A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with Systemic Sclerosis in a large European cohort

por Bossini-Castillo, L, Broen, JCA, Simeon, C P, Beretta, L, Vonk, M C, Ortego-Centeno, N, Espinosa, G, Carreira, P, Camps, M T, Navarrete, N, González-Escribano, M F, Vicente-Rabaneda, E, Rodríguez, L, Tolosa, C, Román-Ivorra, J A, Gómez-Gracia, I, García-Hernández, F J, Castellví, I, Gallego, M, Fernández-Nebro, A, Egurbide, M V, Follonosa, V, García de la Peña, P, Pros, A, González-Gay, M A, Hesselstrand, R, Riemekasten, G, Witte, T, Coenen, MJH, Koeleman, B P, Houssiau, F, Smith, V, De Keyser, F, Westhovens, R, De Langhe, E, Voskuyl, A E, Schuerwegh, A J, Chee, M M, Madhok, R, Shiels, P, Fonseca, C, Denton, C, Claes, K, Padykov, L, Nordin, A, Palm, Ø, Lie, B A, Airó, P, Scorza, R, van Laar, J M, Hunzelmann, N, Kreuter, A, Herrick, A, Worthington, J, Radstake, TRDJ, Martín, J, Rueda, B
Publicado 2010

Identification of novel genetic markers associated with the clinical phenotypes of systemic sclerosis through a genome wide association strategy

por Gorlova, O, Martin, J M, Rueda, B, Koeleman, BPC, Ying, J, Teruel, M, Diaz-Gallo, L M, Broen, J C, Vonk, M C, Simeon, C P, Alizadeh, B Z, Coenen, MJH, Voskuyl, A E, Schuerwegh, A J, van Riel, PLCM, Vanthuyne, M, van ‘t Slot, R, Italiaander, A, Ophoff, R A, Hunzelmann, N, Fonollosa, V, Ortego-Centeno, N, González-Gay, M A, García-Hernández, F J, González-Escribano, M F, Airo, P, van Laar, J, Worthington, J, Hesselstrand, R, Smith, V, De Keyser, F, Houssiau, F, Chee, M M, Madhok, R, Shiels, P, Westhovens, R, Kreuter, A, de Baere, E, Witte, T, Padyukov, L, Nordin, A, Scorza, R, Lunardi, C, Lie, B A, Hoffmann-Vold, A M, García de la Peña, P, Carreira, P, Varga, J, Hinchcliff, M, Lee, A T, Gourh, P, Amos, C I, Riemekasten, G, Herrick, A, Beretta, L, Fonseca, C, Denton, C P, Gregersen, P K, Agarwal, S, Assassi, S, Tan, F K, Arnett, F C, Radstake, TRDJ, Mayes, M D, Martin, J
Publicado 2010