| Common genetic variation in KATNAL1 non‐coding regions is involved in the susceptibility to severe phenotypes of male infertility M Cerván‐Martín, L Bossini‐Castillo, A Guzmán‐Jiménez, R Rivera‐Egea, ... Andrology 10 (7), 1339-1350, 2022 | 4 | 2022 |
| Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility M Cerván-Martín, F Tüttelmann, AM Lopes, L Bossini-Castillo, ... Communications Biology 5 (1), 1220, 2022 | 3 | 2022 |
| Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia A Guzmán-Jiménez, S González-Muñoz, M Cerván-Martín, ... Frontiers in Cell and Developmental Biology 10, 1089782, 2022 | 1 | 2022 |
| Changes in environmental exposures over decades may influence the genetic architecture of severe spermatogenic failure M Cerván-Martín, S González-Muñoz, A Guzmán-Jiménez, ... Human Reproduction 39 (3), 612-622, 2024 | | 2024 |
| Sex-specific association of SELL gene polymorphisms with pattern hair loss in the Thai population: A candidate gene association study and in silico functional characterization C Khantham, W Ruksiriwanich, T Chaitep, P Linsaenkart, ... Journal of dermatological science 109 (2), 102-105, 2023 | | 2023 |
| P-536 Common variation in the PIN1 locus increases the genetic risk to suffer from Sertoli Cell Only syndrome M Cerván Martín, S González-Muñoz, L Bossini-Castillo, ... Human Reproduction 37 (Supplement_1), deac107. 494, 2022 | | 2022 |
| Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome M Cerván-Martín, L Bossini-Castillo, A Guzmán-Jimenez, R Rivera-Egea, ... Journal of Personalized Medicine 12 (6), 932, 2022 | | 2022 |
