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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.; Massey, Thomas H.; Ciosi, Marc; Landwehrmeyer, G. Bernhard; Paulsen, Jane S.; Dorsey, E. Ray; Shoulson, Ira; ... (2022). Genetic modifiers of Huntington disease differentially influence motor and cognitive domains. American journal of human genetics, 109(5), pp. 885-899. Cell Press 10.1016/j.ajhg.2022.03.004
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 (2022). Huntington’s disease age at motor onset is modified by the tandem hexamer repeat in TCERG1. NPJ genomic medicine, 7(1), p. 53. Springer Nature 10.1038/s41525-022-00317-w
Hong, Eun Pyo; Chao, Michael J.; Massey, Thomas; McAllister, Branduff; Lobanov, Sergey; Jones, Lesley; Holmans, Peter; Kwak, Seung; Orth, Michael; Ciosi, Marc; Monckton, Darren G.; Long, Jeffrey D.; Lucente, Diane; Wheeler, Vanessa C.; MacDonald, Marcy E.; Gusella, James F.; 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. IOS Press 10.3233/JHD-210485
Minkova, Lora; Gregory, Sarah; Scahill, Rachael I.; Abdulkadir, Ahmed; Kaller, Christoph P.; Peter, Jessica; Long, Jeffrey D.; Stout, Julie C.; Reilmann, Ralf; Roos, Raymund A.; Durr, Alexandra; Leavitt, Blair R.; Tabrizi, Sarah J.; Klöppel, Stefan (2018). Cross-sectional and longitudinal voxel-based grey matter asymmetries in Huntington's disease. NeuroImage: Clinical, 17, pp. 312-324. Elsevier 10.1016/j.nicl.2017.10.023
