Min Ae Lee-Kirsch

699 total citations
8 papers, 175 citations indexed

About

Min Ae Lee-Kirsch is a scholar working on Immunology, Molecular Biology and Rheumatology. According to data from OpenAlex, Min Ae Lee-Kirsch has authored 8 papers receiving a total of 175 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Immunology, 3 papers in Molecular Biology and 3 papers in Rheumatology. Recurrent topics in Min Ae Lee-Kirsch's work include interferon and immune responses (5 papers), Systemic Lupus Erythematosus Research (3 papers) and RNA regulation and disease (2 papers). Min Ae Lee-Kirsch is often cited by papers focused on interferon and immune responses (5 papers), Systemic Lupus Erythematosus Research (3 papers) and RNA regulation and disease (2 papers). Min Ae Lee-Kirsch collaborates with scholars based in Germany, United States and Argentina. Min Ae Lee-Kirsch's co-authors include Georgia Ramantani, Victoria Tüngler, Franziska Schmidt, Mike Lorenz, Wolfgang Staroske, Martin Häusler, Petra Schwille, Pascal Niggemann, Osvaldo Chara and Barbara Kind and has published in prestigious journals such as Annals of the New York Academy of Sciences, Journal of Molecular Medicine and Journal of Child Neurology.

In The Last Decade

Min Ae Lee-Kirsch

8 papers receiving 168 citations

Peers

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

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8 of 8 papers shown

#	Work	Indexed citations
1	Aicardi-Goutières syndrome due to a paternal mosaic IFIH1 mutation 2019 ·Neurology Genetics ·Victoria Tüngler, (unknown), (unknown), Peter Kaufmann, Christine Wolf, (unknown), Florian Harmuth, Jennifer Reichbauer, Ingeborg Krägeloh‐Mann, Rebecca Schüle, Min Ae Lee-Kirsch	6
2	Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutation 2016 ·Brain and Development ·(unknown), Katja Storch, Gabriele Hahn, Min Ae Lee-Kirsch, Georgia Ramantani, Sandra L. Jackson, Derek Neilson, Maja von der Hagen, Ute Hehr, Martin Smitka	26
3	Phenotypic Variability in a Family with Aicardi-Goutières Syndrome Due to the Common A177T <i>RNASEH2B</i> Mutation 2014 ·Case Reports in Clinical Medicine ·Victoria Tüngler, Franziska Schmidt, (unknown), (unknown), Min Ae Lee-Kirsch	8
4	Epilepsy in Aicardi–Goutières syndrome 2013 ·European Journal of Paediatric Neurology ·Georgia Ramantani, Louis Maillard, Thomas Bast, Ralf A. Husain, Pascal Niggemann, Jürgen Kohlhase, Christoph Hertzberg, (unknown), A. Micheil Innes, (unknown), Andrea Bevot, Celina von Stülpnagel, (unknown), Frank Niemann, Mehmet Ali Ergün, Uta Tacke, Martin Häusler, Chrysanthy Ikonomidou, Rudolf Korinthenberg, Min Ae Lee-Kirsch	18
5	Single-stranded nucleic acids promote SAMHD1 complex formation 2013 ·Journal of Molecular Medicine ·Victoria Tüngler, Wolfgang Staroske, Barbara Kind, (unknown), Stefanie Kretschmer, Franziska Schmidt, (unknown), Mike Lorenz, Osvaldo Chara, Petra Schwille, Min Ae Lee-Kirsch	68
6	Aicardi-Goutières Syndrome and Systemic Lupus Erythematosus (SLE) in a 12-Year-Old Boy With SAMHD1 Mutations 2011 ·Journal of Child Neurology ·Georgia Ramantani, Martin Häusler, Pascal Niggemann, (unknown), (unknown), Michael Mull, Klaus Tenbrock, Min Ae Lee-Kirsch	39
7	Unusual Radiological Presentation of Tuberous Sclerosis Complex With Leptomeningeal Angiomatosis Associated With a Hypomorphic Mutation in the TSC2 Gene 2009 ·Journal of Child Neurology ·Georgia Ramantani, Pascal Niggemann, Gabriele Hahn, Andrea Näke, Raimund Fahsold, Min Ae Lee-Kirsch	3
8	Genetic Dissection of Autoimmune Polyendocrine Syndrome Type 2 2007 ·Annals of the New York Academy of Sciences ·Annalisa Ballarini, Min Ae Lee-Kirsch	7

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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