Miriam Cerván Martín
Biography
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Postdoctoral researcher at GENYO (Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research) since January 2026, with a Junta de Andalucía Junior Postdoctoral contract. Previously Juan de la Cierva postdoctoral researcher at the IPBLN (2024-2025), Fulbright research stay at Boston Children's Hospital (2025), and predoctoral (FPI, 2018-2022) and postdoctoral (2022-2023) researcher at the University of Granada. Collaborating researcher at the Hospital Universitario Virgen de las Nieves (2018-2023), in the recruitment and management of samples for the study of male infertility. Note: at the IPBLN-CSIC from January 2024 to December 2025. (Description curated from publicly available data.) |
Profile
| Institution | IPBLN |
| Position | Postdoctoral Fellow |
| Home page | https://www.linkedin.com/in/miriam-cerv%C3%A1n-mart%C3%ADn-925a12108/ |
| Contact email | Miriam.cervan@ipb.csic.es |
| ORCID | 0000-0001-6033-0587 |
BCB Hub
| BCB Committee | Not a member |
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Research
Research topics
miRNA
Research lines
Publications 11 entries
- A genetic variant in the 3′-UTR of PIWIL4 confers risk for extreme phenotypes of male infertility by altering miR-215 and miR-136 binding affinity Article · 11 Jun 2025
- Changes in environmental exposures over decades may influence the genetic architecture of severe spermatogenic failure Article · 1 Feb 2024
- A comprehensive study of common and rare genetic variants in spermatogenesis-related loci identifies new risk factors for idiopathic severe spermatogenic failure Article · 2024
- Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia Article · 15 Dec 2022
- Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility Article · 10 Nov 2022
View all (6 more)
- Common genetic variation in KATNAL1 non‐coding regions is involved in the susceptibility to severe phenotypes of male infertility Article · 8 Jul 2022
- Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome Article · 4 Jun 2022
- Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort Article · 20 Apr 2021
- Evaluation of Male Fertility-Associated Loci in a European Population of Patients with Severe Spermatogenic Impairment Article · 29 Dec 2020
- Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment Article · Aug 2020
- Genetic Landscape of Nonobstructive Azoospermia and New Perspectives for the Clinic Article · 21 Jan 2020