Joy Read

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

Motor, cognitive, and functional declines contribute to a single progressive factor in early HD

Scott Schobel, Giuseppe Palermo, Peggy Auinger et al. · Neurology · 2017 · 155 citations · Full text

Medicine, Neurology, Neuroscience +17

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

Siblings of young people with Duchenne muscular dystrophy – A qualitative study of impact and coping

Joy Read, Maria Kinali, Francesco Muntoni et al. · European Journal of Paediatric Neurology · 2010 · 57 citations

Nursing, Human Development, Psychology +16