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Issue DateTitleAuthor(s)
29-Aug-2018Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation studyTrajanoska, Katerina; Morris, John A.; Oei, Ling; Zheng, Hou-Feng; Evans, David M.; Kiel, Douglas P.; Ohlsson, Claes; Richards, J. Brent; Rivadeneira, Fernando; GEFOS/GENOMOS consortium; 23andMe Research Team; Balcells Comas, Susana; Grinberg Vaisman, Daniel Raúl
Jan-2019Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorderDemontis, Ditte; Walters, Raymond K.; Martin, Joanna; Mattheisen, Manuel; Als, Thomas D.; Agerbo, Esben; Baldursson, Gísli; Belliveau, Rich; Bybjerg-Grauholm, Jonas; Bækvad-Hansen, Marie; Cerrato, Felicia; Chambert, Kimberly; Churchhouse, Claire; Dumont, Ashley; Eriksson, Nicholas; Gandal, Michael; Goldstein, Jacqueline I.; Grasby, Katrina L.; Grove, Jakob; Gudmundsson, Olafur O.; Hansen, Christine S.; Hauberg, Mads Engel; Hollegaard, Mads V.; Howrigan, Daniel P.; Huang, Hailiang; Maller, Julian B.; Martin, Alicia R.; Martin, Nicholas G.; Moran, Jennifer; Pallesen, Jonatan; Palmer, Duncan S.; Pedersen, Carsten Bøcker; Pedersen, Marianne Giørtz; Poterba, Timothy; Poulsen, Jesper Buchhave; Ripke, Stephan; Robinson, Elise B.; Satterstrom, F. Kyle; Stefansson, Hreinn; Stevens, Christine; Turley, Patrick; Walters, G. Bragi; Won, Hyejung; Wright, Margaret J.; ADHD Working Group of the Psychiatric Genomics Consortium (PGC); Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium; 23andMe Research Team; Andreassen, Ole A.; Asherson, Philip; Burton, Christie L.; Boomsma, Dorret I.; Cormand Rifà, Bru; Dalsgaard, Søren; Franke, Barbara; Gelernter, Joel; Geschwind, Daniel; Hakonarson, Hakon; Haavik, Jan; Kranzler, Henry R.; Kuntsi, Joanna; Langley, Kate; Lesch, Klaus-Peter; Middeldorp, Christel; Reif, Andreas; Rhode, Luis Augusto; Roussos, Panos; Schachar, Russell; Sklar, Pamela; Sonuga-Barke, Edmund J. S; Sullivan, Patrick F.; Thapar, Anita; Tung, Joyce Y.; Waldman, Irwin D.; Medland, Sarah E.; Stefansson, Kari; Nordentoft, Merete; Hougaard, David M.; Werge, Thomas; Mors, Ole; Mortensen, Preben Bo; Daly, Mark J.; Faraone, Stephen V.; Børglum, Anders D.; Neale, Benjamin M.
27-Apr-2020Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease.Bryois, Juliene; Skene, Nathan G.; Folkmann Hansen, Thomas; Kogelman, Lisette J. A.; Watson, Hunna J.; Liu, Zijing; Eating Disorders Working Group of the Psychiatric Genomics Consortium; International Headache Genetics Consortium; 23andMe Research Team; Brueggeman, Leo; Breen, Gerome; Bulik, Cynthia M.; Arenas, Ernest; Hjerling-Leffler, Jens; Sullivan, Patrick F.