Friederike Koerber

2.0k total citations
31 papers, 1.1k citations indexed

About

Friederike Koerber is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Friederike Koerber has authored 31 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 6 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Friederike Koerber's work include Connective tissue disorders research (8 papers), Genetic and Kidney Cyst Diseases (4 papers) and Glioma Diagnosis and Treatment (3 papers). Friederike Koerber is often cited by papers focused on Connective tissue disorders research (8 papers), Genetic and Kidney Cyst Diseases (4 papers) and Glioma Diagnosis and Treatment (3 papers). Friederike Koerber collaborates with scholars based in Germany, Austria and United States. Friederike Koerber's co-authors include Eckhard Schöenau, Oliver Semler, Christian Netzer, Bernd Wollnik, Katharina Zimmermann, Jutta Becker, Brunhilde Wirth, Hanno J. Bolz, Heike Hoyer‐Kuhn and Petra de Vries and has published in prestigious journals such as Journal of Clinical Investigation, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Friederike Koerber

28 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Friederike Koerber Germany 15 677 373 309 159 159 31 1.1k
Moira Cheung United Kingdom 22 752 1.1× 188 0.5× 287 0.9× 125 0.8× 264 1.7× 60 1.2k
Catherine Owen United Kingdom 15 782 1.2× 521 1.4× 220 0.7× 172 1.1× 63 0.4× 22 1.5k
Kentaro Matsuoka Japan 18 300 0.4× 252 0.7× 80 0.3× 193 1.2× 117 0.7× 83 1.1k
Ryan C. Hedgepeth United States 12 549 0.8× 506 1.4× 76 0.2× 224 1.4× 44 0.3× 18 1.1k
Leonid Zeitlin Israel 14 686 1.0× 103 0.3× 348 1.1× 94 0.6× 342 2.2× 32 1.1k
Tetsuya Horita Japan 22 180 0.3× 151 0.4× 1.0k 3.2× 229 1.4× 211 1.3× 79 1.8k
Martin Biosse Duplan France 15 320 0.5× 320 0.9× 308 1.0× 145 0.9× 31 0.2× 31 1.3k
Yutong Su China 19 97 0.1× 317 0.8× 292 0.9× 46 0.3× 163 1.0× 67 999
P. A. Dyer United Kingdom 18 174 0.3× 215 0.6× 248 0.8× 86 0.5× 101 0.6× 50 1.1k
R. Lala Italy 18 123 0.2× 233 0.6× 369 1.2× 162 1.0× 50 0.3× 44 825

Countries citing papers authored by Friederike Koerber

Since Specialization
Citations

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

Fields of papers citing papers by Friederike Koerber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Friederike Koerber

This figure shows the co-authorship network connecting the top 25 collaborators of Friederike Koerber. A scholar is included among the top collaborators of Friederike Koerber 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 Friederike Koerber. Friederike Koerber 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.
Jazmati, Danny, Barbara Hero, Hedwig E. Deubzer, et al.. (2022). Efficacy and Feasibility of Proton Beam Therapy in Relapsed High-Risk Neuroblastoma-Experiences from the Prospective KiProReg Registry. Current Oncology. 29(11). 8222–8234. 3 indexed citations
2.
Jazmati, Danny, Barbara Hero, Christian Bäumer, et al.. (2021). Proton Beam Therapy for Children With Neuroblastoma: Experiences From the Prospective KiProReg Registry. Frontiers in Oncology. 10. 617506–617506. 12 indexed citations
3.
Eifinger, Frank, et al.. (2021). Finding alternative sites for intraosseous infusions in newborns. Resuscitation. 163. 57–63. 7 indexed citations
4.
Koy, Anne, Friederike Koerber, Christoph Huenseler, et al.. (2020). PNPT1 mutations may cause Aicardi-Goutières-Syndrome. Brain and Development. 43(2). 320–324. 24 indexed citations
5.
Koerber, Friederike, et al.. (2019). Unfall oder Kindesmisshandlung? Differenzialdiagnostik bei Frakturen ohne klare Ursache. 14(4). 311–327. 1 indexed citations
6.
Becker, Kerstin, Friederike Koerber, Jörg Dötsch, et al.. (2018). A novel mutation in sphingosine-1-phosphate lyase causing congenital brain malformation. Brain and Development. 40(6). 480–483. 37 indexed citations
7.
Scaal, Martin, et al.. (2018). Anatomical investigations on intraosseous access in stillborns – Comparison of different devices and techniques. Resuscitation. 127. 79–82. 14 indexed citations
8.
Dafinger, Claudia, Friederike Koerber, Bernhard Schermer, et al.. (2017). Challenges in establishing genotype–phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutations. Pediatric Nephrology. 32(7). 1269–1273. 9 indexed citations
9.
Franke, Mareike, Bettina Baeßler, Claudia Dafinger, et al.. (2017). Magnetic resonance T2 mapping and diffusion-weighted imaging for early detection of cystogenesis and response to therapy in a mouse model of polycystic kidney disease. Kidney International. 92(6). 1544–1554. 23 indexed citations
10.
Eifinger, Frank, Anne Vierzig, Bernhard Roth, Martin Scaal, & Friederike Koerber. (2016). The pericardial reflection and the tip of the central venous catheter — topographical analysis in stillborn babies. Pediatric Radiology. 46(11). 1528–1531. 1 indexed citations
11.
Hoyer‐Kuhn, Heike, Oliver Semler, Kathrin Kuhr, et al.. (2015). Comparison of DXA Scans and Conventional X-rays for Spine Morphometry and Bone Age Determination in Children. Journal of Clinical Densitometry. 19(2). 208–215. 18 indexed citations
12.
Hoyer‐Kuhn, Heike, Christian Netzer, Friederike Koerber, Eckhard Schöenau, & Oliver Semler. (2014). Two years’ experience with denosumab for children with Osteogenesis imperfecta type VI. Orphanet Journal of Rare Diseases. 9(1). 145–145. 91 indexed citations
13.
Beck, Bodo B., Sandra Habbig, Katalin Dittrich, et al.. (2012). Liver cell transplantation in severe infantile oxalosis--a potential bridging procedure to orthotopic liver transplantation?. Nephrology Dialysis Transplantation. 27(7). 2984–2989. 34 indexed citations
14.
Semler, Oliver, Lutz Garbes, Katharina Keupp, et al.. (2012). A Mutation in the 5′-UTR of IFITM5 Creates an In-Frame Start Codon and Causes Autosomal-Dominant Osteogenesis Imperfecta Type V with Hyperplastic Callus. The American Journal of Human Genetics. 91(2). 349–357. 184 indexed citations
15.
Semler, Oliver, et al.. (2011). Reshaping of Vertebrae during Treatment with Neridronate or Pamidronate in Children with Osteogenesis Imperfecta. Hormone Research in Paediatrics. 76(5). 321–327. 40 indexed citations
16.
Koerber, Friederike, et al.. (2011). Standard zur Befundung von Röntgenaufnahmen der Wirbelsäule bei Patienten mit Osteogenesis imperfecta. RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren. 183(5). 462–469. 5 indexed citations
17.
Dafinger, Claudia, Max C. Liebau, Solaf M. Elsayed, et al.. (2011). Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics. Journal of Clinical Investigation. 121(7). 2662–2667. 141 indexed citations
18.
Lüers, Jan-Christoffer, B Hoffmann, Friederike Koerber, G Rahimi, & Michael Streppel. (2008). Sinus-piriformis-Fistel als seltene Ursache von Dyspnoe bei einem Neugeborenen. HNO. 56(9). 975–980. 1 indexed citations
19.
Stippel, Dirk L., Christopher Bangard, Karina Schleimer, et al.. (2006). Successful Renal Transplantation in a Child With Thrombosis of the Inferior Vena Cava and Both Iliac Veins. Transplantation Proceedings. 38(3). 688–690. 18 indexed citations
20.
Chefetz, Ilana, Raoul Heller, Assimina Galli‐Τsinopoulou, et al.. (2005). A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcification. Human Genetics. 118(2). 261–266. 89 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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