Marco J. Koudijs

3.6k total citations
45 papers, 2.3k citations indexed

About

Marco J. Koudijs is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Marco J. Koudijs has authored 45 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 16 papers in Cancer Research and 12 papers in Genetics. Recurrent topics in Marco J. Koudijs's work include Cancer Genomics and Diagnostics (14 papers), Acute Lymphoblastic Leukemia research (8 papers) and BRCA gene mutations in cancer (6 papers). Marco J. Koudijs is often cited by papers focused on Cancer Genomics and Diagnostics (14 papers), Acute Lymphoblastic Leukemia research (8 papers) and BRCA gene mutations in cancer (6 papers). Marco J. Koudijs collaborates with scholars based in Netherlands, Germany and United Kingdom. Marco J. Koudijs's co-authors include Edwin Cuppen, Ronald H.A. Plasterk, Erno Wienholds, Fredericus J. M. van Eeden, Fredericus J. M. van Eeden, Nicolle Besselink, Marlous Hoogstraat, Emile E. Voest, Victor Guryev and Isaäc J. Nijman and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Marco J. Koudijs

42 papers receiving 2.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Marco J. Koudijs Netherlands	23	1.4k	781	491	401	243	45	2.3k
Mauro Santibanez‐Koref United Kingdom	36	2.5k 1.8×	810 1.0×	530 1.1×	600 1.5×	198 0.8×	96	3.6k
Ryo Matoba Japan	30	2.8k 2.1×	622 0.8×	461 0.9×	446 1.1×	170 0.7×	69	3.8k
Arthur Gutierrez‐Hartmann United States	27	1.8k 1.3×	497 0.6×	419 0.9×	421 1.0×	179 0.7×	79	2.8k
Georg Beckmann Germany	16	1.5k 1.1×	583 0.7×	549 1.1×	234 0.6×	188 0.8×	36	2.3k
Bernhard Schmierer United Kingdom	19	2.5k 1.9×	323 0.4×	482 1.0×	454 1.1×	227 0.9×	28	3.1k
Piri Welcsh United States	20	2.1k 1.5×	445 0.6×	603 1.2×	930 2.3×	223 0.9×	36	2.9k
Iván del Barco Barrantes Spain	16	1.6k 1.1×	431 0.6×	305 0.6×	353 0.9×	191 0.8×	19	2.3k
Michele Rubini Italy	25	1.7k 1.3×	535 0.7×	664 1.4×	841 2.1×	82 0.3×	76	3.3k
Ma. Xenia G. Ilagan United States	18	3.2k 2.4×	477 0.6×	579 1.2×	397 1.0×	477 2.0×	27	4.3k
Chul Geun Kim South Korea	28	2.4k 1.7×	381 0.5×	431 0.9×	616 1.5×	154 0.6×	120	3.1k

Countries citing papers authored by Marco J. Koudijs

Since Specialization

Citations

This map shows the geographic impact of Marco J. Koudijs's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Marco J. Koudijs with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marco J. Koudijs more than expected).

Fields of papers citing papers by Marco J. Koudijs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marco J. Koudijs. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Marco J. Koudijs. The network helps show where Marco J. Koudijs may publish in the future.

Co-authorship network of co-authors of Marco J. Koudijs

This figure shows the co-authorship network connecting the top 25 collaborators of Marco J. Koudijs. A scholar is included among the top collaborators of Marco J. Koudijs based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marco J. Koudijs. Marco J. Koudijs is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Boer, Judith M., Marco J. Koudijs, Lennart Kester, et al.. (2025). Challenging Conventional Diagnostic Methods by Comprehensive Molecular Diagnostics: A Nationwide Prospective Comparison in Children With ALL. JCO Precision Oncology. 9(9). e2400788–e2400788. 1 indexed citations

Hiemcke‐Jiwa, Laura S., Jayne Y. Hehir‐Kwa, Nathalie Gaspar, et al.. (2025). Prognostic Value of the G2 Expression Signature and MYC Overexpression in Childhood High-Grade Osteosarcoma. JCO Precision Oncology. 9(9). e2400855–e2400855.

Boer, Judith M., Aurélie Boeree, Karin P.S. Langenberg, et al.. (2024). Oncogenic and immunological targets for matched therapy of pediatric blood cancer patients: Dutch iTHER study experience. HemaSphere. 8(7). e122–e122.

Hopman, Saskia, Machteld I. Bosscha, Charlotte J. Dommering, et al.. (2023). Assessment of Cancer Predisposition Syndromes in a National Cohort of Children With a Neoplasm. JAMA Network Open. 6(2). e2254157–e2254157. 19 indexed citations

Morsink, Folkert H.M., Wendy W.J. de Leng, Marco J. Koudijs, et al.. (2023). Diagnostic Utility of Menin Immunohistochemistry in Patients With Multiple Endocrine Neoplasia Type 1 Syndrome. The American Journal of Surgical Pathology. 47(7). 785–791. 3 indexed citations

Heemskerk‐Gerritsen, Bernadette A. M., Antoinette Hollestelle, Christi J. van Asperen, et al.. (2022). Progression-free survival and overall survival after BRCA1/2-associated epithelial ovarian cancer: A matched cohort study. PLoS ONE. 17(9). e0275015–e0275015. 1 indexed citations

Bleiker, Eveline M. A., Jacob P. Hoogendam, Mary E. Velthuizen, et al.. (2022). Mainstream genetic testing for women with ovarian cancer provides a solid basis for patients to make a well-informed decision about genetic testing. Hereditary Cancer in Clinical Practice. 20(1). 33–33. 13 indexed citations

Zweemer, Ronald P., et al.. (2021). Positive experiences of healthcare professionals with a mainstreaming approach of germline genetic testing for women with ovarian cancer. Familial Cancer. 21(3). 295–304. 22 indexed citations

Roosmalen, Markus J. van, Nizar Hami, Ingrid Verlaan-Klink, et al.. (2020). Diverse BRAF Gene Fusions Confer Resistance to EGFR-Targeted Therapy via Differential Modulation of BRAF Activity. Molecular Cancer Research. 18(4). 537–548. 11 indexed citations

10.

Carbo, Ellen C., Joost Frenkel, Morris A. Swertz, et al.. (2019). Gene Mosaicism Screening Using Single-Molecule Molecular Inversion Probes in Routine Diagnostics for Systemic Autoinflammatory Diseases. Journal of Molecular Diagnostics. 21(6). 943–950. 5 indexed citations

11.

Kloosterman, Wigard P., Robert R.J. Coebergh van den Braak, Mark Pieterse, et al.. (2017). A Systematic Analysis of Oncogenic Gene Fusions in Primary Colon Cancer. Cancer Research. 77(14). 3814–3822. 67 indexed citations

12.

Weeber, Fleur, Marco J. Koudijs, Marlous Hoogstraat, et al.. (2015). Effective Therapeutic Intervention and Comprehensive Genetic Analysis of mTOR Signaling in PEComa : A Case Report. Nature Biotechnology. 35(6). 1 indexed citations

13.

Weeber, Fleur, Marco J. Koudijs, Marlous Hoogstraat, et al.. (2015). Effective Therapeutic Intervention and Comprehensive Genetic Analysis of mTOR Signaling in PEComa: A Case Report.. PubMed. 35(6). 3399–403. 3 indexed citations

14.

Hinrichs, John W. J., et al.. (2015). Comparison of Next-Generation Sequencing and Mutation-Specific Platforms in Clinical Practice. American Journal of Clinical Pathology. 143(4). 573–578. 38 indexed citations

15.

Hoogstraat, Marlous, Mirjam S. de Pagter, Geert A. Cirkel, et al.. (2013). Genomic and transcriptomic plasticity in treatment-naïve ovarian cancer. Genome Research. 24(2). 200–211. 63 indexed citations

16.

Vermaat, Joost S.P., Isaäc J. Nijman, Marco J. Koudijs, et al.. (2011). Primary Colorectal Cancers and Their Subsequent Hepatic Metastases Are Genetically Different: Implications for Selection of Patients for Targeted Treatment. Clinical Cancer Research. 18(3). 688–699. 119 indexed citations

17.

Kloosterman, Wigard P., Marlous Hoogstraat, Masoumeh Tavakoli‐Yaraki, et al.. (2011). Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer. Genome biology. 12(10). R103–R103. 161 indexed citations

18.

Koudijs, Marco J., et al.. (2008). Genetic analysis of the two zebrafish patched homologues identifies novel roles for the hedgehog signaling pathway. BMC Developmental Biology. 8(1). 15–15. 59 indexed citations

19.

Guryev, Victor, Marco J. Koudijs, Eugène Berezikov, et al.. (2006). Genetic variation in the zebrafish. Genome Research. 16(4). 491–497. 163 indexed citations

20.

Koudijs, Marco J., et al.. (2005). The Zebrafish Mutants dre, uki, and lep Encode Negative Regulators of the Hedgehog Signaling Pathway. PLoS Genetics. 1(2). e19–e19. 71 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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