| Genetic landscape of nonobstructive azoospermia and new perspectives for the clinic M Cerván-Martín, JA Castilla, RJ Palomino-Morales, FD Carmona Journal of clinical medicine 9 (2), 300, 2020 | 61 | 2020 |
| Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort M Cerván‐Martín, L Bossini‐Castillo, R Rivera‐Egea, N Garrido, S Luján, ... Andrology 9 (4), 1151-1165, 2021 | 12 | 2021 |
| Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment M Cerván-Martín, MI Suazo-Sánchez, R Rivera-Egea, N Garrido, S Luján, ... Fertility and sterility 114 (2), 398-406, 2020 | 12 | 2020 |
| Evaluation of male fertility-associated loci in a European population of patients with severe spermatogenic impairment M Cerván-Martín, L Bossini-Castillo, R Rivera-Egea, N Garrido, S Luján, ... Journal of Personalized Medicine 11 (1), 22, 2020 | 10 | 2020 |
| 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 |
| Genetic basis of idiopathic male infertility M Cerván Martín Universidad de Granada, 2023 | | 2023 |
| KATNAL1 polymorphisms confer susceptibility to severe phenotypes of male infertility in a large European cohort A Guzman Jimenez, M Cervan-Martin, L Bossini-Castillo, N Garrido, ... HUMAN REPRODUCTION 37, I441-I442, 2022 | | 2022 |
| P-538 KATNAL1 polymorphisms confer susceptibility to severe phenotypes of male infertility in a large European cohort A GUZMÁN JIMÉNEZ, M Cerván-Martín, L Bossini-Castillo, N Garrido, ... Human Reproduction 37 (Supplement_1), deac107. 496, 2022 | | 2022 |
| 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 |
| O-118 New insight into the genetic contribution of common variants to the development of extreme phenotypes of unexplained male infertility: a multicenter genome-wide … M Cerván Martín, F Tüttelmann, AM Lopes, L Bossini-Castillo, N Garrido, ... Human Reproduction 36 (Supplement_1), deab126. 027, 2021 | | 2021 |
| New insight into the genetic contribution of common variants to the development of extreme phenotypes of unexplained male infertility: a multicenter genome-wide association study M Cerván-Martín, F Tüttelmann, A Lopes, LB Castillo, N Garrido, S Luján, ... 37th Annual Meeting of the European Society of Human Reproduction and …, 2021 | | 2021 |
