Owen MJ - Search Results

1

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.

Cichon S, Mühleisen TW, Degenhardt FA, Mattheisen M, Miró X, Strohmaier J, Steffens M, Meesters C, Herms S, Weingarten M, Priebe L, Haenisch B, Alexander M, Vollmer J, Breuer R, Schmäl C, Tessmann P, Moebus S, Wichmann HE, Schreiber S, Müller-Myhsok B, Lucae S, Jamain S, Leboyer M, Bellivier F, Etain B, Henry C, Kahn JP, Heath S; Bipolar Disorder Genome Study (BiGS) Consortium; Hamshere M, O'Donovan MC, Owen MJ, Craddock N, Schwarz M, Vedder H, Kammerer-Ciernioch J, Reif A, Sasse J, Bauer M, Hautzinger M, Wright A, Mitchell PB, Schofield PR, Montgomery GW, Medland SE, Gordon SD, Martin NG, Gustafsson O, Andreassen O, Djurovic S, Sigurdsson E, Steinberg S, Stefansson H, Stefansson K, Kapur-Pojskic L, Oruc L, Rivas F, Mayoral F, Chuchalin A, Babadjanova G, Tiganov AS, Pantelejeva G, Abramova LI, Grigoroiu-Serbanescu M, Diaconu CC, Czerski PM, Hauser J, Zimmer A, Lathrop M, Schulze TG, Wienker TF, Schumacher J, Maier W, Propping P, Rietschel M, Nöthen MM. Cichon S, et al. Among authors: owen mj. Am J Hum Genet. 2011 Mar 11;88(3):372-81. doi: 10.1016/j.ajhg.2011.01.017. Epub 2011 Feb 25. Am J Hum Genet. 2011. PMID: 21353194 Free PMC article.

2

Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB).

Rees MI, Lewis TM, Kwok JB, Mortier GR, Govaert P, Snell RG, Schofield PR, Owen MJ. Rees MI, et al. Among authors: owen mj. Hum Mol Genet. 2002 Apr 1;11(7):853-60. doi: 10.1093/hmg/11.7.853. Hum Mol Genet. 2002. PMID: 11929858

3

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. Among authors: owen mj. Hum Genet. 2002 May;110(5):471-8. doi: 10.1007/s00439-002-0706-6. Epub 2002 Mar 23. Hum Genet. 2002. PMID: 12073018

4

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. Among authors: owen r, owen mj. Am J Med Genet. 2002 Jul 8;114(5):491-6. doi: 10.1002/ajmg.10517. Am J Med Genet. 2002. PMID: 12116182

5

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. Among authors: owen mj. 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

6

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. Among authors: owen mj. Hum Genet. 2003 Jul;113(2):149-53. doi: 10.1007/s00439-003-0956-y. Epub 2003 May 1. Hum Genet. 2003. PMID: 12728311

7

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. Among authors: owen mj. Hum Genet. 2003 Aug;113(3):258-67. doi: 10.1007/s00439-003-0960-2. Epub 2003 May 21. Hum Genet. 2003. PMID: 12759818

8

Mutational analysis of two positional candidate susceptibility genes for bipolar disorder on chromosome 12q23-q24: phenylalanine hydroxylase and human LIM-homeobox LHX5.

Green EK, Elvidge GP, Owen MJ, Craddock N. Green EK, et al. Among authors: owen mj. Psychiatr Genet. 2003 Jun;13(2):97-101. doi: 10.1097/01.ypg.0000057882.80011.9e. Psychiatr Genet. 2003. PMID: 12782966

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. Among authors: owen mj. 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. Among authors: owen mj. 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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