Holger Storf

1.2k total citations
64 papers, 439 citations indexed

About

Holger Storf is a scholar working on Molecular Biology, Genetics and Artificial Intelligence. According to data from OpenAlex, Holger Storf has authored 64 papers receiving a total of 439 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 21 papers in Genetics and 16 papers in Artificial Intelligence. Recurrent topics in Holger Storf's work include Genomics and Rare Diseases (21 papers), Biomedical Text Mining and Ontologies (21 papers) and Electronic Health Records Systems (7 papers). Holger Storf is often cited by papers focused on Genomics and Rare Diseases (21 papers), Biomedical Text Mining and Ontologies (21 papers) and Electronic Health Records Systems (7 papers). Holger Storf collaborates with scholars based in Germany, Netherlands and Italy. Holger Storf's co-authors include Jannik Schaaf, Martin Sedlmayr, Thomas Wagner, Martin Becker, Martin Riedl, Jan Zeidler, Johann‐Matthias Graf von der Schulenburg, Hans‐Ulrich Prokosch, Lutz Frölich and Katrin Jekel and has published in prestigious journals such as Journal of Medical Internet Research, Journal of the American Medical Informatics Association and Journal of Alzheimer s Disease.

In The Last Decade

Holger Storf

54 papers receiving 429 citations

Peers

Holger Storf
Michael Mendis United States
Frank Ückert Germany
Josef Schepers Germany
Marjan Mansourvar Denmark
Frank J. Manion United States
Otto Rienhoff Germany
Sylvia Thun Germany
Christine M. Cutillo United States
Fariborz Mokarian Iran
Amy Franklin United States
Michael Mendis United States
Holger Storf
Citations per year, relative to Holger Storf Holger Storf (= 1×) peers Michael Mendis

Countries citing papers authored by Holger Storf

Since Specialization
Citations

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

Fields of papers citing papers by Holger Storf

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Holger Storf

This figure shows the co-authorship network connecting the top 25 collaborators of Holger Storf. A scholar is included among the top collaborators of Holger Storf 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 Holger Storf. Holger Storf 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.
Tyc, Olaf, Hans‐Peter Erasmus, Cristina Ortiz, et al.. (2025). Enterococcus faecium DNA in acute decompensated cirrhosis: a key player in inflammation and kidney dysfunction. Frontiers in Medicine. 12. 1629210–1629210.
2.
Stratmann, Katharina, et al.. (2025). Enhancing diagnostic precision for rare diseases using case-based reasoning. Journal of the American Medical Informatics Association. 33(1). 98–111.
3.
Schaaf, Jannik, et al.. (2024). Initial User-Centred Design of an AI-Based Clinical Decision Support System for Primary Care. Studies in health technology and informatics. 310. 1051–1055. 6 indexed citations
4.
Schaaf, Jannik, et al.. (2024). Exploring patient-centered design solutions of a telehealth app for HIV − A qualitative study. International Journal of Medical Informatics. 189. 105524–105524. 3 indexed citations
5.
Storf, Holger, et al.. (2024). Development and expert inspections of the user interface for a primary care decision support system. International Journal of Medical Informatics. 192. 105651–105651. 1 indexed citations
6.
Németh, Attila, Patrick N. Harter, Katharina J. Weber, et al.. (2023). DistSNE: Distributed computing and online visualization of DNA methylation‐based central nervous system tumor classification. Brain Pathology. 34(3). e13228–e13228. 4 indexed citations
7.
Schaaf, Jannik, et al.. (2023). Interviews with HIV Experts for Development of a Mobile Health Application in HIV Care—A Qualitative Study. Healthcare. 11(15). 2180–2180. 4 indexed citations
8.
Boeker, Martin, et al.. (2023). Machine translation of standardised medical terminology using natural language processing: A scoping review. New Biotechnology. 77. 120–129. 10 indexed citations
9.
Schaaf, Jannik, et al.. (2022). The Use of Computer-Assisted Case-Based Reasoning to Support Clinical Decision-Making – A Scoping Review. Lecture notes in computer science. 395–409. 3 indexed citations
10.
11.
Schaaf, Jannik, et al.. (2020). Diagnosis of Rare Diseases: a scoping review of clinical decision support systems. Orphanet Journal of Rare Diseases. 15(1). 263–263. 32 indexed citations
12.
Schaaf, Jannik, et al.. (2020). Interviews with experts in rare diseases for the development of clinical decision support system software - a qualitative study. BMC Medical Informatics and Decision Making. 20(1). 230–230. 9 indexed citations
13.
Schaaf, Jannik, Martin Sedlmayr, Hans‐Ulrich Prokosch, et al.. (2020). The Status Quo of Rare Diseases Centres for the Development of a Clinical Decision Support System – A Cross-Sectional Study. Studies in health technology and informatics. 271. 176–183. 4 indexed citations
14.
Schaaf, Jannik, et al.. (2019). Diagnosis of Rare Diseases: A scoping review of clinical decision support systems. Research Square. 1 indexed citations
15.
Ganslandt, Thomas, Jannik Schaaf, Josef Schepers, et al.. (2019). Experiences from the National Demonstrator Study within the German Medical Informatics Initiative.. AMIA.
16.
Wagner, Thomas, et al.. (2018). Mapping of Health Care Providers for People with Rare Diseases - From Vision to Implementation.. PubMed. 247. 940–944. 1 indexed citations
17.
18.
Storf, Holger, et al.. (2017). Register für seltene Erkrankungen: OSSE – ein Open-Source-Framework für die technische Umsetzung. Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz. 60(5). 523–531. 1 indexed citations
19.
Jekel, Katrin, Marinella Damian, Holger Storf, Lucrezia Hausner, & Lutz Frölich. (2016). Development of a Proxy-Free Objective Assessment Tool of Instrumental Activities of Daily Living in Mild Cognitive Impairment Using Smart Home Technologies. Journal of Alzheimer s Disease. 52(2). 509–517. 29 indexed citations
20.
Crisler, Matthew C. & Holger Storf. (2012). A Decade of Steering Entropy - Use, Impact, and Further Application. Transportation Research Board 91st Annual MeetingTransportation Research Board. 1 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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