Adriana Prundean

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

Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation

Christophe Verny, Naïg Guegen, Valérie Desquiret‐Dumas et al. · Mitochondrion · 2010 · 89 citations

Life Sciences, Genetics, Neurology +12

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

A randomized, double‐blind, placebo‐controlled trial evaluating cysteamine in Huntington's disease

Christophe Verny, Anne‐Catherine Bachoud‐Lévi, Alexandra Dürr et al. · Movement Disorders · 2017 · 44 citations

Medicine, Neurology, Pharmacology +17

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