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Using rare genetic mutations to revisit structural brain asymmetry.
Kopal J, Kumar K, Shafighi K, Saltoun K, Modenato C, Moreau CA, Huguet G, Jean-Louis M, Martin CO, Saci Z, Younis N, Douard E, Jizi K, Beauchamp-Chatel A, Kushan L, Silva AI, van den Bree MBM, Linden DEJ, Owen MJ, Hall J, Lippé S, Draganski B, Sønderby IE, Andreassen OA, Glahn DC, Thompson PM, Bearden CE, Zatorre R, Jacquemont S, Bzdok D. Kopal J, et al. Among authors: owen mj. Nat Commun. 2024 Mar 26;15(1):2639. doi: 10.1038/s41467-024-46784-w. Nat Commun. 2024. PMID: 38531844 Free PMC article.
Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.
Grozeva D, Kirov G, Ivanov D, Jones IR, Jones L, Green EK, St Clair DM, Young AH, Ferrier N, Farmer AE, McGuffin P, Holmans PA, Owen MJ, O'Donovan MC, Craddock N; Wellcome Trust Case Control Consortium. Grozeva D, et al. Among authors: owen mj. Arch Gen Psychiatry. 2010 Apr;67(4):318-27. doi: 10.1001/archgenpsychiatry.2010.25. Arch Gen Psychiatry. 2010. PMID: 20368508 Free PMC article.
Psychopathology and cognition in children with 22q11.2 deletion syndrome.
Niarchou M, Zammit S, van Goozen SH, Thapar A, Tierling HM, Owen MJ, van den Bree MB. Niarchou M, et al. Among authors: owen mj. Br J Psychiatry. 2014 Jan;204(1):46-54. doi: 10.1192/bjp.bp.113.132324. Epub 2013 Oct 10. Br J Psychiatry. 2014. PMID: 24115343 Free PMC article.
1,096 results