Microduplications of 16p11.2 are associated with schizophrenia

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36. Common variant at 16p11.2 conferring risk of psychosis
    Steinberg, S, de Jong, S, Mattheisen, M, Costas, J, Demontis, D, Jamain, S, Pietiläinen, O P H, Lin, K, Papiol, S, Huttenlocher, J et al. · 2014 · Molecular Psychiatry
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43. Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome
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    Rees, Elliott, Moskvina, Valentina, Owen, Michael J., O'Donovan, Michael C., Kirov, George · 2011 · Biological Psychiatry
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    Diane M. Bushman, Jerold J. M. Chun · 2013 · Seminars in Cell and Developmental Biology
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    Abyzov, Alexej, Li, Shantao, Kim, Daniel Rhee, Mohiyuddin, Marghoob, Stütz, Adrian M., Parrish, Nicholas F., Mu, Xinmeng Jasmine, Clark, Wyatt, Chen, Ken, Hurles, Matthew et al. · 2015 · Nature Communications
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