Leonor Correia Guedes

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

Alessio Di Fonzo, Christan F. Rohé, Joaquim J. Ferreira et al. · The Lancet · 2005 · 529 citations

Molecular Neuroscience, Mendelian Disorder, Autosomal Dominant Parkinson +7

<i>FBXO7</i> mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome

Alessio Di Fonzo, Marieke C. J. Dekker, P. Montagna et al. · Neurology · 2008 · 353 citations

Convergence of miRNA Expression Profiling, α-Synuclein Interacton and GWAS in Parkinson's Disease

Madalena Martins, Alexandra Rosa, Leonor Correia Guedes et al. · PLoS ONE · 2011 · 241 citations · Full text

LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study

Marialuisa Quadri, Wim Mandemakers, Martyna M. Grochowska et al. · The Lancet Neurology · 2018 · 159 citations

Neurodegenerative Diseases, Genetic Disorder, Genetics +9

Posttranslational modifications of blood-derived alpha-synuclein as biochemical markers for Parkinson’s disease

Hugo Vicente Miranda, Rafaela Cássio, Leonor Correia Guedes et al. · Scientific Reports · 2017 · 107 citations · Full text