Josefine Fuchs

1.1k total citations
27 papers, 792 citations indexed

About

Josefine Fuchs is a scholar working on Ophthalmology, Radiology, Nuclear Medicine and Imaging and Genetics. According to data from OpenAlex, Josefine Fuchs has authored 27 papers receiving a total of 792 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Ophthalmology, 11 papers in Radiology, Nuclear Medicine and Imaging and 7 papers in Genetics. Recurrent topics in Josefine Fuchs's work include Retinal Diseases and Treatments (11 papers), Retinal and Optic Conditions (7 papers) and Retinal Imaging and Analysis (7 papers). Josefine Fuchs is often cited by papers focused on Retinal Diseases and Treatments (11 papers), Retinal and Optic Conditions (7 papers) and Retinal Imaging and Analysis (7 papers). Josefine Fuchs collaborates with scholars based in Denmark, Germany and United States. Josefine Fuchs's co-authors include Thomas Rosenberg, Henrik Lund‐Andersen, Michael Larsen, Birgit Sander, Sara Brandi Bloch, Morten la Cour, Ernst Goldschmidt, Peter N. Robinson, Frank Tiecke and Patrick Booms and has published in prestigious journals such as PLoS ONE, Ophthalmology and The American Journal of Human Genetics.

In The Last Decade

Josefine Fuchs

25 papers receiving 763 citations

Peers

Josefine Fuchs

OPHTH

RNMI

GENET

PRM

CCM

Daiju Iwata Japan

Don H. Nicholson United States

Michael Triebwasser United States

Michael Ilsar Israel

Saleh Al-Mesfer Saudi Arabia

J. Maguire United States

Steven R. Bennett United States

G. J. Jaffe United States

M. Ashwin Reddy United Kingdom

Paul J. Bryar United States

Daiju Iwata Japan

Josefine Fuchs

730 ×1.7

OPHTH

209 ×0.6

RNMI

21 ×0.1

GENET

103 ×0.8

PRM

22 ×0.2

CCM

Citations per year, relative to Josefine Fuchs Josefine Fuchs (= 1×) peers Daiju Iwata

Countries citing papers authored by Josefine Fuchs

Since Specialization

Citations

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

Fields of papers citing papers by Josefine Fuchs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Josefine Fuchs

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

All Works

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20 of 20 papers shown

Potapenko, Ivan, Bo Thiesson, Javad Nouri Hajari, et al.. (2022). Automated artificial intelligence‐based system for clinical follow‐up of patients with age‐related macular degeneration. Acta Ophthalmologica. 100(8). 927–936. 7 indexed citations

Potapenko, Ivan, Bo Thiesson, Torben Lykke Sørensen, et al.. (2021). Detection of oedema on optical coherence tomography images using deep learning model trained on noisy clinical data. Acta Ophthalmologica. 100(1). 103–110. 9 indexed citations

Nissen, Janna, Pikka Jokelainen, Christen Rune Stensvold, et al.. (2017). The disease burden of congenital toxoplasmosis in Denmark, 2014. PLoS ONE. 12(5). e0178282–e0178282. 18 indexed citations

Dalvin, Lauren A., et al.. (2016). Retinitis pigmentosa associated with a mutation in BEST1. American Journal of Ophthalmology Case Reports. 2. 11–17. 13 indexed citations

Heim, Nils, Anton Faron, Josefine Fuchs, et al.. (2016). Die Lesbarkeit von onlinebasierten Patienteninformationen in der Augenheilkunde. Der Ophthalmologe. 114(5). 450–456. 7 indexed citations

Rasmussen, Annette, et al.. (2016). Neovascular age‐related macular degeneration treated with ranibizumab or aflibercept in the same large clinical setting: visual outcome and number of injections. Acta Ophthalmologica. 95(2). 128–132. 17 indexed citations

Rasmussen, Annette, et al.. (2015). Visual outcomes in relation to time to treatment in neovascular age‐related macular degeneration. Acta Ophthalmologica. 93(7). 616–620. 40 indexed citations

Rasmussen, Annette, Sara Brandi Bloch, Josefine Fuchs, et al.. (2013). A 4-Year Longitudinal Study of 555 Patients Treated with Ranibizumab for Neovascular Age-related Macular Degeneration. Ophthalmology. 120(12). 2630–2636. 100 indexed citations

Bloch, Sara Brandi, Morten la Cour, Birgit Sander, et al.. (2011). Predictors of 1‐year visual outcome in neovascular age‐related macular degeneration following intravitreal ranibizumab treatment. Acta Ophthalmologica. 91(1). 42–47. 56 indexed citations

10.

Gal, Andreas, Isabella Rau, Hans‐Jürgen Kreienkamp, et al.. (2011). Autosomal-Recessive Posterior Microphthalmos Is Caused by Mutations in PRSS56, a Gene Encoding a Trypsin-Like Serine Protease. The American Journal of Human Genetics. 88(3). 382–390. 60 indexed citations

11.

Fuchs, Josefine, et al.. (2005). Hereditary High Hypermetropia in the Faroe Islands. Ophthalmic Genetics. 26(1). 9–15. 20 indexed citations

12.

Booms, Patrick, Frank Tiecke, Seval Türkmen, et al.. (2002). TGGE screening of the entireFBN1coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies. Human Mutation. 20(3). 197–208. 52 indexed citations

13.

Tiecke, Frank, Patrick Booms, Peter N. Robinson, et al.. (2001). Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype–phenotype correlations in FBN1 exons 24–40. European Journal of Human Genetics. 9(1). 13–21. 98 indexed citations

14.

Tiecke, Frank, Patrick Booms, Thomas Rosenberg, et al.. (2000). Clustering of mutations associated with mild Marfan-like phenotypes in the 3? region ofFBN1 suggests a potential genotype-phenotype correlation. American Journal of Medical Genetics. 91(3). 212–221. 48 indexed citations

15.

Fuchs, Josefine & Thomas Rosenberg. (1998). Congenital ectopia lentis, A Danish national survey. Acta Ophthalmologica Scandinavica. 76(1). 20–26. 60 indexed citations

16.

Fuchs, Josefine. (1997). Marfan syndrome and other systemic disorders with congenital ectopia lentis. A Danish national survey. Acta Paediatrica. 86(9). 947–952. 38 indexed citations

17.

Fuchs, Josefine, et al.. (1992). Glaucoma blindness in Denmark. Acta Ophthalmologica. 70(1). 73–78. 20 indexed citations

18.

Fledelius, Hans C., Josefine Fuchs, & A C Reck. (1990). Refraction in diabetics during metabolic dysregulation, acute or chronic. Acta Ophthalmologica. 68(3). 275–280. 17 indexed citations

19.

Goldschmidt, Ernst, Josefine Fuchs, & Christina Raitta. (1989). Glaucoma prevalence in the Nordic countries. Acta Ophthalmologica. 67(2). 204–210. 17 indexed citations

20.

Fuchs, Josefine. (1973). [A new method for surgery of xanthelasma (author's transl)].. PubMed. 163(3). 324–6. 2 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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