García-Cabrero AM, Marinas A, Guerrero R, Rodríguez de Córdoba S, Serratosa JM, and Sánchez MP
[2012]. Laforin and malin deletions in mice produce similar neurologic impairments. J Neuropathol Exp Neurol 71:413-421
Knecht E, Criado O, Aguado C, Gayarre J, Durán-Trio L, García-Cabrero AM, Vernia S, San Millán B, Heredia M, Romá-Mateo C, Mouron S, Juana-López L, Domínguez M, Navarro C, Serratosa JM, Sánchez M, Sanz P, Bovolenta P and Rodríguez de Córdoba S.
[2012]. Malin knockout mice support a primary role of autophagy in the pathogenesis of Lafora disease. Autophagy 8(4)
Zhou H., Yan H., Stover CM., Montes Fernandez T., Rodríguez de Córdoba S., Song WC., Wu X., Thompson RW., Schwaeble WJ., Atkinson JP., Hourcade DE and Pham C
[2012]. Antibody directs properdin-dependent activation of the complement alternative pathway in a mouse model of abdominal aortic aneurysm. Proc Natl Acad Sci USA 109:E415-22
Martínez-Barricarte R, Recalde S, Fernández-Robredo P, Millán I, Olavarrieta L, Viñuela A, Pérez-Pérez J, García-Layana A, Rodríguez de Córdoba S, on behalf of the Spanish Multi-centre Group of AMD
[2012]. Relevance of complement factor H-related 1 (CFHR1) genotypes in age- related macular degeneration (AMD). Invest Ophthalmol Vis Sci 53:1087-1094
Criado O, Aguado C, Gayarre J, Duran-Trio L, Garcia-Cabrero AM, Vernia S, San Millan B, Heredia M, Roma-Mateo C, Mouron S, Juana-Lopez L, Dominguez M, Navarro C, Serratosa JM, Sanchez M, Sanz P, Bovolenta P, Knecht E and Rodríguez de Córdoba S
[2011]. Lafora bodies and neurological defects in malin-deficient mice correlate with impaired autophagy. Hum Mol Genet 21:1521-1533
Tortajada A, Pinto S, Martínez-Ara J, López-Trascasa M, Sánchez-Corral P, Rodríguez de Córdoba S
[2011]. Complement factor H variants I890 and L1007 while commonly associated with atypical haemolytic uremic syndrome are polymorphisms with no functional significance. Kidney International 81:56-63
Romá-Mateo C, Solaz-Fuster MC, Gimeno-Alcañiz JV, Dukhande V, Donderis J, Worby CA, Marina A, Criado O, Koller A, Rodríguez de Córdoba S, Gentry MS, Sanz P
[2011]. Laforin, a dual specificity protein phosphatase involved in Lafora disease, is phosphorylated at Ser25 by AMP-activated protein kinase. Biochem J 439:265-75
Alcorlo M, Martínez-Barricarte R, Fernández FJ, Rodríguez-Gallego C, Round A, Vega MC, Harris CL, Rodríguez de Córdoba S, Llorca O
[2011]. Unique structure of iC3b resolved at a resolution of 24 A by 3D-electron microscopy. Proc Natl Acad Sci USA 108:13236-40
Layana AG, Zarranz-Ventura J, Robredo PF, Recalde S, Rodríguez de Córdoba S; Grupo Español de Investigación Cooperativa en DMAE
[2011]. Genetics and ARMD: from the laboratory to the Consulting room. Arch Soc Esp Oftalmol. 86:101-102 (Editorial)
Heurich M, Martínez-Barricarte R, Francis NJ, Roberts DL, Rodríguez de Córdoba S, Morgan BP and Harris CL
[2011]. Common polymorphisms in C3, factor B and factor H collaborate to determine systemic complement activity and disease risk. Proc Natl Acad Sci USA 108:8761-8766
Vernia S, Heredia M, Criado O, Rodríguez de Córdoba S, Garcia-Roves PM, Cansell C, Denis R, Luquet S, Foufelle F, Ferre P and Sanz P
[2011]. Laforin, a dual specificity phosphatase involved in Lafora disease, regulates insulin response and whole-body energy balance in mice. Hum Mol Genet 20:2571-2584
Rodríguez de Córdoba S, Harris CL, Morgan BP and Llorca O
[2011]. Lessons from functional and structural analyses of disease-associated genetic variants in the complement alternative pathway. Biochim. Biophys. Acta-Mol. Basis Dis 1812:12-22
Martínez-Barricarte R*, Heurich M*, Valdes-Canedo F, Vázquez-Martul E, Torreira E, Montes T, Tortajada A, Pinto S, López-Trascasa M, Morgan BP, Llorca O, Harris CL, Rodríguez de Córdoba S
[2010]. Human C3 mutation reveals a mechanism of Dense Deposit Disease pathogenesis and provides insights into complement activation and regulation. J Clin Invest 120:3702-3712 (*Equal first author)
Knecht E, Aguado C, Sarkar S, Korolchuk VI, Criado-Garcia O, Vernia S, Boya P, Sanz P, Rodríguez de Córdoba S, Rubinsztein DC
[2010]. Impaired autophagy in Lafora disease. Autophagy 6:991-993
Gale DP*, Goicoechea de Jorge E*, Cook HT, Martínez-Barricarte R, Hadjisavvas A, McLean AG, Pusey CD, Pierides A, Kyriacou K., Athanasiou Y, Voskarides K, Deltas C, Palmer A, Frémeaux-Bacchi V, Rodríguez de Córdoba S, Maxwell PH, Pickering MC
[2010]. Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis. Lancet 376:794-801 (*Equal first author)
Hakobyan S*, Tortajada A*, Harris CL, Rodríguez de Córdoba S, Morgan PB
[2010]. Variant-specific quantification of factor H in plasma identifies null alleles associated with atypical Hemolytic Uremic Syndrome. Kidney International 78:782-788 (*Equal first author)
Aguado C*, Sarkar S*, Korolchuk VI, Criado O, Vernia S, Boya P, Sanz P, Rodríguez de Córdoba S, Knecht E and Rubinsztein DC.
[2010]. Laforin, the most common protein mutated in Lafora disease, regulates autophagy. Hum Mol Genet 19:2867-76 (*Equal first author).
Buil A, Trégouët DA,Souto JC, Saut N, Germain M, Rotival M, Tiret L, Cambien F, Lathrop M, Zeller T, Alessi MC, Rodríguez de Córdoba S, Münzel T, Wild P, Fontcuberta J, Gagnon F, Emmerich J, Almasy L, Blankenberg S, Soria JM, Morange PE
[2010]. C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies. Blood 115:46644-50
Rodríguez de Córdoba S
[2010]. aHUS: a disorder with many risk factors. Blood 115:158-160
Moreno-Navarrete JM, Martínez-Barricarte R, Catalán V, Sabater M, Gómez-Ambrosi J, Ortega FJ, Ricart W, Blüher M, Frühbeck G, Rodríguez de Córdoba S and Fernández-Real JM
[2010]. Complement Factor H is expressed in adipose tissue in association with insulin resistance. Diabetes 59(1):200-9
