4 documents found, page 1 of 1
Common variants in Alzheimer's disease and risk stratification by polygenic ris...
de Rojas, Itziar; Moreno-Grau, Sonia; Tesi, Niccolo; Grenier-Boley, Benjamin; Andrade, Victor; Jansen, Iris E.; Pedersen, Nancy L.; Stringa, NajadaGenetic discoveries of Alzheimer's disease are the drivers of our understanding, and together with polygenetic risk stratification can contribute towards planning of feasible and efficient preventive and curative clinical trials. We first perform a large genetic association study by merging all available case-control datasets and by-proxy study results (discovery n = 409,435 and validation size n = 58,190). Her...
Googling the City: In Search of the Public Interest on Toronto’s ‘Smart’ Waterf...
Morgan, Kevin; Webb, BrianToronto’s Quayside waterfront regeneration project has become an international reference point for the burgeoning debate about the scope and limits of the digitally enabled ‘smart city’ narrative. The project signals the entry of a Google affiliate into the realm of ‘smart urbanism’ in the most dramatic fashion imaginable, by allowing them to potentially realise their long-running dream for “someone to give us ...
Analysis of shared heritability in common disorders of the brain
Anttila, Verneri; Bulik-Sullivan, Brendan; Finucane, Hilary K.; Walters, Raymond K.; Bras, Jose; Duncan, Laramie; Escott-Price, ValentinaDisorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We quantified the genetic sharing of 25 brain disorders from genome-wide association studies of 265,218 patients and 784,643 control participants and assessed their relationship to 17 phenotypes from 1,191,588 individuals. Psychiatric disorders share common varian...
Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical inf...
Sassi, Celeste; Nalls, Michael A.; Ridge, Perry G.; Gibbs, Jesse R.; Lupton, Michelle K.; Troakes, Claire; Lunnon, Katie; Al-Sarraj, SafaMendelian adult-onset leukodystrophies are a spectrum of rare inherited progressive neurodegenerative disorders affecting the white matter of the central nervous system. Among these, cerebral autosomal dominant and recessive arteriopathy with subcortical infarcts and leukoencephalopathy, cerebroretinal vasculopathy, metachromatic leukodystrophy, hereditary diffuse leukoencephalopathy with spheroids, and vanishi...