Functional Polymorphisms Associated with Disease-Free Survival in Resected Carcinoma of the Esophagus

por Boonstra, Jurjen J., van Marion, Ronald, Tilanus, Hugo W., Dinjens, Winand N. M.
Publicado 2010

Mucinous carcinoid of the ovary: report of a case with metastasis in the contralateral ovary after ten years

por Buis, Christien C.M, van Doorn, Helena C, Dinjens, Winand N.M, Ewing, Patricia C
Publicado 2010

“The leading role of pathology in assessing the somatic molecular alterations of cancer: Position Paper of the European Society of Pathology”: letter to the Editor

por Dinjens, Winand N. M., Ligtenberg, Marjolijn J. L., van Wezel, Tom, Schuuring, Ed, Dubbink, Hendrikus Jan
Publicado 2020

Novel EGFR V834L Germline Mutation Associated With Familial Lung Adenocarcinoma

por van der Leest, Cor, Wagner, Anja, Pedrosa, Rute M., Aerts, Joachim G., Dinjens, Winand N.M., Dubbink, Hendrikus J.
Publicado 2018

Mitochondrial D310 mutation as clonal marker for solid tumors

por Geurts-Giele, Willemina R. R., Gathier, Gerard H. G. K., Atmodimedjo, Peggy N., Dubbink, Hendrikus J., Dinjens, Winand N. M.
Publicado 2015

Estrogen receptor variants in ER-positive basal-type breast cancers responding to therapy like ER-negative breast cancers

por Groenendijk, Floris H., Treece, Tina, Yoder, Erin, Baron, Paul, Beitsch, Peter, Audeh, William, Dinjens, Winand N. M., Bernards, Rene, Whitworth, Pat
Publicado 2019

Phenotype or Genotype: Decision‐Making Dilemmas in Hepatocellular Adenoma

por Klompenhouwer, Anne J., Thomeer, Maarten G.J., Dinjens, Winand N.M., de Man, Robert A., Ijzermans, Jan N.M., Doukas, Michail
Publicado 2019

MGMT promoter hypermethylation is a frequent, early, and consistent event in astrocytoma progression, and not correlated with TP53 mutation

por Groenendijk, Floris H., Taal, Walter, Dubbink, Hendrikus J., Haarloo, Cathleen R., Kouwenhoven, Mathilde C., van den Bent, Martin J., Kros, Johan M., Dinjens, Winand N. M.
Publicado 2010

Impact of panel design and cut-off on tumour mutational burden assessment in metastatic solid tumour samples

por Mankor, Joanne M., Paats, Marthe S., Groenendijk, Floris H., Roepman, Paul, Dinjens, Winand N. M., Dubbink, Hendrikus J., Sleijfer, Stefan, Cuppen, Edwin, Lolkema, Martijn P. J. K.
Publicado 2020

Optimal tissue sampling during ERCP and emerging molecular techniques for the differentiation of benign and malignant biliary strictures

por Kamp, Eline J. C. A., Dinjens, Winand N. M., Doukas, Michail, Bruno, Marco J., de Jonge, Pieter Jan F., Peppelenbosch, Maikel P., de Vries, Annemarie C.
Publicado 2021

Early onset esophageal adenocarcinoma: a distinct molecular entity?

por van Nistelrooij, Anna M.J., van Marion, Ronald, Biermann, Katharina, Spaander, Manon C.W., van Lanschot, J. Jan B., Wijnhoven, Bas P.L., Dinjens, Winand N.M.
Publicado 2016

Excluding Lynch syndrome in a female patient with metachronous DNA mismatch repair deficient colon- and ovarian cancer

por Crobach, Stijn, Jansen, Anne M. L., Ligtenberg, Marjolein J. L., Koopmans, Marije, Nielsen, Maartje, Hes, Frederik J., Wijnen, Juul T., Dinjens, Winand N. M., van Wezel, Tom, Morreau, Hans
Publicado 2017

Adrenal Medullary Hyperplasia Is a Precursor Lesion for Pheochromocytoma in MEN2 Syndrome()()

por Korpershoek, Esther, Petri, Bart-Jeroen, Post, Edward, van Eijck, Casper H.J., Oldenburg, Rogier A., Belt, Eric J.T., de Herder, Wouter W., de Krijger, Ronald R., Dinjens, Winand N.M.
Publicado 2014

Clinical evaluation of a dedicated next generation sequencing panel for routine glioma diagnostics

por Synhaeve, Nathalie E., van den Bent, Martin J., French, Pim J., Dinjens, Winand N. M., Atmodimedjo, Peggy N., Kros, Johan M., Verdijk, R., Dirven, Clemens M. F., Dubbink, Hendrikus J.
Publicado 2018

Reclassification of two germline DICER1 splicing variants leads to DICER1 syndrome diagnosis

por Apellaniz-Ruiz, Maria, Sabbaghian, Nelly, Chong, Anne-Laure, de Kock, Leanne, Cetinkaya, Semra, Bayramoğlu, Elvan, Dinjens, Winand N. M., McCluggage, W. Glenn, Wagner, Anja, Yilmaz, Aslihan Arasli, Foulkes, William D.
Publicado 2023

Gynecological Surveillance and Surgery Outcomes in Dutch Lynch Syndrome Carriers

por Eikenboom, Ellis L., van Doorn, Helena C., Dinjens, Winand N. M., Dubbink, Hendrikus J., Geurts-Giele, Willemina R. R., Spaander, Manon C. W., Tops, Carli M. J., Wagner, Anja, Goverde, Anne
Publicado 2021

Primary Sclerosing Cholangitis–Associated Cholangiocarcinoma Demonstrates High Intertumor and Intratumor Heterogeneity

por Kamp, Eline J.C.A., Peppelenbosch, Maikel P., Doukas, Michail, Verheij, Joanne, Ponsioen, Cyriel Y., van Marion, Ronald, Bruno, Marco J., Koerkamp, Bas Groot, Dinjens, Winand N.M., de Vries, Annemarie C.
Publicado 2021

Vascular Pattern Analysis for the Prediction of Clinical Behaviour in Pheochromocytomas and Paragangliomas

por Oudijk, Lindsey, van Nederveen, Francien, Badoual, Cécile, Tissier, Frédérique, Tischler, Arthur S., Smid, Marcel, Gaal, José, Lepoutre-Lussey, Charlotte, Gimenez-Roqueplo, Anne-Paule, Dinjens, Winand N.M., Korpershoek, Esther, de Krijger, Ronald, Favier, Judith
Publicado 2015

Molecular clonality analysis of esophageal adenocarcinoma by multiregion sequencing of tumor samples

por van Nistelrooij, Anna M. J., van Marion, Ronald, Koppert, Linetta B., Biermann, Katharina, Spaander, Manon C. W., Tilanus, Hugo W., van Lanschot, J. Jan B., Wijnhoven, Bas P. L., Dinjens, Winand N. M.
Publicado 2017

Personalised selection of experimental treatment in patients with advanced solid cancer is feasible using whole-genome sequencing

por Pruis, Melinda A., Groenendijk, Floris H., Badloe, K. Sangeeta, van Puffelen, Andrea, Robbrecht, Debbie, Dinjens, Winand N. M., Sleijfer, Stefan, Dingemans, Anne-Marie C., von der Thüsen, Jan H., Roepman, Paul, Lolkema, Martijn P.
Publicado 2022