Microduplications of 16p11.2 are associated with schizophrenia

Wellcome Trust Case Control Consortium, McCarthy, Shane E, Makarov, Vladimir, Kirov, George, Addington, Anjene M, McClellan, Jon, Yoon, Seungtai, Perkins, Diana O +65 more·2009·Nature Genetics

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  14. Consensus paper of the WFSBP Task Force on Biological Markers: Criteria for biomarkers and endophenotypes of schizophrenia part II: Cognition, neuroimaging and genetics
    A. Schmitt, D. Rujescu, M. Gawlik, A. Hasan, K. Hashimoto, Sylvain Iceta, M. Jarema, J. Kambeitz, S. Kasper, D. Keeser et al. · 2016 · World Journal of Biological Psychiatry
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  16. Distribution of Disease-Associated Copy Number Variants Across Distinct Disorders of Cognitive Development
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  25. Schizotypy and altered digit ratios: A second look
    Diane Carol Gooding, Madeline Johnson, Joel S. Peterman · 2010 · Psychiatry Research
  26. Discovery and development of integrative biological markers for schizophrenia
    Viola Oertel‐Knöchel, Robert A. Bittner, Christian Knöchel, David Prvulovic, Harald Juergen Hampel · 2011 · Progress in Neurobiology
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    Danielle P. Moreira, Karina Griesi‐Oliveira, Ana Luiza Bossolani-Martins, Naila Cristina Vilaça Lourenço, Vanessa Takahashi, Katia Maria da Rocha, Eloísa Sá Moreira, Estêvão Vadasz, Joanna Góes Castro Meira, Débora Romeo Bertola et al. · 2014 · PLoS ONE
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