Mette Ramsing

715 total citations
30 papers, 454 citations indexed

About

Mette Ramsing is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mette Ramsing has authored 30 papers receiving a total of 454 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mette Ramsing's work include Renal and related cancers (5 papers), Prenatal Screening and Diagnostics (4 papers) and Genetic Syndromes and Imprinting (3 papers). Mette Ramsing is often cited by papers focused on Renal and related cancers (5 papers), Prenatal Screening and Diagnostics (4 papers) and Genetic Syndromes and Imprinting (3 papers). Mette Ramsing collaborates with scholars based in Denmark, Germany and United States. Mette Ramsing's co-authors include Helga Rehder, Wolfgang Holzgreve, Michael Pedersen, Naja Becher, Mette Sommerlund, Bárbara Fritz, Julie Glavind, Chong J. Kim, W. Lenz and Niels Uldbjerg and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Cell Reports.

In The Last Decade

Mette Ramsing

30 papers receiving 448 citations

Peers

Mette Ramsing
Katherine H. Miller United States
W C Mentzer United States
R. Øyen United States
Mario Vignali Italy
Philippe Tummers Belgium
Thomas L. Morgan United States
Johann Bichler United States
Janis P. O’Malley United States
B G Leventhal United States
Ryo Kitagawa Japan
Katherine H. Miller United States
Mette Ramsing
Citations per year, relative to Mette Ramsing Mette Ramsing (= 1×) peers Katherine H. Miller

Countries citing papers authored by Mette Ramsing

Since Specialization
Citations

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

Fields of papers citing papers by Mette Ramsing

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mette Ramsing

This figure shows the co-authorship network connecting the top 25 collaborators of Mette Ramsing. A scholar is included among the top collaborators of Mette Ramsing 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 Mette Ramsing. Mette Ramsing 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.
Ramsing, Mette, et al.. (2023). Majocchi’s Granuloma – The Great Mimicker: A Case Report. Case Reports in Dermatology. 15(1). 190–193. 2 indexed citations
2.
Herlin, Troels, Mette Holm, Mette Christiansen, et al.. (2020). Idiopathic hypereosinophilic syndrome: A rare diagnosis in children. SHILAP Revista de lepidopterología. 8(10). 2013–2016. 5 indexed citations
3.
Massa, Filippo, Serge Garbay, Mette Ramsing, et al.. (2020). Developmental Renal Glomerular Defects at the Origin of Glomerulocystic Disease. Cell Reports. 33(4). 108304–108304. 3 indexed citations
4.
Hansen, Anette Tarp, Puk Sandager, Mette Ramsing, et al.. (2018). Tinzaparin for the treatment of foetal growth retardation: An open-labelled randomized clinical trial. Thrombosis Research. 170. 38–44. 6 indexed citations
5.
Rasmussen, Maria, Lone Sunde, Mette Ramsing, et al.. (2017). Targeted gene sequencing and whole‐exome sequencing in autopsied fetuses with prenatally diagnosed kidney anomalies. Clinical Genetics. 93(4). 860–869. 40 indexed citations
6.
7.
Becher, Naja, et al.. (2017). First reported case of Simpson–Golabi–Behmel syndrome in a female fetus diagnosed prenatally with chromosomal microarray. Clinical Case Reports. 5(5). 608–612. 9 indexed citations
8.
Christensen, Rikke, David M. Owens, Annette Füchtbauer, et al.. (2017). Constitutive transgene expression of Stem Cell Antigen-1 in the hair follicle alters the sensitivity to tumor formation and progression. Stem Cell Research. 23. 109–118. 4 indexed citations
9.
Cortés, Claudio R., Aideen McInerney‐Leo, Ida Vogel, et al.. (2016). Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function. Scientific Reports. 6(1). 24083–24083. 21 indexed citations
10.
Herlin, Troels, et al.. (2016). Diagnosis and Treatment of Blau Syndrome/Early-onset Sarcoidosis, an Autoinflammatory Granulomatous Disease, in an Infant. Acta Dermato Venereologica. 97(1). 126–127. 11 indexed citations
11.
Loo, Christine, et al.. (2015). The development of hepatic stellate cells in normal and abnormal human fetuses - an immunohistochemical study. Physiological Reports. 3(8). e12504–e12504. 7 indexed citations
12.
Gregersen, Pernille Axél, Mette Sommerlund, Mette Ramsing, et al.. (2013). Diagnostic and Molecular Genetic Challenges in Male Incontinentia Pigmenti: A Case Report. Acta Dermato Venereologica. 93(6). 741–742. 8 indexed citations
13.
Rasmussen, Maria, Mette Ramsing, Olav Bjørn Petersen, Ida Vogel, & Lone Sunde. (2013). A description of a fetal syndrome associated with HNF1B mutation and a wide intrafamilial disease variability. American Journal of Medical Genetics Part A. 161(12). 3191–3195. 9 indexed citations
14.
Riber‐Hansen, Rikke, Nina Hastrup, Ole Clemmensen, et al.. (2011). Treatment influencing down-staging in EORTC Melanoma Group sentinel node histological protocol compared with complete step-sectioning: A national multicentre study. European Journal of Cancer. 48(3). 347–352. 16 indexed citations
15.
Buus, Niels Henrik, et al.. (2011). Antifibrotic effect after low‐dose imatinib mesylate treatment in patients with nephrogenic systemic fibrosis: an open‐label non‐randomized, uncontrolled clinical trial. Journal of the European Academy of Dermatology and Venereology. 27(6). 779–784. 24 indexed citations
16.
Gregersen, Pernille Axél, et al.. (2010). Elastosis Perforans Serpiginosa in a patient with Down syndrome treated with imiquimod 5% cream.. Dermatology Reports. 2(2). e15–e15. 4 indexed citations
17.
Ramsing, Mette, et al.. (2000). Disruptive anomalies in a newborn with focal dermalhypoplasia (Goltz syndrome). European Journal of Dermatology. 7(1). 15–18. 3 indexed citations
18.
Ramsing, Mette, Gabriele Gillessen‐Kaesbach, Wolfgang Holzgreve, Bárbara Fritz, & Helga Rehder. (2000). Variability in the phenotypic expression of Fryns syndrome: A report of two sibships. American Journal of Medical Genetics. 95(5). 415–424. 22 indexed citations
19.
Coerdt, Wiltrud, Mette Ramsing, & Helga Rehder. (1994). Embryopathologische Untersuchungen an induzierten und spontanen Aborten im 1. Schwangerschaftstrimenon. Der Pathologe. 15(1). 32–39. 2 indexed citations
20.
Ramsing, Mette, Helga Rehder, Wolfgang Holzgreve, Peter Meinecke, & W. Lenz. (1990). Fraser syndrome (cryptophthalmos with syndactyly) in the fetus and newborn. Clinical Genetics. 37(2). 84–96. 38 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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