Dennis Hendriksen

627 total citations
15 papers, 334 citations indexed

About

Dennis Hendriksen is a scholar working on Molecular Biology, Genetics and Artificial Intelligence. According to data from OpenAlex, Dennis Hendriksen has authored 15 papers receiving a total of 334 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Artificial Intelligence. Recurrent topics in Dennis Hendriksen's work include Biomedical Text Mining and Ontologies (6 papers), Genomics and Rare Diseases (4 papers) and Semantic Web and Ontologies (4 papers). Dennis Hendriksen is often cited by papers focused on Biomedical Text Mining and Ontologies (6 papers), Genomics and Rare Diseases (4 papers) and Semantic Web and Ontologies (4 papers). Dennis Hendriksen collaborates with scholars based in Netherlands, Canada and United Kingdom. Dennis Hendriksen's co-authors include Morris A. Swertz, Rob J. van der Geest, Patrick Deelen, Harm-Jan Westra, Lude Franke, Marc Jan Bonder, K. Joeri van der Velde, Hans C. van Assen, Bart Charbon and Chao Pang and has published in prestigious journals such as SHILAP Revista de lepidopterología, Bioinformatics and International Journal of Molecular Sciences.

In The Last Decade

Dennis Hendriksen

14 papers receiving 326 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dennis Hendriksen Netherlands	10	115	87	83	63	51	15	334
Giovanna Nicora Italy	9	167 1.5×	53 0.6×	23 0.3×	46 0.7×	30 0.6×	35	434
Gareth Bryson United Kingdom	9	70 0.6×	27 0.3×	15 0.2×	45 0.7×	57 1.1×	20	274
Xiaowei Xu China	10	38 0.3×	16 0.2×	92 1.1×	40 0.6×	33 0.6×	34	435
Tatsuya Matsubara Japan	10	33 0.3×	23 0.3×	43 0.5×	57 0.9×	91 1.8×	28	329
Iain S. Forrest United States	10	78 0.7×	90 1.0×	76 0.9×	35 0.6×	24 0.5×	22	327
Alena Orlenko United States	8	109 0.9×	37 0.4×	113 1.4×	23 0.4×	14 0.3×	12	326
Ho‐Chang Lee South Korea	9	82 0.7×	30 0.3×	16 0.2×	18 0.3×	66 1.3×	20	297
Dexin Lin China	9	80 0.7×	7 0.1×	52 0.6×	50 0.8×	43 0.8×	16	320
Evita Sadimin United States	12	158 1.4×	18 0.2×	12 0.1×	74 1.2×	185 3.6×	36	432
Mei‐Fang Lin China	14	135 1.2×	29 0.3×	15 0.2×	64 1.0×	63 1.2×	25	500

Countries citing papers authored by Dennis Hendriksen

Since Specialization

Citations

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

Fields of papers citing papers by Dennis Hendriksen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dennis Hendriksen. 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 Dennis Hendriksen. The network helps show where Dennis Hendriksen may publish in the future.

Co-authorship network of co-authors of Dennis Hendriksen

This figure shows the co-authorship network connecting the top 25 collaborators of Dennis Hendriksen. A scholar is included among the top collaborators of Dennis Hendriksen 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 Dennis Hendriksen. Dennis Hendriksen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Boer, Eddy N. de, Dennis Hendriksen, Bart Charbon, et al.. (2025). Nanopore Long-Read Sequencing as a First-Tier Diagnostic Test to Detect Repeat Expansions in Neurological Disorders. International Journal of Molecular Sciences. 26(7). 2850–2850. 1 indexed citations

Johansson, Lennart, Bart Charbon, Dennis Hendriksen, et al.. (2025). MOLGENIS VIP: an end-to-end DNA variant interpretation pipeline for research and diagnostics configurable to support rapid implementation of new methods. NAR Genomics and Bioinformatics. 7(2). lqaf087–lqaf087.

Li, Shuang�, K. Joeri van der Velde, Dick de Ridder, et al.. (2020). CAPICE: a computational method for Consequence-Agnostic Pathogenicity Interpretation of Clinical Exome variations. Genome Medicine. 12(1). 75–75. 32 indexed citations

Velde, K. Joeri van der, Freerk van Dijk, Dennis Hendriksen, et al.. (2020). A pipeline‐friendly software tool for genome diagnostics to prioritize genes by matching patient symptoms to literature. SHILAP Revista de lepidopterología. 1(1). e10023–e10023. 4 indexed citations

Velde, K. Joeri van der, Floris Imhann, Bart Charbon, et al.. (2018). MOLGENIS research: advanced bioinformatics data software for non-bioinformaticians. Bioinformatics. 35(6). 1076–1078. 55 indexed citations

Pang, Chao, Fleur Kelpin, David van Enckevort, et al.. (2017). BiobankUniverse: automatic matchmaking between datasets for biobank data discovery and integration. Bioinformatics. 33(22). 3627–3634. 3 indexed citations

Pang, Chao, David van Enckevort, Fleur Kelpin, et al.. (2016). MOLGENIS/connect: a system for semi-automatic integration of heterogeneous phenotype data with applications in biobanks. Bioinformatics. 32(14). 2176–2183. 10 indexed citations

Pang, Chao, Anna Sijtsma, Dennis Hendriksen, et al.. (2015). SORTA: a system for ontology-based re-coding and technical annotation of biomedical phenotype data. Database. 2015. bav089–bav089. 25 indexed citations

Deelen, Patrick, Marc Jan Bonder, Harm-Jan Westra, et al.. (2014). Genotype harmonizer: automatic strand alignment and format conversion for genotype data integration. BMC Research Notes. 7(1). 901–901. 76 indexed citations

10.

Pang, Chao, Dennis Hendriksen, Martijn Dijkstra, et al.. (2014). BiobankConnect: software to rapidly connect data elements for pooled analysis across biobanks using ontological and lexical indexing. Journal of the American Medical Informatics Association. 22(1). 65–75. 20 indexed citations

11.

Geest, Rob J. van der, Arthur J. Scholte, Lucia J.M. Kroft, et al.. (2012). Evaluation of sampling density on the accuracy of aortic pulse wave velocity from velocity‐encoded MRI in patients with Marfan syndrome. Journal of Magnetic Resonance Imaging. 36(6). 1470–1476. 14 indexed citations

12.

Geest, Rob J. van der, Arthur J. Scholte, Peter J. Boogaard, et al.. (2011). Accuracy of aortic pulse wave velocity assessment with velocity-encoded MRI: validation in patients with Marfan syndrome. Journal of Cardiovascular Magnetic Resonance. 13(S1). 2 indexed citations

13.

Westenberg, Jos J.M., Albert de Roos, Heynric B. Grotenhuis, et al.. (2010). Improved aortic pulse wave velocity assessment from multislice two‐directional in‐plane velocity‐encoded magnetic resonance imaging. Journal of Magnetic Resonance Imaging. 32(5). 1086–1094. 47 indexed citations

14.

Hendriksen, Dennis, et al.. (2009). LV Challenge LKEB Contribution: Fully Automated Myocardial Contour Detection. 34 indexed citations

15.

Hendriksen, Dennis, et al.. (2007). Automated Contour Detection in Cardiac MRI Using Active Appearance Models. Investigative Radiology. 42(10). 697–703. 11 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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