O'Donovan MC - Search Results

1

Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13.

Hamshere ML, Bennett P, Williams N, Segurado R, Cardno A, Norton N, Lambert D, Williams H, Kirov G, Corvin A, Holmans P, Jones L, Jones I, Gill M, O'Donovan MC, Owen MJ, Craddock N. Hamshere ML, et al. Arch Gen Psychiatry. 2005 Oct;62(10):1081-8. doi: 10.1001/archpsyc.62.10.1081. Arch Gen Psychiatry. 2005. PMID: 16203953

2

No major schizophrenia locus detected on chromosome 1q in a large multicenter sample.

Levinson DF, Holmans PA, Laurent C, Riley B, Pulver AE, Gejman PV, Schwab SG, Williams NM, Owen MJ, Wildenauer DB, Sanders AR, Nestadt G, Mowry BJ, Wormley B, Bauché S, Soubigou S, Ribble R, Nertney DA, Liang KY, Martinolich L, Maier W, Norton N, Williams H, Albus M, Carpenter EB, DeMarchi N, Ewen-White KR, Walsh D, Jay M, Deleuze JF, O'Neill FA, Papadimitriou G, Weilbaecher A, Lerer B, O'Donovan MC, Dikeos D, Silverman JM, Kendler KS, Mallet J, Crowe RR, Walters M. Levinson DF, et al. Science. 2002 Apr 26;296(5568):739-41. doi: 10.1126/science.1069914. Science. 2002. PMID: 11976456

3

Genome scans and microarrays: converging on genes for schizophrenia?

Williams NM, O'Donovan MC, Owen MJ. Williams NM, et al. Genome Biol. 2002;3(4):REVIEWS1011. doi: 10.1186/gb-2002-3-4-reviews1011. Epub 2002 Mar 27. Genome Biol. 2002. PMID: 11983064 Free PMC article. Review.

4

Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools.

Norton N, Williams NM, Williams HJ, Spurlock G, Kirov G, Morris DW, Hoogendoorn B, Owen MJ, O'Donovan MC. Norton N, et al. Hum Genet. 2002 May;110(5):471-8. doi: 10.1007/s00439-002-0706-6. Epub 2002 Mar 23. Hum Genet. 2002. PMID: 12073018

5

Schizophrenia and functional polymorphisms in the MAOA and COMT genes: no evidence for association or epistasis.

Norton N, Kirov G, Zammit S, Jones G, Jones S, Owen R, Krawczak M, Williams NM, O'Donovan MC, Owen MJ. Norton N, et al. Am J Med Genet. 2002 Jul 8;114(5):491-6. doi: 10.1002/ajmg.10517. Am J Med Genet. 2002. PMID: 12116182

6

Association analysis of monoamine oxidase A and attention deficit hyperactivity disorder.

Lawson DC, Turic D, Langley K, Pay HM, Govan CF, Norton N, Hamshere ML, Owen MJ, O'Donovan MC, Thapar A. Lawson DC, et al. Am J Med Genet B Neuropsychiatr Genet. 2003 Jan 1;116B(1):84-9. doi: 10.1002/ajmg.b.10002. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12497620

7

Cis-acting variation in the expression of a high proportion of genes in human brain.

Bray NJ, Buckland PR, Owen MJ, O'Donovan MC. Bray NJ, et al. Hum Genet. 2003 Jul;113(2):149-53. doi: 10.1007/s00439-003-0956-y. Epub 2003 May 1. Hum Genet. 2003. PMID: 12728311

8

Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease.

Harold D, Peirce T, Moskvina V, Myers A, Jones S, Hollingworth P, Moore P, Lovestone S, Powell J, Foy C, Archer N, Walter S, Edmonson A, McIlroy S, Craig D, Passmore PA, Goate A, Hardy J, O'Donovan M, Williams J, Liddell M, Owen MJ, Jones L. Harold D, et al. Hum Genet. 2003 Aug;113(3):258-67. doi: 10.1007/s00439-003-0960-2. Epub 2003 May 21. Hum Genet. 2003. PMID: 12759818

9

No evidence of association of two 5HT transporter gene polymorphisms and attention deficit hyperactivity disorder.

Langley K, Payton A, Hamshere ML, Pay HM, Lawson DC, Turic D, Ollier W, Worthington J, Owen MJ, O'Donovan MC, Thapar A. Langley K, et al. Psychiatr Genet. 2003 Jun;13(2):107-10. doi: 10.1097/01.ypg.0000056177.32550.a5. Psychiatr Genet. 2003. PMID: 12782968

10

A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain.

Bray NJ, Buckland PR, Williams NM, Williams HJ, Norton N, Owen MJ, O'Donovan MC. Bray NJ, et al. Am J Hum Genet. 2003 Jul;73(1):152-61. doi: 10.1086/376578. Epub 2003 Jun 11. Am J Hum Genet. 2003. PMID: 12802784 Free PMC article.

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