The central role of DNA damage and repair in CAG repeat diseases

por Massey, Thomas H., Jones, Lesley
Publicado 2018

Medication-overuse headache: causes, consequences and management

por Massey, Thomas H., Robertson, Neil P.
Publicado 2021

Dentatorubral-pallidoluysian Atrophy: An Update

por Carroll, Liam S., Massey, Thomas H., Wardle, Mark, Peall, Kathryn J.
Publicado 2018

Rescue of severe brain and cervical cord IRIS by restarting natalizumab in a pregnant MS patient

por Massey, Thomas H., Smith, Rachel, Sadiq, Shaheena, Overton, Christopher, Pearson, Owen R.
Publicado 2017

Mutant huntingtin confers cell-autonomous phenotypes on Huntington’s disease iPSC-derived microglia

por Stöberl, Nina, Donaldson, Jasmine, Binda, Caroline S., McAllister, Branduff, Hall-Roberts, Hazel, Jones, Lesley, Massey, Thomas H., Allen, Nicholas D.
Publicado 2023

Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington Disease

por McAllister, Branduff, Gusella, James F., Landwehrmeyer, G. Bernhard, Lee, Jong-Min, MacDonald, Marcy E., Orth, Michael, Rosser, Anne E., Williams, Nigel M., Holmans, Peter, Jones, Lesley, Massey, Thomas H.
Publicado 2021

Huntington’s disease age at motor onset is modified by the tandem hexamer repeat in TCERG1

por Lobanov, Sergey V., McAllister, Branduff, McDade-Kumar, Mia, Landwehrmeyer, G. Bernhard, Orth, Michael, Rosser, Anne E., Paulsen, Jane S., Lee, Jong-Min, MacDonald, Marcy E., Gusella, James F., Long, Jeffrey D., Ryten, Mina, Williams, Nigel M., Holmans, Peter, Massey, Thomas H., Jones, Lesley
Publicado 2022

Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencing

por 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, Monckton, Darren G, Jones, Lesley, network, REGISTRY Investigators of the European Huntington’s disease, Xenarios, Ioannis, Dion, Vincent
Publicado 2022

Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset

por McAllister, Branduff, Donaldson, Jasmine, Binda, Caroline S., Powell, Sophie, Chughtai, Uroosa, Edwards, Gareth, Stone, Joseph, Lobanov, Sergey, Elliston, Linda, Schuhmacher, Laura-Nadine, Rees, Elliott, Menzies, Georgina, Ciosi, Marc, Maxwell, Alastair, Chao, Michael J., Hong, Eun Pyo, Lucente, Diane, Wheeler, Vanessa, Lee, Jong-Min, MacDonald, Marcy E., Long, Jeffrey D., Aylward, Elizabeth H., Landwehrmeyer, G. Bernhard, Rosser, Anne E., Paulsen, Jane S., Williams, Nigel M., Gusella, James F., Monckton, Darren G., Allen, Nicholas D., Holmans, Peter, Jones, Lesley, Massey, Thomas H.
Publicado 2022