Min Ae Lee‐Kirsch

5.9k total citations
71 papers, 2.7k citations indexed

About

Min Ae Lee‐Kirsch is a scholar working on Molecular Biology, Immunology and Rheumatology. According to data from OpenAlex, Min Ae Lee‐Kirsch has authored 71 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 46 papers in Immunology and 13 papers in Rheumatology. Recurrent topics in Min Ae Lee‐Kirsch's work include interferon and immune responses (32 papers), Inflammasome and immune disorders (22 papers) and RNA regulation and disease (16 papers). Min Ae Lee‐Kirsch is often cited by papers focused on interferon and immune responses (32 papers), Inflammasome and immune disorders (22 papers) and RNA regulation and disease (16 papers). Min Ae Lee‐Kirsch collaborates with scholars based in Germany, United States and Austria. Min Ae Lee‐Kirsch's co-authors include Christine Wolf, Judy Lieberman, Claudia Günther, Nan Yan, Stefanie Kretschmer, M. Cristina Cardoso, N. König, Kerstin Engel, Klaus Lindpaintner and François Gaudet and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Nature Immunology.

In The Last Decade

Min Ae Lee‐Kirsch

67 papers receiving 2.7k citations

Peers

Min Ae Lee‐Kirsch
Moncef Zouali France
Melissa E. Elder United States
Utano Tomaru Japan
Michel Ticchioni France
Anna‐Marie Fairhurst Singapore
Jean‐François Eliaou France
Lynda Bennett United States
Margreet Jonker Netherlands
Dolores Jaraquemada Spain
Joseph Hesselgesser United States
Moncef Zouali France
Min Ae Lee‐Kirsch
Citations per year, relative to Min Ae Lee‐Kirsch Min Ae Lee‐Kirsch (= 1×) peers Moncef Zouali

Countries citing papers authored by Min Ae Lee‐Kirsch

Since Specialization
Citations

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

Fields of papers citing papers by Min Ae Lee‐Kirsch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Min Ae Lee‐Kirsch. 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 Min Ae Lee‐Kirsch. The network helps show where Min Ae Lee‐Kirsch may publish in the future.

Co-authorship network of co-authors of Min Ae Lee‐Kirsch

This figure shows the co-authorship network connecting the top 25 collaborators of Min Ae Lee‐Kirsch. A scholar is included among the top collaborators of Min Ae Lee‐Kirsch 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 Min Ae Lee‐Kirsch. Min Ae Lee‐Kirsch 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.
Seidl, Maximilian, Florian Babor, Stephan Ehl, et al.. (2025). SOCS1 deficiency—crossroads of autoimmunity and autoinflammation—two case reports. Frontiers in Pediatrics. 12. 1516017–1516017. 1 indexed citations
2.
Menzel, Katharina, et al.. (2024). Monogenic lupus – from gene to targeted therapy. SHILAP Revista de lepidopterología. 11(1). 8–8. 1 indexed citations
3.
Lee‐Kirsch, Min Ae, et al.. (2024). Transition database for rare diseases and its use for clinical documentation. Health Informatics Journal. 30(2). 1217744698–1217744698.
4.
Lim, Ee Lyn, Oliver Thieck, Thomas Magg, et al.. (2024). Disrupted degradative sorting of TLR7 is associated with human lupus. Science Immunology. 9(92). eadi9575–eadi9575. 38 indexed citations
5.
Hirota, Keiji, Yasutaka Okabe, Junji Uehori, et al.. (2024). Aberrant RNA sensing in regulatory T cells causes systemic autoimmunity. Science Advances. 10(9). eadk0820–eadk0820. 7 indexed citations
6.
Günther, Claudia, Anja Schnabel, Christine Wolf, et al.. (2023). Rapid and sustained response to JAK inhibition in a child with severe MDA5 + juvenile dermatomyositis. Pediatric Rheumatology. 21(1). 104–104. 2 indexed citations
7.
Wolf, Christine, Jörn‐Sven Kühl, Sarah Koss, et al.. (2023). Hemophagocytic lymphohistiocytosis–like hyperinflammation due to a de novo mutation in DPP9. Journal of Allergy and Clinical Immunology. 152(5). 1336–1344.e5. 5 indexed citations
8.
Broser, Philip J., et al.. (2022). Precision treatment of Singleton Merten syndrome with ruxolitinib: a case report. Pediatric Rheumatology. 20(1). 24–24. 5 indexed citations
9.
Martin, Tamara J., et al.. (2022). Seltene Erkrankungen in den Daten sichtbar machen – Kodierung. Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz. 65(11). 1133–1142. 5 indexed citations
10.
Berndt, Nicole, Christine Wolf, Peter Knuschke, et al.. (2021). Photosensitivity and cGAS-Dependent IFN-1 Activation in Patients with Lupus and TREX1 Deficiency. Journal of Investigative Dermatology. 142(3). 633–640.e6. 18 indexed citations
11.
Fazeli, Walid, Somayeh Bakhtiari, Abbas Tafakhori, et al.. (2021). The phenotypic spectrum of PCDH12 associated disorders - Five new cases and review of the literature. European Journal of Paediatric Neurology. 36. 7–13. 5 indexed citations
12.
Rösen‐Wolff, Angela, Angela Huebner, Eva‐Maria Jacobsen, et al.. (2020). More severe than CVID: Combined immunodeficiency due to a novel NFKB2 mutation. Pediatric Allergy and Immunology. 32(4). 793–797. 7 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.
Achleitner, Martin, Alexander Hennig, Katrin Peschke, et al.. (2017). Lack of Trex1 Causes Systemic Autoimmunity despite the Presence of Antiretroviral Drugs. The Journal of Immunology. 199(7). 2261–2269. 33 indexed citations
15.
Smitka, Martin, Christine Wolf, Victoria Tüngler, et al.. (2017). Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene. European Journal of Paediatric Neurology. 22(1). 186–189. 17 indexed citations
16.
Skrabl‐Baumgartner, Andrea, Barbara Plecko, Wolfgang M. Schmidt, et al.. (2017). Autoimmune phenotype with type I interferon signature in two brothers with ADA2 deficiency carrying a novel CECR1 mutation. Pediatric Rheumatology. 15(1). 67–67. 53 indexed citations
17.
Wolf, Christine, Alexander Rapp, Nicole Berndt, et al.. (2016). RPA and Rad51 constitute a cell intrinsic mechanism to protect the cytosol from self DNA. Nature Communications. 7(1). 11752–11752. 132 indexed citations
18.
Aringer, Martin, Claudia Günther, & Min Ae Lee‐Kirsch. (2012). Innate immune processes in lupus erythematosus. Clinical Immunology. 147(3). 216–222. 25 indexed citations
19.
Lee‐Kirsch, Min Ae, Maolian Gong, Herbert Schulz, et al.. (2006). Familial Chilblain Lupus, a Monogenic Form of Cutaneous Lupus Erythematosus, Maps to Chromosome 3p. The American Journal of Human Genetics. 79(4). 731–737. 91 indexed citations
20.
Lee‐Kirsch, Min Ae, et al.. (2001). Assignment<footref rid="foot01"><sup>1</sup></footref> of the human homeobox 11-like 2 gene (HOX11L2) to chromosome 5q34→q35 by radiation hybrid mapping. Cytogenetic and Genome Research. 92(3-4). 358–358. 3 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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