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Number of items: 32.

Simmonds, Emily, Han, Jun, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Sharp, David J., Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131 and Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 2025. Dementia risk due to traumatic brain injury in subtypes of dementia in the Welsh population. Neurology 105 (3) , e213866. 10.1212/wnl.0000000000213866
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Genetic Modifiers of Huntington’s Disease (GeM-HD) Consortium, Wills, Christopher, Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131 and Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412 2025. Genetic modifiers of somatic expansion and clinical phenotypes in Huntington’s disease highlight shared and tissue-specific effects. Nature Genetics 57 , pp. 1426-1436. 10.1038/s41588-025-02191-5
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Patyjewicz, Marta, Mair, Devan, Zaloum, Safiya A., Onen, Barbara, Walton, Joseph, Dobson, Ruth, Joerres, Christine, Shah, Apeksha Madhusudan, MacCallum, Peter, Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131, Bariana, Tadbir, White, Veronica, De Freitas, Sarah A and Noyce, Alastair 2024. Recreational nitrous oxide and thrombotic events: a case series. BMJ Neurology Open 6 (1) , e000619. 10.1136/bmjno-2023-000619
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Kim, Kyung-Hee, Hong, Eun Pyo, Lee, Yukyeong, McLean, Zachariah, Elezi, Emanuela, Lee, Ramee, Kwak, Seung, McAllister, Branduff, Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131, Lobanov, Sergey, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Orth, Michael, Ciosi, Marc, Monckton, Darren, Long, Jeffrey, Lucente, Diane, Wheeler, Vanessa, MacDonald, Marcy, Gusella, James and Lee, Jong-Min 2024. Posttranscriptional regulation of FAN1 by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington's disease. Proceedings of the National Academy of Sciences 121 (16) , e2322924121. 10.1073/pnas.2322924121
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Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131 and McLauchlan, Duncan J. 2024. Huntington's disease: A clinical primer for acute and general physicians. Clinical Medicine 24 (2) , 100200. 10.1016/j.clinme.2024.100200
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Wheeler, Vanessa C., Stone, Joseph C., Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131 and Mouro Pinto, Ricardo 2024. The instability of the Huntington's disease CAG repeat mutation. Yang, X. William, Thompson, Leslie M. and Heiman, Myriam, eds. Huntington's disease. Pathogenic mechanisms and implications for therapeutics, London, UK: Academic Press, pp. 85-115. (10.1016/B978-0-323-95672-7.00003-0)

Hong, Eun Pyo, Ramos, Eliana Marisa, Aziz, N. Ahmad, Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131, McAllister, Branduff, Lobanov, Sergey ORCID: https://orcid.org/0000-0002-3126-1903, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Kwak, Seung, Orth, Michael, Ciosi, Marc, Lomeikaite, Vilija, Monckton, Darren G., Long, Jeffrey D., Lucente, Diane, Wheeler, Vanessa C., Gillis, Tammy, MacDonald, Marcy E., Sequeiros, Jorge, Gusella, James F. and Lee, Jong-Min 2024. Modification of Huntington's disease by short tandem repeats. Brain Communications 6 (2) , fcae016. 10.1093/braincomms/fcae016
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Stöberl, Nina, Donaldson, Jasmine ORCID: https://orcid.org/0000-0001-6699-0674, Binda, Caroline S., McAllister, Branduff, Hall-Roberts, Hazel, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131 and Allen, Nicholas D. ORCID: https://orcid.org/0000-0003-4009-186X 2023. Mutant huntingtin confers cell-autonomous phenotypes on Huntington’s disease iPSC-derived microglia. Scientific Reports 13 , 20477. 10.1038/s41598-023-46852-z
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Taylor, Alysha S., Barros, Dinis, Gobet, Nastassia, Schuepbach, Thierry, McAllister, Branduff, Aeschbach, Lorene, Randall, Emma L., Trofimenko, Evgeniya, Heuchan, Eleanor R., Barszcz, Paula, Ciosi, Marc, Morgan, Joanne, Hafford-Tear, Nathaniel J., Davidson, Alice E., Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131, Monckton, Darren G., Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, network, REGISTRY Investigators of the European Huntington's disease, Xenarios, Ioannis and Dion, Vincent ORCID: https://orcid.org/0000-0003-4953-7637 2022. Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencing. NAR Genomics and Bioinformatics 4 (4) , lqac089. 10.1093/nargab/lqac089
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Lobanov, Sergey ORCID: https://orcid.org/0000-0002-3126-1903, McAllister, Branduff, McDade-Kumar, Mia, Landwehrmeyer, Bernhard, Orth, Michael, Rosser, Anne ORCID: https://orcid.org/0000-0002-4716-4753, Paulsen, Jane, Lee, Jong-Min, MacDonald, Marcy, Gusella, James, Long, Jeffrey, Ryten, Mina, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131 and Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 2022. Huntington’s disease age at motor onset is modified by the tandem hexamer repeat in TCERG1. npj Genomic Medicine 7 , 53. 10.1038/s41525-022-00317-w
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Lee, Jong-Min, Huang, Yuan, Orth, Michael, Gillis, Tammy, Siciliano, Jacqueline, Hong, Eunpyo, Mysore, Jayalakshmi Srinidhi, Lucente, Diane, Wheeler, Vanessa C., Seong, Ihn Sik, McLean, Zachariah L., Mills, James A., McAllister, Branduff, Lobanov, Sergey V. ORCID: https://orcid.org/0000-0002-3126-1903, Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131, Ciosi, Marc, Landwehrmeyer, G. Bernhard, Paulsen, Jane S., Dorsey, E. Ray, Shoulson, Ira, Sampaio, Cristina, Monckton, Darren G., Kwak, Seung, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, MacDonald, Marcy E., Long, Jeffrey D. and Gusella, James F. 2022. Genetic modifiers of Huntington disease differentially influence motor and cognitive domains. American Journal of Human Genetics 109 (5) , pp. 885-899. 10.1016/j.ajhg.2022.03.004
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McAllister, Branduff, Donaldson, Jasmine ORCID: https://orcid.org/0000-0001-6699-0674, Binda, Caroline, Powell, Sophie, Chughtai, Uroosa, Edwards, Gareth, Stone, Joseph, Lobanov, Sergey ORCID: https://orcid.org/0000-0002-3126-1903, Elliston, Linda, Schuhmacher, Laura, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Menzies, Georgina ORCID: https://orcid.org/0000-0002-6600-6507, Ciosi, Marc, Maxwell, Alastair, Chao, Michael, Eun Pyo, Hong, Lucente, Diane, Wheeler, Vanessa, Jong-Min, Lee, MacDonald, Marcy, Long, Jeffrey, Aylward, Elizabeth, Landwehrmeyer, G. Bernhard, Rosser, Anne ORCID: https://orcid.org/0000-0002-4716-4753, REGISTRY Investigators of the European Huntington’s disease netw, Paulsen, Jane, PREDICT-HD Investigators of the Huntington Study Group, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Gusella, James, Monckton, Darren, Allen, Nicholas, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 and Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131 2022. Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset. Nature Neuroscience 25 , pp. 446-457. 10.1038/s41593-022-01033-5
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Cooper, Miriam ORCID: https://orcid.org/0000-0002-4695-5481, Gale, Katherine, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Broughton, Thomas, Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131, Hall, Nicola J. and Jones, Catherine R.G. ORCID: https://orcid.org/0000-0003-0541-0431 2022. How to do it: the neurological consultation with an autistic patient. Practical Neurology 22 , pp. 120-125. 10.1136/practneurol-2020-002856
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Steventon, J.J., Chandler, H.L., Foster, C. ORCID: https://orcid.org/0000-0003-1609-9458, Dingsdale, H. ORCID: https://orcid.org/0000-0002-2919-8722, Germuska, M. ORCID: https://orcid.org/0000-0003-0580-4350, Massey, T. ORCID: https://orcid.org/0000-0002-9804-2131, Parker, G., Wise, R.G. ORCID: https://orcid.org/0000-0003-1700-2144 and Murphy, K. 2021. Changes in white matter microstructure and MRI-derived cerebral blood flow after one-week of exercise training. Scientific Reports 11 , 22061. 10.1038/s41598-021-01630-7
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Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131 and Robertson, Neil P. ORCID: https://orcid.org/0000-0002-5409-4909 2021. Medication-overuse headache: causes, consequences and management. Journal of Neurology 268 (9) , 3505–3507. 10.1007/s00415-021-10720-5
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McAllister, Branduff, Gusella, James F., Landwehrmeyer, G. Bernhard, Lee, Jong-Min, MacDonald, Marcy E., Orth, Michael, Rosser, Anne E. ORCID: https://orcid.org/0000-0002-4716-4753, Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 and Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131 2021. Timing and impact of psychiatric, cognitive, and motor abnormalities in Huntington disease. Neurology 96 (19) , e2395-e2406. 10.1212/WNL.0000000000011893
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Hong, Eun Pyo, Chao, Michael J., Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131, McAllister, Branduff, Lobanov, Sergey ORCID: https://orcid.org/0000-0002-3126-1903, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Kwak, Seung, Orth, Michael, Ciosi, Marc, Monckton, Darren G., Long, Jeffrey D., Lucente, Diane, Wheeler, Vanessa C., MacDonald, Marcy E., Gusella, James F. and Lee, Jong-Min 2021. Association analysis of chromosome X to identify genetic modifiers of Huntington's disease. Journal of Huntington's Disease 10 (3) , pp. 367-375. 10.3233/JHD-210485
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Cunningham, Adam, Fung, Wilson, Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 and Peall, Kathryn ORCID: https://orcid.org/0000-0003-4749-4944 2020. Movement disorder phenotypes in children with 22q11.2 deletion syndrome. Movement Disorders 35 (7) , pp. 1272-1274. 10.1002/mds.28078
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Ellis, Natalie, Tee, Amelia, McAllister, Branduff, Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131, McLauchlan, Duncan, Stone, Timothy, Correia, Kevin, Loupe, Jacob, Kim, Kyung-Hee, Barker, Douglas, Hong, Eun Pyo, Chao, Michael, Long, Jeffrey, Lucente, Diane, Vonsattel, Jean Paul, Pinto, Ricardo, Elneel, Kawther Abu, Ramos, Eliana Marisa, Mysore, Jayalakshmi Srinidhi, Gillis, Tammy, Wheeler, Vanessa, Medway, Christopher, Hall, Lynsey, Kwak, Seung, Sampaio, Cristina, Ciosi, Marc, Maxwell, Alastair, Chatzi, Afroditi, Monckton, Darren, Orth, Michael, Landwehrmeyer, G. Bernhard, Paulsen, Jane, Shoulson, Ira, Myers, Richard, van Duijn, Erik, Rickards, Hugh, MacDonald, Marcy, Lee, Jong-min, Gusella, James, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 and Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412 2020. Genetic risk underlying psychiatric and cognitive symptoms in Huntington’s Disease. Biological Psychiatry 87 (9) , pp. 857-865. 10.1016/j.biopsych.2019.12.010
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Massey, T. H. ORCID: https://orcid.org/0000-0002-9804-2131 and Robertson, N. P. ORCID: https://orcid.org/0000-0002-5409-4909 2020. Restless legs syndrome: causes and consequences. Journal of Neurology 267 (2) , pp. 575-577. 10.1007/s00415-019-09682-6
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McAllister, Branduff, Gusella, James F., Landwehrmeyer, G. Bernhard, Lee, Jong-Min, MacDonald, Marcy E., Orth, Michael, Rosser, Anne E. ORCID: https://orcid.org/0000-0002-4716-4753, Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 and Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131 2020. The onset and prevalence of motor and psychiatric symptoms in Huntington’s disease. [Online]. bioRxiv.
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Lee, Jong-Min, Correia, Kevin, Loupe, Jacob, Kim, Kyung, Barker, Douglas, Hong, Eun Pyo, Chao, Michael, Long, Jeffery, Lucente, Diane, Vonsattel, Jean, Pinto, Richardo, Ehiana, Ramos, Mysore, Jayalakshmi, Gillis, Tammy, Wheeler, Vanessa, MacDonald, Marcy, Gusella, James, McAllister, Branduff, Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131, Medway, Christopher ORCID: https://orcid.org/0000-0002-1764-0587, Stone, Timothy, Hall, Lynsey, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Kwark, Seung, Ehrhardt, Anka, Sampaio, Cristina, Ciosi, Marc, Maxwell, Alastair, Chatzi, Afroditi, Monckton, Darren, Orth, Michael, Landwehrmeyer, Bernhard and Paulsen, Jane 2019. CAG repeat not polyglutamine length determines timing of Huntington’s disease onset. Cell 178 (4) , 887-099.e14. 10.1016/j.cell.2019.06.036
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Cronin, Thomas ORCID: https://orcid.org/0000-0001-9522-3992, Rosser, Anne ORCID: https://orcid.org/0000-0002-4716-4753 and Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131 2019. Clinical presentation and features of Juvenile-onset Huntington's disease: a systematic review. Journal of Huntington's Disease 8 (2) , pp. 171-179. 10.3233/JHD-180339
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Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131, McAllister, Branduff and Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 2018. Methods for assessing DNA repair and repeat expansion in Huntington's Disease. Precious, Sophie V., Rosser, Anne E. ORCID: https://orcid.org/0000-0002-4716-4753 and Dunnett, Stephen B. ORCID: https://orcid.org/0000-0003-1826-1578, eds. Huntington’s Disease, Vol. 1780. Methods in Molecular Biology, Humana Press, pp. 483-495. (10.1007/978-1-4939-7825-0_22)
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Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131 and Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909 2018. Repurposing drugs to treat neurological diseases. Journal of Neurology 265 (2) , pp. 446-448. 10.1007/s00415-018-8732-z
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Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131 and Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 2018. The central role of DNA damage and repair in CAG repeat diseases. Disease Models & Mechanisms 11 (1) , dmm031930. 10.1242/dmm.031930
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Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Massey, Thomas H. ORCID: https://orcid.org/0000-0002-9804-2131 and Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 2017. Genetic modifiers of Mendelian disease: Huntington's disease and the trinucleotide repeat disorders. Human Molecular Genetics 26 (R2) , R83-R90. 10.1093/hmg/ddx261
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van de Zande, N. A., Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131, McLauchlan, Duncan, Pryce Roberts, A., Zutt, R., Wardle, Mark, Payne, G. C., Clenaghan, Catherine, Tijssen, M. A. J., Rosser, Anne Elizabeth ORCID: https://orcid.org/0000-0002-4716-4753 and Peall, Kathryn J. ORCID: https://orcid.org/0000-0003-4749-4944 2017. Clinical characterization of dystonia in adult patients with Huntington's disease. European Journal of Neurology 24 (9) , pp. 1140-1147. 10.1111/ene.13349
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Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131 and Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909 2017. Why antisense could make sense for neurodegeneration. Journal of Neurology 264 (7) , pp. 1542-1544. 10.1007/s00415-017-8515-y
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Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131, Smith, Rachel, Sadiq Shaheena, Shaheena, Overton, Christopher and Pearson, Owen R. 2017. Rescue of severe brain and cervical cord IRIS by restarting natalizumab in a pregnant MS patient. Neurology 88 (7) , pp. 711-713. 10.1212/WNL.0000000000003604
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Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131 and Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909 2016. Zika virus and neurology: proving cause and effect. Journal of Neurology 263 (6) , pp. 1255-1257. 10.1007/s00415-016-8165-5
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Massey, Thomas ORCID: https://orcid.org/0000-0002-9804-2131, Pickersgill, Trevor T and Peall, Kathryn J ORCID: https://orcid.org/0000-0003-4749-4944 2016. Nitrous oxide misuse and vitamin B12 deficiency. BMJ Case Reports , 215728. 10.1136/bcr-2016-215728
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This list was generated on Mon Oct 27 10:03:35 2025 GMT.


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