Cytogenetically cryptic ZMYM2-FLT3 and DIAPH1-PDGFRB gene fusions in myeloid neoplasms with eosinophilia by Jawhar, M, Naumann, N, Knut, M, Score, J, Ghazzawi, M, Schneider, B, Kreuzer, K-A, Hallek, M, Drexler, H G, Chacko, J, Wallis, L, Fabarius, A, Metzgeroth, G, Hofmann, W-K, Chase, A, Tapper, W, Reiter, A, Cross, N C P

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Ethnicity and outcome of young breast cancer patients in the United Kingdom: the POSH study by Copson, E, Maishman, T, Gerty, S, Eccles, B, Stanton, L, Cutress, R I, Altman, D G, Durcan, L, Simmonds, P, Jones, L, Tapper, W, Eccles, Diana

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Longitudinal copy number, whole exome and targeted deep sequencing of 'good risk' IGHV-mutated CLL patients with progressive disease by Rose-Zerilli, M J J, Gibson, J, Wang, J, Tapper, W, Davis, Z, Parker, H, Larrayoz, M, McCarthy, H, Walewska, R, Forster, J, Gardiner, A, Steele, A J, Chelala, C, Ennis, S, Collins, A, Oakes, C C, Oscier, D G, Strefford, J C

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A Map of the Human Genome in Linkage Disequilibrium Units by Tapper, W., Collins, A., Gibson, J., Maniatis, N., Ennis, S., Morton, N. E.

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The First Linkage Disequilibrium (LD) Maps: Delineation of Hot and Cold Blocks by Diplotype Analysis by Maniatis, N., Collins, A., C.-F. Xu, McCarthy, L. C., Hewett, D. R., Tapper, W., Ennis, S., Ke, X., Morton, N. E.

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Profound parental bias associated with chromosome 14 acquired uniparental disomy indicates targeting of an imprinted locus by Chase, A, Leung, W, Tapper, W, Jones, A V, Knoops, L, Rasi, C, Forsberg, L A, Guglielmelli, P, Zoi, K, Hall, V, Chiecchio, L, Eder-Azanza, L, Bryant, C, Lannfelt, L, Docherty, L, White, H E, Score, J, Mackay, D J G, Vannucchi, A M, Dumanski, J P, Cross, N C P

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Preliminary analysis of an expanded corona database for Venus by Stofan, Ellen R., Smrekar, Suzanne E., Tapper, Simon W., Guest, John E., Grindrod, Peter M.

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A Metric Linkage Disequilibrium Map of a Human Chromosome by Tapper, W. J., Maniatis, N., Morton, N. E., Collins, A.

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Linkage Disequilibrium in Human Populations by Lonjou, Christine, Zhang, Weihua, Collins, Andrew, Tapper, William J., Elahi, Eiram, Maniatis, Nikolas, Morton, Newton E.

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Exome sequence read depth methods for identifying copy number changes by Kadalayil, Latha, Rafiq, Sajjad, Rose-Zerilli, Matthew J J, Pengelly, Reuben J, Parker, Helen, Oscier, David, Strefford, Jonathan C, Tapper, William J, Gibson, Jane, Ennis, Sarah, Collins, Andrew

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Variability of sexual phenotype in 46,XX(SRY+) patients: the influence of spreading X inactivation versus position effects by Sharp, A, Kusz, K, Jaruzelska, J, Tapper, W, Szarras-Czapnik, M, Wolski, J, Jacobs, P

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Cross‐Ancestry Genome‐Wide Association Study Defines the Extended CYP2D6 Locus as the Principal Genetic Determinant of Endoxifen Plasma Concentrations by Khor, Chiea Chuen, Winter, Stefan, Sutiman, Natalia, Mürdter, Thomas E., Chen, Sylvia, Lim, Joanne Siok Liu, Li, Zheng, Li, Jingmei, Sim, Kar Seng, Ganchev, Boian, Eccles, Diana, Eccles, Bryony, Tapper, William, Zgheib, Nathalie K., Tfayli, Arafat, Ng, Raymond Chee Hui, Yap, Yoon Sim, Lim, Elaine, Wong, Mabel, Wong, Nan Soon, Ang, Peter Cher Siang, Dent, Rebecca, Tremmel, Roman, Klein, Kathrin, Schaeffeler, Elke, Zhou, Yitian, Lauschke, Volker M., Eichelbaum, Michel, Schwab, Matthias, Brauch, Hiltrud B., Chowbay, Balram, Schroth, Werner

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Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis by Shu, Xiang, Wu, Lang, Khankari, Nikhil K, Shu, Xiao-Ou, Wang, Thomas J, Michailidou, Kyriaki, Bolla, Manjeet K, Wang, Qin, Dennis, Joe, Milne, Roger L, Schmidt, Marjanka K, Pharoah, Paul D P, Andrulis, Irene L, Hunter, David J, Simard, Jacques, Easton, Douglas F, Zheng, Wei

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Breast Cancer Risk Factors and Survival by Tumor Subtype: Pooled Analyses from the Breast Cancer Association Consortium by Morra, Anna, Jung, Audrey Y, Behrens, Sabine, Keeman, Renske, Ahearn, Thomas U, Anton-Culver, Hoda, Arndt, Volker, Augustinsson, Annelie, Auvinen, Päivi K, Beane Freeman, Laura E, Becher, Heiko, Beckmann, Matthias W, Blomqvist, Carl, Bojesen, Stig E, Bolla, Manjeet K, Brenner, Hermann, Briceno, Ignacio, Brucker, Sara Y, Camp, Nicola J, Campa, Daniele, Canzian, Federico, Castelao, Jose E, Chanock, Stephen J, Choi, Ji-Yeob, Clarke, Christine L, Couch, Fergus J, Cox, Angela, Cross, Simon S, Czene, Kamila, Dörk, Thilo, Dunning, Alison M, Dwek, Miriam, Easton, Douglas F, Eccles, Diana M, Egan, Kathleen M, Evans, D Gareth, Fasching, Peter A, Flyger, Henrik, Gago-Dominguez, Manuela, Gapstur, Susan M, García-Sáenz, José A, Gaudet, Mia M, Giles, Graham G, Grip, Mervi, Guénel, Pascal, Haiman, Christopher A, Håkansson, Niclas, Hall, Per, Hamann, Ute, Han, Sileny N, Hart, Steven N, Hartman, Mikael, Heyworth, Jane S, Hoppe, Reiner, Hopper, John L, Hunter, David J, Ito, Hidemi, Jager, Agnes, Jakimovska, Milena, Jakubowska, Anna, Janni, Wolfgang, Kaaks, Rudolf, Kang, Daehee, Kapoor, Pooja Middha, Kitahara, Cari M, Koutros, Stella, Kraft, Peter, Kristensen, Vessela N, Lacey, James V, Lambrechts, Diether, Le Marchand, Loic, Li, Jingmei, Lindblom, Annika, Lubiński, Jan, Lush, Michael, Mannermaa, Arto, Manoochehri, Mehdi, Margolin, Sara, Mariapun, Shivaani, Matsuo, Keitaro, Mavroudis, Dimitrios, Milne, Roger L, Muranen, Taru A, Newman, William G, Noh, Dong-Young, Nordestgaard, Børge G, Obi, Nadia, Olshan, Andrew F, Olsson, Håkan, Park-Simon, Tjoung-Won, Petridis, Christos, Pharoah, Paul D P, Plaseska-Karanfilska, Dijana, Presneau, Nadege, Rashid, Muhammad U, Rennert, Gad, Rennert, Hedy S, Rhenius, Valerie, Romero, Atocha, Saloustros, Emmanouil

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Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer by Couch, Fergus J., Mendoza-Fandino, Gustavo A., Nord, Silje, Hallberg, Emily, Agata, Simona, Ahsan, Habibul, Aittomäki, Kristiina, Andrulis, Irene L., Anton-Culver, Hoda, Arndt, Volker, Arver, Brita, Barile, Monica, Benitez, Javier, Blank, Stephanie V., Blomqvist, Carl, Bonanni, Bernardo, Brauch, Hiltrud, Brenner, Hermann, Burwinkel, Barbara, Caligo, Maria A., Claes, Kathleen B. M., Cross, Simon S., Darabi, Hatef, de la Hoya, Miguel, Devilee, Peter, Dolcetti, Riccardo, Dorfling, Cecilia M., Försti, Asta, Foulkes, William D., Friebel, Tara, Gabrielson, Marike, Garber, Judy, Gaudet, Mia M., Gerdes, Anne-Marie, Ghoussaini, Maya, Goldgar, David E., Haeberle, Lothar, Hart, Steven, Healey, Sue, Herzog, Josef, Hogervorst, Frans B. L., Hopper, John L., Huzarski, Tomasz, Jakubowska, Anna, Janavicius, Ramunas, Jones, Michael, Kar, Siddhartha, Karlan, Beth Y., Knight, Julia A., Ko, Yon-Dschun, Konstantopoulou, Irene, Kwong, Ava, Liu, Jianjun, Manoukian, Siranoush, Margolin, Sara, Marme, Frederik, Miller, Austin, Montagna, Marco, Mulligan, Anna M., Nathanson, Katherine L., Olson, Janet E., Osorio, Ana, Park, Sue K., Peto, Julian, Pilarski, Robert, Poppe, Bruce, Rappaport, Christine, Rennert, Gad, Richardson, Andrea, Robson, Mark, Romieu, Isabelle, Rutgers, Emiel J., Sanchez, Maria-Jose, Sawyer, Elinor J., Schmidt, Marjanka K., Schmutzler, Rita K., Scott, Rodney, Senter, Leigha, Simard, Jacques, Sinilnikova, Olga M., Szabo, Csilla I., Tapper, William, Teixeira, Manuel R., Thomassen, Mads, Thompson, Deborah, Truong, Thérèse, Tsimiklis, Helen, Turnbull, Clare, Ursin, Giski, Weitzel, Jeffrey N., Whittemore, Alice, Wildiers, Hans, Yang, Xiaohong R., Zheng, Wei, Hall, Per, Kraft, Peter, Vachon, Celine, Slager, Susan, Monteiro, Alvaro A. N., Easton, Douglas F.

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Recombination, interference and sequence: comparison of chromosomes 21 and 22 by TAPPER, W. J., KE, X., MORTON, N. E., COLLINS, A.

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The impact of SNP density on fine-scale patterns of linkage disequilibrium by Ke, Xiayi, Hunt, Sarah, Tapper, William, Lawrence, Robert, Stavrides, George, Ghori, Jilur, Whittaker, Pamela, Collins, Andrew, Morris, Andrew P., Bentley, David, Cardon, Lon R., Deloukas, Panos

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LDB2000: sequence-based integrated maps of the human genome by Ke, Xiayi, Tapper, William, Collins, Andrew

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Abstract S2-03: Does BRCA status affect outcome in young breast cancer patients? Results from the prospective study of outcomes in sporadic and hereditary breast cancer (POSH) by Eccles, DM, Copson, ER, Maishman, T, Tapper, W, Cutress, R, Gerty, S, Stanton, L, Altman, DG, Durcan, L, Simmonds, P, Decker, B, Allen, J, Luccarini, C, Easton, D, Dunning, A

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A sequence-based integrated map of chromosome 22 by Tapper, W J, Morton, N E, Dunham, I, Ke, X, Collins, A

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