Adrián Alcalá San Martín
Ayudante de investigación
Research group
Professional network profiles
Last Publications
- Soliani L, Alcalá-San Martin A, Balsells S, Hernando-Davalillo C and Ortigoza-Escobar JD Chromosome Microarray Analysis for the Investigation of Deletions in Pediatric Movement Disorders: A Systematic Review of the Literature Movement Disorders Clinical Practice . 10(4): 547-557.
- 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.
- Pijuan-Marquilles J, Ortigoza-Escobar JD, Juan Jairo Ortiz Guerra, Alcalá-San Martin A, Calvo MJ, Cubells M, Hernando-Davalillo C, Palau F and Hoenicka J PLXNA2 and LRRC40 as candidate genes in autism spectrum disorder. AUTISM RESEARCH . 14(6): 1088-1100.
Projects
- Project name:
- SGR 2022-2024_Precision Medicine of Genetic and Rare Diseases (PrecisionRare)
- Leader
- Francesc Palau Martínez
- Funding entities:
- Agaur - Agència de Gestió d'Ajuts Universitaris i de Recerca
- Code
- 2021 SGR 01610
- Starting - finishing date:
- 2022 - 2025