Catherine Clenaghan

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

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

Clinical manifestations of intermediate allele carriers in Huntington disease

Esther Cubo, María A. Ramos-Arroyo, Saül Martínez‐Horta et al. · Neurology · 2016 · 54 citations

Life Sciences, Genetics, Neurology +13

Clinical characterization of dystonia in adult patients with Huntington's disease

Nadine A van de Zande, Thomas H. Massey, Duncan McLauchlan et al. · European Journal of Neurology · 2017 · 37 citations · Full text

Medicine, Neurology, Neuroscience +16

Reduced Cancer Incidence in Huntington’s Disease: Analysis in the Registry Study

Paul McNulty, Richard Pilcher, Renata Necuiniate et al. · Journal of Huntington s Disease · 2018 · 37 citations · Full text

Medicine, Oncology, Cancer Epidemiology +16