The age factor in Alzheimer’s disease

par Guerreiro, Rita, Bras, Jose
Publié dans Genome Med (2015)

GENETIC SUSCEPTIBILITY IN PARKINSON’S DISEASE

par Bras, Jose Miguel, Singleton, Andrew
Publié 2008

Genetics Underlying Atypical Parkinsonism and Related Neurodegenerative Disorders

par Scholz, Sonja W., Bras, Jose
Publié dans Int J Mol Sci (2015)

Exome Sequencing in Parkinson’s disease

par Bras, Jose M, Singleton, Andrew B
Publié 2011

The Genetics of Dementia with Lewy Bodies: Current Understanding and Future Directions

par Orme, Tatiana, Guerreiro, Rita, Bras, Jose
Publié dans Curr Neurol Neurosci Rep (2018)

How understudied populations have contributed to our understanding of Alzheimer’s disease genetics

par Dehghani, Nadia, Bras, Jose, Guerreiro, Rita
Publié dans Brain (2021)

Next generation sequencing techniques in neurological diseases: redefining clinical and molecular associations

par Guerreiro, Rita, Brás, José, Hardy, John, Singleton, Andrew
Publié 2014

POTENTIAL ROLE OF CERAMIDE METABOLISM IN LEWY BODY DISEASE

par Bras, Jose, Singleton, Andrew, Cookson, Mark R, Hardy, John
Publié 2008

Late-onset and acute presentation of Brown-Vialetto-Van Laere syndrome in a Brazilian family

par Camargos, Sarah, Guerreiro, Rita, Bras, Jose, Mageste, Luis Sergio
Publié dans Neurol Genet (2018)

Genetic Variants and Related Biomarkers in Sporadic Alzheimer’s Disease

par Guerreiro, Rita, Bras, Jose, Toombs, Jamie, Heslegrave, Amanda, Hardy, John, Zetterberg, Henrik
Publié dans Curr Genet Med Rep (2014)

Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis

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

A nonsense mutation in PRNP associated with clinical Alzheimer's disease()

par Guerreiro, Rita, Brás, José, Wojtas, Aleksandra, Rademakers, Rosa, Hardy, John, Graff-Radford, Neill
Publié 2014

Current concepts and controversies in the pathogenesis of Parkinson’s disease dementia and Dementia with Lewy Bodies

par Weil, Rimona S., Lashley, Tammaryn L., Bras, Jose, Schrag, Anette E., Schott, Jonathan M.
Publié dans F1000Res (2017)

Psychiatric Manifestations of ATP13A2 Mutations

par Balint, Bettina, Damasio, Joana, Magrinelli, Francesca, Guerreiro, Rita, Bras, Jose, Bhatia, Kailash P.
Publié dans Mov Disord Clin Pract (2020)

Analysis of Nigerians with Apparently Sporadic Parkinson Disease for Mutations in LRRK2, PRKN and ATXN3

par Okubadejo, Njideka, Britton, Angela, Crews, Cynthia, Akinyemi, Rufus, Hardy, John, Singleton, Andrew, Bras, Jose
Publié 2008

Mutation of TBCK causes a rare recessive developmental disorder

par Guerreiro, Rita J., Brown, Rachel, Dian, Donnai, de Goede, Christian, Bras, Jose, Mole, Sara E.
Publié dans Neurol Genet (2016)

Genetic architecture of common non-Alzheimer’s disease dementias

par Guerreiro, Rita, Gibbons, Elizabeth, Tábuas-Pereira, Miguel, Kun-Rodrigues, Celia, Santo, Gustavo C., Bras, Jose
Publié dans Neurobiol Dis (2020)

CLN6 disease caused by the same mutation originating in Pakistan has varying pathology

par Guerreiro, Rita, Bras, Jose T., Vieira, Mariana, Warrier, Varun, Agrawal, Shakti, Stewart, Helen, Anderson, Glenn, Mole, Sara E.
Publié 2013

AP4S1 splice-site mutation in a case of spastic paraplegia type 52 with polymicrogyria

par Carmona, Susana, Marecos, Clara, Amorim, Marta, Ferreira, Ana C., Conceição, Carla, Brás, José, Duarte, Sofia T., Guerreiro, Rita
Publié dans Neurol Genet (2018)

Coding Variation in GBA Explains the Majority of the SYT11-GBA Parkinson’s Disease GWAS Locus

par Blauwendraat, Cornelis, Bras, Jose M., Nalls, Mike A., Lewis, Patrick A., Hernandez, Dena G., Singleton, Andrew B.
Publié dans Mov Disord (2018)