Hospital Universitario y Politécnico La Fe | Spain
Dr. Ramiro Quiroga is a highly experienced medical professional specializing in Gynecology, Obstetrics, and Clinical Analysis, with a PhD in Medicine from the University of Valencia. Accredited in Human Genetics by the Spanish Association of Human Genetics, his main expertise lies in prenatal diagnosis and the application of genetics in human reproduction. He serves as a consultant for the Orphanet Spain Network for Rare Diseases and as a member of expert committees for FEDER and the National Commission on Assisted Human Reproduction. In addition to his clinical practice at Hospital Universitario y Politécnico La Fe, he contributes to teaching and research at the University of Valencia, with numerous publications, book chapters, and conference presentations. Fluent in Spanish and English, Dr. Ramiro Quiroga combines his medical, academic, and research experience to advance the fields of human genetics and prenatal medicine.
Profile: Orcid
Featured Publications
S. Menao Guillén, L. Pedrola, C. Orellana, M. Roselló, M. Arruebo, C. Lahuerta Pueyo, M. Sobreviela Laserrada, B. Marcos, J. Pascual Mancho, J. V. Cervera, et al. (2025). Clinical utility of opportunistic genome-wide cfDNA prenatal screening in intermediate-risk pregnancies. Genes.
Vendrell, X., Abulí, A., Serra, C., Guillén, J. J., Rueda, J., García-Planells, J., Santos-Simarro, F., Quiroga, R., Abellán, F., Oancea-Ionescu, R., et al. (2025). Population-based genetic carrier screening: A consensus statement from the Spanish societies AEGH, AEDP, ASEBIR, SEAGEN, SEF, and SEGCD. European Journal of Human Genetics.
Pedrola Vidal, L., Roselló Piera, M., Martín-Grau, C., Rubio Moll, J. S., Gómez Portero, R., Marcos Puig, B., Cervera Zamora, J. V., Quiroga, R., & Orellana Alonso, C. (2024). Prenatal genome-wide cell-free DNA screening: Three years of clinical experience in a hospital prenatal diagnostic unit in Spain. Genes.
Martín-Grau, C., Orellana Alonso, C., Roselló Piera, M., Pedrola Vidal, L., Llorens-Salvador, R., Quiroga, R., Marín Reina, P., Rubio Moll, J. S., Gómez Portero, R., & Martínez-Castellano, F. (2023). Expanding the phenotype of PIGP deficiency to multiple congenital anomalies-hypotonia-seizures syndrome. Clinical Genetics.