van den Bree MBM - Search Results

1

Childhood cognitive development in 22q11.2 deletion syndrome: case-control study.

Chawner SJRA, Doherty JL, Moss H, Niarchou M, Walters JTR, Owen MJ, van den Bree MBM. Chawner SJRA, et al. Among authors: van den bree mbm. Br J Psychiatry. 2017 Oct;211(4):223-230. doi: 10.1192/bjp.bp.116.195651. Epub 2017 Sep 7. Br J Psychiatry. 2017. PMID: 28882829 Free PMC article.

2

Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22.

Turic D, Robinson L, Duke M, Morris DW, Webb V, Hamshere M, Milham C, Hopkin E, Pound K, Fernando S, Grierson A, Easton M, Williams N, Van Den Bree M, Chowdhury R, Gruen J, Stevenson J, Krawczak M, Owen MJ, O'Donovan MC, Williams J. Turic D, et al. Mol Psychiatry. 2003 Feb;8(2):176-85. doi: 10.1038/sj.mp.4001216. Mol Psychiatry. 2003. PMID: 12610650

3

The future of psychiatric genetics.

van den Bree MB, Owen MJ. van den Bree MB, et al. Ann Med. 2003;35(2):122-34. doi: 10.1080/07853890310010023. Ann Med. 2003. PMID: 12795340 Free article. Review.

4

No evidence of association between HLA-DRB1 and attention deficit hyperactivity disorder.

Payton A, Turic D, Langley K, Mills S, Lawson DC, Van den Bree M, Owen MJ, O'Donovan MC, Ollier W, Worthington J, Thapar A. Payton A, et al. Psychiatr Genet. 2003 Sep;13(3):183-5. doi: 10.1097/00041444-200309000-00009. Psychiatr Genet. 2003. PMID: 12960752

5

Association of the dopamine D4 receptor gene 7-repeat allele with neuropsychological test performance of children with ADHD.

Langley K, Marshall L, van den Bree M, Thomas H, Owen M, O'Donovan M, Thapar A. Langley K, et al. Am J Psychiatry. 2004 Jan;161(1):133-8. doi: 10.1176/appi.ajp.161.1.133. Am J Psychiatry. 2004. PMID: 14702261

6

Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD.

Turic D, Langley K, Mills S, Stephens M, Lawson D, Govan C, Williams N, Van Den Bree M, Craddock N, Kent L, Owen M, O'Donovan M, Thapar A. Turic D, et al. Mol Psychiatry. 2004 Feb;9(2):169-73. doi: 10.1038/sj.mp.4001387. Mol Psychiatry. 2004. PMID: 14966475

7

No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: a case-control study.

Mills S, Langley K, Van den Bree M, Street E, Turic D, Owen MJ, O'Donovan MC, Thapar A. Mills S, et al. BMC Psychiatry. 2004 Jun 7;4:15. doi: 10.1186/1471-244X-4-15. BMC Psychiatry. 2004. PMID: 15182372 Free PMC article.

8

No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia.

Cope NA, Hill G, van den Bree M, Harold D, Moskvina V, Green EK, Owen MJ, Williams J, O'Donovan MC. Cope NA, et al. Mol Psychiatry. 2005 Mar;10(3):237-8. doi: 10.1038/sj.mp.4001596. Mol Psychiatry. 2005. PMID: 15477871 No abstract available.

9

Catechol O-methyltransferase gene variant and birth weight predict early-onset antisocial behavior in children with attention-deficit/hyperactivity disorder.

Thapar A, Langley K, Fowler T, Rice F, Turic D, Whittinger N, Aggleton J, Van den Bree M, Owen M, O'Donovan M. Thapar A, et al. Arch Gen Psychiatry. 2005 Nov;62(11):1275-8. doi: 10.1001/archpsyc.62.11.1275. Arch Gen Psychiatry. 2005. PMID: 16275815

10

Agreement between maternal report and antenatal records for a range of pre and peri-natal factors: the influence of maternal and child characteristics.

Rice F, Lewis A, Harold G, van den Bree M, Boivin J, Hay DF, Owen MJ, Thapar A. Rice F, et al. Early Hum Dev. 2007 Aug;83(8):497-504. doi: 10.1016/j.earlhumdev.2006.09.015. Epub 2006 Oct 30. Early Hum Dev. 2007. PMID: 17071023

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