Cecilie Bredrup

2.4k total citations · 1 hit paper
34 papers, 1.4k citations indexed

About

Cecilie Bredrup is a scholar working on Radiology, Nuclear Medicine and Imaging, Molecular Biology and Cell Biology. According to data from OpenAlex, Cecilie Bredrup has authored 34 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Radiology, Nuclear Medicine and Imaging, 13 papers in Molecular Biology and 8 papers in Cell Biology. Recurrent topics in Cecilie Bredrup's work include Corneal Surgery and Treatments (11 papers), Corneal surgery and disorders (9 papers) and Proteoglycans and glycosaminoglycans research (6 papers). Cecilie Bredrup is often cited by papers focused on Corneal Surgery and Treatments (11 papers), Corneal surgery and disorders (9 papers) and Proteoglycans and glycosaminoglycans research (6 papers). Cecilie Bredrup collaborates with scholars based in Norway, United States and Germany. Cecilie Bredrup's co-authors include Per M. Knappskog, Helge Boman, Eyvind Rødahl, Tero Kivelä, Walter Lisch, Massimo Busin, Berthold Seitz, Christopher J. Rapuano, Shigeru Kinoshita and Jayne S. Weiss and has published in prestigious journals such as PLoS ONE, Diabetes Care and FEBS Letters.

In The Last Decade

Cecilie Bredrup

31 papers receiving 1.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

IC3D Classification of Corneal Dystrophies—Edition 2

2015 323 citations Jayne S. Weiss, Hans Ulrik Møller et al. Cornea profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Cecilie Bredrup Norway	14	674	434	370	205	195	34	1.4k
Ulrich Welge‐Lüßen Germany	24	596 0.9×	901 2.1×	1.1k 3.0×	109 0.5×	190 1.0×	60	1.8k
Gulab Zode United States	25	460 0.7×	1.1k 2.6×	1.3k 3.6×	145 0.7×	467 2.4×	45	2.2k
Toshiyuki Oshitari Japan	29	1.1k 1.6×	690 1.6×	1.5k 4.2×	170 0.8×	111 0.6×	125	2.4k
Weiming Mao United States	18	243 0.4×	511 1.2×	519 1.4×	44 0.2×	178 0.9×	55	1.0k
Xi Shen China	22	322 0.5×	492 1.1×	709 1.9×	123 0.6×	52 0.3×	102	1.5k
Deborah Wallace Ireland	22	219 0.3×	711 1.6×	578 1.6×	45 0.2×	221 1.1×	46	1.2k
Zhiqi Chen China	22	311 0.5×	248 0.6×	465 1.3×	88 0.4×	61 0.3×	79	1.4k
Jian Ye China	18	238 0.4×	273 0.6×	421 1.1×	116 0.6×	65 0.3×	102	983
E. Balestrazzi Italy	26	1.2k 1.8×	363 0.8×	1.5k 4.1×	224 1.1×	36 0.2×	117	2.3k
Shlomo Melamed Israel	30	1.2k 1.8×	428 1.0×	2.0k 5.4×	265 1.3×	82 0.4×	98	2.5k

Countries citing papers authored by Cecilie Bredrup

Since Specialization

Citations

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

Fields of papers citing papers by Cecilie Bredrup

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cecilie Bredrup

This figure shows the co-authorship network connecting the top 25 collaborators of Cecilie Bredrup. A scholar is included among the top collaborators of Cecilie Bredrup 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 Cecilie Bredrup. Cecilie Bredrup 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

Rødahl, Eyvind, et al.. (2025). Variable response of germline activating PDGFRB variants to receptor tyrosine kinase inhibitors: implications for treatment. European Journal of Human Genetics. 33(12). 1668–1676.

Aukrust, Ingvild, Laurie L. Molday, Siren Berland, et al.. (2024). Functional Characterization of ABCA4 Missense Variants Aids Variant Interpretation and Phenotype Prediction in Patients With ABCA4-Retinal Dystrophies. Investigative Ophthalmology & Visual Science. 65(10). 2–2.

Bruland, Ove, et al.. (2023). Corneal Vascularization Associated With a Novel PDGFRB Variant. Investigative Ophthalmology & Visual Science. 64(14). 9–9. 3 indexed citations

Bredrup, Cecilie, et al.. (2023). Functional characterization of all‐trans retinoic acid‐induced differentiation factor (ATRAID). FEBS Open Bio. 13(10). 1874–1886. 2 indexed citations

Abarca-Barriga, Hugo Hernán, Dorien J.M. Peters, Gunnar Houge, et al.. (2023). A Pellino‐2 variant is associated with constitutive NLRP3 inflammasome activation in a family with ocular pterygium–digital keloid dysplasia. FEBS Letters. 597(9). 1290–1299. 1 indexed citations

Bruland, Ove, et al.. (2021). K⁺ regulates relocation of Pellino‐2 to the site of NLRP3 inflammasome activation in macrophages. FEBS Letters. 595(19). 2437–2446. 6 indexed citations

Jensen, Hanne, Jennifer J. Johnston, Emilio Di Maria, et al.. (2018). Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome. The American Journal of Human Genetics. 103(6). 976–983. 18 indexed citations

Bredrup, Cecilie, Tomasz Stokowy, Julie McGaughran, et al.. (2018). A tyrosine kinase-activating variant Asn666Ser in PDGFRB causes a progeria-like condition in the severe end of Penttinen syndrome. European Journal of Human Genetics. 27(4). 574–581. 20 indexed citations

Kamma‐Lorger, Christina S., Christian Pinali, Juan Carlos Martínez, et al.. (2016). Role of Decorin Core Protein in Collagen Organisation in Congenital Stromal Corneal Dystrophy (CSCD). PLoS ONE. 11(2). e0147948–e0147948. 23 indexed citations

10.

Weiss, Jayne S., Hans Ulrik Møller, Anthony J. Aldave, et al.. (2015). IC3D Classification of Corneal Dystrophies—Edition 2. Cornea. 34(2). 117–159. 323 indexed citations breakdown →

11.

Bruland, Ove, Anni Vedeler, Jaakko Saraste, et al.. (2015). Development of Congenital Stromal Corneal Dystrophy Is Dependent on Export and Extracellular Deposition of Truncated Decorin. Investigative Ophthalmology & Visual Science. 56(5). 2909–2909. 19 indexed citations

12.

Bredrup, Cecilie, Stefan Johansson, Laurence A. Bindoff, et al.. (2015). High Myopia–Excavated Optic Disc Anomaly Associated With a Frameshift Mutation in the MYC-Binding Protein 2 Gene (MYCBP2). American Journal of Ophthalmology. 159(5). 973–979.e2. 9 indexed citations

13.

Abarca-Barriga, Hugo Hernán, Olav H. Haugen, Gunnar Høvding, et al.. (2014). Ocular pterygium—Digital keloid dysplasia. American Journal of Medical Genetics Part A. 164(11). 2901–2907. 7 indexed citations

14.

Rødahl, Eyvind, Per M. Knappskog, Cecilie Bredrup, & Helge Boman. (2012). Congenital Stromal Corneal Dystrophy. Europe PMC (PubMed Central). 2 indexed citations

15.

Bredrup, Cecilie, et al.. (2011). Early panretinal photocoagulation for ERG‐verified ischaemic central retinal vein occlusion. Acta Ophthalmologica. 91(1). 37–41. 10 indexed citations

16.

Fiskerstrand, Torunn, Dorra H’mida-Ben Brahim, Stefan Johansson, et al.. (2010). Mutations in ABHD12 Cause the Neurodegenerative Disease PHARC: An Inborn Error of Endocannabinoid Metabolism. The American Journal of Human Genetics. 87(3). 410–417. 162 indexed citations

17.

Vesterhus, Mette, Helge Ræder, Harald Aurlien, et al.. (2008). Neurological Features and Enzyme Therapy in Patients With Endocrine and Exocrine Pancreas Dysfunction Due to CEL Mutations. Diabetes Care. 31(9). 1738–1740. 10 indexed citations

18.

Bredrup, Cecilie, et al.. (2007). Photopic 30 Hz flicker electroretinography predicts ocular neovascularization in central retinal vein occlusion. Acta Ophthalmologica Scandinavica. 85(6). 640–643. 25 indexed citations

19.

Rødahl, Eyvind, Rita Van Ginderdeuren, Per M. Knappskog, Cecilie Bredrup, & Helge Boman. (2006). A Second Decorin Frame Shift Mutation in a Family With Congenital Stromal Corneal Dystrophy. American Journal of Ophthalmology. 142(3). 520–521. 51 indexed citations

20.

Bredrup, Cecilie, Per M. Knappskog, Jacek Majewski, Eyvind Rødahl, & Helge Boman. (2005). Congenital Stromal Dystrophy of the Cornea Caused by a Mutation in the Decorin Gene. Investigative Ophthalmology & Visual Science. 46(2). 420–420. 126 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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