New methods for finding disease-susceptibility genes: impact and potential. by McCarthy, M, Smedley, D, Hide, W

Application of eVOC: controlled vocabularies for unifying gene expression data. by Hide, W, Smedley, D, Mccarthy, M, Kelso, J

Nanoparticles filled epoxy-based adhesive for in situ timber bonding. by Ahmad, Zakiah, Ansell, M. P., Smedley, D., Md. Tahir, Paridah

Variation at the IRF2 gene and susceptibility to psoriasis in chromosome 4q-linked families. by Parkinson, J, Charon, C, Baker, B, Powles, A, Rogers, S, Caird, A, Smedley, D, Halford, S, Fry, L, McCarthy, M

Association and haplotype analysis of the insulin-degrading enzyme (IDE) gene, a strong positional and biological candidate for type 2 diabetes susceptibility. by Groves, C, Wiltshire, S, Smedley, D, Owen, K, Frayling, T, Walker, M, Hitman, G, Levy, J, O'Rahilly, S, Menzel, S, Hattersley, A, McCarthy, M

eVOC: a controlled vocabulary for unifying gene expression data. by Kelso, J, Visagie, J, Theiler, G, Christoffels, A, Bardien, S, Smedley, D, Otgaar, D, Greyling, G, Jongeneel, C, McCarthy, M, Hide, T, Hide, W

Linkage analysis in the Diabetes (UK) Warren 2 sibpair repository supports localisation of a type 2 diabetes susceptibility gene to chromosome 1q21-24. by McCarthy, M, Hattersley, A, Walker, M, Hitman, G, Levy, J, O'Rahilly, S, Lathrop, G, Simecek, N, Wishart, M, Dhillon, R, Fletcher, C, Frayling, T, Bennett, A, Groves, C, Smedley, D, Menzel, S, Wiltshire, S

The 100,000 genomes pilot on rare disease diagnosis in healthcare – a preliminary report by Smedley, D, Smith, KR, Rueda Martin, A, Buchanan, J, Wordsworth, S, de Burca, A, Davies, J, Crichton, C, Welch, J, Woods, K, Campbell, C, Camps, C, Gibson, K, Lester, T, Patel, S, Roy, NBA, Sen, A, Németh, AH, Taylor, J, Caulfield, M

A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of... by Wiltshire, S, Hattersley, A, Hitman, G, Walker, M, Levy, J, Sampson, M, O'Rahilly, S, Frayling, T, Bell, J, Lathrop, G, Bennett, A, Dhillon, R, Fletcher, C, Groves, C, Jones, E, Prestwich, P, Simecek, N, Rao, P, Wishart, M, Bottazzo, G, Foxon, R, Howell, S, Smedley, D, Cardon, L, Menzel, S

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants by Aragam, KG, Jiang, T, Goel, A, Kanoni, S, Wolford, BN, Atri, DS, Weeks, EM, Wang, M, Hindy, G, Zhou, W, Grace, C, Roselli, C, Marston, NA, Kamanu, FK, Surakka, I, Venegas, LM, Sherliker, P, Koyama, S, Ishigaki, K, Åsvold, BO, Brown, MR, Brumpton, B, de Vries, PS, Giannakopoulou, O, Giardoglou, P, Gudbjartsson, DF, Güldener, U, Haider, SMI, Helgadottir, A, Ibrahim, M, Kastrati, A, Kessler, T, Kyriakou, T, Konopka, T, Li, L, Ma, L, Meitinger, T, Mucha, S, Munz, M, Murgia, F, Nielsen, JB, Nöthen, MM, Pang, S, Reinberger, T, Schnitzler, G, Smedley, D, Thorleifsson, G, von Scheidt, M, Ulirsch, JC, Biobank Japan, Hopewell, JC, Clarke, R, Watkins, H

Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy by Park, J, Tucci, A, Cipriani, V, Demidov, G, Rocca, C, Senderek, J, Butryn, M, Velic, A, Lam, T, Galanaki, E, Cali, E, Vestito, L, Maroofian, R, Deininger, N, Rautenberg, M, Admard, J, Hahn, G-A, Bartels, C, van Os, NJH, Horvath, R, Chinnery, PF, Tiet, MY, Hewamadduma, C, Hadjivassiliou, M, Tofaris, GK, Genomics England Research Consortium, Wood, NW, Hayer, SN, Bender, F, Menden, B, Cordts, I, Klein, K, Nguyen, HP, Krauss, JK, Blahak, C, Strom, TM, Sturm, M, van de Warrenburg, B, Lerche, H, Maček, B, Synofzik, M, Ossowski, S, Timmann, D, Wolf, ME, Smedley, D, Riess, O, Schöls, L, Houlden, H, Haack, TB, Hengel, H