Franziska Ringpfeil

1.4k total citations
18 papers, 916 citations indexed

About

Franziska Ringpfeil is a scholar working on Genetics, Cell Biology and Molecular Biology. According to data from OpenAlex, Franziska Ringpfeil has authored 18 papers receiving a total of 916 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 15 papers in Cell Biology and 6 papers in Molecular Biology. Recurrent topics in Franziska Ringpfeil's work include Skin and Cellular Biology Research (13 papers), Dermatological and Skeletal Disorders (12 papers) and Autoimmune Bullous Skin Diseases (4 papers). Franziska Ringpfeil is often cited by papers focused on Skin and Cellular Biology Research (13 papers), Dermatological and Skeletal Disorders (12 papers) and Autoimmune Bullous Skin Diseases (4 papers). Franziska Ringpfeil collaborates with scholars based in United States, Germany and Australia. Franziska Ringpfeil's co-authors include Jouni Uitto, Mark Lebwohl, Angela M. Christiano, Leena Pulkkinen, Jouni Uitto, Aoi Nakano, Jouni Uitto, Leena Pulkkinen, Lea Pulkkinen and Dessislava Markova and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The American Journal of Human Genetics and Journal of Investigative Dermatology.

In The Last Decade

Franziska Ringpfeil

18 papers receiving 900 citations

Peers

Franziska Ringpfeil
L Amato Italy
Marieke Levitus Netherlands
Lin Gao China
Peter L. Samuels United States
Lisa M. Vincent United States
Sylvia A. Bleuming Netherlands
S B Deak United States
Franziska Ringpfeil
Citations per year, relative to Franziska Ringpfeil Franziska Ringpfeil (= 1×) peers Marilyn McLeod

Countries citing papers authored by Franziska Ringpfeil

Since Specialization
Citations

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

Fields of papers citing papers by Franziska Ringpfeil

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Franziska Ringpfeil

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

All Works

18 of 18 papers shown
1.
Alexeev, Vitali, Leonie F. A. Huitema, Franziska Ringpfeil, et al.. (2022). T‐cell activation and bacterial infection in skin wounds of recessive dystrophic epidermolysis bullosa patients. Experimental Dermatology. 31(9). 1431–1442. 8 indexed citations
2.
Huitema, Leonie F. A., Franziska Ringpfeil, Bahar Dasgeb, et al.. (2020). Aberrant recruitment of leukocytes defines poor wound healing in patients with recessive dystrophic epidermolysis bullosa. Journal of Dermatological Science. 100(3). 209–216. 12 indexed citations
3.
Ringpfeil, Franziska, et al.. (2011). The necrolytic erythemas: a continuous spectrum?. PubMed. 88(4). 185–8. 1 indexed citations
4.
Ringpfeil, Franziska, et al.. (2010). Pseudoxanthoma Elasticum: A Streamlined, Ethnicity‐based Mutation Detection Strategy. Clinical and Translational Science. 3(6). 295–298. 10 indexed citations
5.
Ringpfeil, Franziska, et al.. (2008). Large, Papillomatous, Pedunculated Nevus Sebaceus: A New Phenotype. Pediatric Dermatology. 25(3). 355–358. 13 indexed citations
6.
Ringpfeil, Franziska, et al.. (2006). Pseudoxanthoma Elasticum Is a Recessive Disease Characterized by Compound Heterozygosity. Journal of Investigative Dermatology. 126(4). 782–786. 42 indexed citations
7.
Ringpfeil, Franziska. (2005). Selected disorders of connective tissue: pseudoxanthoma elasticum, cutis laxa, and lipoid proteinosis. Clinics in Dermatology. 23(1). 41–46. 26 indexed citations
8.
Markova, Dessislava, Yaqun Zou, Franziska Ringpfeil, et al.. (2003). Genetic Heterogeneity of Cutis Laxa: A Heterozygous Tandem Duplication within the Fibulin-5 (FBLN5) Gene. The American Journal of Human Genetics. 72(4). 998–1004. 106 indexed citations
9.
Pulkkinen, Leena, Franziska Ringpfeil, & Jouni Uitto. (2002). Progress in heritable skin diseases: Molecular bases and clinical implications. Journal of the American Academy of Dermatology. 47(1). 91–104. 25 indexed citations
10.
Uitto, Jouni, Leena Pulkkinen, & Franziska Ringpfeil. (2002). Progress in Molecular Genetics of Heritable Skin Diseases: The Paradigms of Epidermolysis Bullosa and Pseudoxanthoma Elasticum. Journal of Investigative Dermatology Symposium Proceedings. 7(1). 6–16. 8 indexed citations
11.
Ringpfeil, Franziska, Lea Pulkkinen, & Jouni Uitto. (2001). Molecular genetics of pseudoxanthoma elasticum. Experimental Dermatology. 10(4). 221–228. 52 indexed citations
12.
Ringpfeil, Franziska, John J. DiGiovanna, Bernhard Korge, et al.. (2001). Darier disease – novel mutations in ATP2A2 and genotype–phenotype correlation. Experimental Dermatology. 10(1). 19–27. 70 indexed citations
13.
Uitto, Jouni, Leena Pulkkinen, & Franziska Ringpfeil. (2001). Molecular genetics of pseudoxanthoma elasticum: a metabolic disorder at the environment–genome interface?. Trends in Molecular Medicine. 7(1). 13–17. 102 indexed citations
14.
Ringpfeil, Franziska, Aoi Nakano, Jouni Uitto, & Leena Pulkkinen. (2001). Compound Heterozygosity for a Recurrent 16.5-kb Alu-Mediated Deletion Mutation and Single-Base-Pair Substitutions in the ABCC6 Gene Results in Pseudoxanthoma Elasticum. The American Journal of Human Genetics. 68(3). 642–652. 66 indexed citations
15.
Pulkkinen, Leena, Aoi Nakano, Franziska Ringpfeil, & Jouni Uitto. (2001). Identification of ABCC6 pseudogenes on human chromosome 16p: implications for mutation detection in pseudoxanthoma elasticum. Human Genetics. 109(3). 356–365. 71 indexed citations
16.
Ringpfeil, Franziska, et al.. (2001). Ibuprofen-induced bullous leukocytoclastic vasculitis.. PubMed. 67(4). 303–7. 9 indexed citations
17.
Ringpfeil, Franziska, Mark Lebwohl, & Jouni Uitto. (2000). Mutations in the MRP6 Gene Cause Pseudoxanthoma Elasticum.. Journal of Investigative Dermatology. 115(2). 332–332. 3 indexed citations
18.
Ringpfeil, Franziska, Mark Lebwohl, Angela M. Christiano, & Jouni Uitto. (2000). Pseudoxanthoma elasticum: Mutations in the MRP6 gene encoding a transmembrane ATP-binding cassette (ABC) transporter. Proceedings of the National Academy of Sciences. 97(11). 6001–6006. 292 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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