Owen MJ - Search Results

1

Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence.

Kopal J, Kumar K, Saltoun K, Modenato C, Moreau CA, Martin-Brevet S, Huguet G, Jean-Louis M, Martin CO, Saci Z, Younis N, Tamer P, Douard E, Maillard AM, Rodriguez-Herreros B, Pain A, Richetin S, 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, Jacquemont S, Bzdok D. Kopal J, et al. Among authors: owen mj. Nat Hum Behav. 2023 Jun;7(6):1001-1017. doi: 10.1038/s41562-023-01541-9. Epub 2023 Mar 2. Nat Hum Behav. 2023. PMID: 36864136 Free PMC article.

2

Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1.

Bray NJ, Holmans PA, van den Bree MB, Jones L, Elliston LA, Hughes G, Richards AL, Williams NM, Craddock N, Owen MJ, O'Donovan MC. Bray NJ, et al. Among authors: owen mj. Hum Mol Genet. 2008 Apr 15;17(8):1169-74. doi: 10.1093/hmg/ddn006. Epub 2008 Jan 8. Hum Mol Genet. 2008. PMID: 18182443

3

Psychopathy traits in adolescents with childhood attention-deficit hyperactivity disorder.

Fowler T, Langley K, Rice F, Whittinger N, Ross K, van Goozen S, Owen MJ, O'Donovan MC, van den Bree MB, Thapar A. Fowler T, et al. Among authors: owen mj. Br J Psychiatry. 2009 Jan;194(1):62-7. doi: 10.1192/bjp.bp.107.046870. Br J Psychiatry. 2009. PMID: 19118328

4

Psychopathy trait scores in adolescents with childhood ADHD: the contribution of genotypes affecting MAOA, 5HTT and COMT activity.

Fowler T, Langley K, Rice F, van den Bree MB, Ross K, Wilkinson LS, Owen MJ, O'Donovan MC, Thapar A. Fowler T, et al. Among authors: owen mj. Psychiatr Genet. 2009 Dec;19(6):312-9. doi: 10.1097/YPG.0b013e3283328df4. Psychiatr Genet. 2009. PMID: 19829167

5

The internet is parents' main source of information about psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS).

van den Bree MB, Miller G, Mansell E, Thapar A, Flinter F, Owen MJ. van den Bree MB, et al. Among authors: owen mj. Eur J Med Genet. 2013 Aug;56(8):439-41. doi: 10.1016/j.ejmg.2013.05.001. Epub 2013 May 22. Eur J Med Genet. 2013. PMID: 23707654 Free PMC article.

6

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.

7

Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome.

Monks S, Niarchou M, Davies AR, Walters JT, Williams N, Owen MJ, van den Bree MB, Murphy KC. Monks S, et al. Among authors: owen mj. Schizophr Res. 2014 Mar;153(1-3):231-6. doi: 10.1016/j.schres.2014.01.020. Epub 2014 Feb 15. Schizophr Res. 2014. PMID: 24534796

8

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

9

Genetic risk for schizophrenia: convergence on synaptic pathways involved in plasticity.

Hall J, Trent S, Thomas KL, O'Donovan MC, Owen MJ. Hall J, et al. Among authors: owen mj. Biol Psychiatry. 2015 Jan 1;77(1):52-8. doi: 10.1016/j.biopsych.2014.07.011. Epub 2014 Jul 18. Biol Psychiatry. 2015. PMID: 25152434 Review.

10

Alzheimer's disease risk variant in CLU is associated with neural inefficiency in healthy individuals.

Lancaster TM, Brindley LM, Tansey KE, Sims RC, Mantripragada K, Owen MJ, Williams J, Linden DE. Lancaster TM, et al. Among authors: owen mj. Alzheimers Dement. 2015 Oct;11(10):1144-52. doi: 10.1016/j.jalz.2014.10.012. Epub 2014 Dec 10. Alzheimers Dement. 2015. PMID: 25496871

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