Núria Brandi Tarrrau
Investigador
Research group
The researcher Núria Brandi Tarrau graduated in Biology in 1984 from the Central University of Barcelona and obtained her PhD in Biology from the University of Barcelona in 2010.
Since 1989 she has been an Administration and Services Personnel at the University of Barcelona, Faculty of Medicine.
Last Publications
- Pascual-Alonso A, Blasco-Perez L, Vidal-Falcó S, Gean Molins E, Rubio P, O'Callaghan-Gordo M, Martinez-Monseny T, Castells AA, Xiol-Viñas C, Català V, Brandi-Tarrau N, Pacheco-Fernández P, Ros C, Del Campo M, Guillén E, Ibañez S, Sánchez MJ, Lapunzina P, Nevado J, Santos F, Lloveras E, Ortigoza-Escobar JD, Tejada MI, Maortua H, Martínez F, Orellana C, Roselló M, Mesas MA, Obón M, Plaja A, Fernández-Ramos JA, Tizzano E, Marín R, Peña-Segura JL, Alcántara S and Armstrong-Moron J Molecular characterization of Spanish patients with MECP2 duplication syndrome. CLINICAL GENETICS . 97(4): 610-620.
- Pillai NR, Yubero-Siles D, Shayota BJ, De Oyarzabal-Sanz AL, Ghosh R, Sun Q, Azamian MS, Arjona-Fernandez C, Brandi-Tarrau N, Palau F, Lalani SR, Artuch-Iriberri R, Garcia-Cazorla A and Scott DA Loss of CLTRN function produces a neuropsychiatric disorder and a biochemical phenotype that mimics Hartnup disease AMERICAN JOURNAL OF MEDICAL GENETICS PART A . 179(12): 2459-2468.
- Xiol-Viñas C, Vidal-Falcó S, Pascual-Alonso A, Blasco-Perez L, Brandi-Tarrau N, Pacheco-Fernández P, Gerotina E, O'Callaghan-Gordo M, Pineda M and Armstrong-Moron J X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients. SCIENTIFIC REPORTS . 9(1): 11983-11983.
Projects
- Project name:
- Identificación de biomarcadores y dianas terapéuticas a través del análisis integrado de multiómica de la huella molecular del síndrome de Rett y trastornos del neurodesarrollo.
- Leader
- Judith Silvia Armstrong Morón
- Funding entities:
- Armstrong Morón, Judith Silvia, Instituto de Salud Carlos III (ISCIII), Fundació Privada per a la Recerca i la Docència Sant Joan de Déu - FSJD
- Code
- PI23/00108
- Starting - finishing date:
- 2024 - 2026
- 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:
- Estudio de pacientes dentro del Espectro Rett mediante un enfoque multiómico integrativo: delucidar la huella molecular de la via funcional.
- Leader
- Judith Silvia Armstrong Morón
- Funding entities:
- Instituto de Salud Carlos III (ISCIII)
- Code
- PI20/00389
- Starting - finishing date:
- 2021 - 2024