Microbial and metabolic multi‐omic correlations in systemic sclerosis patients von Bellocchi, Chiara, Fernández‐Ochoa, Álvaro, Montanelli, Gaia, Vigone, Barbara, Santaniello, Alessandro, Milani, Christian, Quirantes‐Piné, Rosa, Borrás‐Linares, Isabel, Ventura, Marco, Segura‐Carrettero, Antonio, Alarcón‐Riquelme, Marta Eugenia, Beretta, Lorenzo

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Genome-wide meta-analysis reveals shared new loci in systemic seropositive rheumatic diseases von Acosta-Herrera, M, Kerick, M, Gonzalez-Serna, D, Wijmenga, C, Franke, A, Gregersen, PK, Padyukov, L, Worthington, J, Vyse, TJ, Alarcon-Riquelme, ME, Mayes, MD, Martin, J, Miller, FW, Chen, W, O'Hanlon, TP, Cooper, RG, Vencovsky, J, Rider, LG, Danko, K, Wedderburn, LR, Lundberg, IE, Pachman, LM, Reed, AM, Ytterberg, SR, Selva-O'Callaghan, A, Radstake, TR, Isenberg, DA, Chinoy, H, Ollier, WER, Scheet, P, Peng, B, Lee, A, Lamb, JA, Amos, CI, Denton, C, Hilton-Jones, D, Plotz, PH, Varsani, H, Radstake, TRDJ, Gorlova, O, Rueda, B, Martin, JE, Alizadeh, BZ, Palomino-Morales, R, Coenen, MJ, Vonk, MC, Voskuyl, AE, Scheurwegh, AJ, Broen, JC, van Riel, PLCM, van 't Slot, R, Italiaander, A, Ophoff, RA, Riemekasten, G, Hunzelmann, N, Simeon, CP, Ortego-Centeno, N, Gonzalez-Gay, MA, Gonzalez-Escribano, MF, Airo, P, van Laar, J, Herrick, A, Hesselstrand, R, Smith, V, de Keyser, F, Houssiau, F, Chee, MM, Madhok, R, Shiels, P, Westhovens, R, Kreuter, A, Kiener, H, de Baere, E, Witte, T, Klareskog, L, Beretta, L, Scorza, R, Lie, BA, Hoffman-Vold, AM, Carreira, P, Varga, J, Hinchcliff, M, Lee, AT, Ying, J, Han, Y, Weng, SF, Wigley, FM, Hummers, L, Nelson, JL, Agarwal, SK, Assassi, S, Gourh, P, Tan, FK, Koeleman, BPC, Arnett, FC

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Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis von Kerick, Martin, Acosta-Herrera, Marialbert, Simeón-Aznar, Carmen Pilar, Callejas, José Luis, Assassi, Shervin, Proudman, Susanna M., Nikpour, Mandana, Hunzelmann, Nicolas, Moroncini, Gianluca, de Vries-Bouwstra, Jeska K., Orozco, Gisela, Barton, Anne, Herrick, Ariane L., Terao, Chikashi, Allanore, Yannick, Fonseca, Carmen, Alarcón-Riquelme, Marta Eugenia, Radstake, Timothy R. D. J., Beretta, Lorenzo, Denton, Christopher P., Mayes, Maureen D., Martin, Javier

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Systemic lupus erythematosus. “What do we know and where are we heading?” von Alarcón Riquelme, Marta Eugenia

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Genética del lupus eritematoso generalizado. ¿Qué se sabe y a dónde se va? von Alarcón Riquelme, Marta Eugenia

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Genome-wide whole blood transcriptome profiling in a large European cohort of systemic sclerosis patients von Beretta, Lorenzo, Barturen, Guillermo, Vigone, Barbara, Bellocchi, Chiara, Hunzelmann, Nicolas, De Langhe, Ellen, Cervera, Ricard, Gerosa, Maria, Kovacs, Laszlo, Ortega Castro, Rafaela, Almeida, Isabel, Cornec, Divi, Chizzolini, Carlo, Pers, Jacques-Olivier, Makowska, Zuzanna, Lesche, Ralf, Kerick, Martin, Eugenia Alarcon-Riquelme, Marta, Martin, Javier

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Genome-wide meta-analysis reveals shared new loci in systemic seropositive rheumatic diseases von Acosta-Herrera, Marialbert, Kerick, Martin, Gonzalez-Serna, David, Wijmenga, Cisca, Franke, Andre, Gregersen, Peter K, Padyukov, Leonid, Worthington, Jane, Vyse, Timothy James, Eugenia Alarcon-Riquelme, Marta, Mayes, Maureen D, Martin, Javier, Miller, Frederick W, Chen, Wei, O'Hanlon, Terrance P, Cooper, Robert G, Vencovsky, Jiri, Rider, Lisa G, Danko, Katalin, Wedderburn, Lucy R, Lundberg, Ingrid E, Pachman, Lauren M, Reed, Ann M, Ytterberg, Steven R, Selva-O'Callaghan, Albert, Radstake, Timothy R, Isenberg, David A, Chinoy, Hector, Ollier, William E.R, Scheet, Paul, Peng, Bo, Lee, Annette, Lamb, Janine A, Amos, Christopher I, Denton, Christopher, Hilton-Jones, David, Plotz, Paul H, Varsani, Hemlata, Radstake, Timothy R.D.J, Gorlova, Olga, Rueda, Blanca, Martin, Jose-Ezequiel, Alizadeh, Behrooz Z, Palomino-Morales, Rogelio, Coenen, Marieke J, Vonk, Madelon C, Voskuyl, Alexandre E, Scheurwegh, Annemie J, Broen, Jasper C, van Riel, Piet L.C.M, van 't Slot, Ruben, Italiaander, Annet, Ophoff, Roel A, Riemekasten, Gabriela, Hunzelmann, Nico, Simeon, Carmen P, Ortego-Centeno, Norberto, Gonzalez-Gay, Miguel A, Gonzalez-Escribano, Maria F, Airo, Paolo, van Laar, Jaap, Herrick, Ariane, Hesselstrand, Roger, Smith, Vanessa, de Keyser, Filip, Houssiau, Fredric, Chee, Meng May, Madhok, Rajan, Shiels, Paul, Westhovens, Rene, Kreuter, Alexander, Kiener, Hans, de Baere, Elfride, Witte, Torsten, Klareskog, Lars, Beretta, Lorenzo, Scorza, Rafaella, Lie, Benedicte A, Hoffman-Vold, Anna-Maria, Carreira, Patricia, Varga, John, Hinchcliff, Monique, Lee, Annette T, Ying, Jun, Han, Younghun, Weng, Shih-Feng, Wigley, Fredrick M, Hummers, Laura, Nelson, J. Lee, Agarwal, Sandeep K, Assassi, Shervin, Gourh, Pravitt, Tan, Filemon K, Koeleman, Bobby P.C, Arnett, Frank C

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USE OF ALLELIC VARIANTS (SNPS) IN THE REGION 6P21.33 FOR THE DIAGNOSIS, PROGNOSIS AND TREATMENT OF MÉNIÈRE'S DISEASE von CABRERA MARTÍNEZ, Sonia, ALARCÓN RIQUELME, Marta Eugenia, LÓPEZ ESCÁMEZ, José Antonio, REQUENA NAVARRO, María Teresa

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Uso de variantes alélicas (SNPs) en la región 6p21.33 para el diagnóstico, pronóstico y tratamiento de la Enfermedad de Ménière von López Escámez, José Antonio, Cabrera Martínez, Sonia, Alarcón Riquelme, Marta Eugenia, Requena Navarro, María Teresa

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USE OF ALLELIC VARIANTS (SNPS) IN THE REGION 6P21.33 FOR THE DIAGNOSIS, PROGNOSIS AND TREATMENT OF MÉNIÈRE'S DISEASE von CABRERA MARTÍNEZ, Sonia, ALARCÓN RIQUELME, Marta Eugenia, LÓPEZ ESCÁMEZ, José Antonio, REQUENA NAVARRO, María Teresa

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USE OF POLYMORPHISMS OF THE GENE NFKB1 FOR AUDITORY PROGNOSIS FOR MENIÈRE'S DISEASE von CABRERA MARTÍNEZ, Sonia, ALARCÓN RIQUELME, Marta Eugenia, LÓPEZ ESCÁMEZ, José Antonio, REQUENA NAVARRO, María Teresa, ESPINOSA SÁNCHEZ, Juan Manuel, SÁNCHEZ RODRÍGUEZ, Elena

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USE OF POLYMORPHISMS OF THE GENE NFKB1 FOR AUDITORY PROGNOSIS FOR MENIÈRE'S DISEASE von CABRERA MARTÍNEZ, Sonia, ALARCÓN RIQUELME, Marta Eugenia, LÓPEZ ESCÁMEZ, José Antonio, REQUENA NAVARRO, María Teresa, ESPINOSA SÁNCHEZ, Juan Manuel, SÁNCHEZ RODRÍGUEZ, Elena

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USE OF POLYMORPHISMS OF THE GENE NFKB1 FOR AUDITORY PROGNOSIS FOR MENIÈRE'S DISEASE von ESPINOSA SÁNCHEZ, JUAN MANUEL, ALARCÓN RIQUELME, MARTA EUGENIA, LÓPEZ ESCÁMEZ, JOSÉ ANTONIO, REQUENA NAVARRO, MARÍA TERESA, SÁNCHEZ RODRÍGUEZ, ELENA, CABRERA MARTÍNEZ, SONIA

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Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis von Kerick, Martin, Acosta-Herrera, Marialbert, Pilar Simeon-Aznar, Carmen, Luis Callejas, Jose, Assassi, Shervin, Proudman, Susanna M, Nikpour, Mandana, Hunzelmann, Nicolas, Moroncini, Gianluca, de Vries-Bouwstra, Jeska K, Orozco, Gisela, Barton, Anne, Herrick, Ariane L, Terao, Chikashi, Allanore, Yannick, Fonseca, Carmen, Eugenia Alarcon-Riquelme, Marta, Radstake, Timothy RDJ, Beretta, Lorenzo, Denton, Christopher P, Mayes, Maureen D, Martin, Javier

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Use of allelic variants (snps) in the 6p21.33 region for the diagnosis, prognosis and treatment of m¿ni¿re's disease. (Machine-translation by Google Translate, not legally binding)... von López Escámez, José Antonio, Cabrera Martínez, Sonia, Alarcón Riquelme, Marta Eugenia, Requena Navarro, María Teresa

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POLYMORPHISMS OF PD-1 von PROKUNINA, LUDMILA, ALARCON-RIQUELME, MARTA, EUGENIA

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Polymorphisms of pd-1 von LUDMILA PROKUNINA, MARTA EUGENIA ALARCON-RIQUELME

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POLYMORPHISMS OF PD-1 von PROKUNINA, LUDMILA, ALARCON-RIQUELME, MARTA, EUGENIA

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