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 · 531 citations

Life Sciences, Genetics, Molecular Genetics +12

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion

J.-M. Lee, E.M. Ramos, J.-H. Lee et al. · Neurology · 2012 · 391 citations · Full text

Life Sciences, Genetics, Neurology +15

<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 · 362 citations

Life Sciences, Genetics, Neurology +14

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

Davina J. Hensman Moss, Antonio F. Pardiñas, Douglas R. Langbehn et al. · The Lancet Neurology · 2017 · 332 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

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 · 242 citations · Full text

Life Sciences, Molecular Biology, Neuroscience +17