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Premature death in adults with 22q11.2 deletion syndrome.
Bassett AS, Chow EW, Husted J, Hodgkinson KA, Oechslin E, Harris L, Silversides C. Bassett AS, et al. Among authors: husted j. J Med Genet. 2009 May;46(5):324-30. doi: 10.1136/jmg.2008.063800. Epub 2009 Feb 25. J Med Genet. 2009. PMID: 19246480 Free PMC article.
The schizophrenia phenotype in 22q11 deletion syndrome.
Bassett AS, Chow EW, AbdelMalik P, Gheorghiu M, Husted J, Weksberg R. Bassett AS, et al. Among authors: husted j. Am J Psychiatry. 2003 Sep;160(9):1580-6. doi: 10.1176/appi.ajp.160.9.1580. Am J Psychiatry. 2003. PMID: 12944331 Free PMC article.
Clinical features of 78 adults with 22q11 Deletion Syndrome.
Bassett AS, Chow EW, Husted J, Weksberg R, Caluseriu O, Webb GD, Gatzoulis MA. Bassett AS, et al. Among authors: husted j. Am J Med Genet A. 2005 Nov 1;138(4):307-13. doi: 10.1002/ajmg.a.30984. Am J Med Genet A. 2005. PMID: 16208694 Free PMC article.
Postmaturity in a genetic subtype of schizophrenia.
Chow EW, Husted J, Weksberg R, Bassett AS. Chow EW, et al. Among authors: husted j. Acta Psychiatr Scand. 2003 Oct;108(4):260-8. doi: 10.1034/j.1600-0447.2003.00124.x. Acta Psychiatr Scand. 2003. PMID: 12956826 Free PMC article.
Heritability of neurocognitive traits in familial schizophrenia.
Husted JA, Lim S, Chow EW, Greenwood C, Bassett AS. Husted JA, et al. Am J Med Genet B Neuropsychiatr Genet. 2009 Sep 5;150B(6):845-53. doi: 10.1002/ajmg.b.30907. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19180565 Free PMC article.
Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays.
Costain G, Lionel AC, Merico D, Forsythe P, Russell K, Lowther C, Yuen T, Husted J, Stavropoulos DJ, Speevak M, Chow EW, Marshall CR, Scherer SW, Bassett AS. Costain G, et al. Among authors: husted j. Hum Mol Genet. 2013 Nov 15;22(22):4485-501. doi: 10.1093/hmg/ddt297. Epub 2013 Jun 27. Hum Mol Genet. 2013. PMID: 23813976 Free PMC article.
115 results