Kathrin Rommel

636 total citations
12 papers, 411 citations indexed

About

Kathrin Rommel is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Oncology. According to data from OpenAlex, Kathrin Rommel has authored 12 papers receiving a total of 411 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 4 papers in Pulmonary and Respiratory Medicine and 3 papers in Oncology. Recurrent topics in Kathrin Rommel's work include Connective tissue disorders research (5 papers), Genomics and Rare Diseases (4 papers) and Protease and Inhibitor Mechanisms (3 papers). Kathrin Rommel is often cited by papers focused on Connective tissue disorders research (5 papers), Genomics and Rare Diseases (4 papers) and Protease and Inhibitor Mechanisms (3 papers). Kathrin Rommel collaborates with scholars based in Germany, Canada and France. Kathrin Rommel's co-authors include Jörg Schmidtke, Mine Arslan‐Kirchner, Matthias Karck, Axel Haverich, Krishna K. Singh, Anjali Mishra, Valérie Serrière-Lanneau, Sophie Höhn, Sonia Pavan and Ana Rath and has published in prestigious journals such as PLoS ONE, Human Mutation and European Journal of Human Genetics.

In The Last Decade

Kathrin Rommel

11 papers receiving 402 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kathrin Rommel Germany 6 320 152 118 115 69 12 411
Helle Wulf-Johansson Denmark 8 56 0.2× 100 0.7× 29 0.2× 85 0.7× 48 0.7× 11 262
Frank Richard Germany 9 67 0.2× 105 0.7× 21 0.2× 116 1.0× 77 1.1× 17 372
Naomi L. Sharma United Kingdom 7 72 0.2× 305 2.0× 12 0.1× 222 1.9× 119 1.7× 12 452
Emanuela Fantinel Italy 11 31 0.1× 299 2.0× 47 0.4× 121 1.1× 118 1.7× 29 409
Joe Dennis United Kingdom 9 109 0.3× 30 0.2× 18 0.2× 88 0.8× 61 0.9× 24 247
Pierre‐Marie Morice France 7 35 0.1× 39 0.3× 81 0.7× 97 0.8× 44 0.6× 21 382
Raffaella Toso United States 14 104 0.3× 70 0.5× 40 0.3× 76 0.7× 21 0.3× 23 613
Anh Tuan Huynh Austria 8 33 0.1× 168 1.1× 48 0.4× 110 1.0× 58 0.8× 14 356
Vicky Kang United States 5 54 0.2× 210 1.4× 28 0.2× 38 0.3× 62 0.9× 12 315
M Izuo Japan 12 101 0.3× 55 0.4× 13 0.1× 50 0.4× 103 1.5× 82 425

Countries citing papers authored by Kathrin Rommel

Since Specialization
Citations

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

Fields of papers citing papers by Kathrin Rommel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kathrin Rommel

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

All Works

12 of 12 papers shown
1.
Martin, Tamara J., et al.. (2022). Seltene Erkrankungen in den Daten sichtbar machen – Kodierung. Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz. 65(11). 1133–1142. 5 indexed citations
2.
Rommel, Kathrin, et al.. (2018). Drei Fälle von schwerer chronischer Diarrhö mit seltener Ursache und einfacher Therapie. Der Internist. 59(9). 961–966.
3.
Pavan, Sonia, et al.. (2017). Clinical Practice Guidelines for Rare Diseases: The Orphanet Database. PLoS ONE. 12(1). e0170365–e0170365. 113 indexed citations
4.
Storf, Holger, et al.. (2014). Se-atlas-cartographic representation of experts for rare diseases. Orphanet Journal of Rare Diseases. 9(Suppl 1). P1–P1. 4 indexed citations
5.
Rommel, Kathrin, et al.. (2011). Funding of rare disease research in Germany: a pilot study. Journal of Community Genetics. 2(2). 101–105. 3 indexed citations
6.
7.
Singh, Krishna K., Praphulla Chandra Shukla, Kathrin Rommel, Jörg Schmidtke, & Mine Arslan‐Kirchner. (2006). Sequence variations in the 5′ upstream regions of the FBN1 gene associated with Marfan syndrome. European Journal of Human Genetics. 14(7). 876–879. 10 indexed citations
8.
Singh, Krishna K., Kathrin Rommel, Anjali Mishra, et al.. (2006). TGFBR1andTGFBR2mutations in patients with features of Marfan syndrome and Loeys-Dietz syndrome. Human Mutation. 27(8). 770–777. 137 indexed citations
9.
Rommel, Kathrin, Matthias Karck, Axel Haverich, et al.. (2005). Identification of 29 novel and nine recurrent fibrillin-1 (FBN1) mutations and genotype-phenotype correlations in 76 patients with Marfan syndrome. Human Mutation. 26(6). 529–539. 78 indexed citations
10.
Rommel, Kathrin, Matthias Karck, Axel Haverich, Jörg Schmidtke, & Mine Arslan‐Kirchner. (2002). Mutation screening of the fibrillin-1 (FBN1) gene in 76 unrelated patients with Marfan syndrome or Marfanoid features leads to the identification of 11 novel and three previously reported mutations. Human Mutation. 20(5). 406–407. 36 indexed citations
11.
Rommel, Kathrin. (1978). [The extent of the effect of clinical-chemical parameters].. PubMed. 29(1). 25–30. 1 indexed citations
12.
Burkhardt, Heinrich, et al.. (1970). Diagnostik der Knochenbeteiligung beim Morbus Hodgkin*. DMW - Deutsche Medizinische Wochenschrift. 95(18). 1009–1011. 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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