Delilah Hendriks

3.6k total citations · 2 hit papers
28 papers, 2.1k citations indexed

About

Delilah Hendriks is a scholar working on Molecular Biology, Hepatology and Surgery. According to data from OpenAlex, Delilah Hendriks has authored 28 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Hepatology and 7 papers in Surgery. Recurrent topics in Delilah Hendriks's work include Liver physiology and pathology (10 papers), Pluripotent Stem Cells Research (9 papers) and CRISPR and Genetic Engineering (8 papers). Delilah Hendriks is often cited by papers focused on Liver physiology and pathology (10 papers), Pluripotent Stem Cells Research (9 papers) and CRISPR and Genetic Engineering (8 papers). Delilah Hendriks collaborates with scholars based in Netherlands, Sweden and Switzerland. Delilah Hendriks's co-authors include Magnus Ingelman‐Sundberg, Benedetta Artegiani, Hans Clevers, Volker M. Lauschke, Catherine C. Bell, Susana M. Chuva de Sousa Lopes, Tommy B. Andersson, Åsa Nordling, Souren Mkrtchian and Christopher E. Goldring and has published in prestigious journals such as Cell, Nature Communications and Nature Biotechnology.

In The Last Decade

Delilah Hendriks

28 papers receiving 2.0k citations

Hit Papers

Characterization of primary human hepatocyte spheroids as... 2016 2026 2019 2022 2016 2023 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Delilah Hendriks Netherlands 19 780 746 693 419 418 28 2.1k
Simon Messner Switzerland 17 386 0.5× 446 0.6× 1.3k 1.9× 296 0.7× 764 1.8× 26 2.5k
Peggy Papeleu Belgium 18 378 0.5× 125 0.2× 957 1.4× 155 0.4× 172 0.4× 31 1.6k
Karl‐Dimiter Bissig United States 23 396 0.5× 173 0.2× 883 1.3× 76 0.2× 260 0.6× 43 1.8k
Guangfu Li United States 28 216 0.3× 183 0.2× 984 1.4× 30 0.1× 821 2.0× 96 2.4k
Baohong Zhang China 24 78 0.1× 137 0.2× 579 0.8× 46 0.1× 305 0.7× 77 1.6k
Dieter Paul Germany 20 188 0.2× 85 0.1× 731 1.1× 59 0.1× 216 0.5× 46 1.3k
Shinji Iwasaki Japan 22 371 0.5× 25 0.0× 530 0.8× 92 0.2× 353 0.8× 80 1.9k
Nai Yang Fu Singapore 26 68 0.1× 99 0.1× 1.5k 2.1× 91 0.2× 920 2.2× 43 2.3k
Jonathan Larkin United States 22 155 0.2× 66 0.1× 423 0.6× 28 0.1× 135 0.3× 45 1.4k

Countries citing papers authored by Delilah Hendriks

Since Specialization
Citations

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

Fields of papers citing papers by Delilah Hendriks

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Delilah Hendriks

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

All Works

20 of 20 papers shown
1.
Artegiani, Benedetta, et al.. (2025). Generation of human fetal brain organoids and their CRISPR engineering for brain tumor modeling. Nature Protocols. 20(7). 1846–1883. 2 indexed citations
2.
Artegiani, Benedetta, et al.. (2025). Emerging approaches to enhance human brain organoid physiology. Trends in Cell Biology. 35(6). 483–499. 6 indexed citations
3.
Artegiani, Benedetta & Delilah Hendriks. (2025). Organoids from pluripotent stem cells and human tissues: When two cultures meet each other. Developmental Cell. 60(4). 493–511. 6 indexed citations
4.
Hendriks, Delilah, Carmen López‐Iglesias, Jeff DeMartino, et al.. (2024). Human fetal brain self-organizes into long-term expanding organoids. Cell. 187(3). 712–732.e38. 52 indexed citations
5.
Hendriks, Delilah, et al.. (2024). Mapping of mitogen and metabolic sensitivity in organoids defines requirements for human hepatocyte growth. Nature Communications. 15(1). 4034–4034. 17 indexed citations
6.
Yang, Annie, Devanjali Dutta, Kai Kretzschmar, et al.. (2023). Development of Plasmodium falciparum liver-stages in hepatocytes derived from human fetal liver organoid cultures. Nature Communications. 14(1). 4631–4631. 13 indexed citations
7.
Geurts, Maarten H., Shashank Gandhi, Matteo Boretto, et al.. (2023). One-step generation of tumor models by base editor multiplexing in adult stem cell-derived organoids. Nature Communications. 14(1). 4998–4998. 32 indexed citations
8.
Hendriks, Delilah, Jos F. Brouwers, Karien M. Hamer, et al.. (2023). Engineered human hepatocyte organoids enable CRISPR-based target discovery and drug screening for steatosis. Nature Biotechnology. 41(11). 1567–1581. 125 indexed citations breakdown →
9.
Lopes, Susana M. Chuva de Sousa, et al.. (2023). Organoid models of fibrolamellar carcinoma mutations reveal hepatocyte transdifferentiation through cooperative BAP1 and PRKAR2A loss. Nature Communications. 14(1). 2377–2377. 22 indexed citations
10.
Ardisasmita, Arif Ibrahim, Imre F. Schene, Indi P. Joore, et al.. (2022). A comprehensive transcriptomic comparison of hepatocyte model systems improves selection of models for experimental use. Communications Biology. 5(1). 1094–1094. 15 indexed citations
11.
Artegiani, Benedetta, Delilah Hendriks, Joep Beumer, et al.. (2020). Fast and efficient generation of knock-in human organoids using homology-independent CRISPR–Cas9 precision genome editing. Nature Cell Biology. 22(3). 321–331. 210 indexed citations
12.
Hendriks, Delilah, Benedetta Artegiani, Huili Hu, Susana M. Chuva de Sousa Lopes, & Hans Clevers. (2020). Establishment of human fetal hepatocyte organoids and CRISPR–Cas9-based gene knockin and knockout in organoid cultures from human liver. Nature Protocols. 16(1). 182–217. 119 indexed citations
13.
Hendriks, Delilah, Hans Clevers, & Benedetta Artegiani. (2020). CRISPR-Cas Tools and Their Application in Genetic Engineering of Human Stem Cells and Organoids. Cell stem cell. 27(5). 705–731. 126 indexed citations
14.
Baze, Audrey, C. Parmentier, Delilah Hendriks, et al.. (2018). Three-Dimensional Spheroid Primary Human Hepatocytes in Monoculture and Coculture with Nonparenchymal Cells. Tissue Engineering Part C Methods. 24(9). 534–545. 70 indexed citations
15.
Parmentier, C., Delilah Hendriks, Bruno Heyd, et al.. (2018). Inter-individual differences in the susceptibility of primary human hepatocytes towards drug-induced cholestasis are compound and time dependent. Toxicology Letters. 295. 187–194. 18 indexed citations
16.
Hendriks, Delilah, et al.. (2016). Hepatic 3D spheroid models for the detection and study of compounds with cholestatic liability. Scientific Reports. 6(1). 35434–35434. 122 indexed citations
17.
Bell, Catherine C., Delilah Hendriks, Sabrina Moro, et al.. (2016). Characterization of primary human hepatocyte spheroids as a model system for drug-induced liver injury, liver function and disease. Scientific Reports. 6(1). 25187–25187. 517 indexed citations breakdown →
18.
Hendriks, Delilah, et al.. (2016). 3D hepatic spheroid models for the detection and study of compounds with cholestatic liability. Toxicology Letters. 258. S134–S135. 1 indexed citations
19.
Neve, Etienne P.A., Harald Köfeler, Delilah Hendriks, et al.. (2015). Expression and Function of mARC: Roles in Lipogenesis and Metabolic Activation of Ximelagatran. PLoS ONE. 10(9). e0138487–e0138487. 24 indexed citations
20.
Hendriks, Delilah, et al.. (2014). Human NAD(P)H:quinone Oxidoreductase 1 (NQO1)-Mediated Inactivation of Reactive Quinoneimine Metabolites of Diclofenac and Mefenamic Acid. Chemical Research in Toxicology. 27(4). 576–586. 27 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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