Platelet and Neutrophil Antigens by Allen, D, Lucas, G, Murphy, M, Ouwehand, W

Dindel: accurate indel calls from short-read data. by Albers, C, Lunter, G, MacArthur, D, McVean, G, Ouwehand, W, Durbin, R

A naturally occurring Arg -> Gln substitution at position 93 of platelet beta 3 integrin abolishes anti-HPA-1a binding. by Watkins, N, Schaffner-Reckinger, E, Allen, D, Metcalfe, P, Murphy, M, Kieffer, N, Ouwehand, W

Efficiency and safety of varying the frequency of whole blood donation: randomised trial of 45,000 donors by Di Angelantonio, E, Thompson, S, Kaptoge, S, Moore, C, Walker, M, Armitage, J, Ouwehand, W, Roberts, D, Danesh, J

The effect of treatment with Campath-1H in patients with autoimmune cytopenias. by Willis, F, Marsh, J, Bevan, D, Killick, S, Lucas, G, Griffiths, R, Ouwehand, W, Hale, G, Waldmann, H, Gordon-Smith, E

Longer-term efficiency and safety of increasing the frequency of whole blood donation (INTERVAL): extension study of a randomised trial of 20 757 blood donors by Kaptoge, S, Di Angelantonio, E, Moore, C, Walker, M, Armitage, J, Ouwehand, W, Roberts, D, Danesh, J, Thompson, S, INTERVAL Trial Group

HPA-1a phenotype-genotype discrepancy reveals a naturally occurring Arg93Gln substitution in the platelet beta 3 integrin that disrupts the HPA-1a epitope. by Watkins, N, Schaffner-Reckinger, E, Allen, D, Howkins, G, Brons, N, Smith, G, Metcalfe, P, Murphy, M, Kieffer, N, Ouwehand, W

Guidelines for the investigation and management of idiopathic thrombocytopenic purpura in adults, children and in pregnancy by Provan, D, Newland, A, Norfolk, D, Bolton-Maggs, P, Lilleyman, J, Greer, I, May, A, Murphy, M, Ouwehand, W, Watson, S, Haematology, B

Combinatorial transcriptional control in blood stem/progenitor cells: genome-wide analysis of ten major transcriptional regulators. by Wilson, N, Foster, S, Wang, X, Knezevic, K, Schütte, J, Kaimakis, P, Chilarska, P, Kinston, S, Ouwehand, W, Dzierzak, E, Pimanda, J, de Bruijn, M, Göttgens, B

Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies. by Sarwar, N, Sandhu, MS, Ricketts, S, Butterworth, A, Di Angelantonio, E, Boekholdt, S, Ouwehand, W, Watkins, H, Samani, N, Saleheen, D, Lawlor, D, Reilly, M, Hingorani, A, Talmud, P, Danesh, J

Glucophosphate isomerase deficiency identified by next‐generation sequencing by Vora, S, Proven, M, Hipkiss, R, Ware, P, Howard, K, Dreau, H, Baird, S, Ouwehand, W, Megy, K, Stirrups, K, Lim, D, Norton, A, Kumar, A, Roberts, I, Layton, M, Roy, N

Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. by Timpson, N, Lindgren, C, Weedon, M, Randall, J, Ouwehand, W, Strachan, D, Rayner, N, Walker, M, Hitman, G, Doney, A, Palmer, C, Morris, A, Hattersley, A, Zeggini, E, Frayling, T, McCarthy, M

The BEACH-domain containing protein, Nbeal2, interacts with Dock7, Sec16a and Vac14 by Mayer, L, Jasztal, M, Pardo, M, Aguera de Haro, S, Collins, J, Bariana, T, Smethurst, P, Grassi, L, Petersen, R, Nurden, P, Favier, R, Yu, L, Meacham, S, Astle, W, Choudhary, J, Yue, W, Ouwehand, W, Guerrero, J

Association of variants in the fat mass and obesity associated (FTO) gene with polycystic ovary syndrome. by Barber, T, Bennett, A, Groves, C, Sovio, U, Ruokonen, A, Martikainen, H, Pouta, A, Hartikainen, A, Elliott, P, Lindgren, C, Freathy, R, Koch, K, Ouwehand, W, Karpe, F, Conway, G, Wass, J, Järvelin, MR, Franks, S, McCarthy, M

Genome-wide association analysis identifies 20 loci that influence adult height. by Weedon, M, Lango, H, Lindgren, C, Wallace, C, Evans, D, Mangino, M, Freathy, R, Perry, JR, Stevens, S, Hall, A, Samani, N, Shields, B, Prokopenko, I, Farrall, M, Dominiczak, A, Johnson, T, Bergmann, S, Beckmann, J, Vollenweider, P, Waterworth, D, Mooser, V, Palmer, C, Morris, A, Ouwehand, W, Zhao, J

Novel loci and biomedical consequences of iron homoeostasis variation by Allara, E, Bell, S, Smith, R, Keene, SJ, Gill, D, Gaziano, L, Morselli Gysi, D, Wang, F, Tragante, V, Mason, A, Karthikeyan, S, Lumbers, RT, Bonglack, E, Ouwehand, W, Roberts, DJ, Dowsett, J, Ostrowski, SR, Larsen, MH, Ullum, H, Pedersen, OB, Brunak, S, Banasik, K, Erikstrup, C, Mitchell, J

Chromosome contacts in activated T cells identify autoimmune disease candidate genes by Burren, O, Rubio García, A, Javierre, B, Rainbow, D, Cairns, J, Cooper, N, Lambourne, J, Schofield, E, Castro Dopico, X, Ferreira, R, Coulson, R, Burden, F, Rowlston, S, Downes, K, Wingett, S, Frontini, M, Ouwehand, W, Fraser, P, Spivakov, M, Todd, J, Wicker, L, Cutler, A, Wallace, C

Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship. by Anderson, C, Massey, D, Barrett, J, Prescott, N, Tremelling, M, Fisher, SA, Gwilliam, R, Jacob, J, Nimmo, E, Drummond, H, Lees, C, Onnie, C, Hanson, C, Blaszczyk, K, Ravindrarajah, R, Hunt, S, Varma, D, Hammond, N, Lewis, G, Attlesey, H, Watkins, N, Ouwehand, W, Strachan, D, McArdle, W, Lewis, C

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. by Burton, P, Clayton, D, Cardon, L, Craddock, N, Deloukas, P, Duncanson, A, Kwiatkowski, D, McCarthy, M, Ouwehand, W, Samani, N, Todd, J, Donnelly, P, Barrett, J, Davison, D, Easton, D, Evans, D, Leung, H, Marchini, J, Morris, A, Spencer, C, Tobin, MD, Attwood, A, Boorman, J, Cant, B, Everson, U

eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic Data by Breeze, C, Paul, D, van Dongen, J, Butcher, L, Ambrose, J, Barrett, J, Lowe, R, Rakyan, V, Iotchkova, V, Frontini, M, Downes, K, Ouwehand, W, Laperle, J, Jacques, P, Bourque, G, Bergmann, A, Siebert, R, Vellenga, E, Saeed, S, Matarese, F, Martens, J, Stunnenberg, H, Teschendorff, A, Herrero, J, Birney, E, Dunham, I, Beck, S