Gatekeeper role of gastroenterologists and surgeons in recognising and discussing familial colorectal cancer

por Douma, Kirsten F. L., Dekker, Evelien, Smets, Ellen M. A., Aalfs, Cora M.
Publicado 2015

An E-Learning Module to Improve Nongenetic Health Professionals’ Assessment of Colorectal Cancer Genetic Risk: Feasibility Study

por Douma, Kirsten Freya Lea, Aalfs, Cora M, Dekker, Evelien, Tanis, Pieter J, Smets, Ellen M
Publicado 2017

Informing relatives about their hereditary or familial cancer risk: study protocol for a randomized controlled trial

por de Geus, Eveline, Aalfs, Cora M, Verdam, Mathilde GE, de Haes, Hanneke CJM, Smets, Ellen MA
Publicado 2014

Uncertainty related to multigene panel testing for cancer: a qualitative study on counsellors’ and counselees’ views

por Medendorp, Niki M., Hillen, Marij A., Murugesu, Laxsini, Aalfs, Cora M., Stiggelbout, Anne M., Smets, Ellen M. A.
Publicado 2018

A scoping review of practice recommendations for clinicians’ communication of uncertainty

por Medendorp, Niki M., Stiggelbout, Anne M., Aalfs, Cora M., Han, Paul K. J., Smets, Ellen M. A., Hillen, Marij A.
Publicado 2021

Design and Feasibility of an Intervention to Support Cancer Genetic Counselees in Informing their At-Risk Relatives

por de Geus, Eveline, Eijzenga, Willem, Menko, Fred H., Sijmons, Rolf H., de Haes, Hanneke C. J. M., Aalfs, Cora M., Smets, Ellen M. A.
Publicado 2016

Addition of an online, validated family history questionnaire to the Dutch FIT-based screening programme did not improve its diagnostic yield

por Roos, Victorine H., Kallenberg, Frank G. J., van der Vlugt, Manon, Bongers, Evelien J. C., Aalfs, Cora M., Bossuyt, Patrick M. M., Dekker, Evelien
Publicado 2020

Prophylactic total pancreatectomy in individuals at high risk of pancreatic ductal adenocarcinoma (PROPAN): systematic review and shared decision-making programme using decision ta...

por Scholten, Lianne, Latenstein, Anouk EJ, Aalfs, Cora M, Bruno, Marco J, Busch, Olivier R, Bonsing, Bert A., Koerkamp, Bas Groot, Molenaar, I Quintus, Ubbink, Dirk T, van Hooft, Jeanin E, Fockens, Paul, Glas, Jolanda, DeVries, J Hans, Besselink, Marc G
Publicado 2020

Effect of a health literacy training program for surgical oncologists and specialized nurses on disparities in referral to breast cancer genetic testing

por van der Giessen, Jeanine A.M., van Dulmen, Sandra, Velthuizen, Mary E., van den Muijsenbergh, Maria E.T.C., van Engelen, Klaartje, Collée, Margriet, van Dalen, Thijs, Aalfs, Cora M., Hooning, Maartje J., Spreeuwenberg, Peter M.M., Fransen, Mirjam P., Ausems, Margreet G.E.M.
Publicado 2021

‘We don’t know for sure’: discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations

por 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.
Publicado 2019

Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case–control study

por Potjer, Thomas P, van der Stoep, Nienke, Houwing-Duistermaat, Jeanine J, Konings, Ingrid C A W, Aalfs, Cora M, van den Akker, Peter C, Ausems, Margreet G, Dommering, Charlotte J, van der Kolk, Lizet E, Maiburg, Merel C, Spruijt, Liesbeth, Wagner, Anja, Vasen, Hans F A, Hes, Frederik J
Publicado 2015

Factors associated with cancer worries in individuals participating in annual pancreatic cancer surveillance

por Konings, Ingrid C.A.W., Harinck, Femme, Kuenen, Marianne A., Sidharta, Grace N., Kieffer, Jacobien M., Aalfs, Cora M., Poley, Jan-Werner, Smets, Ellen M.A., Wagner, Anja, van Rens, Anja, Vleggaar, Frank P., Ausems, Margreet G.E.M., Fockens, Paul, van Hooft, Jeanin E., Bruno, Marco J., Bleiker, Eveline M.A.
Publicado 2016

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...

por 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.
Publicado 2018

Online decision support for persons having a genetic predisposition to cancer and their partners during reproductive decision‐making

por 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.
Publicado 2018

Reproductive decision-making in the context of hereditary cancer: the effects of an online decision aid on informed decision-making

por 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.
Publicado 2020

Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS): a prospective, observational, multi-center study

por Postema, Floor A. M., Hopman, Saskia M. J., de Borgie, Corianne A. J. M., Aalfs, Cora M., Anninga, Jakob K., Berger, Lieke P. V., Bleeker, Fonnet E., Dommering, Charlotte J., van Eijkelenburg, Natasha K. A., Hammond, Peter, van den Heuvel-Eibrink, Marry M., Hol, Janna A., Kors, Wijnanda A., Letteboer, Tom G. W., Loeffen, Jan L. C. M., Meijer, Lisethe, Olderode-Berends, Maran J. W., Wagner, Anja, Hennekam, Raoul C., Merks, Johannes H. M.
Publicado 2021

Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility

por 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
Publicado 2018

Validation of a clinical screening instrument for tumour predisposition syndromes in patients with childhood cancer (TuPS): protocol for a prospective, observational, multicentre s...

por Postema, Floor A M, Hopman, Saskia M J, de Borgie, Corianne A J M, Hammond, Peter, Hennekam, Raoul C, Merks, Johannes H M, Aalfs, Cora M, Anninga, Jakob K, Berger, Lieke PV, Bleeker, Fonnet E, de Bont, Eveline SJM, de Borgie, Corianne AJM, Dommering, Charlotte J, van Eijkelenburg, Natasha KA, Hammond, Peter, Hennekam, Raoul C, van den Heuvel-Eibrink, Marry M, Hopman, Saskia MJ, Jongmans, Marjolijn CJ, Kors, Wijnanda A, Letteboer, Tom GW, Loeffen, Jan LCM, Merks, Johannes HM, Olderode-Berends, Maran JW, Postema, Floor AM, Wagner, Anja
Publicado 2017

Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing

por Vogelaar, Ingrid P, van der Post, Rachel S, van Krieken, J Han JM, Spruijt, Liesbeth, van Zelst-Stams, Wendy AG, Kets, C Marleen, Lubinski, Jan, Jakubowska, Anna, Teodorczyk, Urszula, Aalfs, Cora M, van Hest, Liselotte P, Pinheiro, Hugo, Oliveira, Carla, Jhangiani, Shalini N, Muzny, Donna M, Gibbs, Richard A, Lupski, James R, de Ligt, Joep, Vissers, Lisenka E L M, Hoischen, Alexander, Gilissen, Christian, van de Vorst, Maartje, Goeman, Jelle J, Schackert, Hans K, Ranzani, Guglielmina N, Molinaro, Valeria, 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, Bjørnevoll, Inga, Høberg-Vetti, Hildegunn, van Kessel, Ad Geurts, Kuiper, Roland P, Ligtenberg, Marjolijn J L, Hoogerbrugge, Nicoline
Publicado 2017

Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers

por Walker, Logan C, Fredericksen, Zachary S, Wang, Xianshu, Tarrell, Robert, Pankratz, Vernon S, Lindor, Noralane M, Beesley, Jonathan, Healey, Sue, Chen, Xiaoqing, Stoppa-Lyonnet, Dominique, Tirapo, Carole, Giraud, Sophie, Mazoyer, Sylvie, Muller, Danièle, Fricker, Jean-Pierre, Delnatte, Capucine, Schmutzler, Rita K, Wappenschmidt, Barbara, Engel, Christoph, Schönbuchner, Ines, Deissler, Helmut, Meindl, Alfons, Hogervorst, Frans B, Verheus, Martijn, Hooning, Maartje J, van den Ouweland, Ans MW, Nelen, Marcel R, Ausems, Margreet GEM, Aalfs, Cora M, van Asperen, Christi J, Devilee, Peter, Gerrits, Monique M, Waisfisz, Quinten, Szabo, Csilla I, Easton, Douglas F, Peock, Susan, Cook, Margaret, Oliver, Clare T, Frost, Debra, Harrington, Patricia, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Chu, Carol, Davidson, Rosemarie, Eccles, Diana, Ong, Kai-Ren, Cook, Jackie, Rebbeck, Tim, Nathanson, Katherine L, Domchek, Susan M, Singer, Christian F, Gschwantler-Kaulich, Daphne, Dressler, Anne-Catharina, Pfeiler, Georg, Godwin, Andrew K, Heikkinen, Tuomas, Nevanlinna, Heli, Agnarsson, Bjarni A, Caligo, Maria Adelaide, Olsson, Håkan, Kristoffersson, Ulf, Liljegren, Annelie, Arver, Brita, Karlsson, Per, Melin, Beatrice, Sinilnikova, Olga M, McGuffog, Lesley, Antoniou, Antonis C, Chenevix-Trench, Georgia, Spurdle, Amanda B, Couch, Fergus J
Publicado 2010