A comprehensive study of common and rare genetic variants in spermatogenesis-related loci identifies new risk factors for idiopathic severe spermatogenic failure

Can genome-wide genotyping data be analysed using a hypothesis-driven approach to enhance the understanding of the genetic basis of severe spermatogenic failure (SPGF) in male infertility?

Detalles Bibliográficos
Autores: Guzmán-Jimenez, Andrea, González-Muñoz, Sara, Cerván-Martín, Miriam, Garrido, Nicolás, Castilla, José A., Gonzalvo, María Carmen, Clavero, Ana, Molina, Marta, Luján, Saturnino, Santos-Ribeiro, Samuel, Vilches, Miguel Ángel, Espuch, Andrea, Maldonado, Vicente, Galiano-Gutiérrez, Noelia, Santamaría-López, Esther, González-Ravina, Cristina, Quintana-Ferraz, Fernando, Gómez, Susana, Amorós, David, Martínez-Granados, Luis, Ortega-González, Yanira, Burgos, Miguel, Pereira-Caetano, Iris, Bulbul, Ozgur, Castellano, Stefano, Romano, Massimo, Albani, Elena, Bassas, Lluis, Seixas, Susana, Gonçalves, João, Lopes, Alexandra M., Larriba, Sara, Palomino-Morales, Rogelio, Carmona, Francisco David, Bossini-Castillo, Lara
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2024
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/391794
Acceso en línea:http://hdl.handle.net/10261/391794
https://api.elsevier.com/content/abstract/scopus_id/85212334340
Access Level:acceso abierto
Palabra clave:Genetics
Idiopathic spermatogenic failure
Male infertility
Monogenic mutations
Polygenic susceptibility
Spermatogenesis
Descripción
Sumario:Can genome-wide genotyping data be analysed using a hypothesis-driven approach to enhance the understanding of the genetic basis of severe spermatogenic failure (SPGF) in male infertility?