BRCA1 -Mutated Estrogen Receptor-Positive Breast Cancer Shows BRCAness, Suggesting Sensitivity to Drugs Targeting Homologous Recombination Deficiency
Lips, Esther H, Debipersad, Rashmie D, Scheerman, Caroline E, Mulder, Lennart, Sonke, Gabe S, van der Kolk, Lizet E, Wesseling, Jelle, Hogervorst, Frans B L, Nederlof, Petra M
Published in Clinical cancer research (01.03.2017)
Published in Clinical cancer research (01.03.2017)
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Clinical Impact of Prospective Whole Genome Sequencing in Sarcoma Patients
Schipper, Luuk J, Monkhorst, Kim, Samsom, Kris G, Bosch, Linda J W, Snaebjornsson, Petur, van Boven, Hester, Roepman, Paul, van der Kolk, Lizet E, van Houdt, Winan J, van der Graaf, Winette T A, Meijer, Gerrit A, Voest, Emile E
Published in Cancers (16.01.2022)
Published in Cancers (16.01.2022)
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The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice
Menko, Fred H, ter Stege, Jacqueline A, van der Kolk, Lizet E, Jeanson, Kiki N, Schats, Winnie, Moha, Daoud Ait, Bleiker, Eveline M A
Published in Familial cancer (01.01.2019)
Published in Familial cancer (01.01.2019)
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Outcomes of screening gastroscopy in first-degree relatives of patients fulfilling hereditary diffuse gastric cancer criteria
van der Post, Rachel S., MD, van Dieren, Jolanda, MD, PhD, Grelack, Anna, MD, Hoogerbrugge, Nicoline, MD, PhD, van der Kolk, Lizet E., MD, PhD, Snaebjornsson, Petur, MD, PhD, Lansdorp-Vogelaar, Iris, PhD, van Krieken, J. Han, MD, PhD, Bisseling, Tanya M., MD, PhD, Cats, Annemieke, MD, PhD
Published in Gastrointestinal endoscopy (01.02.2018)
Published in Gastrointestinal endoscopy (01.02.2018)
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Feasibility of whole‐genome sequencing‐based tumor diagnostics in routine pathology practice
Samsom, Kris G, Schipper, Luuk J, Roepman, Paul, Bosch, Linda JW, Lalezari, Ferry, Klompenhouwer, Elisabeth G, Langen, Adrianus J, Buffart, Tineke E, Riethorst, Immy, Schoenmaker, Lieke, Schout, Daoin, Noort, Vincent, Berg, Jose G, Bruijn, Ewart, Hoeven, Jacobus JM, Snellenberg, Hans, Kolk, Lizet E, Cuppen, Edwin, Voest, Emile E, Meijer, Gerrit A, Monkhorst, Kim
Published in The Journal of pathology (01.10.2022)
Published in The Journal of pathology (01.10.2022)
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First estimates of diffuse gastric cancer risks for carriers of CTNNA1 germline pathogenic variants
Coudert, Marie, Drouet, Youenn, Delhomelle, Hélène, Svrcek, Magali, Benusiglio, Patrick R, Coulet, Florence, Clark, Dana Farengo, Katona, Bryson W, van Hest, Liselotte P, van der Kolk, Lizet E, Cats, Annemieke, van Dieren, Jolanda M, Nehoray, Bita, Slavin, Thomas, Spier, Isabel, Hüneburg, Robert, Lobo, Silvana, Oliveira, Carla, Boussemart, Lise, Masson, Laure, Chiesa, Jean, Schwartz, Mathias, Buecher, Bruno, Golmard, Lisa, Bouvier, Anne-Marie, Bonadona, Valérie, Stoppa-lyonnet, Dominique, Lasset, Christine, Colas, Chrystelle
Published in Journal of medical genetics (01.12.2022)
Published in Journal of medical genetics (01.12.2022)
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The uptake of predictive DNA testing in 40 families with a pathogenic BRCA1/BRCA2 variant. An evaluation of the proband-mediated procedure
Menko, Fred H, Jeanson, Kiki N, Bleiker, Eveline M A, van Tiggelen, Carla W M, Hogervorst, Frans B L, Ter Stege, Jacqueline A, Ait Moha, Daoud, van der Kolk, Lizet E
Published in European journal of human genetics : EJHG (01.08.2020)
Published in European journal of human genetics : EJHG (01.08.2020)
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Genotype-phenotype correlations for pancreatic cancer risk in Dutch melanoma families with pathogenic CDKN2A variants
Overbeek, Kasper A, Rodríguez-Girondo, Mar DM, Wagner, Anja, van der Stoep, Nienke, van den Akker, Peter C, Oosterwijk, Jan C, van Os, Theo A, van der Kolk, Lizet E, Vasen, Hans F A, Hes, Frederik J, Cahen, Djuna L, Bruno, Marco J, Potjer, Thomas P
Published in Journal of medical genetics (01.04.2021)
Published in Journal of medical genetics (01.04.2021)
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Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility
Weren, Robbert D A, van der Post, Rachel S, Vogelaar, Ingrid P, van Krieken, J Han, Spruijt, Liesbeth, Lubinski, Jan, Jakubowska, Anna, Teodorczyk, Urszula, Aalfs, Cora M, van Hest, Liselotte P, Oliveira, Carla, Kamping, Eveline J, Schackert, Hans K, Ranzani, Guglielmina N, Gómez García, Encarna B, Hes, Frederik J, Holinski-Feder, Elke, Genuardi, Maurizio, Ausems, Margreet G E M, Sijmons, Rolf H, Wagner, Anja, van der Kolk, Lizet E, Cats, Annemieke, Bjørnevoll, Inga, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J L
Published in Journal of medical genetics (01.10.2018)
Published in Journal of medical genetics (01.10.2018)
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Does a proactive procedure lead to a higher uptake of predictive testing in families with a pathogenic BRCA1/BRCA2 variant? A family cancer clinic evaluation
Menko, Fred H., Velden, Sophie L., Griffioen, Diana N., Ait Moha, Daoud, Jeanson, Kiki N., Hogervorst, Frans B. L., Giesbertz, Noor A. A., Bleiker, Eveline M. A., Kolk, Lizet E.
Published in Journal of genetic counseling (01.06.2024)
Published in Journal of genetic counseling (01.06.2024)
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‘We don’t know for sure’: discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations
Medendorp, Niki M., Hillen, Marij A., van Maarschalkerweerd, Pomme E. A., Aalfs, Cora M., Ausems, Margreet G. E. M., Verhoef, Senno, van der Kolk, Lizet E., Berger, Lieke P. V., Wevers, Marijke R., Wagner, Anja, Caanen, Barbara A. H., Stiggelbout, Anne M., Smets, Ellen M. A.
Published in Familial cancer (01.01.2020)
Published in Familial cancer (01.01.2020)
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Study protocol: Whole genome sequencing Implementation in standard Diagnostics for Every cancer patient (WIDE)
Samsom, Kris G, Bosch, Linda J W, Schipper, Luuk J, Roepman, Paul, de Bruijn, Ewart, Hoes, Louisa R, Riethorst, Immy, Schoenmaker, Lieke, van der Kolk, Lizet E, Retèl, Valesca P, Frederix, Geert W J, Buffart, Tineke E, van der Hoeven, Jacobus J M, Voest, Emile E, Cuppen, Edwin, Monkhorst, Kim, Meijer, Gerrit A
Published in BMC medical genomics (10.11.2020)
Published in BMC medical genomics (10.11.2020)
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Effect of routine assessment of specific psychosocial problems on personalized communication, counselors’ awareness, and distress levels in cancer genetic counseling practice: a randomized controlled trial
Eijzenga, Willem, Aaronson, Neil K, Hahn, Daniela E E, Sidharta, Grace N, van der Kolk, Lizet E, Velthuizen, Mary E, Ausems, Margreet G E M, Bleiker, Eveline M A
Published in Journal of clinical oncology (20.09.2014)
Published in Journal of clinical oncology (20.09.2014)
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Reproductive decision-making in the context of hereditary cancer: the effects of an online decision aid on informed decision-making
Reumkens, Kelly, Tummers, Marly H. E., Severijns, Yil, Gietel-Habets, Joyce J. G., van Kuijk, Sander M. J., Aalfs, Cora M., van Asperen, Christi J., Ausems, Margreet G. E. M., Collée, Margriet, Dommering, Charlotte J., Kets, Marleen, van der Kolk, Lizet E., Oosterwijk, Jan C., Tjan-Heijnen, Vivianne C. G., van der Weijden, Trudy, de Die-Smulders, Christine E. M., van Osch, Liesbeth A. D. M.
Published in Journal of community genetics (01.01.2021)
Published in Journal of community genetics (01.01.2021)
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The development of an online decision aid to support persons having a genetic predisposition to cancer and their partners during reproductive decision-making: a usability and pilot study
Reumkens, Kelly, Tummers, Marly H. E., Gietel-Habets, Joyce J. G., van Kuijk, Sander M. J., Aalfs, Cora M., van Asperen, Christi J., Ausems, Margreet G. E. M., Collée, Margriet, Dommering, Charlotte J., Kets, C. Marleen, van der Kolk, Lizet E., Oosterwijk, Jan C., Tjan-Heijnen, Vivianne C. G., van der Weijden, Trudy, de Die-Smulders, Christine E. M., van Osch, Liesbeth A. D. M.
Published in Familial cancer (01.01.2019)
Published in Familial cancer (01.01.2019)
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Online decision support for persons having a genetic predisposition to cancer and their partners during reproductive decision‐making
Reumkens, Kelly, Tummers, Marly H. E., Gietel‐Habets, Joyce J. G., van Kuijk, Sander M. J., Aalfs, Cora M., van Asperen, Christi J., Ausems, Margreet G. E. M., Collée, Margriet, Dommering, Charlotte J., Kets, C. Marleen, van der Kolk, Lizet E., Oosterwijk, Jan C., Tjan‐Heijnen, Vivianne C. G., van der Weijden, Trudy, de Die‐Smulders, Christine E. M., van Osch, Liesbeth A. D. M.
Published in Journal of genetic counseling (01.06.2019)
Published in Journal of genetic counseling (01.06.2019)
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SNP association study in PMS2-associated Lynch syndrome
ten Broeke, Sanne W., Elsayed, Fadwa A., Pagan, Lisa, Olderode-Berends, Maran J. W., Garcia, Encarna Gomez, Gille, Hans J. P., van Hest, Liselot P., Letteboer, Tom G. W., van der Kolk, Lizet E., Mensenkamp, Arjen R., van Os, Theo A., Spruijt, Liesbeth, Redeker, Bert J. W., Suerink, Manon, Vos, Yvonne J., Wagner, Anja, Wijnen, Juul T., Steyerberg, E. W., Tops, Carli M. J., van Wezel, Tom, Nielsen, Maartje
Published in Familial cancer (01.10.2018)
Published in Familial cancer (01.10.2018)
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Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK21100delC Carriers
Schmidt, Marjanka K, Hogervorst, Frans, van Hien, Richard, Cornelissen, Sten, Broeks, Annegien, Adank, Muriel A, Meijers, Hanne, Waisfisz, Quinten, Hollestelle, Antoinette, Schutte, Mieke, van den Ouweland, Ans, Hooning, Maartje, Andrulis, Irene L, Anton-Culver, Hoda, Antonenkova, Natalia N, Antoniou, Antonis C, Arndt, Volker, Bermisheva, Marina, Bogdanova, Natalia V, Bolla, Manjeet K, Brauch, Hiltrud, Brenner, Hermann, Brüning, Thomas, Burwinkel, Barbara, Chang-Claude, Jenny, Chenevix-Trench, Georgia, Couch, Fergus J, Cox, Angela, Cross, Simon S, Czene, Kamila, Dunning, Alison M, Fasching, Peter A, Figueroa, Jonine, Fletcher, Olivia, Flyger, Henrik, Galle, Eva, García-Closas, Montserrat, Giles, Graham G, Haeberle, Lothar, Hall, Per, Hillemanns, Peter, Hopper, John L, Jakubowska, Anna, John, Esther M, Jones, Michael, Khusnutdinova, Elza, Knight, Julia A, Kosma, Veli-Matti, Kristensen, Vessela, Lee, Andrew, Lindblom, Annika, Lubinski, Jan, Mannermaa, Arto, Margolin, Sara, Meindl, Alfons, Milne, Roger L, Muranen, Taru A, Newcomb, Polly A, Offit, Kenneth, Park-Simon, Tjoung-Won, Peto, Julian, Pharoah, Paul D P, Robson, Mark, Rudolph, Anja, Sawyer, Elinor J, Schmutzler, Rita K, Seynaeve, Caroline, Soens, Julie, Southey, Melissa C, Spurdle, Amanda B, Surowy, Harald, Swerdlow, Anthony, Tollenaar, Rob A E M, Tomlinson, Ian, Trentham-Dietz, Amy, Vachon, Celine, Wang, Qin, Whittemore, Alice S, Ziogas, Argyrios, van der Kolk, Lizet, Nevanlinna, Heli, Dörk, Thilo, Bojesen, Stig, Easton, Douglas F
Published in Journal of clinical oncology (10.08.2016)
Published in Journal of clinical oncology (10.08.2016)
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Gastroscopic surveillance with targeted biopsies compared with random biopsies in CDH1 mutation carriers
van Dieren, Jolanda M, Kodach, Liudmila L, den Hartog, Peggy, van der Kolk, Lizet E, Sikorska, Karolina, van Velthuysen, Marie-Louise F, van Sandick, Johanna W, Koemans, Willem J, Snaebjornsson, Petur, Cats, Annemieke
Published in Endoscopy (01.10.2020)
Published in Endoscopy (01.10.2020)
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Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk
Wilcox, Naomi, Dumont, Martine, González-Neira, Anna, Carvalho, Sara, Joly Beauparlant, Charles, Crotti, Marco, Luccarini, Craig, Soucy, Penny, Dubois, Stéphane, Nuñez-Torres, Rocio, Pita, Guillermo, Gardner, Eugene J., Dennis, Joe, Alonso, M. Rosario, Álvarez, Nuria, Baynes, Caroline, Collin-Deschesnes, Annie Claude, Desjardins, Sylvie, Becher, Heiko, Behrens, Sabine, Bolla, Manjeet K., Castelao, Jose E., Chang-Claude, Jenny, Cornelissen, Sten, Dörk, Thilo, Engel, Christoph, Gago-Dominguez, Manuela, Guénel, Pascal, Hadjisavvas, Andreas, Hahnen, Eric, Hartman, Mikael, Herráez, Belén, Jung, Audrey, Keeman, Renske, Kiechle, Marion, Li, Jingmei, Loizidou, Maria A., Lush, Michael, Michailidou, Kyriaki, Panayiotidis, Mihalis I., Sim, Xueling, Teo, Soo Hwang, Tyrer, Jonathan P., van der Kolk, Lizet E., Wahlström, Cecilia, Wang, Qin, Perry, John R. B., Benitez, Javier, Schmidt, Marjanka K., Schmutzler, Rita K., Pharoah, Paul D. P., Droit, Arnaud, Dunning, Alison M., Kvist, Anders, Devilee, Peter, Easton, Douglas F., Simard, Jacques
Published in Nature genetics (01.09.2023)
Published in Nature genetics (01.09.2023)
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