Authors: Rees, MI Lewis, TM Vafa, B Ferrie, C Corry, P Muntoni, F Jungbluth, H Stephenson, JBP Kerr, M Snell, RG Schofield, RR Owen, MJ

Citation: Mi. Rees et al., Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexia, HUM GENET, 109(3), 2001, pp. 267-270

Authors: 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

Citation: Ag. Cardno et al., A genomewide linkage study of age at onset in schizophrenia, AM J MED G, 105(5), 2001, pp. 439-445

Authors: Baker, KL Rees, MI Thompson, PW Howell, RT Cole, TR Hughes, HE Upadhyaya, M Ravine, D

Citation: Kl. Baker et al., Chromosome 2 interstitial deletion (del(2) (q14.1q21)) associated with connective tissue laxity and an attention deficit disorder, J MED GENET, 38(7), 2001, pp. 493-496

Authors: Rees, MI Watts, P Fenton, I Clarke, A Snell, RG Owen, MJ Gray, J

Citation: Mi. Rees et al., Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA(3)), HUM GENET, 106(2), 2000, pp. 206-209

Authors: Rees, MI Fenton, I Williams, NM Holmans, P Norton, N Cardno, A Asherson, P Spurlock, G Roberts, E Parfitt, E Mant, P Vallada, H Dawson, E Li, MW Collier, DA Powell, JF Nanko, S Gill, M McGuffin, P Owen, MJ

Citation: Mi. Rees et al., Autosome search for schizophrenia susceptibility genes in multiply affected families, MOL PSYCHI, 4(4), 1999, pp. 353-359

Authors: 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

Citation: Nm. Williams et al., A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs, HUM MOL GEN, 8(9), 1999, pp. 1729-1739