Mar Borregán Prats
Investigador post-doc
Grup de recerca
Perfils professionals a les xarxes
Últimes publicacions
- 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.
- 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.
- 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.
Projectes
- Nom del projecte:
- SGR 2022-2024_Precision Medicine of Genetic and Rare Diseases (PrecisionRare)
- Investigador/a principal
- Francesc Palau Martínez
- Entitat/es finançadora/es:
- Agaur - Agència de Gestió d'Ajuts Universitaris i de Recerca
- Codi
- 2021 SGR 01610
- Data de inici-fi:
- 2022 - 2025