Mireia Navarro-Boluda

Valencia, VC, Spain

Last Updated: 09/26/2026

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Found 8 publications

Timing matters: molecular signatures linked to developmental and implantation processes in day 5 and day 6 blastocysts.

Timing matters: molecular signatures linked to developmental and implantation processes in day 5 and day 6 blastocysts.

Journal: F&S science

Published: May 19, 2026

Euploid but failing to implant? Insights from trophectoderm transcriptomics of euploid blastocysts using an in vitro model.

Euploid but failing to implant? Insights from trophectoderm transcriptomics of euploid blastocysts using an in vitro model.

Journal: F&S science

Published: July 08, 2025

Olink® Explore for High-Throughput Protein Biomarker Discovery in Cerebrospinal Fluid.

Olink® Explore for High-Throughput Protein Biomarker Discovery in Cerebrospinal Fluid.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: April 01, 2025

A pilot study of transcriptomic preimplantation genetic testing (PGT-T): towards a new step in embryo selection?

A pilot study of transcriptomic preimplantation genetic testing (PGT-T): towards a new step in embryo selection?

Journal: Human reproduction (Oxford, England)

Published: February 20, 2024

Potentially toxic element bioaccumulation in consumed indoor shrimp farming associated with diet, water and sediment levels.

Potentially toxic element bioaccumulation in consumed indoor shrimp farming associated with diet, water and sediment levels.

Journal: Environmental science and pollution research international

Published: July 19, 2023

A Single-Run Next-Generation Sequencing (NGS) Assay for the Simultaneous Detection of Both Gene Mutations and Large Chromosomal Abnormalities in Patients with Myelodysplastic Syndromes (MDS) and Related Myeloid Neoplasms.

A Single-Run Next-Generation Sequencing (NGS) Assay for the Simultaneous Detection of Both Gene Mutations and Large Chromosomal Abnormalities in Patients with Myelodysplastic Syndromes (MDS) and Related Myeloid Neoplasms.

Journal: Cancers

Published: March 23, 2021

Case Report: Partial Uniparental Disomy Unmasks a Novel Recessive Mutation in the LYST Gene in a Patient With a Severe Phenotype of Chédiak-Higashi Syndrome.

Case Report: Partial Uniparental Disomy Unmasks a Novel Recessive Mutation in the LYST Gene in a Patient With a Severe Phenotype of Chédiak-Higashi Syndrome.

Journal: Frontiers in immunology

Published: November 03, 2020

Analysis of SNP Array Abnormalities in Patients with DE NOVO Acute Myeloid Leukemia with Normal Karyotype.

Analysis of SNP Array Abnormalities in Patients with DE NOVO Acute Myeloid Leukemia with Normal Karyotype.

Journal: Scientific reports

Published: September 11, 2018

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Last Updated: 09/26/2026