Owen MJ - Search Results

1

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.

2

Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder.

Langley K, Fowler TA, Grady DL, Moyzis RK, Holmans PA, van den Bree MB, Owen MJ, O'Donovan MC, Thapar A. Langley K, et al. Among authors: owen mj. Eur Child Adolesc Psychiatry. 2009 Jan;18(1):26-32. doi: 10.1007/s00787-008-0698-4. Epub 2008 Jun 18. Eur Child Adolesc Psychiatry. 2009. PMID: 18563476

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

Schizophrenia genetics: new insights from new approaches.

Williams HJ, Owen MJ, O'Donovan MC. Williams HJ, et al. Among authors: owen mj. Br Med Bull. 2009;91:61-74. doi: 10.1093/bmb/ldp017. Epub 2009 May 14. Br Med Bull. 2009. PMID: 19443537 Review.

5

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

6

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.

7

A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk.

Chapman J, Rees E, Harold D, Ivanov D, Gerrish A, Sims R, Hollingworth P, Stretton A; GERAD1 Consortium; Holmans P, Owen MJ, O'Donovan MC, Williams J, Kirov G. Chapman J, et al. Among authors: owen mj. Hum Mol Genet. 2013 Feb 15;22(4):816-24. doi: 10.1093/hmg/dds476. Epub 2012 Nov 11. Hum Mol Genet. 2013. PMID: 23148125 Free PMC article.

8

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.

9

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.

10

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

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