Katharina Eirich

629 total citations
8 papers, 389 citations indexed

About

Katharina Eirich is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Katharina Eirich has authored 8 papers receiving a total of 389 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Surgery. Recurrent topics in Katharina Eirich's work include DNA Repair Mechanisms (5 papers), BRCA gene mutations in cancer (3 papers) and CRISPR and Genetic Engineering (2 papers). Katharina Eirich is often cited by papers focused on DNA Repair Mechanisms (5 papers), BRCA gene mutations in cancer (3 papers) and CRISPR and Genetic Engineering (2 papers). Katharina Eirich collaborates with scholars based in Germany, United States and Austria. Katharina Eirich's co-authors include Detlev Schindler, Beatrice Schuster, John Rouse, Johan P. de Winter, Jûrgen Steltenpool, Martin A. Rooimans, Thomas Bettecken, Chantal Stoepker, Anneke B. Oostra and Aggie Nieuwint and has published in prestigious journals such as Nature Genetics, Oncogene and Human Molecular Genetics.

In The Last Decade

Katharina Eirich

8 papers receiving 381 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Katharina Eirich Germany	6	313	145	83	65	34	8	389
Irina Kholodnyuk Sweden	10	195 0.6×	83 0.6×	60 0.7×	64 1.0×	46 1.4×	18	278
Hannah F. Almubarak Saudi Arabia	5	252 0.8×	94 0.6×	110 1.3×	60 0.9×	31 0.9×	7	371
Ian Kesterton United Kingdom	6	352 1.1×	137 0.9×	128 1.5×	100 1.5×	38 1.1×	8	444
Jenni Nikkilä Finland	10	337 1.1×	195 1.3×	83 1.0×	121 1.9×	66 1.9×	11	433
Svenja Leible Germany	7	366 1.2×	48 0.3×	64 0.8×	88 1.4×	54 1.6×	10	509
Ingrid Stec Netherlands	7	422 1.3×	142 1.0×	44 0.5×	46 0.7×	48 1.4×	9	527
Swarna Gogineni United States	8	181 0.6×	114 0.8×	56 0.7×	71 1.1×	47 1.4×	19	322
Landon Wark Canada	10	206 0.7×	47 0.3×	46 0.6×	79 1.2×	35 1.0×	15	313
G. Liu United States	10	255 0.8×	163 1.1×	119 1.4×	117 1.8×	17 0.5×	15	381
Mika Bessho United States	10	344 1.1×	96 0.7×	77 0.9×	143 2.2×	21 0.6×	15	414

Countries citing papers authored by Katharina Eirich

Since Specialization

Citations

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

Fields of papers citing papers by Katharina Eirich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katharina Eirich

This figure shows the co-authorship network connecting the top 25 collaborators of Katharina Eirich. A scholar is included among the top collaborators of Katharina Eirich 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 Katharina Eirich. Katharina Eirich 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

1.

Sattler, Horst, Marcus E. Kleber, Katharina Eirich, et al.. (2018). Recurrent tendosynovitis as a rare manifestation of a lipid disorder. Journal of clinical lipidology. 13(1). 54–61. 4 indexed citations

2.

Bernuth, Horst von, Sebastian Fröhler, Nadine Krämer, et al.. (2014). Combined immunodeficiency develops with age in Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2). Orphanet Journal of Rare Diseases. 9(1). 116–116. 31 indexed citations

3.

Böhringer, Michael, Nicholas B. Griner, Ellen S. Dickinson, et al.. (2013). siRNA screening identifies differences in the Fanconi anemia pathway in BALB/c-Trp53+/− with susceptibility versus C57BL/6-Trp53+/− mice with resistance to mammary tumors. Oncogene. 32(48). 5458–5470. 7 indexed citations

4.

Serra, Annalisa, Katharina Eirich, Annika Winkler, et al.. (2012). Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi Anemia. Molecular Syndromology. 3(3). 120–130. 13 indexed citations

5.

Osório, Ana, Daniela Endt, Fernando Fernández, et al.. (2012). Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families. Human Molecular Genetics. 21(13). 2889–2898. 76 indexed citations

6.

Meindl, Alfons, Katharina Eirich, Stefanie Engert, et al.. (2012). Germline RAD51C mutations confer susceptibility to ovarian cancer. Nature Genetics. 44(5). 476–476. 5 indexed citations

7.

Stoepker, Chantal, Beatrice Schuster, Yvonne Hilhorst‐Hofstee, et al.. (2011). SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype. Nature Genetics. 43(2). 138–141. 233 indexed citations

8.

Kopic, Sascha, Katharina Eirich, Beatrice Schuster, et al.. (2010). Hepatoblastoma in a 4‐year‐old girl with Fanconi anaemia. Acta Paediatrica. 100(5). 780–783. 20 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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