| CAG repeat not polyglutamine length determines timing of Huntington’s disease onset JM Lee, K Correia, J Loupe, KH Kim, D Barker, EP Hong, MJ Chao, ... Cell 178 (4), 887-900. e14, 2019 | 273 | 2019 |
| Timing and impact of psychiatric, cognitive, and motor abnormalities in Huntington disease B McAllister, JF Gusella, GB Landwehrmeyer, JM Lee, ME MacDonald, ... Neurology 96 (19), e2395-e2406, 2021 | 70 | 2021 |
| Genetic modifiers of Huntington disease differentially influence motor and cognitive domains JM Lee, Y Huang, M Orth, T Gillis, J Siciliano, E Hong, JS Mysore, ... The American Journal of Human Genetics 109 (5), 885-899, 2022 | 33 | 2022 |
| Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset B McAllister, J Donaldson, CS Binda, S Powell, U Chughtai, G Edwards, ... Nature neuroscience 25 (4), 446-457, 2022 | 33 | 2022 |
| Genetic risk underlying psychiatric and cognitive symptoms in Huntington’s disease N Ellis, A Tee, B McAllister, T Massey, D McLauchlan, T Stone, K Correia, ... Biological Psychiatry 87 (9), 857-865, 2020 | 30 | 2020 |
| Methods for assessing DNA repair and repeat expansion in Huntington’s disease T Massey, B McAllister, L Jones Huntington’s Disease, 483-495, 2018 | 8 | 2018 |
| Huntington’s disease onset is determined by length of uninterrupted CAG, not encoded polyglutamine, and is modified by DNA maintenance mechanisms Genetic Modifiers of Huntington’s Disease (GeM-HD) Consortium, JM Lee, ... bioRxiv, 529768, 2019 | 6 | 2019 |
| Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencing AS Taylor, D Barros, N Gobet, T Schuepbach, B McAllister, L Aeschbach, ... NAR Genomics and Bioinformatics 4 (4), lqac089, 2022 | 5 | 2022 |
| Huntington’s disease age at motor onset is modified by the tandem hexamer repeat in TCERG1 SV Lobanov, B McAllister, M McDade-Kumar, GB Landwehrmeyer, M Orth, ... NPJ genomic medicine 7 (1), 53, 2022 | 5 | 2022 |
| Association analysis of chromosome X to identify genetic modifiers of Huntington’s disease EP Hong, MJ Chao, T Massey, B McAllister, S Lobanov, L Jones, ... Journal of Huntington's disease 10 (3), 367-375, 2021 | 5 | 2021 |
| FAN1 nuclease activity affects CAG expansion and age at onset of Huntington’s disease B McAllister, J Donaldson, CS Binda, S Powell, U Chughtai, G Edwards, ... bioRxiv, 2021.04. 13.439716, 2021 | 4 | 2021 |
| Modification of Huntington's disease by short tandem repeats EP Hong, EM Ramos, NA Aziz, TH Massey, B McAllister, S Lobanov, ... Brain communications, 2024 | 1 | 2024 |
| The onset and prevalence of motor and psychiatric symptoms in Huntington’s disease B McAllister, JF Gusella, GB Landwehrmeyer, JM Lee, ME MacDonald, ... BioRxiv, 2020 | 1 | 2020 |
| Posttranscriptional regulation of FAN1 by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington’s disease KH Kim, EP Hong, Y Lee, ZL McLean, E Elezi, R Lee, S Kwak, ... Proceedings of the National Academy of Sciences 121 (16), e2322924121, 2024 | | 2024 |
| Mutant huntingtin confers cell-autonomous phenotypes on Huntington’s disease iPSC-derived microglia N Stöberl, J Donaldson, CS Binda, B McAllister, H Hall-Roberts, L Jones, ... Scientific Reports 13 (1), 20477, 2023 | | 2023 |
| Upregulated NF-κB pathway proteins may underlie APOE44 associated astrocyte phenotypes in sporadic Alzheimer’s disease AP Roberts, K Dec, V Tyrrell, VB O’Donnell, A Harwood, J Williams bioRxiv, 2023.04. 19.537428, 2023 | | 2023 |
| C01 Exome sequencing of individuals with Huntington’s disease implicates fan1 nuclease activity in slowing CAG expansion and disease onset T Massey, B McAllister, J Donaldson, C Binda, J Stone, N Allen, ... Journal of Neurology, Neurosurgery & Psychiatry 93 (Suppl 1), A16-A16, 2022 | | 2022 |
| C03 FAN1 coding variants identified in individuals with Huntington’s disease implicate its nuclease activity and dna binding in age at onset CS Binda, B McAllister, G Menzies, G Edwards, J Davies, L Jones, ... Journal of Neurology, Neurosurgery & Psychiatry 93 (Suppl 1), A17-A17, 2022 | | 2022 |
| Rare genetic modifiers of Huntington’s disease reveal novel pathological mechanisms T Massey, B McAllister, C Binda, J Donaldson, U Chughtai, P Holmans, ... Journal of Neurology, Neurosurgery & Psychiatry 93 (6), A4-A5, 2022 | | 2022 |
| Author Response: Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington Disease TH Massey, B McAllister, AE Rosser, L Jones Neurology 98 (12), 515-515, 2022 | | 2022 |
