Laia Pedrola Vidal (Laia Pedrola, L Pedrola)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 7

Top Venues

Genes

Ophthalmic genetics

PloS one

This page only lists publications with an associated author ORCID identifier.

Publications

Laia Pedrola Vidal, Mónica Roselló Piera, Carla Martín Grau, Juan S Rubio Moll, Rosa Gómez Portero, Beatriz Marcos Puig, José Vicente Cervera, Ramiro Quiroga, Carmen Orellana Alonso
Prenatal Genome-Wide Cell-Free DNA Screening: Three Years of Clinical Experience in a Hospital Prenatal Diagnostic Unit in Spain. Genes 15 (5) (2024)
Laia Pedrola Vidal, Mónica Roselló Piera, Carla Martín Grau, Juan S Rubio Moll, Rosa Gómez Portero, Beatriz Marcos Puig, José Vicente Cervera, Ramiro Quiroga, Carmen Orellana Alonso
Prenatal Genome-Wide Cell-Free DNA Screening: Three Years of Clinical Experience in a Hospital Prenatal Diagnostic Unit in Spain. Genes 15 (5) (2024)
Alba Gabaldon-Albero, Lourdes Cordon, Amparo Sempere, Laia Pedrola Vidal, Carla Martín Grau, Silvestre Oltra, Sandra Monfort, Alfonso Caro-Llopis, Marta Dominguez-Martinez, Sara Hernandez-Muela, Monica Rosello, Carmen Orellana, Francisco Martinez
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 Caused by a Novel PIGA Variant Not Associated with a Skewed X-Inactivation Pattern. Genes 15 (6) (2024)
Laia Pedrola Vidal, Mónica Roselló Piera, Carla Martín Grau, Juan S Rubio Moll, Rosa Gómez Portero, Beatriz Marcos Puig, José Vicente Cervera, Ramiro Quiroga, Carmen Orellana Alonso
Prenatal Genome-Wide Cell-Free DNA Screening: Three Years of Clinical Experience in a Hospital Prenatal Diagnostic Unit in Spain. Genes 15 (5) (2024)
Alba Gabaldon-Albero, Lourdes Cordon, Amparo Sempere, Laia Pedrola Vidal, Carla Martín Grau, Silvestre Oltra, Sandra Monfort, Alfonso Caro-Llopis, Marta Dominguez-Martinez, Sara Hernandez-Muela, Monica Rosello, Carmen Orellana, Francisco Martinez
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 Caused by a Novel PIGA Variant Not Associated with a Skewed X-Inactivation Pattern. Genes 15 (6) (2024)
V Hernández, I Pascual-Camps, M J Aparisi, M Martínez-Matilla, F Martínez, J A Cerón, Laia Pedrola Vidal
Great clinical variability of Nance Horan syndrome due to deleterious NHS mutations in two unrelated Spanish families. Ophthalmic genetics 40 (6) (2019)
Sarah Moreau-Le Lan, Elena Aller, Ines Calabria, Lola Gonzalez-Tarancon, Cristina Cardona-Gay, Marina Martinez-Matilla, Maria J Aparisi, Jorge Selles, Lydia Sagath, Inmaculada Pitarch, Nuria Muelas, Jose V Cervera, Jose M Millan, Laia Pedrola Vidal
New mutations found by Next-Generation Sequencing screening of Spanish patients with Nemaline Myopathy. PloS one 13 (12) (2018)

Laia Pedrola Vidal.css-eqlu8i{font-size:small;padding-left:4px;} (Laia Pedrola, L Pedrola)

Publication Activity (10 Years)

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Laia Pedrola Vidal (Laia Pedrola, L Pedrola)