Publications
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Hernando-Davalillo C, Alcalá-San Martin A, Borregán M and Ortigoza-Escobar JD.
De novo 4q35.2 duplication containing FAT1 is associated with autism spectrum disorder.
CLINICAL GENETICS . 102(5): 434-437. Number of citations: 2
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Casas G, Limeres J, Oristrell G, Gutierrez-Garcia L, Andreini D, Borregán M, Larrañaga-Moreira JM, Lopez-Sainz A, Codina-Solà M, Teixido-Tura G, Sorolla-Romero JA, Fernández-Álvarez P, González-Carrillo J, Guala A, La Mura L, Soler-Fernández R, Sao Avilés A, Santos-Mateo JJ, Marsal JR, Ribera A, de la Pompa JL, Villacorta E, Jiménez-Jáimez J, Ripoll-Vera T, Bayes-Genis A, Garcia-Pinilla JM, Palomino-Doza J, Tiron C, Pontone G, Bogaert J, Aquaro GD, Gimeno-Blanes JR, Zorio E, Garcia-Pavia P, Barriales-Villa R, Evangelista A, Masci PG, Ferreira-González I and Rodríguez-Palomares JF.
Clinical Risk Prediction in Patients With Left Ventricular Myocardial Noncompaction.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY . 78(7): 643-662. Number of citations: 28
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Rovira-Moreno, E, Abuli, A, Codina-Sola, M, Valenzuela, I, Serra-Juhe, C, Cusco, I, Borregán M, Cueto-Gonzalez, A, Vendrell, T, Lopez-Grondona, F, Brun-Gasca, C, Brignani, E, Martinez-Ribot, L, Garci-Espejo, R, Cruz, J, Garcia-Arumi, E and Tizzano, EF.
Beyond the disease itself: A cross-cutting educational initiative for patients and families with rare diseases
JOURNAL OF GENETIC COUNSELING . 30(3): 693-700. Number of citations: 1