Laura Marti Sanchez
Investigador post-doc
Research group
Researcher Laura Martí Sánchez graduated in Biochemistry and Biomedical Sciences in 2004 from the University of Valencia. That same year he took two postgraduate courses belonging to the same university: Postgraduate in Genetic Diagnostic Techniques and Postgraduate in Medical Genetics. During those years, various internships have been carried out: (1) in the clinical field in the Laboratory of Clinical Analysis and Microbiology of the Hospital de Manises (Valencia), (2) performing cytogenetic techniques in the Radiological Protection Department of the La Fe hospital (Valencia), (3) in the Sequencing and Arrays service of the La Fe hospital (Valencia), (4) in the production and diagnosis service of the company Progenie Molecular (Valencia) and (5) performing basic research techniques in the Príncipe Felipe Research Center (Valencia).
Potentially, the researcher completed the "Advanced Genetics" master's degree from the Autonomous University of Barcelona.
Currently, the researcher is studying her last year of doctoral studies at the Faculty of Medicine of the University of Barcelona.
Professional network profiles
Last Publications
- Nou-Fontanet L, Marti-Sanchez L, Martorell-Sampol L, Casas J and Ortigoza-Escobar JD Atypical Mowat-Wilson Syndrome: Dystonia, Choreoathetosis and Cognitive Features. Movement Disorders Clinical Practice . 11(7): 889-893.
- Pata S, Flores-Rojas K, Gil A, López-Laso E, Marti-Sanchez L, Baide-Mairena H, Pérez-Dueñas B and Gil-Campos M Clinical improvements after treatment with a low-valine and low-fat diet in a pediatric patient with enoyl-CoA hydratase, short chain 1 (ECHS1) deficiency ORPHANET JOURNAL OF RARE DISEASES . 17(1): 340-340.
- Baide-Mairena H, Marti-Sanchez L, Marcé-Grau A, Cazurro-Gutiérrez A, Sanchez-Montanez A, Delgado I, Moreno-Galdó A, Macaya-Ruiz A, García-Arumí E and Pérez-Dueñas B Genetic diagnosis of basal ganglia disease in childhood DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY . 64(6): 743-752.
Projects
- Project name:
- Mapas de conectividad funcional cerebral y neurodesarrollo en epilepsias pediátricas de debut precoz (Proyecto EPI-NEUROMAPS)
- Leader
- Maria del Carmen Fons Estupiña
- Funding entities:
- Instituto de Salud Carlos III (ISCIII)
- Code
- PI22/01441
- Starting - finishing date:
- 2023 - 2025
- 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
- Project name:
- Biomarcadores y genes en la necrosis estriatal bilateral de la infancia
- Leader
- Belén Pérez Dueñas, Rafael Artuch Iriberri
- Funding entities:
- Hospital Sant Joan de Déu - Esplugues HSJD
- Code
- BR201602
- Starting - finishing date:
- 2017 - 2020