Damian Heine-Suñer

10PUBLICATIONS
63CO-AUTHORS
Developmental genetics (incl. sex determination)Infant and child healthGenetics not elsewhere classifiedPredictive and prognostic markersCardiology (incl. cardiovascular diseases)
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Publications (10)

|Mar 27, 2026
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Jhih-Rong Lin, Daniella Miller, Dana Luong

|Nov 13, 2025
Maternal Genotype and Dietary Vitamin A Modify Aortic Arch Phenotypes in a Mouse Model of 22q11DS.

Emilia Amengual-Cladera, Maria Victòria Llull-Alberti, Marc Ventayol-Guirado

|Mar 13, 2025
The Triad of Blood-Brain Barrier Integrity: Endothelial Cells, Astrocytes, and Pericytes in Perinatal Stroke Pathophysiology.

Tania Garcia-Martínez, Denise G Gornatti, Marina Ortiz

|Apr 27, 2024
Phenotypic Expression and Outcomes in Patients with the p.Arg301Gln GLA Variant in Anderson-Fabry Disease.

Rocío Blanco, Yolanda Rico-Ramírez, Álvaro Hermida-Ameijeiras

|Jun 10, 2023
Identification of Driver Epistatic Gene Pairs Combining Germline and Somatic Mutations in Cancer.

Jairo Rocha, Jaume Sastre, Emilia Amengual-Cladera

|May 27, 2023
NOTCH1 Gene as a Novel Cause of Thoracic Aortic Aneurysm in Patients with Tricuspid Aortic Valve: Two Cases Reported.

Laura Torres-Juan, Yolanda Rico, Elena Fortuny

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Frequent Collaborators

5 joint publications

Tomas Ripoll-Vera

5 joint publications

Laura Torres-Juan

3 joint publications

Fiama Giuliana Caimi-Martinez

2 joint publications

Bernice E Morrow