Laia Pedrola Vidal

8PUBLICATIONS
24CO-AUTHORS
Foetal development and medicineGene expression (incl. microarray and other genome-wide approaches)NeurogeneticsGene mappingEpigenetics (incl. genome methylation and epigenomics)
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Publications (8)

|Apr 09, 2026
Protocol for a prospective observational cohort study to assess clinical applications of expanded noninvasive prenatal testing (NIPT) in pregnancies with placental dysfunction.

Ana Villalba, M Ángeles Sánchez-Durán, Carmen Orellana

|Nov 27, 2025
Clinical Utility of Opportunistic Genome-Wide cfDNA Prenatal Screening in Intermediate-Risk Pregnancies.

S Menao Guillén, L Pedrola, C Orellana

|Jul 07, 2025
Genetic landscape of hereditary transthyretin amyloidosis in Spain: a multicentric retrospective study.

Marta Domínguez-Martínez, Alfonso Caro-Llopis, Carla Martín-Grau

|Feb 13, 2025
Utility of Optical Genome Mapping for Accurate Detection and Fine-Mapping of Structural Variants in Elusive Rare Diseases.

Carmen Orellana, Monica Rosello, Amparo Sanchis

|Jun 27, 2024
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 Caused by a Novel <i>PIGA</i> Variant Not Associated with a Skewed X-Inactivation Pattern.

Alba Gabaldon-Albero, Lourdes Cordon, Amparo Sempere

|May 25, 2024
Prenatal Genome-Wide Cell-Free DNA Screening: Three Years of Clinical Experience in a Hospital Prenatal Diagnostic Unit in Spain.

Laia Pedrola Vidal, Mónica Roselló Piera, Carla Martín-Grau

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Frequent Collaborators

4 joint publications

Carmen Orellana

4 joint publications

Carla Martin-Grau

3 joint publications

Monica Rosello

2 joint publications

Jose V Cervera Zamora