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01/01/2023
Sperm DNA methylome abnormalities occur both pre- and post-treatment in men with Hodgkin disease and testicular cancer
Chan D., Oros Klein K., Riera-Escamilla A., Krausz C., O’Flaherty C., Chan P., Robaire B., Trasler J.M.. Sperm DNA methylome abnormalities occur both pre- and post-treatment in men with Hodgkin disease and testicular cancer. Clinical Epigenetics. 2023; 15(1)DOI:10.1186/s13148-022-01417-1. PMID:36611168. IF:4.800(Q1/2D).
26/12/2022
Diverse monogenic subforms of human spermatogenic failure
Nagirnaja, L, Lopes, AM, Charng, WL, Miller, B, Stakaitis, R, Golubickaite, I, Stendahl, A, Luan, TPC, Friedrich, C, Mahyari, E, Fadial, E, Kasak, L, Vigh-Conrad, K, Oud, MS, Xavier, MJ, Cheers, SR, James, ER, Guo, JT, Jenkins, TG, Riera-Escamilla, A, Barros, A, Carvalho, F, Fernandes, S, Goncalves, J, Gurnett, CA, Jorgensen, N, Jezek, D, Jungheim, ES, Kliesch, S, McLachlan, RI, Omurtag, KR, Pilatz, A, Sandlow, J, Smith, J, Eisenberg, ML, Hotaling, JM, Jarvi, KA, Punab, M, Rajpert-De Meyts, E, Carrell, DT, Krausz, C, Laan, M, O'Bryan, MK, Schlegel, PN, Tuttelmann, F, Veltman, JA, Almstrup, K, Aston, KI, Conrad, DF. Diverse monogenic subforms of human spermatogenic failure. Nature Communications. 2022; 13(1)DOI:10.1038/s41467-022-35661-z. PMID:36572685. IF:16.600(Q1/1D).
15/12/2022
Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia
Guzman-Jimenez, A, Gonzalez-Munoz, S, Cervan-Martin, M, Rivera-Egea, R, Garrido, N, Lujan, S, Santos-Ribeiro, S, Castilla, JA, Gonzalvo, MC, Clavero, A, Vicente, FJ, Maldonado, V, Villegas-Salmeron, J, 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, Lopes, AM, Larriba, S, Palomino-Morales, RJ, Carmona, FD, Bossini-Castillo, L. Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia. Frontiers in Cell and Developmental Biology. 2022; 10DOI:10.3389/fcell.2022.1089782. PMID:36589743. IF:5.500(Q1/2D).
10/11/2022
Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility
Cervan-Martin, M, Tuttelmann, F, Lopes, AM, Bossini-Castillo, L, Rivera-Egea, R, Garrido, N, Lujan, S, Romeu, G, Santos-Ribeiro, S, Castilla, JA, Gonzalvo, MC, Clavero, A, Maldonado, V, Vicente, FJ, Gonzalez-Munoz, S, Guzman-Jimenez, A, Burgos, M, Jimenez, R, Pacheco, A, Gonzalez, C, Gomez, S, Amoros, D, Aguilar, J, Quintana, F, Calhaz-Jorge, C, Aguiar, A, Nunes, J, Sousa, S, Pereira, I, Pinto, MG, Correia, S, Sanchez-Curbelo, J, Lopez-Rodrigo, O, Martin, J, Pereira-Caetano, I, Marques, PI, Carvalho, F, Barros, A, Gromoll, J, Bassas, L, Seixas, S, Goncalves, J, Larriba, S, Kliesch, S, Palomino-Morales, RJ, Carmona, FD. Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility. Communications Biology. 2022; 5(1)DOI:10.1038/s42003-022-04192-0. PMID:36357561. IF:5.900(Q1/2D).
31/10/2022
Standards in semen examination: publishing reproducible and reliable data based on high-quality methodology
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. Standards in semen examination: publishing reproducible and reliable data based on high-quality methodology. HUMAN REPRODUCTION. 2022; 37(11)DOI:10.1093/humrep/deac189. PMID:36112046. IF:6.100(Q1/2D).
01/10/2022
Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility
Cervan-Martin, M, Bossini-Castillo, L, Guzman-Jimenez, A, Rivera-Egea, R, Garrido, N, Lujan, S, Romeu, G, Santos-Ribeiro, S, Castilla, JA, Gonzalvo, MD, Clavero, A, Maldonado, V, Vicente, FJ, Burgos, M, Jimenez, R, Gonzalez-Munoz, S, 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, Palomino-Morales, RJ, Carmona, FD. Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility. Andrology. 2022; 10(7)DOI:10.1111/andr.13221. PMID:35752927. IF:4.500(Q1/3D).