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Genome-wide association study of multiplex schizophrenia pedigrees

Douglas F Levinson, Jianxin Shi, Kai Wang, Sang Oh, Brien Riley, Ann E Pulver, Dieter B Wildenauer, Claudine Laurent, Bryan J Mowry, Pablo V Gejman, Michael J Owen, Kenneth S Kendler, Gerald Nestadt, Sibylle G Schwab, Jacques Mallet, Deborah Nertney, Alan R Sanders, Nigel M Williams, Brandon Wormley, Virginia K LasseterMargot Albus, Stephanie Godard-Bauché, Madeline Alexander, Jubao Duan, Michael C O'Donovan, Dermot Walsh, Anthony O'Neill, George N Papadimitriou, Dimitris Dikeos, Wolfgang Maier, Bernard Lerer, Dominique Campion, David Cohen, Maurice Jay, Ayman Fanous, Peter Eichhammer, Jeremy M Silverman, Nadine Norton, Nancy Zhang, Hakon Hakonarson, Cynthia Gao, Ami Citri, Mark Hansen, Stephan Ripke, Frank Dudbridge, Peter A Holmans, Schizophrenia Psychiatric GWAS Consortium

56 Citations (Scopus)

Abstract

The authors used a genome-wide association study (GWAS) of multiply affected families to investigate the association of schizophrenia to common single-nucleotide polymorphisms (SNPs) and rare copy number variants (CNVs).
Original languageEnglish
JournalThe American journal of psychiatry
Volume169
Issue number9
Pages (from-to)963-73
Number of pages11
DOIs
Publication statusPublished - Sept 2012

Keywords

  • African Continental Ancestry Group
  • Case-Control Studies
  • DNA Copy Number Variations
  • European Continental Ancestry Group
  • Female
  • Genetic Predisposition to Disease
  • Genome-Wide Association Study
  • Genotype
  • Humans
  • Male
  • Pedigree
  • Polymorphism, Single Nucleotide
  • Schizophrenia

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