Alastair Maxwell
University of Glasgow(GB)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, DNA Repair Mechanisms, Muscle Physiology and Disorders, CRISPR and Genetic Engineering
Most-Cited Works
- → CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset(2019)541 cited
- → A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes(2019)175 cited
- → Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset(2022)82 cited
- → DNA methylation study of Huntington’s disease and motor progression in patients and in animal models(2020)79 cited
- → Genetic Risk Underlying Psychiatric and Cognitive Symptoms in Huntington’s Disease(2019)44 cited
- → A probable cis-acting genetic modifier of Huntington disease frequent in individuals with African ancestry(2022)21 cited
- → Huntington’s disease onset is determined by length of uninterrupted CAG, not encoded polyglutamine, and is modified by DNA maintenance mechanisms(2019)11 cited
- → FAN1 nuclease activity affects CAG expansion and age at onset of Huntington’s disease(2021)3 cited
- → A2 Cryptic polyglutamine repeat sequence variation and somatic instability in huntington’s disease: drivers of pathology?(2016)2 cited