Natalie Arran

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

MSH3 modifies somatic instability and disease severity in Huntington’s and myotonic dystrophy type 1

Michael Flower, Vilija Lomeikaite, Marc Ciosi et al. · Brain · 2019 · 169 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Reliability and Factor Structure of the Short Problem Behaviors Assessment for Huntington’s Disease (PBA-s) in the TRACK-HD and REGISTRY studies

Jenny Callaghan, Cheryl Stopford, Natalie Arran et al. · Journal of Neuropsychiatry · 2015 · 87 citations

Social Sciences, Behavioral Sciences, Psychology +17

Illness perceptions, coping styles and psychological distress in adults with Huntington’s disease

Natalie Arran, David Craufurd, Jane Simpson · Psychology Health & Medicine · 2013 · 70 citations

Social Sciences, Behavioral Sciences, Psychology +16