Rees MI - Search Results

1

Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophrenia.

Anney RJ, Rees MI, Bryan E, Spurlock G, Williams N, Norton N, Williams H, Cardno A, Zammit S, Jones S, Jones G, Hoogendoorn B, Smith K, Hamshere ML, Coleman S, Guy C, O'Donovan MC, Owen MJ, Buckland PR. Anney RJ, et al. Among authors: rees mi. Mol Psychiatry. 2002;7(5):493-502. doi: 10.1038/sj.mp.4001003. Mol Psychiatry. 2002. PMID: 12082567

2

Autosome search for schizophrenia susceptibility genes in multiply affected families.

Rees MI, Fenton I, Williams NM, Holmans P, Norton N, Cardno A, Asherson P, Spurlock G, Roberts E, Parfitt E, Mant R, Vallada H, Dawson E, Li MW, Collier DA, Powell JF, Nanko S, Gill M, McGuffin P, Owen MJ. Rees MI, et al. Mol Psychiatry. 1999 Jul;4(4):353-9. doi: 10.1038/sj.mp.4000521. Mol Psychiatry. 1999. PMID: 10483052

3

Association studies of bipolar disorder at the human serotonin transporter gene (hSERT; 5HTT).

Rees M, Norton N, Jones I, McCandless F, Scourfield J, Holmans P, Moorhead S, Feldman E, Sadler S, Cole T, Redman K, Farmer A, McGuffin P, Owen MJ, Craddock N. Rees M, et al. Mol Psychiatry. 1997 Sep;2(5):398-402. doi: 10.1038/sj.mp.4000256. Mol Psychiatry. 1997. PMID: 9322234

4

A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs.

Williams NM, Rees MI, Holmans P, Norton N, Cardno AG, Jones LA, Murphy KC, Sanders RD, McCarthy G, Gray MY, Fenton I, McGuffin P, Owen MJ. Williams NM, et al. Among authors: rees mi. Hum Mol Genet. 1999 Sep;8(9):1729-39. doi: 10.1093/hmg/8.9.1729. Hum Mol Genet. 1999. PMID: 10441337

5

A genomewide linkage study of age at onset in schizophrenia.

Cardno AG, Holmans PA, Rees MI, Jones LA, McCarthy GM, Hamshere ML, Williams NM, Norton N, Williams HJ, Fenton I, Murphy KC, Sanders RD, Gray MY, O'Donovan MC, McGuffin P, Owen MJ. Cardno AG, et al. Among authors: rees mi. Am J Med Genet. 2001 Jul 8;105(5):439-45. doi: 10.1002/ajmg.1404. Am J Med Genet. 2001. PMID: 11449396

6

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. Hum Mol Genet. 2002 Apr 1;11(7):853-60. doi: 10.1093/hmg/11.7.853. Hum Mol Genet. 2002. PMID: 11929858

7

Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor.

Rees MI, Andrew M, Jawad S, Owen MJ. Rees MI, et al. Hum Mol Genet. 1994 Dec;3(12):2175-9. doi: 10.1093/hmg/3.12.2175. Hum Mol Genet. 1994. PMID: 7881416

8

Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3).

Rees MI, Watts P, Fenton I, Clarke A, Snell RG, Owen MJ, Gray J. Rees MI, et al. Hum Genet. 2000 Feb;106(2):206-9. doi: 10.1007/s004390051029. Hum Genet. 2000. PMID: 10746562

9

No evidence for allelic association between bipolar disorder and monoamine oxidase A gene polymorphisms.

Craddock N, Daniels J, Roberts E, Rees M, McGuffin P, Owen MJ. Craddock N, et al. Am J Med Genet. 1995 Aug 14;60(4):322-4. doi: 10.1002/ajmg.1320600412. Am J Med Genet. 1995. PMID: 7485269

10

Bipolar disorder and the serotonin transporter gene: a family-based association study.

Kirov G, Rees M, Jones I, MacCandless F, Owen MJ, Craddock N. Kirov G, et al. Psychol Med. 1999 Sep;29(5):1249-54. doi: 10.1017/s003329179900882x. Psychol Med. 1999. PMID: 10576317

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