Autor Título Original / Colaboración Selecciona una opción Original Colaboración Año Selecciona un año20152016201720182019202020212022202320242025 Cuartil Selecciona un cuartilD1Q1Q2Q3Q4 Tipo Selecciona un tipo#N/DArticleArtículoBook ChapterBook ReviewClinical TrialCommentaryCorrectionData PaperEditorialEditorial MaterialExpression of ConcernLetterProceedings PaperReprintReview Revista Transcriptional and Epigenetic Response to Sedentary Behavior and Physical Activity in Children and Adolescents: A Systematic Review Autores: Plaza-Florido, A; Perez-Prieto, I; Molina-Garcia, P; Radom-Aizik, S; Ortega, FB; Altmaee, S Transcriptional and epigenetic response to sedentary behavior and physical activity in children and adolescents: A systematic review (vol 10, 917152, 2022) Autores: Plaza-Florido, A; Perez-Prieto, I; Molina-Garcia, P; Radom-Aizik, S; Ortega, FB; Altmae, S Recent advances in elucidating the genetic basis of systemic sclerosis Autores: Villanueva-Martin, G; Martin, J; Bossini-Castillo, L Story of two sisters with kidney disease: genetics command Autores: Barral-Jueza, M; Garcia-Rabaneda, C; Poyatos-Andujar, AM; Martinez-Atienza, M; Morales-Garcia, AI; Morales-Santana, S; Bellido-Diaz, ML; Bravo-Soto, JA; Esteban-de la Rosa, RJ Targeting HIF-1 alpha Function in Cancer through the Chaperone Action of NQO1: Implications of Genetic Diversity of NQO1 Autores: Salido, E; Timson, DJ; Betancor-Fernandez, I; Palomino-Morales, R; Anoz-Carbonell, E; Pacheco-Garcia, JL; Medina, M; Pey, AL Standards in semen examination: publishing reproducible and reliable data based on high-quality methodology Autores: Bjorndahl, L; Barratt, CLR; Mortimer, D; Agarwal, A; Aitken, RJ; Alvarez, JG; Aneck-Hahn, N; Arver, S; Baldi, E; Bassas, L; Boitrelle, F; Bornman, R; Carrell, DT; Castilla, JA; Parra, GC; Check, JH; Cuasnicu, PS; Darney, SP; de Jager, C; De Jonge, CJ; Drevet, JR; Drobnis, EZ; Du Plessis, SS; Eisenberg, ML; Esteves, SC; Evgeni, EA; Ferlin, A; Garrido, N; Giwercman, A; Goovaerts, IGF; Haugen, TB; Henkel, R; Henningsohn, L; Hofmann, MC; Hotaling, JM; Jedrzejczak, P; Jouannet, P; Jorgensen, N; Brown, JCK; Krausz, C; Kurpisz, M; Kvist, U; Lamb, DJ; Levine, H; Loveland, KL; McLachlan, RI; Mahran, A; Maree, L; da Silva, SM; Mbizvo, MT; Meinhardt, A; Menkveld, R; Mortimer, ST; Moskovtsev, S; Muller, CH; Munuce, MJ; Muratori, M; Niederberger, C; O'Flaherty, C; Oliva, R; Ombelet, W; Pacey, AA; Palladino, MA; Ramasamy, R; Ramos, L; Rives, N; Roldan, ER; Rothmann, S; Sakkas, D; Salonia, A; Sanchez-Pozo, MC; Sapiro, R; Schlatt, S; Schlegel, PN; Schuppe, HC; Shah, R; Skakkebaek, NE; Teerds, K; Toskin, I; Tournaye, H; Turek, PJ; van der Horst, G; Vazquez-Levin, M; Wang, C; Wetzels, A; Zeginiadou, T; Zini, A Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome Autores: Cervan-Martin, M; Bossini-Castillo, L; Guzman-Jimenez, A; Rivera-Egea, R; Garrido, N; Lujan, S; Romeu, G; Santos-Ribeiro, S; Castilla, JA; Gonzalvo, MC; Clavero, A; Vicente, FJ; Maldonado, V; Gonzalez-Munoz, S; Rodriguez-Martin, I; Burgos, M; Jimenez, R; Pinto, MG; Pereira, I; Nunes, J; Sanchez-Curbelo, J; Lopez-Rodrigo, O; Pereira-Caetano, I; Marques, PI; Carvalho, F; Barros, A; Bassas, L; Seixas, S; Goncalves, J; Larriba, S; Lopes, AM; Carmona, FD; Palomino-Morales, RJ < 1 2 … 634 635 636 … 1.706 1.707 >