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Brain functional connectivity mirrors genetic pleiotropy in psychiatric conditions.
Moreau CA, Kumar K, Harvey A, Huguet G, Urchs SGW, Schultz LM, Sharmarke H, Jizi K, Martin CO, Younis N, Tamer P, Martineau JL, Orban P, Silva AI, Hall J, van den Bree MBM, Owen MJ, Linden DEJ, Lippé S, Bearden CE, Almasy L, Glahn DC, Thompson PM, Bourgeron T, Bellec P, Jacquemont S. Moreau CA, et al. Among authors: owen mj. Brain. 2023 Apr 19;146(4):1686-1696. doi: 10.1093/brain/awac315. Brain. 2023. PMID: 36059063 Free PMC article.
SGCE mutations cause psychiatric disorders: clinical and genetic characterization.
Peall KJ, Smith DJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP, Smith M, Whone A, Pall H, White C, Lux A, Jardine P, Bajaj N, Lynch B, Kirov G, O'Riordan S, Samuel M, Lynch T, King MD, Chinnery PF, Warner TT, Blake DJ, Owen MJ, Morris HR. Peall KJ, et al. Among authors: owen mj. Brain. 2013 Jan;136(Pt 1):294-303. doi: 10.1093/brain/aws308. Brain. 2013. PMID: 23365103 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.
Exploring the indirect effects of catechol-O-methyltransferase (COMT) genotype on psychotic experiences through cognitive function and anxiety disorders in a large birth cohort of children.
Niarchou M, Zammit S, Escott-Price V, Owen MJ, van den Bree MB. Niarchou M, et al. Among authors: owen mj. Am J Med Genet B Neuropsychiatr Genet. 2014 Jul;165B(5):410-20. doi: 10.1002/ajmg.b.32245. Epub 2014 May 27. Am J Med Genet B Neuropsychiatr Genet. 2014. PMID: 24862404
1,104 results