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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
Anttila, Verneri; Bulik-Sullivan, Brendan; Finucane, Hilary K; Walters, Raymond K; Bras, Jose; Duncan, Laramie; Escott-Price, Valentina; Falcone, Guido J; Gormley, Padhraig; Malik, Rainer; Patsopoulos, Nikolaos A; Ripke, Stephan; Wei, Zhi; Yu, Dongmei; Lee, Phil H; Turley, Patrick; Grenier-Boley, Benjamin; Chouraki, Vincent; Kamatani, Yoichiro; Berr, Claudine; ... (2018). Analysis of shared heritability in common disorders of the brain. Science, 360(6395) American Association for the Advancement of Science 10.1126/science.aap8757
Moss, Davina J Hensman; Pardiñas, Antonio F; Langbehn, Douglas; Lo, Kitty; Leavitt, Blair R; Roos, Raymund; Durr, Alexandra; Mead, Simon; Holmans, Peter; Jones, Lesley; Tabrizi, Sarah J (2017). Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study. The Lancet. Neurology, 16(9), pp. 701-711. The Lancet Publishing Group 10.1016/S1474-4422(17)30161-8
