MicroRNAs as possible indicators of drug sensitivity in breast cancer cell lines von Uhr, Katharina, Prager-van der Smissen, Wendy J C, Heine, Anouk A J, Ozturk, Bahar, van Jaarsveld, Marijn T M, Boersma, Antonius W M, Jager, Agnes, Wiemer, Erik A C, Smid, Marcel, Foekens, John A, Martens, John W M

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miRNA expression profiling of 51 human breast cancer cell lines reveals subtype and driver mutation-specific miRNAs von Riaz, Muhammad, van Jaarsveld, Marijn T M, Hollestelle, Antoinette, Prager-van der Smissen, Wendy J C, Heine, Anouk A J, Boersma, Antonius W M, Liu, Jingjing, Helmijr, Jean, Ozturk, Bahar, Smid, Marcel, Wiemer, Erik A, Foekens, John A, Martens, John W M

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Breast cancer genomes from CHEK2 c.1100delC mutation carriers lack somatic TP53 mutations and display a unique structural variant size distribution profile von Smid, Marcel, Schmidt, Marjanka K, Prager-van der Smissen, Wendy J C, Ruigrok-Ritstier, Kirsten, Schreurs, Maartje A C, Cornelissen, Sten, Garcia, Aida Marsal, Broeks, Annegien, Timmermans, A Mieke, Trapman-Jansen, Anita M A C, Collée, J Margriet, Adank, Muriel A, Hooning, Maartje J, Martens, John W M, Hollestelle, Antoinette

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A pipeline for copy number profiling of single circulating tumour cells to assess intrapatient tumour heterogeneity von Deger, Teoman, Mendelaar, Pauline A. J., Kraan, Jaco, Prager‐van der Smissen, Wendy J. C., Vlugt‐Daane, Michelle, Bindels, Eric M. J., Sieuwerts, Anieta M., Sleijfer, Stefan, Wilting, Saskia M., Hollestelle, Antoinette, Martens, John W. M.

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Metabotropic glutamate receptor 1 is associated with unfavorable prognosis in ER-negative and triple-negative breast cancer von Bastiaansen, Anna E. M., Timmermans, A. Mieke, Smid, Marcel, van Deurzen, Carolien H. M., Hulsenboom, Esther S. P., Prager-van der Smissen, Wendy J. C., Foekens, Renée, Trapman-Jansen, Anita M. A. C., Sillevis Smitt, Peter A. E., Luider, Theo M., Martens, John W. M., vanDuijn, Martijn M.

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GATA3 mRNA expression, but not mutation, associates with longer progression-free survival in ER-positive breast cancer patients treated with first-line tamoxifen for recurrent dise... von Liu, Jingjing, Prager – van der Smissen, Wendy J.C, Look, Maxime P, Sieuwerts, Anieta M, Smid, Marcel, Meijer – van Gelder, Marion E, Foekens, John A, Hollestelle, Antoinette, Martens, John W.M

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Functional Homologous Recombination (HR) Screening Shows the Majority of BRCA1/2 -Mutant Breast and Ovarian Cancer Cell Lines Are HR-Proficient von Meijer, Titia G, Martens, John W M, Prager-van der Smissen, Wendy J C, Verkaik, Nicole S, Beaufort, Corine M, van Herk, Stanley, Robert-Finestra, Teresa, Hoogenboezem, Remco M, Ruigrok-Ritstier, Kirsten, Paul, Maarten W, Gribnau, Joost, Bindels, Eric M J, Kanaar, Roland, Jager, Agnes, van Gent, Dik C, Hollestelle, Antoinette

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Expression and Localization of Ferritin-Heavy Chain Predicts Recurrence for Breast Cancer Patients with a BRCA1/2 Mutation von Qu, Shuoying, Timmermans, A Mieke, Heemskerk-Gerritsen, Bernadette A M, Trapman-Jansen, Anita M A C, Broeren-Foekens, Renée, Prager-van der Smissen, Wendy J C, El Hassnaoui, Hoesna, van Tienhoven, Tim, Bes-Stobbe, Claudia K, Westenend, Pieter J, van Deurzen, Carolien H M, Martens, John W M, Hooning, Maartje J, Hollestelle, Antoinette

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CD49f-based selection of circulating tumor cells (CTCs) improves detection across breast cancer subtypes von Mostert, Bianca, Kraan, Jaco, Sieuwerts, Anieta M, van der Spoel, Petra, Bolt-de Vries, Joan, Prager-van der Smissen, Wendy J.C, Smid, Marcel, Timmermans, Annemieke M, Martens, John W.M, Gratama, Jan W, Foekens, John A, Sleijfer, Stefan

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Understanding drugs in breast cancer through drug sensitivity screening von Uhr, Katharina, Prager-van der Smissen, Wendy J. C., Heine, Anouk A. J., Ozturk, Bahar, Smid, Marcel, Göhlmann, Hinrich W. H., Jager, Agnes, Foekens, John A., Martens, John W. M.

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Recurrent HOXB13 mutations in the Dutch population do not associate with increased breast cancer risk von Liu, Jingjing, Prager–van der Smissen, Wendy J. C., Schmidt, Marjanka K., Collée, J. Margriet, Cornelissen, Sten, Lamping, Roy, Nieuwlaat, Anja, Foekens, John A., Hooning, Maartje J., Verhoef, Senno, van den Ouweland, Ans M. W., Hogervorst, Frans B. L., Martens, John W. M., Hollestelle, Antoinette

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The circular RNome of primary breast cancer von Smid, Marcel, Wilting, Saskia M, Uhr, Katharina, Rodríguez-González, F Germán, de Weerd, Vanja, Prager-Van der Smissen, Wendy J C, van der Vlugt-Daane, Michelle, van Galen, Anne, Nik-Zainal, Serena, Butler, Adam, Martin, Sancha, Davies, Helen R, Staaf, Johan, van de Vijver, Marc J, Richardson, Andrea L, MacGrogan, Gaëten, Salgado, Roberto, van den Eynden, Gert G G M, Purdie, Colin A, Thompson, Alastair M, Caldas, Carlos, Span, Paul N, Sweep, Fred C G J, Simpson, Peter T, Lakhani, Sunil R, Van Laere, Steven, Desmedt, Christine, Paradiso, Angelo, Eyfjord, Jorunn, Broeks, Annegien, Vincent-Salomon, Anne, Futreal, Andrew P, Knappskog, Stian, King, Tari, Viari, Alain, Børresen-Dale, Anne-Lise, Stunnenberg, Hendrik G, Stratton, Mike, Foekens, John A, Sieuwerts, Anieta M, Martens, John W M

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Breast cancer genome and transcriptome integration implicates specific mutational signatures with immune cell infiltration von Smid, Marcel, Rodríguez-González, F. Germán, Sieuwerts, Anieta M., Salgado, Roberto, Prager-Van der Smissen, Wendy J. C., Vlugt-Daane, Michelle van der, van Galen, Anne, Nik-Zainal, Serena, Staaf, Johan, Brinkman, Arie B., van de Vijver, Marc J., Richardson, Andrea L., Fatima, Aquila, Berentsen, Kim, Butler, Adam, Martin, Sancha, Davies, Helen R., Debets, Reno, Gelder, Marion E. Meijer-Van, van Deurzen, Carolien H. M., MacGrogan, Gaëtan, Van den Eynden, Gert G. G. M., Purdie, Colin, Thompson, Alastair M., Caldas, Carlos, Span, Paul N., Simpson, Peter T., Lakhani, Sunil R., Van Laere, Steven, Desmedt, Christine, Ringnér, Markus, Tommasi, Stefania, Eyford, Jorunn, Broeks, Annegien, Vincent-Salomon, Anne, Futreal, P. Andrew, Knappskog, Stian, King, Tari, Thomas, Gilles, Viari, Alain, Langerød, Anita, Børresen-Dale, Anne-Lise, Birney, Ewan, Stunnenberg, Hendrik G., Stratton, Mike, Foekens, John A., Martens, John W. M.

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Functional Homologous Recombination Screening Shows the Majority of IBRCA1/2/I-Mutant Breast and Ovarian Cancer Cell Lines Are HR-Proficient von Meijer, Titia G, Martens, John W. M, Prager-van der Smissen, Wendy J. C, Verkaik, Nicole S, Beaufort, Corine M, van Herk, Stanley, Robert-Finestra, Teresa, Hoogenboezem, Remco M, Ruigrok-Ritstier, Kirsten, Paul, Maarten W, Gribnau, Joost, Bindels, Eric M. J, Kanaar, Roland, Jager, Agnes, van Gent, Dik C, Hollestelle, Antoinette

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Expression and Localization of Ferritin-Heavy Chain Predicts Recurrence for Breast Cancer Patients with a IBRCA1/2/I Mutation von Qu, Shuoying, Timmermans, A. Mieke, Heemskerk-Gerritsen, Bernadette A. M, Trapman-Jansen, Anita M. A. C, Broeren-Foekens, Renée, Prager-van der Smissen, Wendy J. C, El Hassnaoui, Hoesna, van Tienhoven, Tim, Bes-Stobbe, Claudia K, Westenend, Pieter J, van Deurzen, Carolien H. M, Martens, John W. M, Hooning, Maartje J, Hollestelle, Antoinette

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A pipeline for copy number profiling of single circulating tumor cells to assess intra-patient tumor heterogeneity von Deger, Teoman, Mendelaar, Pauline A J, Kraan, Jaco, Prager-van der Smissen, Wendy J C, van der Vlugt-Daane, Michelle, Bindels, Eric M J, Sieuwerts, Anieta M, Sleijfer, Stefan, Wilting, Saskia M, Hollestelle, Antoinette, Martens, John W M

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Abstract 2793: Not HOXB13 p.G84E, but p.R217C appears to be associated with increased breast cancer risk in the Dutch population von Liu, Jingjing, Prager-van der Smissen, Wendy JC, Cornelissen, Sten, Collee, Margriet J., van den Ouweland, Ans W.M., Schmidt, Marjanka K., Martens, John W.M., Hollestelle, Antoinette

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Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk von Liu, Jingjing, Prager-van der Smissen, Wendy JC, Collée, J Margriet, Bolla, Manjeet K, Michailidou, Kyriaki, Dennis, Joe, Ahearn, Thomas U, Aittomäki, Kristiina, Anton-Culver, Hoda, Aronson, Kristan J, Augustinsson, Annelie, Auvinen, Päivi, Bermisheva, Marina, Bernstein, Leslie, Bogdanova-Markov, Nadja, Brenner, Hermann, Brucker, Sara Y, Brüning, Thomas, Burwinkel, Barbara, Cai, Qiuyin, Campa, Daniele, Canzian, Federico, Castelao, Jose E, Chang-Claude, Jenny, Chanock, Stephen J, Choi, Ji-Yeob, Christiaens, Melissa, Clarke, Christine L, Couch, Fergus J, Czene, Kamila, Daly, Mary B, Dwek, Miriam, Eliassen, A Heather, Figueroa, Jonine, Flyger, Henrik, Fritschi, Lin, Gapstur, Susan M, García-Closas, Montserrat, García-Sáenz, José A, Goldberg, Mark S, Goldgar, David E, Haiman, Christopher A, Hall, Per, Hart, Steven N, Hillemanns, Peter, Hopper, John L, Hunter, David J, ABCTB Investigators, Ito, Hidemi, John, Esther M, Kang, Daehee, Khusnutdinova, Elza, Kraft, Peter, Kurian, Allison W, Li, Jingmei, Lindblom, Annika, Lophatananon, Artitaya, Lubiński, Jan, Manoukian, Siranoush, Margolin, Sara, Mariapun, Shivaani, Meindl, Alfons, Menon, Usha, Muir, Kenneth, Mulligan, Anna Marie, Neuhausen, Susan L, Olsson, Håkan, Park, Sue K, Peto, Julian, Plaseska-Karanfilska, Dijana, Presneau, Nadege, Rau-Murthy, Rohini, Rennert, Gad, Ruebner, Matthias, Schmutzler, Rita K, Schneeweiss, Andreas, Scott, Christopher, Shen, Chen-Yang, Shu, Xiao-Ou, Simard, Jacques, Sohn, Christof, Southey, Melissa C, Spinelli, John J, Tamimi, Rulla M, Tapper, William J, Teo, Soo H, Terry, Mary Beth, Torres, Diana, Truong, Thérèse, Untch, Michael, van Asperen, Christi J, Wolk, Alicja, Yamaji, Taiki, Zheng, Wei, Ziogas, Argyrios, Torres-Mejía, Gabriela, Dörk, Thilo, Swerdlow, Anthony J, Martens, John WM, Hollestelle, Antoinette

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Additional file 3 of Breast cancer genomes from CHEK2 c.1100delC mutation carriers lack somatic TP53 mutations and display a unique structural variant size distribution profile von Smid, Marcel, Schmidt, Marjanka K., Prager-van der Smissen, Wendy J. C., Ruigrok-Ritstier, Kirsten, Schreurs, Maartje A. C., Cornelissen, Sten, Garcia, Aida Marsal, Broeks, Annegien, Timmermans, A. Mieke, Trapman-Jansen, Anita M. A. C., Collée, J. Margriet, Adank, Muriel A., Hooning, Maartje J., Martens, John W. M., Hollestelle, Antoinette

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Additional file 1 of Breast cancer genomes from CHEK2 c.1100delC mutation carriers lack somatic TP53 mutations and display a unique structural variant size distribution profile von Smid, Marcel, Schmidt, Marjanka K., Prager-van der Smissen, Wendy J. C., Ruigrok-Ritstier, Kirsten, Schreurs, Maartje A. C., Cornelissen, Sten, Garcia, Aida Marsal, Broeks, Annegien, Timmermans, A. Mieke, Trapman-Jansen, Anita M. A. C., Collée, J. Margriet, Adank, Muriel A., Hooning, Maartje J., Martens, John W. M., Hollestelle, Antoinette

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