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M. Koudijs · SciRah

Researcher profile · Semantic Scholar

M. Koudijs

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M. Koudijs — researcher profile on SciRah

h-index: 32
Works: 91
Citations: 3,527

Most-cited papers

The microRNA-producing enzyme Dicer1 is essential for zebrafish development
Erno Wienholds, M. Koudijs, F. V. van Eeden, E. Cuppen +1 more
2003Nature Genetics511 citations
Semantic Scholar
Ovarian Cancer Cell Line Panel (OCCP): Clinical Importance of In Vitro Morphological Subtypes
C. Beaufort, J. Helmijr, A. Piskorz, M. Hoogstraat +10 more
2014PLoS ONE389 citations Open access
Semantic Scholar
Genetic variation in the zebrafish.
V. Guryev, M. Koudijs, Eugene Berezikov, Stephen L. Johnson +3 more
2006Genome Research211 citations Open access
Semantic Scholar
Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer
W. Kloosterman, M. Hoogstraat, Oscar Paling, Masoumeh Tavakoli-Yaraki +12 more
2011Genome Biology201 citations Open access
Semantic Scholar
Primary Colorectal Cancers and Their Subsequent Hepatic Metastases Are Genetically Different: Implications for Selection of Patients for Targeted Treatment
J. Vermaat, I. Nijman, M. Koudijs, F. L. Gerritse +9 more
2011Clinical Cancer Research155 citations Open access
Semantic Scholar
Glycosylation Is Important for Cell Surface Expression of the Water Channel Aquaporin-2 but Is Not Essential for Tetramerization in the Endoplasmic Reticulum*
G. Hendriks, M. Koudijs, B. V. van Balkom, V. Oorschot +3 more
2004Journal of Biological Chemistry154 citations Open access
Semantic Scholar
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
D. Barnes, M. Rookus, L. McGuffog, Goska Leslie +190 more
2020Genetics in Medicine116 citations Open access
Semantic Scholar
Hedgehog signaling plays a cell-autonomous role in maximizing cardiac developmental potential
Natalie A. Thomas, M. Koudijs, F. V. van Eeden, A. Joyner +1 more
2008Development106 citations Open access
Semantic Scholar
RAS pathway mutations as a predictive biomarker for treatment adaptation in pediatric B-cell precursor acute lymphoblastic leukemia
I. Jerchel, Alex Q. Hoogkamer, I. Ariës, E. Steeghs +13 more
2017Leukemia100 citations Open access
Semantic Scholar
The Zebrafish Mutants dre, uki, and lep Encode Negative Regulators of the Hedgehog Signaling Pathway
M. Koudijs, M. J. den Broeder, A. Keijser, Erno Wienholds +4 more
2005PLoS Genetics91 citations Open access
Semantic Scholar
Targeted Next Generation Sequencing as a Reliable Diagnostic Assay for the Detection of Somatic Mutations in Tumours Using Minimal DNA Amounts from Formalin Fixed Paraffin Embedded Material
W. D. de Leng, C. G. Gadellaa-van Hooijdonk, Françoise A. S. Barendregt-Smouter, M. Koudijs +13 more
2016PLoS ONE85 citations Open access
Semantic Scholar
A Systematic Analysis of Oncogenic Gene Fusions in Primary Colon Cancer.
W. Kloosterman, Robert R. J. Coebergh van den Braak, Mark Pieterse, Markus J. van Roosmalen +15 more
2017Cancer Research81 citations Open access
Semantic Scholar
Genomic and transcriptomic plasticity in treatment-naïve ovarian cancer
M. Hoogstraat, Mirjam de Pagter, G. Cirkel, Markus J. van Roosmalen +16 more
2014Genome Research81 citations Open access
Semantic Scholar
Next generation sequencing of triple negative breast cancer to find predictors for chemotherapy response
E. Lips, M. Michaut, M. Hoogstraat, L. Mulder +9 more
2015Breast Cancer Research71 citations Open access
Semantic Scholar
Insertional mutagenesis identifies drivers of a novel oncogenic pathway in invasive lobular breast carcinoma
S. Kas, J. D. de Ruiter, Koen Schipper, S. Annunziato +12 more
2017Nature Genetics69 citations Open access
Semantic Scholar
Genetic analysis of the two zebrafish patched homologues identifies novel roles for the hedgehog signaling pathway
M. Koudijs, M. J. den Broeder, E. Groot, F. V. van Eeden
2008BMC Developmental Biology69 citations Open access
Semantic Scholar
Implementation of paediatric precision oncology into clinical practice: The Individualized Therapies for Children with cancer program ‘iTHER’
K. Langenberg, M. Meister, J. Bakhuizen, J. Boer +50 more
2022European Journal of Cancer64 citations Open access
Semantic Scholar
Prevalence of (Epi)genetic Predisposing Factors in a 5-Year Unselected National Wilms Tumor Cohort: A Comprehensive Clinical and Genomic Characterization
J. Hol, R. Kuiper, F. van Dijk, E. Waanders +12 more
2022Journal of Clinical Oncology59 citations Open access
Semantic Scholar
Mosaicism of de novo pathogenic SCN1A variants in epilepsy is a frequent phenomenon that correlates with variable phenotypes
I. D. de Lange, M. Koudijs, R. Slot, B. Gunning +12 more
2018Epilepsia57 citations Open access
Semantic Scholar
High-throughput semiquantitative analysis of insertional mutations in heterogeneous tumors.
M. Koudijs, C. Klijn, L. van der Weyden, Jaap Kool +10 more
2011Genome Research49 citations Open access
Semantic Scholar
Comparison of next-generation sequencing and mutation-specific platforms in clinical practice.
J. Hinrichs, W. V. van Blokland, M. J. Moons, R. Radersma +7 more
2015American Journal of Clinical Pathology47 citations Open access
Semantic Scholar
JAK2 aberrations in childhood B-cell precursor acute lymphoblastic leukemia
E. Steeghs, I. Jerchel, Willemieke de Goffau-Nobel, Alex Q. Hoogkamer +10 more
2016OncoTarget46 citations Open access
Semantic Scholar
Assessment of Cancer Predisposition Syndromes in a National Cohort of Children With a Neoplasm
J. Bakhuizen, S. Hopman, M. Bosscha, C. Dommering +14 more
2023JAMA Network Open44 citations Open access
Semantic Scholar
Hedgehog signalling via a calcitonin receptor-like receptor can induce arterial differentiation independently of VEGF signalling in zebrafish
R. Wilkinson, M. Koudijs, R. Patient, P. Ingham +2 more
2012Blood42 citations Open access
Semantic Scholar
Clinicogenomic associations in childhood Langerhans cell histiocytosis: an international cohort study
P. Kemps, T. Zondag, H. Arnardóttir, Nienke Solleveld-Westerink +27 more
2022Blood Advances41 citations Open access
Semantic Scholar
The molecular genetic make-up of male breast cancer
C. Moelans, J. de Ligt, P. van der Groep, P. Prins +21 more
2019Endocrine-Related Cancer41 citations Open access
Semantic Scholar
Simultaneous detection of clinically relevant mutations and amplifications for routine cancer pathology.
M. Hoogstraat, J. Hinrichs, N. Besselink, Joyce H. Radersma-van Loon +8 more
2015Journal of Molecular Diagnostics41 citations Open access
Semantic Scholar
Towards personalized therapy in pediatric acute lymphoblastic leukemia: RAS mutations and prednisolone resistance
I. Ariës, R. van den Dungen, M. Koudijs, E. Cuppen +5 more
2014Haematologica40 citations Open access
Semantic Scholar
The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
Inge M. M. Lakeman, A. J. van den Broek, J. A. Vos, D. Barnes +210 more
2021Genetics in Medicine37 citations Open access
Semantic Scholar
Improved Gene Fusion Detection in Childhood Cancer Diagnostics Using RNA Sequencing
J. Hehir-Kwa, M. Koudijs, E. Verwiel, L. Kester +13 more
2022JCO Precision Oncology36 citations Open access
Semantic Scholar
Comparison of intramedullary myeloma and corresponding extramedullary soft tissue plasmacytomas using genetic mutational panel analyses
S. D. de Haart, S. Willems, T. Mutis, M. Koudijs +4 more
2016Blood Cancer Journal36 citations Open access
Semantic Scholar
Implementation of a Multicenter Biobanking Collaboration for Next-Generation Sequencing-Based Biomarker Discovery Based on Fresh Frozen Pretreatment Tumor Tissue Biopsies.
S. Bins, G. Cirkel, C. G. Gadellaa-van Hooijdonk, F. Weeber +18 more
2017The Oncologist33 citations Open access
Semantic Scholar
Positive experiences of healthcare professionals with a mainstreaming approach of germline genetic testing for women with ovarian cancer
K. Bokkers, R. Zweemer, M. Koudijs, S. Stehouwer +3 more
2021Familial Cancer31 citations Open access
Semantic Scholar
Tumor heterogeneity and personalized cancer medicine: are we being outnumbered?
G. Cirkel, C. G. Gadellaa-van Hooijdonk, M. Koudijs, S. Willems +1 more
2014Future Oncology31 citations
Semantic Scholar
Functional Categorization of BRCA1 Variants of Uncertain Clinical Significance in Homologous Recombination Repair Complementation Assays
P. Bouwman, I. van der Heijden, H. van der Gulden, Roebi de Bruijn +25 more
2020Clinical Cancer Research29 citations Open access
Semantic Scholar
Detailed imaging and genetic analysis reveal a secondary BRAFL505H resistance mutation and extensive intrapatient heterogeneity in metastatic BRAF mutant melanoma patients treated with vemurafenib
M. Hoogstraat, C. G. Gadellaa-van Hooijdonk, I. Ubink, N. Besselink +13 more
2015Pigment Cell & Melanoma Research27 citations Open access
Semantic Scholar
Analysis of Tumor Heterogeneity and Cancer Gene Networks Using Deep Sequencing of MMTV-Induced Mouse Mammary Tumors
C. Klijn, M. Koudijs, Jaap Kool, J. T. ten Hoeve +11 more
2013PLoS ONE23 citations Open access
Semantic Scholar
Diverse BRAF Gene Fusions Confer Resistance to EGFR-Targeted Therapy via Differential Modulation of BRAF Activity
Christina Stangl, J. Post, Markus J. van Roosmalen, N. Hami +7 more
2020Molecular Cancer Research19 citations Open access
Semantic Scholar
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
C. Hakkaart, J. Pearson, L. Marquart, J. Dennis +157 more
2022Communications Biology18 citations Open access
Semantic Scholar
Assessment of parental mosaicism in SCN1A-related epilepsy by single-molecule molecular inversion probes and next-generation sequencing
I. D. de Lange, M. Koudijs, R. van 't Slot, Anja C. M. Sonsma +9 more
2018Journal of Medical Genetics18 citations Open access
Semantic Scholar
Mainstream genetic testing for women with ovarian cancer provides a solid basis for patients to make a well-informed decision about genetic testing
K. Bokkers, E. Bleiker, J. Hoogendam, M. Velthuizen +7 more
2022Hereditary Cancer in Clinical Practice17 citations Open access
Semantic Scholar
Recurrent ETV3::NCOA2 fusions and MAPK pathway mutations in indeterminate dendritic cell histiocytosis
P. Kemps, F. S. Woei-A-Jin, K. Quint, C. van den Bos +19 more
2024Blood Advances14 citations Open access
Semantic Scholar
Challenging Conventional Diagnostic Methods by Comprehensive Molecular Diagnostics: A Nationwide Prospective Comparison in Children With ALL
J. Boer, M. Koudijs, L. Kester, Edwin Sonneveld +9 more
2025JCO Precision Oncology12 citations Open access
Semantic Scholar
Prognostic Value of the G2 Expression Signature and MYC Overexpression in Childhood High-Grade Osteosarcoma
R. van Ewijk, L. Hiemcke-Jiwa, Jayne Y. Hehir-Kwa, Nathalie Gaspar +12 more
2025JCO Precision Oncology11 citations Open access
Semantic Scholar
Gene Mosaicism Screening Using Single Molecule Molecular Inversion Probes in Routine Diagnostics for Systemic Autoinflammatory Diseases.
Benjamin Kant, E. Carbo, I. Kokmeijer, J. M. Oosterman +6 more
2019Journal of Molecular Diagnostics11 citations Open access
Semantic Scholar
Identifying transposon insertions and their effects from RNA-sequencing data
J. D. de Ruiter, S. Kas, Eva Schut, D. Adams +3 more
2017Nucleic Acids Research9 citations Open access
Semantic Scholar
Effective Therapeutic Intervention and Comprehensive Genetic Analysis of mTOR Signaling in PEComa: A Case Report.
F. Weeber, M. Koudijs, M. Hoogstraat, N. Besselink +5 more
2015Anticancer Research9 citations
Semantic Scholar
Progression-free survival and overall survival after BRCA1/2-associated epithelial ovarian cancer: A matched cohort study
B. Heemskerk-Gerritsen, A. Hollestelle, C. V. van Asperen, I. Van Den Beek +8 more
2022PLoS ONE8 citations Open access
Semantic Scholar
Comparison of clinical selection-based genetic testing with phenotype-agnostic extensive germline sequencing to diagnose genetic predisposition in children with cancer: a prospective diagnostic study.
J. Bakhuizen, F. van Dijk, M. Koudijs, R. Bladergroen +13 more
2024The Lancet Child & Adolescent Health7 citations
Semantic Scholar
Recontacting non-BRCA1/2 breast cancer patients for germline CHEK2 c.1100del pathogenic variant testing: uptake and patient experiences
M. Velthuizen, R. B. van der Luijt, Beja J. de Vries, M. Koudijs +2 more
2021Hereditary Cancer in Clinical Practice7 citations Open access
Semantic Scholar

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