2020
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Brasó-Vives M, Povolotskaya IS, Hartasánchez DA, Farré X, Fernandez-Callejo M, Raveendran M, Harris RA, Rosene DL, Lorente-Galdos B, Navarro A, Marques-Bonet T, Rogers J, Juan D. Copy number variants and fixed duplications among 198 rhesus macaques (Macaca mulatta). PLoS Genetics 2020; 16(5).
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Gelabert P, Sandoval-Velasco M, Serres A, de Manuel M, Renom P, Margaryan A, Stiller J, de-Dios T, Fang Q, Feng S, Mañosa S, Pacheco G, Ferrando-Bernal M, Shi G, Hao F, Chen X, Petersen B, Olsen RA, Navarro A, Deng Y, Dalén L, Marquès-Bonet T, Zhang G, Antunes A, Gilbert MTP, Lalueza-Fox C. Evolutionary history, genomic adaptation to toxic diet, and extinction of the Carolina Parakeet. Current Biology 2020; 30(1): 108-114.
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Gil-Varea E, Fedetz M, Eixarch H, Spataro N, Villar LM, Urcelay E, Saiz A, Fernández O, Leyva L, Ramió-Torrentà Ll, Vandenbroeck K, Otaegui D, Castillo-Triviño T, Izquierdo G, Malhotra S, Bosch E, Navarro A, Alcina A, Montalban X, Matesanz F, Comabella, M. A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells.. Journal of clinical medicine 2020; 9(3).
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Gil-Varea, E; Spataro, N; Villar, LM; Tejeda-Velarde, A; Midaglia, L; Matesanz, F; Malhotra, S; Eixarch, H; Patsopoulos, N; Fernández, O; Oliver-Martos, B; Saiz, A; Llufriu, S; Ramió-Torrentà, L; Quintana, E; Izquierdo, G; Alcina, A; Bosch, E; Navarro, A; Montalban, X; Comabella, M. Targeted resequencing reveals rare variants enrichment in multiple sclerosis susceptibility genes. Human Mutation 2020; 41(7): 1308-20.
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Peroni S, Sorosina M, Malhotra S, Clarelli F, Osiceanu AM, Ferrè L, Roostaei T, Rio J, Midaglia L, Villar LM, Álvarez-Cermeño JC, Guaschino C, Radaelli M, Citterio L, Lechner-Scott J, Spataro N, Navarro A, Martinelli V, Montalban X, Weiner HL, de Jager P, Comi G, Esposito F, Comabella M, Martinelli-Boneschi F. A pharmacogenetic study implicates NINJ2 in the response to Interferon-ß in multiple sclerosis Multiple Sclerosis 2020; 26(9): 1074-82.
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