Increased frequency of repeat expansion mutations across different populations
Kristina Ibáñez(Queen Mary University of London), Arianna Tucci(Genomics England), Bharati Jadhav(Child Health and Development Institute), Andrea Cortese(University of Pavia), Douglas R. Langbehn(University of Iowa), Matteo Zanovello(National Hospital for Neurology and Neurosurgery), John Hardy(UK Dementia Research Institute), Valentina Escott‐Price(Cardiff University), Delia Gagliardi(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Loukas Moutsianas(Genomics England), Jeffrey D. Long(University of Iowa), Anupriya Dalmia(Queen Mary University of London), Sarah J. Tabrizi(Huntington's Disease Association), Clarissa Rocca(Institute of Human Genetics), Paras Garg(Icahn School of Medicine at Mount Sinai), Pietro Fratta, Jana Vandrovcová(Texas Tech University), Alejandro Martin-Trujillo(Institut d'Investigació Biomédica de Bellvitge), Maryam Shoai(University College London), Andrew J. Sharp(University of Geneva), Mark J. Caulfield(Queen Mary University of London), Henry Houlden(Queen Mary University of London), Helen Walker(Newcastle upon Tyne Hospitals NHS Foundation Trust), Chiara Marini‐Bettolo(Newcastle upon Tyne Hospitals NHS Foundation Trust), Stefano Facchini(University College London), Chris Turner(National Hospital for Neurology and Neurosurgery), Christopher Clarkson, Scott J Gies(Child Health and Development Institute), Davina J. Hensman Moss(St George's, University of London), Valentina Galassi Deforie(National Hospital for Neurology and Neurosurgery)
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