Maarten P.G. Massink

1.2k total citations
21 papers, 588 citations indexed

About

Maarten P.G. Massink is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Maarten P.G. Massink has authored 21 papers receiving a total of 588 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Oncology and 6 papers in Genetics. Recurrent topics in Maarten P.G. Massink's work include Cancer Genomics and Diagnostics (5 papers), DNA Repair Mechanisms (3 papers) and BRCA gene mutations in cancer (3 papers). Maarten P.G. Massink is often cited by papers focused on Cancer Genomics and Diagnostics (5 papers), DNA Repair Mechanisms (3 papers) and BRCA gene mutations in cancer (3 papers). Maarten P.G. Massink collaborates with scholars based in Netherlands, United States and United Kingdom. Maarten P.G. Massink's co-authors include Hanne Meijers‐Heijboer, Gijs van Haaften, Irsan Kooi, Quinten Waisfisz, Josephine C. Dorsman, Jacqueline Cloos, Gertjan J.L. Kaspers, Hein te Riele, Berber M. Mol and John W.M. Martens and has published in prestigious journals such as Nature Genetics, The Journal of Experimental Medicine and PLoS ONE.

In The Last Decade

Maarten P.G. Massink

21 papers receiving 581 citations

Peers

Maarten P.G. Massink

ONCOL

GENET

OPHTH

Tie Ke China

A Munnich France

Yong Sam Shin South Korea

Henrik Landgren Sweden

María José Gamundi Spain

Robert F. Willenbucher United States

Esther Kinning United Kingdom

Shehla Mohammed United Kingdom

Terri L. Young United States

Tie Ke China

Maarten P.G. Massink

704 ×2.0

40 ×0.2

ONCOL

117 ×0.9

GENET

49 ×0.4

OPHTH

89 ×1.1

Citations per year, relative to Maarten P.G. Massink Maarten P.G. Massink (= 1×) peers Tie Ke

Countries citing papers authored by Maarten P.G. Massink

Since Specialization

Citations

This map shows the geographic impact of Maarten P.G. Massink'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 Maarten P.G. Massink with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maarten P.G. Massink more than expected).

Fields of papers citing papers by Maarten P.G. Massink

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maarten P.G. Massink. 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 Maarten P.G. Massink. The network helps show where Maarten P.G. Massink may publish in the future.

Co-authorship network of co-authors of Maarten P.G. Massink

This figure shows the co-authorship network connecting the top 25 collaborators of Maarten P.G. Massink. A scholar is included among the top collaborators of Maarten P.G. Massink 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 Maarten P.G. Massink. Maarten P.G. Massink 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

McDonald, Jamie, Carmelo Bernabéu, Carla Olivieri, et al.. (2024). Specifications of the ACMG/AMP Variant Curation Guidelines for Hereditary Hemorrhagic Telangiectasia Genes—ENG and ACVRL1. Human Mutation. 2024. 1–13. 5 indexed citations

Wagener, Frank A. D. T. G., Maarten P.G. Massink, Willem Fennis, et al.. (2023). Concurrent de novo ZFHX4 variant and 16q24.1 deletion in a patient with orofacial clefting; a potential role of ZFHX4 and USP10. American Journal of Medical Genetics Part A. 191(4). 1083–1088. 1 indexed citations

Dooren, M. F. van, Augusta M.A. Lachmeijer, Virginie J. M. Verhoeven, et al.. (2023). Diagnostic Gene Panel Testing in (Non)-Syndromic Patients with Cleft Lip, Alveolus and/or Palate in the Netherlands. Molecular Syndromology. 14(4). 270–282. 3 indexed citations

Vis, Joanne J. van der, Karin M. Kazemier, Marjolein J. W. de Bruijn, et al.. (2023). A new variant in theZCCHC8gene: diverse clinical phenotypes and expression in the lung. ERJ Open Research. 10(1). 487–2023. 2 indexed citations

Vis, Joanne J. van der, Louise C. Showe, Andrew V. Kossenkov, et al.. (2022). Telomere dysfunction implicates POT1 in patients with idiopathic pulmonary fibrosis. The Journal of Experimental Medicine. 219(5). 25 indexed citations

Wiame, Elsa, Sabine A. Fuchs, Maarten P.G. Massink, et al.. (2021). NAA80 bi-allelic missense variants result in high-frequency hearing loss, muscle weakness and developmental delay. Brain Communications. 3(4). fcab256–fcab256. 17 indexed citations

Li, Rachel, Scott A. Turner, Richard H. van Jaarsveld, et al.. (2020). HNRNPH1 ‐related syndromic intellectual disability: Seven additional cases suggestive of a distinct syndromic neurodevelopmental syndrome. Clinical Genetics. 98(1). 91–98. 18 indexed citations

Hammerl, Dora, Maarten P.G. Massink, Marcel Smid, et al.. (2019). Clonality, Antigen Recognition, and Suppression of CD8+ T Cells Differentially Affect Prognosis of Breast Cancer Subtypes. Clinical Cancer Research. 26(2). 505–517. 37 indexed citations

Broekema, Marjoleine F., Maarten P.G. Massink, Cinzia Donato, et al.. (2018). Natural helix 9 mutants of PPARγ differently affect its transcriptional activity. Molecular Metabolism. 20. 115–127. 14 indexed citations

10.

Broekema, Marjoleine F., Maarten P.G. Massink, Joep de Ligt, et al.. (2018). A Single Complex Agpat2 Allele in a Patient With Partial Lipodystrophy. Frontiers in Physiology. 9. 1363–1363. 7 indexed citations

11.

Tessadori, Federico, Jacques C. Giltay, Jane A. Hurst, et al.. (2017). Germline mutations affecting the histone H4 core cause a developmental syndrome by altering DNA damage response and cell cycle control. Nature Genetics. 49(11). 1642–1646. 34 indexed citations

12.

Kooi, Irsan, Berber M. Mol, Maarten P.G. Massink, et al.. (2016). Somatic genomic alterations in retinoblastoma beyond RB1 are rare and limited to copy number changes. Scientific Reports. 6(1). 25264–25264. 74 indexed citations

13.

Kooi, Irsan, Berber M. Mol, Maarten P.G. Massink, et al.. (2016). A Meta-Analysis of Retinoblastoma Copy Numbers Refines the List of Possible Driver Genes Involved in Tumor Progression. PLoS ONE. 11(4). e0153323–e0153323. 56 indexed citations

14.

Massink, Maarten P.G., Irsan Kooi, John W.M. Martens, Quinten Waisfisz, & Hanne Meijers‐Heijboer. (2015). Genomic profiling of CHEK2*1100delC-mutated breast carcinomas. BMC Cancer. 15(1). 877–877. 36 indexed citations

15.

Massink, Maarten P.G., Marijn Créton, Willem Fennis, et al.. (2015). Loss-of-Function Mutations in the WNT Co-receptor LRP6 Cause Autosomal-Dominant Oligodontia. The American Journal of Human Genetics. 97(4). 621–626. 87 indexed citations

16.

Mol, Berber M., Irsan Kooi, Maarten P.G. Massink, et al.. (2014). Coregulation of FANCA and BRCA1 in human cells. SpringerPlus. 3(1). 381–381. 5 indexed citations

17.

Mol, Berber M., Maarten P.G. Massink, Annemarie H. van der Hout, et al.. (2013). High resolution SNP array profiling identifies variability in retinoblastoma genome stability. Genes Chromosomes and Cancer. 53(1). 1–14. 21 indexed citations

18.

Warmoes, Marc O., Janneke E. Jaspers, Thang V. Pham, et al.. (2012). Proteomics of Mouse BRCA1-deficient Mammary Tumors Identifies DNA Repair Proteins with Potential Diagnostic and Prognostic Value in Human Breast Cancer. Molecular & Cellular Proteomics. 11(7). M111.013334–1. 24 indexed citations

19.

Soufan, Alexandre T., Gert van den Berg, Perry D. Moerland, et al.. (2007). Three‐dimensional measurement and visualization of morphogenesis applied to cardiac embryology. Journal of Microscopy. 225(3). 269–274. 26 indexed citations

20.

Houweling, Arjan C., Semir Somi, Maarten P.G. Massink, et al.. (2005). Comparative analysis of the natriuretic peptide precursor gene cluster in vertebrates reveals loss of ANF and retention of CNP‐3 in chicken. Developmental Dynamics. 233(3). 1076–1082. 26 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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