Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

the European Alzheimer's Disease Initiative Investigators; Jean‐Charles Lambert; Simon Heath; Gaël Even; Dominique Campion; Kristel Sleegers; Mikko Hiltunen; Onofre Combarros; Diana Zélénika; María J. Bullido; Béatrice Tavernier; Luc Letenneur; Karolien Bettens; Claudine Berr; Florence Pasquier; Nathalie Fiévet; Pascale Barberger‐Gateau; Sebastiaan Engelborghs; Peter Paul De Deyn; Ignacio Mateo; A. Franck; Seppo Helisalmi; Elisa Porcellini; Olivier Hanon; Marian M. de Pancorbo; Corinne Lendon; Carole Dufouil; Céline Jaillard; Thierry Léveillard; Victoria Álvarez; Paolo Bosco; Michelangelo Mancuso; Francesco Panza; Benedetta Nacmias; Paola Bossù; Paola Piccardi; Giorgio Annoni; Davide Seripa; Daniela Galimberti; Didier Hannequin; Federico Licastro; Hilkka Soininen; Karen Ritchie; Hélène Blanché; Jean‐François Dartigues; Christophe Tzourio; Marta Gut; Christine Van Broeckhoven; Annick Alpérovitch; Mark Lathrop; Philippe Amouyel

doi:10.1038/ng.439

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

the European Alzheimer's Disease Initiative Investigators(Inserm), Jean‐Charles Lambert(Inserm), Simon Heath(Inserm), Gaël Even(Inserm), Dominique Campion(VIB-UAntwerp Center for Molecular Neurology), Kristel Sleegers(Helmholtz Zentrum München), Mikko Hiltunen(Universidad de Cantabria), Onofre Combarros, Diana Zélénika(Consejo Superior de Investigaciones Científicas), María J. Bullido(CHU Dijon Bourgogne), Béatrice Tavernier(Inserm), Luc Letenneur(VIB-UAntwerp Center for Molecular Neurology), Karolien Bettens(Inserm), Claudine Berr(Université de Lille), Florence Pasquier(Institut Pasteur de Lille), Nathalie Fiévet(Inserm), Pascale Barberger‐Gateau(University of Antwerp), Sebastiaan Engelborghs(University of Antwerp), Peter Paul De Deyn(Universidad de Cantabria), Ignacio Mateo(Hospital Universitario La Paz), A. Franck(Kuopio University Hospital), Seppo Helisalmi(University of Bologna), Elisa Porcellini(Délégation Paris 5), Olivier Hanon(University of the Basque Country), Marian M. de Pancorbo(QIMR Berghofer Medical Research Institute), Corinne Lendon(Inserm), Carole Dufouil(Institut de la Vision), Céline Jaillard(Institut de la Vision), Thierry Léveillard(Hospital Universitario Central de Asturias), Victoria Álvarez(Oasi Maria SS), Paolo Bosco(University of Pisa), Michelangelo Mancuso(University of Bari Aldo Moro), Francesco Panza, Benedetta Nacmias(Fondazione Santa Lucia), Paola Bossù(University of Cagliari), Paola Piccardi(University of Milano-Bicocca), Giorgio Annoni(Casa Sollievo della Sofferenza), Davide Seripa(University of Milan), Daniela Galimberti(Inserm), Didier Hannequin(University of Bologna), Federico Licastro(Kuopio University Hospital), Hilkka Soininen(Inserm), Karen Ritchie(Fondation Jean Dausset-CEPH), Hélène Blanché(Inserm), Jean‐François Dartigues(Inserm), Christophe Tzourio, Marta Gut(University of Antwerp), Christine Van Broeckhoven(Inserm), Annick Alpérovitch(Fondation Jean Dausset-CEPH), Mark Lathrop(Centre Hospitalier Universitaire de Lille), Philippe Amouyel

Nature Genetics

September 6, 2009

10.1038/ng.439

Cited by 2,266Open Access

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