Natalie Arran
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Neurological disorders and treatments, Fibromyalgia and Chronic Fatigue Syndrome Research, DNA Repair Mechanisms
Most-Cited Works
- → Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study(2017)328 cited
- → MSH3 modifies somatic instability and disease severity in Huntington’s and myotonic dystrophy type 1(2019)162 cited
- → Reliability and Factor Structure of the Short Problem Behaviors Assessment for Huntington’s Disease (PBA-s) in the TRACK-HD and REGISTRY studies(2015)84 cited
- → Illness perceptions, coping styles and psychological distress in adults with Huntington’s disease(2013)69 cited
- → Longitudinal expression changes are weak correlates of disease progression in Huntington’s disease(2020)9 cited
- → Intellectual enrichment and genetic modifiers of cognition and brain volume in Huntington’s disease(2022)4 cited
- → Test user experience: The Oxford Cognitive Screen(2018)1 cited
- → Peer supervision: An assistants’ perspective(2007)
- → Poster 8: Reliability of the Problem Behaviours Assessment for HD (short version)–Data From the TRACK-HD Study(2010)