complement pathway exacerbate autoimmune diseases?. Autoimmunity Reviews. 22:103241. doi: 10.1016/j.autrev.2022.103241.

Rodríguez de Córdoba, S. [2023]. Genetic variability shapes the alternative pathway complement activity and predisposition to complement-related diseases. Immunological Reviews. 313:71-90.

Cavero, T., Auñón, P., Caravaca-Fontán, F., Trujillo, H., Arjona, E., Morales, E., Guillén, E., Blasco, M., Rabasco, C., Espinosa, M., Blanco, M., Rodríguez-Magariños, C., Cao, M., Ávila, A., Huerta, A., Rubio, E., Cabello, V., Barros, X., Goicoechea De Jorge, E., Rodríguez De Córdoba, S., Praga, M. [2023]. Thrombotic microangiopathy in patients with malignant hypertension. Nephrology Dialysis Transplantation. 38:1217-1226.

Kuźniewska, A., Thiel, M., Kowalska, D., Felberg-Miętka, A., Szynkowski, P., Ołdziej, S., Arjona, E., Jongerius, I., Rodriguez de Córdoba, S., Okrój, M., Urban, A. [2022]. Substitutions at position 263 within the von Willebrand factor type A domain determine the functionality of complement C2 protein. Frontiers in Immunology. 13:1061696. doi: 10.3389/fimmu.2022.1061696.

Caravaca-Fontán, F., Rivero, M., Cavero, T., Díaz-Encarnación, M., Cabello, V., Ariceta, G., Quintana, L.F., Marco, H., Barros, X., Ramos, N., Rodríguez-Mendiola, N., Cruz, S., Fernández-Juárez, G., Rodríguez, A., De José, A.P., Rabasco, C., Rodado, R., Fernández, L., PCrossed D Sign©rez-Gómez, V., Ávila, A., Bravo, L., Espinosa, N., Allende, N., De La Nieta, M.D.S., Rodríguez, E., Olea, T., Melgosa, M., Huerta, A., Miquel, R., Mon, C., Fraga, G., De Lorenzo, A., Draibe, J., González, F., Shabaka, A., López-Rubio, M.E., Fenollosa, M.Á., Martín-Penagos, L., Da Silva, I., Alonso Titos, J., De Córdoba, S.R., De Jorge, E.G., Praga, M. [2022]. Development and validation of a nomogram to predict kidney survival at baseline in patients with C3 glomerulopathy. Clinical Kidney Journal. 15:1737-1746.

Serrano, I., Luque, A., Mitjavila, F., Blom, A.M., Rodríguez de Córdoba, S., Vega, M.C., Torras, J., Aran, J.M. [2022]. The Hidden Side of Complement Regulator C4BP: Dissection and Evaluation of Its Immunomodulatory Activity. Frontiers in Immunology. 13:883743. doi: 10.3389/fimmu.2022.883743 .

Marquez-Tirado, B., Gutierrez-Tenorio, J., Tortajada, A., Continente, L.L., Caravaca-Fontan, F., Malik, T.H., Montero, R.R., Elıas, S., Gonzalez, A.S., Fernandez-Juarez, G., Sanchez-Corral, P., Pickering, M.C., Praga, M., de Cordoba, S.R., de Jorge, E.G. [2022]. Factor H–Related Protein 1 Drives Disease Susceptibility and Prognosis in C3 Glomerulopathy. Journal of the American Society of Nephrology. 33:1137-1153.

Fernández, F.J., Santos-López, J., Martínez-Barricarte, R., Querol-García, J., Martín-Merinero, H., Navas-Yuste, S., Savko, M., Shepard, W.E., Rodríguez de Córdoba, S., Vega, M.C. [2022]. The crystal structure of iC3b-CR3 αI reveals a modular recognition of the main opsonin iC3b by the CR3 integrin receptor. Nature Communications. 13(1):1955. doi: 10.1038/s41467-022-29580-2.

Urban, A., Kowalska, D., Stasiłojć, G., Kuźniewska, A., Skrobińska, A., Arjona, E., Alonso, E.C., Fenollosa Segarra, M.Á., Jongerius, I., Spaapen, R., Satchell, S., Thiel, M., Ołdziej, S., Rodriguez de Córdoba, S., Okrój, M. [2021]. Gain-of-Function Mutations R249C and S250C in Complement C2 Protein Increase C3 Deposition in the Presence of C-Reactive Protein. Frontiers in Immunology. 12:724361 doi.org/10.3389/fimmu.2021.724361.

López-Trascasa, M., Alonso-Melgar, Á., Melgosa-Hijosa, M., Espinosa-Román, L., Lledín-Barbancho, M.D., García-Fernández, E., Rodríguez de Córdoba, S., Sánchez-Corral, P. [2021]. Case Report: Combined Liver-Kidney Transplantation to Correct a Mutation in Complement Factor B in an Atypical Hemolytic Uremic Syndrome Patient. Frontiers in Immunology. doi: 10.3389/fimmu.2021.751093

Corvillo, F., González-Sánchez, L., López-Lera, A., Arjona, E., Ceccarini, G., Santini, F., Araújo-Vilar, D., Brown, R.J., Villarroya, J., Villarroya, F., de Córdoba, S.R., Caballero, T., Nozal, P., López-Trascasa, M. [2021]. Complement factor d (Adipsin) levels are elevated in acquired partial lipodystrophy (barraquer–simons syndrome). International Journal of Molecular Sciences. 22(12):6608. doi: 10.3390/ijms22126608.

Martín-Merinero, H., Zhang, Y., Arjona, E., del Angel, G., Goodfellow, R., Gómez-Rubio, E., Ji, RR., Michelena, M., Smith, RJH., Rodríguez de Córdoba, S. [2021]. Functional characterization of 105 Factor H variants associated with atypical haemolytic uremic syndrome; lessons for variant classification. Blood doi: 10.1182/blood.2021012037.

García-Fernández, J., Vilches-Arroyo, S., Olavarrieta, L., Pérez-Pérez, J., Rodríguez de Córdoba, S. [2021]. Detection of Genetic Rearrangements in the Regulators of Complement Activation RCA Cluster by High-Throughput Sequencing and MLPA. Methods in Molecular Biology. 2227:159-178.

Caravaca-Fontán, F., Díaz-Encarnación, M., Cabello, V., Ariceta, G., Quintana, L., Marco, H., Barros, X., Ramos Terrada, N., Rodríguez-Mendiola, N., Cruz, S., Fernández-Juarez, G., Rodríguez, A., Pérez de José, A., Rabasco, C., Rodado, R., Fernández Lorente, ML., Pérez Gómez, V., Avila, A., Bravo, L., Espinosa, N., Allende, N., Sánchez de la Nieta, M., Rodríguez, E., Olea, T., Melgosa, M., Huerta, A., Miquel-Rodríguez, R., Mon, C., Fraga, G., de Lorenzo, A., Bordignon, J., Cano Megías, M., González, F., Shabaka, A., Fenollosa, MA., Martín-Penagos, L., Da Silva, I., Alonso Titos, J., Rodríguez de Córdoba, S., Goicoechea de Jorge, E. Praga, M.,, on behalf of the Spanish Group for the Study of Glomerular Diseases (GLOSEN). [2021]. Longitudinal Change in Proteinuria and Kidney Outcomes in C3 Glomerulopathy. Nephrol. Dial Transplant. doi: 10.1093/ndt/gfab075.

Martín-Merinero, H., Subías, M., Pereda, A., Gómez-Rubio, E., Juana-López, L., Fernández Rivera, C., Goicoechea de Jorge, E., Martín-Santamaría, S., Cañada, FJ, Rodríguez de Córdoba, S. [2021]. Molecular bases for the association of FHR-1 with atypical hemolytic uremic syndrome and other diseases. Blood 137:3484-3494.