Mette Jorgensen

1.2k total citations
7 papers, 100 citations indexed

About

Mette Jorgensen is a scholar working on Pathology and Forensic Medicine, Molecular Biology and Cancer Research. According to data from OpenAlex, Mette Jorgensen has authored 7 papers receiving a total of 100 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pathology and Forensic Medicine, 4 papers in Molecular Biology and 2 papers in Cancer Research. Recurrent topics in Mette Jorgensen's work include Tumors and Oncological Cases (3 papers), Hedgehog Signaling Pathway Studies (2 papers) and Chromatin Remodeling and Cancer (2 papers). Mette Jorgensen is often cited by papers focused on Tumors and Oncological Cases (3 papers), Hedgehog Signaling Pathway Studies (2 papers) and Chromatin Remodeling and Cancer (2 papers). Mette Jorgensen collaborates with scholars based in United Kingdom, Netherlands and France. Mette Jorgensen's co-authors include D. Gareth Evans, Aslam Sohaib, Louise Izatt, Rosalind A. Eeles, S. L. Gibson, Angela F. Brady, Marc Tischkowitz, Helen Hanson, Vita Ridola and Steffen Hirsch and has published in prestigious journals such as European Journal of Cancer, Journal of Medical Genetics and Eye.

In The Last Decade

Mette Jorgensen

7 papers receiving 98 citations

Peers

Mette Jorgensen

MB

PFM

ONCOL

GENET

NEURO

Zsolt Nagy Hungary

Eugenia García‐Fernández Spain

Emma Miles United Kingdom

Stuart Cramer United States

Lara Rodríguez‐Laguna Spain

Riki Nishimura Japan

Maie Walsh Australia

Salvatore Serravalle Italy

Hana Pálová Czechia

Julia Balaguer Spain

Zsolt Nagy Hungary

Mette Jorgensen

32 ×0.7

MB

31 ×1.1

PFM

18 ×0.6

ONCOL

23 ×1.0

GENET

14 ×0.7

NEURO

Citations per year, relative to Mette Jorgensen Mette Jorgensen (= 1×) peers Zsolt Nagy

Countries citing papers authored by Mette Jorgensen

Since Specialization

Citations

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

Fields of papers citing papers by Mette Jorgensen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mette Jorgensen

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

All Works

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7 of 7 papers shown

1.

Habermann, Stephanie, Claudia Craven, Paul O’Hare, et al.. (2023). Atypical teratoid rhabdoid tumours (ATRTs)—a 21-year institutional experience. Child s Nervous System. 39(6). 1509–1518. 4 indexed citations

2.

Bowman, Richard, Brandon J. Walters, Victoria Smith, et al.. (2022). Visual outcomes and predictors in optic pathway glioma: a single centre study. Eye. 37(6). 1178–1183. 6 indexed citations

3.

Frühwald, Michael C., Karolina Nemes, Heidrun Boztug, et al.. (2021). Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group. Familial Cancer. 20(4). 305–316. 25 indexed citations

4.

Slater, Olga, J. Gains, Anna Kelsey, et al.. (2021). Localised rhabdomyosarcoma in infants (<12 months) and young children (12–36 months of age) treated on the EpSSG RMS 2005 study. European Journal of Cancer. 160. 206–214. 13 indexed citations

5.

Guerrini‐Rousseau, Léa, Miriam J. Smith, Christian P. Kratz, et al.. (2021). Current recommendations for cancer surveillance in Gorlin syndrome: a report from the SIOPE host genome working group (SIOPE HGWG). Familial Cancer. 20(4). 317–325. 17 indexed citations

6.

Sudhakar, Sniya, Kshitij Mankad, Mette Jorgensen, et al.. (2020). Constitutional mismatch repair deficiency (CMMRD) presenting with high-grade glioma, multiple developmental venous anomalies and malformations of cortical development—a multidisciplinary/multicentre approach and neuroimaging clues to clinching the diagnosis. Child s Nervous System. 37(7). 2375–2379. 4 indexed citations

7.

Hanson, Helen, Angela F. Brady, Rosalind A. Eeles, et al.. (2020). UKCGG Consensus Group guidelines for the management of patients with constitutional TP53 pathogenic variants. Journal of Medical Genetics. 58(2). 135–139. 31 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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