Elucidating the Underlying Functional Mechanisms of Breast Cancer Susceptibility Through Post-GWAS Analyses

Autor Rivandi, Mahdi, Martens, John W. M., Hollestelle, Antoinette
Vydáno v Front Genet (2018)

Low-risk susceptibility alleles in 40 human breast cancer cell lines

Autor Riaz, Muhammad, Elstrodt, Fons, Hollestelle, Antoinette, Dehghan, Abbas, Klijn, Jan GM, Schutte, Mieke
Vydáno 2009

Analysis of TP53 Mutation Status in Human Cancer Cell Lines: A Reassessment

Autor Leroy, Bernard, Girard, Luc, Hollestelle, Antoinette, Minna, John D., Gazdar, Adi F., Soussi, Thierry
Vydáno v Hum Mutat (2014)

The 29.5 kb APOBEC3B Deletion Polymorphism Is Not Associated with Clinical Outcome of Breast Cancer

Autor Liu, Jingjing, Sieuwerts, Anieta M., Look, Maxime P., van der Vlugt-Daane, Michelle, Meijer-van Gelder, Marion E., Foekens, John A., Hollestelle, Antoinette, Martens, John W. M.
Vydáno v PLoS One (2016)

Rare BRCA1 haplotypes including 3′UTR SNPs associated with breast cancer risk

Autor Pelletier, Cory, Speed, William C, Paranjape, Trupti, Keane, Katie, Blitzblau, Rachel, Hollestelle, Antoinette, Safavi, Kyan, van den Ouweland, Ans, Zelterman, Daniel, Slack, Frank J, Kidd, Kenneth K, Weidhaas, Joanne B
Vydáno 2011

Exon Expression Arrays as a Tool to Identify New Cancer Genes

Autor Schutte, Mieke, Elstrodt, Fons, Bralten, Linda B. C., Nagel, Jord H. A., Duijm, Elza, Hollestelle, Antoinette, Vuerhard, Maartje J., Wasielewski, Marijke, Peeters, Justine K., van der Spek, Peter, Sillevis Smitt, Peter A., French, Pim J.
Vydáno 2008

miRNA expression profiling of 51 human breast cancer cell lines reveals subtype and driver mutation-specific miRNAs

Autor Riaz, Muhammad, van Jaarsveld, Marijn TM, Hollestelle, Antoinette, Prager-van der Smissen, Wendy JC, Heine, Anouk AJ, Boersma, Antonius WM, Liu, Jingjing, Helmijr, Jean, Ozturk, Bahar, Smid, Marcel, Wiemer, Erik A, Foekens, John A, Martens, John WM
Vydáno 2013

Prevalence of the variant allele rs61764370 T>G in the 3′UTR of KRAS among Dutch BRCA1, BRCA2 and non-BRCA1/BRCA2 breast cancer families

Autor Hollestelle, Antoinette, Pelletier, Cory, Hooning, Maartje, Crepin, Ellen, Schutte, Mieke, Look, Maxime, Collee, J. Margriet, Nieuwlaat, Anja, Dorssers, Lambert C. J., Seynaeve, Caroline, Aulchenko, Yurii S., Martens, John W. M., van den Ouweland, Ans M. W., Weidhaas, Joanne B.
Vydáno 2010

Sensitivity to systemic therapy for metastatic breast cancer in CHEK2 1100delC mutation carriers

Autor Kriege, Mieke, Jager, Agnes, Hollestelle, Antoinette, Berns, Els M. J. J., Blom, Jannet, Meijer-van Gelder, Marion E., Sieuwerts, Anieta M., van den Ouweland, Ans, Collée, J. Margriet, Kroep, Judith R., Martens, John W. M., Hooning, Maartje J., Seynaeve, Caroline
Vydáno v J Cancer Res Clin Oncol (2015)

A 3′-untranslated region KRAS variant and triple-negative breast cancer: a case-control and genetic analysis

Autor Paranjape, Trupti, Heneghan, Helen, Lindner, Robert, Keane, Florence K, Hoffman, Aaron, Hollestelle, Antoinette, Dorairaj, Jemima, Geyda, Kimberly, Pelletier, Cory, Nallur, Sunitha, Martens, John W M, Hooning, Maartje J, Kerin, Michael, Zelterman, Daniel, Zhu, Yong, Tuck, David, Harris, Lyndsay, Miller, Nicola, Slack, Frank, Weidhaas, Joanne
Vydáno 2011

Recurrent HOXB13 mutations in the Dutch population do not associate with increased breast cancer risk

Autor 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
Vydáno v Sci Rep (2016)

The Prevalence of CD146 Expression in Breast Cancer Subtypes and Its Relation to Outcome

Autor de Kruijff, Ingeborg E., Timmermans, Anna M., den Bakker, Michael A., Trapman-Jansen, Anita M.A.C., Foekens, Renée, Meijer-Van Gelder, Marion E., Oomen-de Hoop, Esther, Smid, Marcel, Hollestelle, Antoinette, van Deurzen, Carolien H.M., Foekens, John A., Martens, John W.M., Sleijfer, Stefan
Vydáno v Cancers (Basel) (2018)

CHEK2*1100delC homozygosity in the Netherlands—prevalence and risk of breast and lung cancer

Autor Huijts, Petra EA, Hollestelle, Antoinette, Balliu, Brunilda, Houwing-Duistermaat, Jeanine J, Meijers, Caro M, Blom, Jannet C, Ozturk, Bahar, Krol-Warmerdam, Elly MM, Wijnen, Juul, Berns, Els MJJ, Martens, John WM, Seynaeve, Caroline, Kiemeney, Lambertus A, van der Heijden, Henricus F, Tollenaar, Rob AEM, Devilee, Peter, van Asperen, Christi J
Vydáno 2014

The CHEK2 1100delC Mutation Identifies Families with a Hereditary Breast and Colorectal Cancer Phenotype

Autor Meijers-Heijboer, Hanne, Wijnen, Juul, Vasen, Hans, Wasielewski, Marijke, Wagner, Anja, Hollestelle, Antoinette, Elstrodt, Fons, van den Bos, Renate, de Snoo, Anja, Tjon A Fat, Grace, Brekelmans, Cecile, Jagmohan, Shantie, Franken, Patrick, Verkuijlen, Paul, van den Ouweland, Ans, Chapman, Pamela, Tops, Carli, Möslein, Gabriela, Burn, John, Lynch, Henry, Klijn, Jan, Fodde, Riccardo, Schutte, Mieke
Vydáno 2003

A genome-wide association scan on estrogen receptor-negative breast cancer

Autor Li, Jingmei, Humphreys, Keith, Darabi, Hatef, Rosin, Gustaf, Hannelius, Ulf, Heikkinen, Tuomas, Aittomäki, Kristiina, Blomqvist, Carl, Pharoah, Paul DP, Dunning, Alison M, Ahmed, Shahana, Hooning, Maartje J, Hollestelle, Antoinette, Oldenburg, Rogier A, Alfredsson, Lars, Palotie, Aarno, Peltonen-Palotie, Leena, Irwanto, Astrid, Low, Hui Qi, Teoh, Garrett HK, Thalamuthu, Anbupalam, Kere, Juha, D'Amato, Mauro, Easton, Douglas F, Nevanlinna, Heli, Liu, Jianjun, Czene, Kamila, Hall, Per
Vydáno 2010

Genetically Predicted Levels of DNA Methylation Biomarkers and Breast Cancer Risk: Data From 228 951 Women of European Descent

Autor Yang, Yaohua, Wu, Lang, Shu, Xiao-Ou, Cai, Qiuyin, Shu, Xiang, Li, Bingshan, Guo, Xingyi, Ye, Fei, Michailidou, Kyriaki, Bolla, Manjeet K, Wang, Qin, Dennis, Joe, Andrulis, Irene L, Brenner, Hermann, Chenevix-Trench, Georgia, Campa, Daniele, Castelao, Jose E, Gago-Dominguez, Manuela, Dörk, Thilo, Hollestelle, Antoinette, Lophatananon, Artitaya, Muir, Kenneth, Neuhausen, Susan L, Olsson, Håkan, Sandler, Dale P, Simard, Jacques, Kraft, Peter, Pharoah, Paul D P, Easton, Douglas F, Zheng, Wei, Long, Jirong
Vydáno v J Natl Cancer Inst (2019)

Etiology of hormone receptor positive breast cancer differs by levels of histologic grade and proliferation

Autor Abubakar, Mustapha, Chang‐Claude, Jenny, Ali, H. Raza, Chatterjee, Nilanjan, Coulson, Penny, Daley, Frances, Blows, Fiona, Benitez, Javier, Milne, Roger L., Brenner, Hermann, Stegmaier, Christa, Mannermaa, Arto, Rudolph, Anja, Sinn, Peter, Couch, Fergus J., Devilee, Peter, Tollenaar, Rob A.E.M., Seynaeve, Caroline, Figueroa, Jonine, Lissowska, Jolanta, Hewitt, Stephen, Hooning, Maartje J., Hollestelle, Antoinette, Foekens, Renée, Koppert, Linetta B., Investigators, kConFab, Bolla, Manjeet K., Wang, Qin, Jones, Michael E., Schoemaker, Minouk J., Keeman, Renske, Easton, Douglas F., Swerdlow, Anthony J., Sherman, Mark E., Schmidt, Marjanka K., Pharoah, Paul D., Garcia‐Closas, Montserrat
Vydáno v Int J Cancer (2018)

Common Susceptibility Loci for Male Breast Cancer

Autor Maguire, Sarah, Perraki, Eleni, Tomczyk, Katarzyna, Jones, Michael E, Fletcher, Olivia, Pugh, Matthew, Winter, Timothy, Thompson, Kyle, Cooke, Rosie, Trainer, Alison, James, Paul, Bojesen, Stig, Flyger, Henrik, Nevanlinna, Heli, Mattson, Johanna, Friedman, Eitan, Laitman, Yael, Palli, Domenico, Masala, Giovanna, Zanna, Ines, Ottini, Laura, Silvestri, Valentina, Hollestelle, Antoinette, Hooning, Maartje J, Novaković, Srdjan, Krajc, Mateja, Gago-Dominguez, Manuela, Castelao, Jose Esteban, Olsson, Hakan, Hedenfalk, Ingrid, Saloustros, Emmanouil, Georgoulias, Vasilios, Easton, Douglas F, Pharoah, Paul, Dunning, Alison M, Bishop, D Timothy, Neuhausen, Susan L, Steele, Linda, Ashworth, Alan, Garcia Closas, Montserrat, Houlston, Richard, Swerdlow, Anthony, Orr, Nick
Vydáno v J Natl Cancer Inst (2020)

Genome-wide association study identifies a novel variant in RAD51B associated with male breast cancer risk

Autor Orr, Nick, Lemnrau, Alina, Cooke, Rosie, Fletcher, Olivia, Tomczyk, Katarzyna, Jones, Michael, Johnson, Nichola, Lord, Christopher J, Mitsopoulos, Costas, Zvelebil, Marketa, McDade, Simon S, Buck, Gemma, Blancher, Christine, Consortium, KConFab, Trainer, Alison H, James, Paul A, Bojesen, Stig E, Bokmand, Susanne, Nevanlinna, Heli, Mattson, Johanna, Friedman, Eitan, Laitman, Yael, Palli, Domenico, Masala, Giovanna, Zanna, Ines, Ottini, Laura, Giannini, Giuseppe, Hollestelle, Antoinette, van den Ouweland, Ans M.W., Novaković, Srdjan, Krajc, Mateja, Gago-Dominguez, Manuela, Castelao, Jose Esteban, Olsson, Håkan, Hedenfalk, Ingrid, Easton, Douglas F, Pharoah, Paul DP, Dunning, Alison M, Bishop, D Timothy, Neuhausen, Susan L, Steele, Linda, Houlston, Richard S, Garcia-Closas, Montserrat, Ashworth, Alan, Swerdlow, Anthony J
Vydáno 2012

A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients

Autor Seibold, Petra, Schmezer, Peter, Behrens, Sabine, Michailidou, Kyriaki, Bolla, Manjeet K., Wang, Qin, Flesch-Janys, Dieter, Nevanlinna, Heli, Fagerholm, Rainer, Aittomäki, Kristiina, Blomqvist, Carl, Margolin, Sara, Mannermaa, Arto, Kataja, Vesa, Kosma, Veli-Matti, Hartikainen, Jaana M., Lambrechts, Diether, Wildiers, Hans, Kristensen, Vessela, Alnæs, Grethe Grenaker, Nord, Silje, Borresen-Dale, Anne-Lise, Hooning, Maartje J., Hollestelle, Antoinette, Jager, Agnes, Seynaeve, Caroline, Li, Jingmei, Liu, Jianjun, Humphreys, Keith, Dunning, Alison M., Rhenius, Valerie, Shah, Mitul, Kabisch, Maria, Torres, Diana, Ulmer, Hans-Ulrich, Hamann, Ute, Schildkraut, Joellen M., Purrington, Kristen S., Couch, Fergus J., Hall, Per, Pharoah, Paul, Easton, Doug F., Schmidt, Marjanka K., Chang-Claude, Jenny, Popanda, Odilia
Vydáno v BMC Cancer (2015)