Transcriptomic analysis of repeat expansion-ataxias uncovers distinct non-neuronal cell type-specific signatures of disease across the human brain
Zhongbo Chen(Institute of Human Genetics), Mina Ryten(National Hospital for Neurology and Neurosurgery), Jonathan Brenton(Great Ormond Street Hospital), John Hardy(UK Dementia Research Institute), Johan Jakobsson(Lund University), Juan A. Botía(University College London), Stéphanie Efthymiou(Queen Mary University of London), Suran Nethisinghe(National Hospital for Neurology and Neurosurgery), Sonia García-Ruiz(Great Ormond Street Hospital), Natalia Dominik(National Hospital for Neurology and Neurosurgery), Regina H. Reynolds(Great Ormond Street Hospital), Clarissa Rocca(Institute of Human Genetics), Raquel Garza(Wallenberg Wood Science Center), Kylie Montgomery(New England Biolabs (United States)), Claire Anderson(Great Ormond Street Hospital), David Murphy(University of Nottingham), Aine Fairbrother-Browne(European Bioinformatics Institute), Daria Gavriouchkina(UK Dementia Research Institute), Paola Giunti(National Hospital for Neurology and Neurosurgery), Jasmaine Lee(Queen Mary University of London), Melissa Grant‐Peters(Great Ormond Street Hospital), Zane Jaunmuktane(King's College London), Andrea Cortese(National Hospital for Neurology and Neurosurgery), Nicholas Wood(National Hospital for Neurology and Neurosurgery), Hannah Macpherson(University College London), Fairlie Hinton(Florey Institute of Neuroscience and Mental Health), Emil K. Gustavsson(University of British Columbia), Henry Houlden(Queen Mary University of London), Arianna Tucci(Genomics England), Toby J Curless(Neurosciences Institute), Sonia Gandhi(The Francis Crick Institute), Catriona McLean(Florey Institute of Neuroscience and Mental Health), Huihui Luo(Queen Mary University of London), Amy R. Hicks(National Hospital for Neurology and Neurosurgery), Modesta Blunskyte-Hendley(UK Dementia Research Institute), G Rocamora-Perez(University of Cambridge)
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