Laura Trujillano

5PUBLICATIONS
41CO-AUTHORS
Neurology and neuromuscular diseasesInfant and child healthCancer geneticsEpigenetics (incl. genome methylation and epigenomics)
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Publications (5)

|Jul 17, 2026
NKX2-1 Downstream Regulatory Structural Variants Explain a Substantial Proportion of Molecular Diagnoses in Patients With Benign Hereditary Chorea.

|Feb 27, 2026
Assessing Quality of Life in PACS1 Syndrome Using the KidsLife Scale from Mothers' and Fathers' Perspectives.

Julia Del Rincón, Laura Trujillano, Cristina Lucia-Campos

|Jun 28, 2023
Heart Disease Characterization and Myocardial Strain Analysis in Patients with PACS1 Neurodevelopmental Disorder.

Ana Latorre-Pellicer, Laura Trujillano, Julia Del Rincón

|Dec 09, 2022
Endocrine Evaluation and Homeostatic Model Assessment in Patients with Cornelia de Lange Syndrome

Ángela Ascaso, Ana Latorre-Pellicer, Beatriz Puisac

|Aug 26, 2022
A Novel Intragenic Duplication in the HDAC8 Gene Underlying a Case of Cornelia de Lange Syndrome.

Cristina Lucia-Campos, Irene Valenzuela, Ana Latorre-Pellicer

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Frequent Collaborators

4 joint publications

Ana Latorre-Pellicer

4 joint publications

María Arnedo

4 joint publications

Feliciano J Ramos

4 joint publications

Juan Pié Juste