Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis

por Bras, Jose, Verloes, Alain, Schneider, Susanne A., Mole, Sara E., Guerreiro, Rita J.
Publicado 2012

TDP-43 Is Not a Common Cause of Sporadic Amyotrophic Lateral Sclerosis

por Guerreiro, Rita J., Schymick, Jennifer C., Crews, Cynthia, Singleton, Andrew, Hardy, John, Traynor, Bryan J.
Publicado 2008

Mutation of TBCK causes a rare recessive developmental disorder

por Guerreiro, Rita J., Brown, Rachel, Dian, Donnai, de Goede, Christian, Bras, Jose, Mole, Sara E.
Publicado 2016

CLN8 disease caused by large genomic deletions

por Beesley, Clare, Guerreiro, Rita J., Bras, Jose T., Williams, Ruth E., Taratuto, Ana Lia, Eltze, Christin, Mole, Sara E.
Publicado 2016

Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort

por Guerreiro, Rita J, Bras, Jose M, Santana, Isabel, Januario, Cristina, Santiago, Beatriz, Morgadinho, Ana S, Ribeiro, Maria H, Hardy, John, Singleton, Andrew, Oliveira, Catarina
Publicado 2006

An Aged Canid with Behavioral Deficits Exhibits Blood and Cerebrospinal Fluid Amyloid Beta Oligomers

por Rusbridge, Clare, Salguero, Francisco J., David, Monique Antoinette, Faller, Kiterie M. E., Bras, Jose T., Guerreiro, Rita J., Richard-Londt, Angela C., Grainger, Duncan, Head, Elizabeth, Brandner, Sebastian G. P., Summers, Brian, Hardy, John, Tayebi, Mourad
Publicado 2018

Genetic Variability in CLU and Its Association with Alzheimer's Disease

por Guerreiro, Rita J., Beck, John, Gibbs, J. Raphael, Santana, Isabel, Rossor, Martin N., Schott, Jonathan M., Nalls, Michael A., Ribeiro, Helena, Santiago, Beatriz, Fox, Nick C., Oliveira, Catarina, Collinge, John, Mead, Simon, Singleton, Andrew, Hardy, John
Publicado 2010