C. Simòn

Improved clinical utility of preimplantation genetic testing through the integration of ploidy and common pathogenic microdeletions analyses.

J. Jimenez-Almazan, C. Rubio, L. Rienzi, 2023, Human reproduction.

Integrative Genomic and Transcriptomic Profiling Reveals a Differential Molecular Signature in Uterine Leiomyoma versus Leiomyosarcoma

J. Jimenez-Almazan, A. Mas, V. Lago, 2022, International journal of molecular sciences.

Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects

I. Barshack, E. Eyal, N. Amariglio, 2016, The Journal of experimental medicine.

Maternal exome analysis for the diagnosis of oocyte maturation defects and early embryonic developmental arrest.

V. Colonna, A. Capalbo, M. Figliuzzi, 2022, Reproductive biomedicine online.

O8 Accuracy rates in biopsies performed on day-3 and day-5 embryos using CGHarray technology for PGS

A. Mercader, C. Rubio, L. Rodrigo, 2012 .