Antoni Borrell

24PUBLICATIONS
34CO-AUTHORS
Respiratory diseasesGene expression (incl. microarray and other genome-wide approaches)Epidemiological modellingEpigenetics (incl. genome methylation and epigenomics)Neurogenetics
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Publications (24)

|Aug 05, 2026
The Diagnosis and Prenatal Management of Non-RHD Alloimmunizations.

|Jan 28, 2026
Prenatal Use of Exome Sequencing and Chromosomal Microarray Analysis: Indications, Interpretation, and Gene Selection Strategies.

Laia Rodriguez-Revenga, Victoria Ardiles-Ruesjas, Antoni Borrell

|Jan 04, 2026
Gene List Selection Matters: Missed Diagnoses in Prenatal Exome Sequencing-PanelApp R21 and HPO-Driven Versus OMIM-Based Gene Lists.

Victoria Ardiles-Ruesjas, Laia Rodriguez-Revenga, Montse Pauta

|Aug 15, 2025
Efficacy of Fetal Ear Length as a Prenatal Marker of Chromosomal Anomalies: A Prospective, Multicenter Cohort Study in a Southern European Population.

Elisabet Baldrich, Montse Comas, Alicia Maldonado

|Jul 08, 2025
Performance of international phenotypic criteria for prenatal exome sequencing: systematic review and comparative diagnostic accuracy study using historical individual participant data.

K Reilly, D L Rolnik, S Allen

|Jan 20, 2025
Fetal Corpus Callosum Anomalies: A Review of Underlying Genetic Disorders and Prenatal Testing Options.

Valeria Lanzarone, Elisenda Eixarch, Antoni Borrell

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Frequent Collaborators

11 joint publications

Montse Pauta

6 joint publications

Raigam Jafet Martinez-Portilla

3 joint publications

Victoria Ardiles-Ruesjas

3 joint publications

Laia Rodriguez-Revenga