Regulation of DNA-End Resection by hnRNPU-like Proteins Promotes DNA Double-Strand Break Signaling and Repair von Polo, Sophie E., Blackford, Andrew N., Chapman, J. Ross, Baskcomb, Linda, Gravel, Serge, Rusch, Andre, Thomas, Anoushka, Blundred, Rachel, Smith, Philippa, Kzhyshkowska, Julia, Dobner, Thomas, Taylor, A. Malcolm R., Turnell, Andrew S., Stewart, Grant S., Grand, Roger J., Jackson, Stephen P.

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Stratification of Wilms tumor by genetic and epigenetic analysis von Scott, Richard H, Murray, Anne, Baskcomb, Linda, Turnbull, Clare, Loveday, Chey, Al-Saadi, Reem, Williams, Richard, Breatnach, Fin, Gerrard, Mary, Hale, Juliet, Kohler, Janice, Lapunzina, Pablo, Levitt, Gill A, Picton, Sue, Pizer, Barry, Ronghe, Milind D, Traunecker, Heidi, Williams, Denise, Kelsey, Anna, Vujanic, Gordan M, Sebire, Neil J, Grundy, Paul, Stiller, Charles A, Pritchard-Jones, Kathy, Douglas, Jenny, Rahman, Nazneen

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Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor von Scott, Richard H, Douglas, Jenny, Baskcomb, Linda, Huxter, Nikki, Barker, Karen, Hanks, Sandra, Craft, Alan, Gerrard, Mary, Kohler, Janice A, Levitt, Gill A, Picton, Sue, Pizer, Barry, Ronghe, Milind D, Williams, Denise, Cook, Jackie A, Pujol, Pascal, Maher, Eamonn R, Birch, Jillian M, Stiller, Charles A, Pritchard-Jones, Kathy, Rahman, Nazneen

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Regulation of DNA-damage responses and cell-cycle progression by the chromatin remodelling factor CHD4 von Polo, Sophie E, Kaidi, Abderrahmane, Baskcomb, Linda, Galanty, Yaron, Jackson, Stephen P

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PHOX2B analysis in non-syndromic neuroblastoma cases shows novel mutations and genotype-phenotype associations von McConville, Carmel, Reid, Sarah, Baskcomb, Linda, Douglas, Jenny, Rahman, Nazneen

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Proteomic Investigations Reveal a Role for RNA Processing Factor THRAP3 in the DNA Damage Response von Beli, Petra, Lukashchuk, Natalia, Wagner, Sebastian A., Weinert, Brian T., Olsen, Jesper V., Baskcomb, Linda, Mann, Matthias, Jackson, Stephen P., Choudhary, Chunaram

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A genome wide linkage search for breast cancer susceptibility genes von Smith, Paula, McGuffog, Lesley, Easton, Douglas F., Mann, Graham J., Pupo, Gulietta M., Newman, Beth, Chenevix-Trench, Georgia, Szabo, Csilla, Southey, Melissa, Renard, Hélène, Odefrey, Fabrice, Lynch, Henry, Stoppa-Lyonnet, Dominique, Couch, Fergus, Hopper, John L., Giles, Graham G., McCredie, Margaret R. E., Buys, Saundra, Andrulis, Irene, Senie, Ruby, Goldgar, David E., Oldenburg, Rogier, Kroeze-Jansema, Karin, Kraan, Jaennelle, Meijers-Heijboer, Hanne, Klijn, Jan G. M., van Asperen, Christi, van Leeuwen, Inge, Vasen, Hans F. A., Cornelisse, Cees J., Devilee, Peter, Baskcomb, Linda, Seal, Sheila, Barfoot, Rita, Mangion, Jon, Hall, Anita, Edkins, Sarah, Rapley, Elizabeth, Wooster, Richard, Chang-Claude, Jenny, Eccles, Diana, Evans, D. Gareth, Futreal, P. Andrew, Nathanson, Katherine L., Weber, Barbara L., Rahman, Nazneen, Stratton, Michael R.

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Evaluation of RAD50 in familial breast cancer predisposition von Tommiska, Johanna, Seal, Sheila, Renwick, Anthony, Barfoot, Rita, Baskcomb, Linda, Jayatilake, Hiran, Bartkova, Jirina, Tallila, Jonna, Kaare, Milja, Tamminen, Anitta, Heikkilä, Päivi, Evans, D. Gareth, Eccles, Diana, Aittomäki, Kristiina, Blomqvist, Carl, Bartek, Jiri, Stratton, Michael R., Nevanlinna, Heli, Rahman, Nazneen

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Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor von Scott, Richard H, Douglas, Jenny, Baskcomb, Linda, Huxter, Nikki, Barker, Karen, Hanks, Sandra, Craft, Alan, Gerrard, Mary, Kohler, Janice A, Levitt, Gill A, Picton, Sue, Pizer, Barry, Ronghe, Milind D, Williams, Denise, Cook, Jackie A, Pujol, Pascal, Maher, Eamonn R, Birch, Jillian M, Stiller, Charles A, Pritchard-Jones, Kathy, Rahman, Nazneen

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