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 2012-12-01

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

External Quality Assessment Unravels Interlaboratory Differences in Quality of RAS Testing for Anti-EGFR Therapy in Colorectal Cancer

por Tack, Véronique, Ligtenberg, Marjolijn J.L., Tembuyser, Lien, Normanno, Nicola, Vander Borght, Sara, Han van Krieken, J., Dequeker, Elisabeth M.C.
Publicado en Oncologist (2015)

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 en Oncotarget (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 en Hered Cancer Clin Pract (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 en Cancer Biol Ther (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

Lynch Syndrome-Associated Extracolonic Tumors Are Rare in Two Extended Families With the Same EPCAM Deletion

por Lynch, Henry T., Riegert-Johnson, Douglas L., Snyder, Carrie, Lynch, Jane F., Hagenkord, Jill, Boland, C. Richard, Rhees, Jennifer, Thibodeau, Stephen N., Boardman, Lisa A., Davies, Janine, Kuiper, Roland P., Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J.L.
Publicado 2011

Candidate colorectal cancer predisposing gene variants in Chinese early-onset and familial cases

por Zhang, Jun-Xiao, Fu, Lei, de Voer, Richarda M, Hahn, Marc-Manuel, Jin, Peng, Lv, Chen-Xi, Verwiel, Eugène TP, Ligtenberg, Marjolijn JL, Hoogerbrugge, Nicoline, Kuiper, Roland P, Sheng, Jian-Qiu, Geurts van Kessel, Ad
Publicado en World J Gastroenterol (2015)

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 en BMC Cancer (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

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 en Pancreas (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 en Int J Cancer (2020)

External Quality Assessment for KRAS Testing Is Needed: Setup of a European Program and Report of the First Joined Regional Quality Assessment Rounds

por Bellon, Ellen, Ligtenberg, Marjolijn J.L., Tejpar, Sabine, Cox, Karen, de Hertogh, Gert, de Stricker, Karin, Edsjö, Anders, Gorgoulis, Vassilis, Höfler, Gerald, Jung, Andreas, Kotsinas, Athanassios, Laurent-Puig, Pierre, López-Ríos, Fernando, Hansen, Tine Plato, Rouleau, Etienne, Vandenberghe, Peter, van Krieken, Johan J.M., Dequeker, Elisabeth
Publicado 2011

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 en Sci Rep (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 en Hum Mutat (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 en Oncotarget (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 en Virchows Arch (2016)

Revertant Somatic Mosaicism by Mitotic Recombination in Dyskeratosis Congenita

por Jongmans, Marjolijn C.J., Verwiel, Eugene T.P., Heijdra, Yvonne, Vulliamy, Tom, Kamping, Eveline J., Hehir-Kwa, Jayne Y., Bongers, Ernie M.H.F., Pfundt, Rolph, van Emst, Liesbeth, van Leeuwen, Frank N., van Gassen, Koen L.I., Geurts van Kessel, Ad, Dokal, Inderjeet, Hoogerbrugge, Nicoline, Ligtenberg, Marjolijn J.L., Kuiper, Roland P.
Publicado 2012