Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe
M. Rietschel(Heidelberg University), W. Maier(University of Bonn), Ditte Demontis(Broad Institute), Richard Bruggeman, Ole Mors(Aarhus University), Piotr M. Czerski(Poznan University of Medical Sciences), Preben Bo Mortensen(Aarhus University), Per Hoffmann(Genomics (United Kingdom)), André G. Uitterlinden(Erasmus MC), Stefan Herms(University of Bonn), Thomas W. Mühleisen(University of Bonn), Don Linszen, J A. Nikitopoulos(University of Bonn), René Breuer(Heidelberg University), Paweł Kapelski(Poznan University of Medical Sciences), Michael P. Alexander(University of Bonn), Andreas J. Forstner(University of Bonn), Peter Kirsch(Heidelberg University), Lydia Krabbendam(Maastricht University), J Hauser(Poznan University of Medical Sciences), Fernando Rivandeneira(Erasmus MC), Christine Esslinger(Aarhus University), Susanne Moebus(University of Bonn), Manuel Mattheisen(Aarhus University), C Schmael(Aarhus University), Lutz Priebe(University of Bonn), René S. Kahn(University Medical Center Utrecht), F B Basmanav(University of Bonn), H-E Wichmann(Erasmus MC), Britta Haenisch(Poznan University of Medical Sciences), E Strengman(Aarhus University Hospital), T. F. Wienker(Poznan University of Medical Sciences), S Meier(Heidelberg University), J Strohmaier(Heidelberg University), Jim van Os, Lieuwe de Haan, S. Schreiber(Erasmus MC), J Schumacher(University of Bonn), F. Degenhardt(University of Bonn), D M Hougaard(Statens Serum Institut), Wiepke Cahn, A. Hofman(University of Bonn), I Giegling(Ludwig-Maximilians-Universität München), R Mössner(University of Bonn), Torben Ørntoft(Aarhus University Hospital), Inez Myin‐Germeys(KU Leuven), Durk Wiersma(University of Groningen), Michael Steffens(University of Bonn)
Cited by 116
Related Papers
Identification of common genetic risk variants for autism spectrum disorder
|Nature Genetics|2019|2.6k
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
|Nature Genetics|2018|2.3k
Genome-wide association study reveals genetic risk underlying Parkinson's disease
|Nature Genetics|2009|2k
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
|Nature Genetics|2018|1.7k
Common variants conferring risk of schizophrenia
|Nature|2009|1.7k