Rogelio Palomino
Universidad de Granada
H-index: 26
Europe-Spain
Top articles of Rogelio Palomino
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Changes in environmental exposures over decades may influence the genetic architecture of severe spermatogenic failure | Human Reproduction | Miriam Cerván-Martín Sara González-Muñoz Andrea Guzmán-Jiménez Inmaculada Higueras-Serrano José A Castilla | 2024/3/1 |
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 | Journal of Dermatological Science | Chiranan Khantham Warintorn Ruksiriwanich Tanakarn Chaitep Pichchapa Linsaenkart Anurak Muangsanguan | 2023/2/1 |
Targeting HIF-1α function in cancer through the chaperone action of NQO1: implications of genetic diversity of NQO1 | Eduardo Salido David J Timson Isabel Betancor-Fernández Rogelio Palomino-Morales Ernesto Anoz-Carbonell | 2022/5/5 | |
A GWAS in idiopathic/unexplained infertile men detects a genomic region determining Follicle-stimulating hormone levels | The Journal of Clinical Endocrinology & Metabolism | Maria Schubert Lina Pérez Lanuza Marius Wöste Martin Dugas F David Carmona | 2022/8 |
P-538 KATNAL1 polymorphisms confer susceptibility to severe phenotypes of male infertility in a large European cohort | Human Reproduction | A GUZMÁN JIMÉNEZ M Cerván-Martín L Bossini-Castillo N Garrido S Luján | 2022/7 |
Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia | Frontiers in Cell and Developmental Biology | Andrea Guzmán-Jiménez Sara González-Muñoz Miriam Cerván-Martín Rocío Rivera-Egea Nicolás Garrido | 2022/12/15 |
P-536 Common variation in the PIN1 locus increases the genetic risk to suffer from Sertoli Cell Only syndrome | Human Reproduction | M Cerván Martín S González-Muñoz L Bossini-Castillo A Guzmán-Jime'nez N Garrido | 2022/7 |
Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility | Communications Biology | Miriam Cerván-Martín Frank Tüttelmann Alexandra M Lopes Lara Bossini-Castillo Rocío Rivera-Egea | 2022/11/10 |
Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome | Journal of Personalized Medicine | Miriam Cerván-Martín Lara Bossini-Castillo Andrea Guzmán-Jimenez Rocío Rivera-Egea Nicolás Garrido | 2022/6/4 |
Different phenotypic outcome due to site-specific phosphorylation in the cancer-associated NQO1 enzyme studied by phosphomimetic mutations | Ángel Luis Pey Rodríguez Juan Luis Pacheco García Rogelio Jesús Palomino Morales | 2022/10/30 | |
Allosteric communication in the multifunctional and redox NQO1 protein studied by cavity-making mutations | Antioxidants | Juan Luis Pacheco-Garcia Dmitry S Loginov Ernesto Anoz-Carbonell Pavla Vankova Rogelio Palomino-Morales | 2022/6/2 |
Common genetic variation in KATNAL1 non‐coding regions is involved in the susceptibility to severe phenotypes of male infertility | Andrology | Miriam Cerván‐Martín Lara Bossini‐Castillo Andrea Guzmán‐Jiménez Rocío Rivera‐Egea Nicolás Garrido | 2022/10 |
Structural basis of the pleiotropic and specific phenotypic consequences of missense mutations in the multifunctional NAD (P) H: quinone oxidoreductase 1 and their … | Redox Biology | Juan Luis Pacheco-Garcia Ernesto Anoz-Carbonell Pavla Vankova Adithi Kannan Rogelio Palomino-Morales | 2021/10/1 |
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 … | Human Reproduction | M Cerván Martín F Tüttelmann AM Lopes L Bossini-Castillo N Garrido | 2021/7 |
Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort | Andrology | Miriam Cerván‐Martín Lara Bossini‐Castillo Rocío Rivera‐Egea Nicolas Garrido Saturnino Luján | 2021/7 |
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 | 37th Annual Meeting of the European Society of Human Reproduction and Embryology (ESHRE), 26 June-1 July 2021 (Online) | Miriam Cerván-Martín Frank Tüttelmann Alexandra Lopes Lara B Castillo Nicolás Garrido | 2021 |
Evaluation of male fertility-associated loci in a European population of patients with severe spermatogenic impairment | Journal of Personalized Medicine | Miriam Cerván-Martín Lara Bossini-Castillo Rocío Rivera-Egea Nicolás Garrido Saturnino Luján | 2020/12/29 |
Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment | Fertility and sterility | Miriam Cerván-Martín M Irene Suazo-Sánchez Rocío Rivera-Egea Nicolás Garrido Saturnino Luján | 2020/8/1 |
Deficiency of the onco-miRNA cluster, miR-106b∼25, causes oligozoospermia and the cooperative action of miR-106b∼25 and miR-17∼92 is required to … | Molecular Human Reproduction | Alicia Hurtado Rogelio Palomino Ina Georg Miguel Lao Francisca M Real | 2020/6 |
Genetic landscape of nonobstructive azoospermia and new perspectives for the clinic | Miriam Cerván-Martín José A Castilla Rogelio J Palomino-Morales F David Carmona | 2020/2 |
