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Hendrikus J. Dubbink

Erasmus MC · NL
Area of research
Genetics · Pulmonary and Respiratory Medicine · imunotherapy
Research interest
Research interests include Glioma Diagnosis and Treatment, Cancer Genomics and Diagnostics, Radiomics and Machine Learning in Medical Imaging, and Brain Metastases and Treatment.
h-index
46
citations
7,788
works
214
NIH funding
primary concept
Medicine
email

Recent publications

Concurrent and adjuvant temozolomide for 1p/19q non-co-deleted anaplastic glioma (CATNON; EORTC study 26053-22054): final and exploratory analyses of a randomised, open-label, phase 3 trial
The Lancet Oncology 2025cited by 5position: middledoi
Temozolomide and Radiotherapy versus Radiotherapy Alone in Patients with Glioblastoma, <i>IDH</i> -wildtype: <i>Post Hoc</i> Analysis of the EORTC Randomized Phase III CATNON Trial
Clinical Cancer Research 2022cited by 71position: middledoi
Adjuvant and concurrent temozolomide for 1p/19q non-co-deleted anaplastic glioma (CATNON; EORTC study 26053-22054): second interim analysis of a randomised, open-label, phase 3 study
The Lancet Oncology 2021cited by 323position: middledoi
Prognostic significance of genome-wide DNA methylation profiles within the randomized, phase 3, EORTC CATNON trial on non-1p/19q deleted anaplastic glioma
Neuro-Oncology 2021cited by 62position: middledoi
Non-IDH1-R132H IDH1/2 mutations are associated with increased DNA methylation and improved survival in astrocytomas, compared to IDH1-R132H mutations
Acta Neuropathologica 2021cited by 55position: middledoi
The clonal relation of primary upper urinary tract urothelial carcinoma and paired urothelial carcinoma of the bladder
International Journal of Cancer 2020cited by 24position: middledoi
Plasma Predictive Features in Treating EGFR-Mutated Non-Small Cell Lung Cancer.
Cancers 2020cited by 0position: contributordoi
Interim results from the CATNON trial (EORTC study 26053-22054) of treatment with concurrent and adjuvant temozolomide for 1p/19q non-co-deleted anaplastic glioma: a phase 3, randomised, open-label intergroup study
The Lancet 2017cited by 397position: middledoi
Functional analysis of <i>MSH2</i> unclassified variants found in suspected Lynch syndrome patients reveals pathogenicity due to attenuated mismatch repair
Journal of Medical Genetics 2014cited by 14position: middledoi
Interlaboratory comparison of IDH mutation detection
Journal of Neuro-Oncology 2013cited by 67position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Winand N.M. Dinjens · AbbVie (United States)2 papers (2014–2020) · 1 papers (2014–2014)Harmen J.G. van de Werken · Utrecht University1 papers (2020–2020)Kevin C. Halling · Roswell Park Comprehensive Cancer Center1 papers (2013–2013)Christian Hartmann · Medizinische Hochschule Hannover1 papers (2013–2013)Martin J. van den Bent · St James's University Hospital1 papers (2013–2013) · 1 papers (2014–2014)Jan Hettinger · German Cancer Research Center1 papers (2014–2014)Job van Riet · German Cancer Research Center1 papers (2020–2020)Marjolijn J. L. Ligtenberg · ERN GENTURIS1 papers (2014–2014)Tahlita C.M. Zuiverloon · University of Colorado Denver1 papers (2020–2020)Arjen R. Mensenkamp · Eunice Kennedy Shriver National Institute of Child Health and Human Development1 papers (2014–2014) · 1 papers (2014–2014) · 1 papers (2020–2020)Antoine G. van der Heijden · Radboud University Nijmegen1 papers (2020–2020)Andreas von Deimling · Stiftung Schleswig-Holsteinische Landesmuseen1 papers (2013–2013)Anja Wagner · Ludwig-Maximilians-Universität München1 papers (2014–2014)Judith B. Prins · Radboud University Nijmegen1 papers (2014–2014)Matthias Preusser · Comprehensive Cancer Center Vienna1 papers (2013–2013)Thomas Ströbel · Indiana University School of Medicine1 papers (2013–2013)