Universal genetic assessment for women with ovarian cancer not yet achieved: The promises of universal tumor DNA testing

por Witjes, Vera M., Vos, Janet R., Ligtenberg, Marjolijn J.L., Hoogerbrugge, Nicoline
Publicado 2021

Mismatch repair deficiency in early‐onset duodenal, ampullary, and pancreatic carcinomas is a strong indicator for a hereditary defect

por Kryklyva, Valentyna, Brosens, Lodewijk AA, Marijnissen‐van Zanten, Monica AJ, Ligtenberg, Marjolijn JL, Nagtegaal, Iris D
Publicado 2021

Familial gastric cancer: detection of a hereditary cause helps to understand its etiology

por Vogelaar, Ingrid P, van der Post, Rachel S, Bisseling, Tanya M, van Krieken, J Han JM, Ligtenberg, Marjolijn JL, Hoogerbrugge, Nicoline
Publicado 2012

RAS testing in metastatic colorectal cancer: excellent reproducibility amongst 17 Dutch pathology centers

por Boleij, Annemarie, Tops, Bastiaan B.J., Rombout, Paul D.M., Dequeker, Elizabeth M., Ligtenberg, Marjolijn J.L., van Krieken, J. Han
Publicado 2015

High sensitivity of both sequencing and real-time PCR analysis of KRAS mutations in colorectal cancer tissue

por Tol, Jolien, Dijkstra, Jeroen R, Vink-Börger, Marianne E, Nagtegaal, Iris D, Punt, Cornelis JA, Van Krieken, Johan HJM, Ligtenberg, Marjolijn JL
Publicado 2010

Germline MUTYH gene mutations are not frequently found in unselected patients with papillary breast carcinoma

por Boesaard, Ewout P, Vogelaar, Ingrid P, Bult, Peter, Wauters, Carla AP, van Krieken, J Han JM, Ligtenberg, Marjolijn JL, van der Post, Rachel S, Hoogerbrugge, Nicoline
Publicado 2014

Pancreatic acinar cell carcinoma is associated with BRCA2 germline mutations: a case report and literature review

por Kryklyva, Valentyna, Haj Mohammad, Nadia, Morsink, Folkert H.M., Ligtenberg, Marjolijn J.L., Offerhaus, G. Johan A., Nagtegaal, Iris D., de Leng, Wendy W.J., Brosens, Lodewijk A.A.
Publicado 2019

Improving calculation, interpretation and communication of familial colorectal cancer risk: Protocol for a randomized controlled trial

por Dekker, Nicky, Hermens, Rosella PMG, Elwyn, Glyn, van der Weijden, Trudy, Nagengast, Fokko M, van Duijvendijk, Peter, Salemink, Simone, Adang, Eddy, van Krieken, J Han JM, Ligtenberg, Marjolijn JL, Hoogerbrugge, Nicoline
Publicado 2010

Cost-Effectiveness of Parallel Versus Sequential Testing of Genetic Aberrations for Stage IV Non–Small-Cell Lung Cancer in the Netherlands

por Wolff, Henri B., Steeghs, Elisabeth M.P., Mfumbilwa, Zakile A., Groen, Harry J.M., Adang, Eddy M., Willems, Stefan M., Grünberg, Katrien, Schuuring, Ed, Ligtenberg, Marjolijn J.L., Tops, Bastiaan B.J., Coupé, Veerle M.H.
Publicado 2022

Development of a semi-conductor sequencing-based panel for genotyping of colon and lung cancer by the Onconetwork consortium

por Tops, Bastiaan BJ, Normanno, Nicola, Kurth, Henriette, Amato, Eliana, Mafficini, Andrea, Rieber, Nora, Le Corre, Delphine, Rachiglio, Anna Maria, Reiman, Anne, Sheils, Orla, Noppen, Christoph, Lacroix, Ludovic, Cree, Ian A, Scarpa, Aldo, Ligtenberg, Marjolijn JL, Laurent-Puig, Pierre
Publicado 2015

Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation

por Jongmans, Marjolijn C J, van der Burgt, Ineke, Hoogerbrugge, Peter M, Noordam, Kees, Yntema, Helger G, Nillesen, Willy M, Kuiper, Roland P, Ligtenberg, Marjolijn JL, van Kessel, Ad Geurts, van Krieken, J Han JM, Kiemeney, Lambertus ALM, Hoogerbrugge, Nicoline
Publicado 2011

Clinical Validity of Tumor-Informed Circulating Tumor DNA Analysis in Patients Undergoing Surgery of Colorectal Metastases

por Hofste, Lisa S.M., Geerlings, Maartje J., Kamping, Eveline J., Kouwenhoven, Nadine D.H., von Rhein, Daniel, Jansen, Erik A.M., Garms, Linda M., Nagtegaal, Iris D., van der Post, Rachel S., de Wilt, Johannes H.W., Klarenbeek, Bastiaan R., Ligtenberg, Marjolijn J.L.
Publicado 2022

Medullary Pancreatic Carcinoma Due to Somatic POLE Mutation: A Distinctive Pancreatic Carcinoma With Marked Long-Term Survival

por Kryklyva, Valentyna, ter Linden, Esther, Kroeze, Leonie I., de Voer, Richarda M., van der Kolk, B. Marion, Stommel, Martijn W.J., Hermans, John J., Luchini, Claudio, Wood, Laura D., Hruban, Ralph H., Nagtegaal, Iris D., Ligtenberg, Marjolijn J.L., Brosens, Lodewijk A.A.
Publicado 2020

Molecular profiling identifies synchronous endometrial and ovarian cancers as metastatic endometrial cancer with favorable clinical outcome

por Reijnen, Casper, Küsters‐Vandevelde, Heidi V.N., Ligtenberg, Marjolijn J.L., Bulten, Johan, Oosterwegel, Marloes, Snijders, Marc P.L.M., Sweegers, Sanne, de Hullu, Joanne A., Vos, Maria C., van der Wurff, Anneke A.M., van Altena, Anne M., Eijkelenboom, Astrid, Pijnenborg, Johanna M.A.
Publicado 2020

Deleterious Germline BLM Mutations and the Risk for Early-onset Colorectal Cancer

por de Voer, Richarda M., Hahn, Marc-Manuel, Mensenkamp, Arjen R., Hoischen, Alexander, Gilissen, Christian, Henkes, Arjen, Spruijt, Liesbeth, van Zelst-Stams, Wendy A., Marleen Kets, C., Verwiel, Eugene T., Nagtegaal, Iris D., Schackert, Hans K., van Kessel, Ad Geurts, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J.L., Kuiper, Roland P.
Publicado 2015

Novel BRCA1 and BRCA2 Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas

por Weren, Robbert D.A., Mensenkamp, Arjen R., Simons, Michiel, Eijkelenboom, Astrid, Sie, Aisha S., Ouchene, Hicham, van Asseldonk, Monique, Gomez‐Garcia, Encarna B., Blok, Marinus J., de Hullu, Joanne A., Nelen, Marcel R., Hoischen, Alexander, Bulten, Johan, Tops, Bastiaan B.J., Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J.L.
Publicado 2016

A molecular inversion probe-based next-generation sequencing panel to detect germline mutations in Chinese early-onset colorectal cancer patients

por Zhang, Junxiao, Wang, Xiaoyan, de Voer, Richarda M, Hehir-Kwa, Jayne Y., Kamping, Eveline J, Weren, Robbert D.A., Nelen, Marcel, Hoischen, Alexander, Ligtenberg, Marjolijn J.L., Hoogerbrugge, Nicoline, Yang, Xiangling, Yang, Zihuan, Fan, Xinjuan, Wang, Lei, Liu, Huanliang, Wang, Jianping, Kuiper, Roland P., van Kessel, Ad Geurts
Publicado 2017

Integration of next-generation sequencing in clinical diagnostic molecular pathology laboratories for analysis of solid tumours; an expert opinion on behalf of IQN Path ASBL

por Deans, Zandra C, Costa, Jose Luis, Cree, Ian, Dequeker, Els, Edsjö, Anders, Henderson, Shirley, Hummel, Michael, Ligtenberg, Marjolijn JL, Loddo, Marco, Machado, Jose Carlos, Marchetti, Antonio, Marquis, Katherine, Mason, Joanne, Normanno, Nicola, Rouleau, Etienne, Schuuring, Ed, Snelson, Keeda-Marie, Thunnissen, Erik, Tops, Bastiaan, Williams, Gareth, van Krieken, Han, Hall, Jacqueline A
Publicado 2016

An evaluation of the challenges to developing tumor BRCA1 and BRCA2 testing methodologies for clinical practice

por Ellison, Gillian, Ahdesmäki, Miika, Luke, Sally, Waring, Paul M., Wallace, Andrew, Wright, Ronnie, Röthlisberger, Benno, Ludin, Katja, Merkelbach‐Bruse, Sabine, Heydt, Carina, Ligtenberg, Marjolijn J.L., Mensenkamp, Arjen R., de Castro, David Gonzalez, Jones, Thomas, Vivancos, Ana, Kondrashova, Olga, Pauwels, Patrick, Weyn, Christine, Hahnen, Eric, Hauke, Jan, Soong, Richie, Lai, Zhongwu, Dougherty, Brian, Carr, T. Hedley, Johnson, Justin, Mills, John, Barrett, J. Carl
Publicado 2017

Germline deletions in the tumour suppressor gene FOCAD are associated with polyposis and colorectal cancer development

por Weren, Robbert DA, Venkatachalam, Ramprasath, Cazier, Jean‐Baptiste, Farin, Henner F, Kets, C Marleen, de Voer, Richarda M, Vreede, Lilian, Verwiel, Eugène TP, van Asseldonk, Monique, Kamping, Eveline J, Kiemeney, Lambertus A, Neveling, Kornelia, Aben, Katja KH, Carvajal‐Carmona, Luis, Nagtegaal, Iris D, Schackert, Hans K, Clevers, Hans, van de Wetering, Marc, Tomlinson, Ian P, Ligtenberg, Marjolijn JL, Hoogerbrugge, Nicoline, Geurts van Kessel, Ad, Kuiper, Roland P
Publicado 2015