Ulrike Gamerdinger

580 total citations
20 papers, 398 citations indexed

About

Ulrike Gamerdinger is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Ulrike Gamerdinger has authored 20 papers receiving a total of 398 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Plant Science. Recurrent topics in Ulrike Gamerdinger's work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (7 papers) and Prenatal Screening and Diagnostics (3 papers). Ulrike Gamerdinger is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (7 papers) and Prenatal Screening and Diagnostics (3 papers). Ulrike Gamerdinger collaborates with scholars based in Germany, Iran and Poland. Ulrike Gamerdinger's co-authors include Thomas Dreyer, Irina Fenic, Klaus Steger, Eva Penelo, U. Stahl, Joachim Woenckhaus, Hartmut Engels, M. Hansmann, Gabriele Lasczkowski and Stefan Gattenlöhner and has published in prestigious journals such as Cancer Research, The Journal of Pathology and Oral Oncology.

In The Last Decade

Ulrike Gamerdinger

19 papers receiving 389 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ulrike Gamerdinger Germany 11 190 105 94 74 60 20 398
Christine R. Bryke United States 13 268 1.4× 229 2.2× 102 1.1× 63 0.9× 45 0.8× 31 529
Jacqueline R. Batanian United States 15 206 1.1× 186 1.8× 82 0.9× 92 1.2× 104 1.7× 56 568
Mamoru Ozaki Japan 12 152 0.8× 142 1.4× 64 0.7× 53 0.7× 33 0.6× 38 389
Shunsuke Kimura Japan 13 203 1.1× 144 1.4× 71 0.8× 25 0.3× 31 0.5× 40 476
Hasan Acar Türkiye 12 139 0.7× 82 0.8× 30 0.3× 75 1.0× 24 0.4× 69 429
P. Mollevanger Netherlands 13 196 1.0× 189 1.8× 52 0.6× 30 0.4× 95 1.6× 19 428
Ellen Kater‐Baats Netherlands 6 244 1.3× 93 0.9× 56 0.6× 78 1.1× 21 0.3× 8 401
Javier Suela Spain 13 268 1.4× 145 1.4× 61 0.6× 56 0.8× 28 0.5× 31 539
Timothy J. Vyse United Kingdom 10 186 1.0× 298 2.8× 31 0.3× 34 0.5× 49 0.8× 11 619
Paola Angelini Italy 15 189 1.0× 65 0.6× 74 0.8× 52 0.7× 14 0.2× 33 643

Countries citing papers authored by Ulrike Gamerdinger

Since Specialization
Citations

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

Fields of papers citing papers by Ulrike Gamerdinger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulrike Gamerdinger

This figure shows the co-authorship network connecting the top 25 collaborators of Ulrike Gamerdinger. A scholar is included among the top collaborators of Ulrike Gamerdinger 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 Ulrike Gamerdinger. Ulrike Gamerdinger 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.
Pscherer, Sibylle, Ulrike Gamerdinger, Andrea Teigler‐Schlegel, et al.. (2021). Parallel evaluation of cell‑based phage display panning strategies: Optimized selection and depletion steps result in AML blast‑binding consensus antibodies. Molecular Medicine Reports. 24(5). 5 indexed citations
2.
Dreyer, Thomas, Moritz Meyer, Alexander Brobeil, et al.. (2020). Das Mukoepidermoidkarzinom – Bedeutung der Molekularpathologie. Laryngo-Rhino-Otologie. 99(3). 144–148. 5 indexed citations
3.
Wagner, Steffen, Ulrike Gamerdinger, Sarah Sandmann, et al.. (2019). Genetic alterations in human papillomavirus-associated oropharyngeal squamous cell carcinoma of patients with treatment failure. Oral Oncology. 93. 59–65. 10 indexed citations
4.
Harth, Sebastian, et al.. (2015). Dedifferentiated Liposarcoma of the Anterior Mediastinum: A Rare Case. RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren. 188(1). 95–97. 7 indexed citations
5.
Sharma, Shachi Jenny, et al.. (2014). Compound lesion of a basal cell carcinoma and a malignant melanoma: Is there a common genetic origin?. European Archives of Oto-Rhino-Laryngology. 272(2). 505–509.
6.
Spieker, Tilmann, Ulrike Gamerdinger, Johannes Berger, et al.. (2014). A Recurrent Activating PLCG1 Mutation in Cardiac Angiosarcomas Increases Apoptosis Resistance and Invasiveness of Endothelial Cells. Cancer Research. 74(21). 6173–6183. 53 indexed citations
7.
Gamerdinger, Ulrike, Alexander Brobeil, Mehmet Kemal Tur, et al.. (2014). Detection of an activated JAK3 variant and a Xq26.3 microdeletion causing loss of PHF6 and miR-424 expression in myelodysplastic syndromes by combined targeted next generation sequencing and SNP array analysis. Pathology - Research and Practice. 210(6). 369–376. 10 indexed citations
8.
Schwanitz, Gesa, Isa Abdi Rad, Mir Davood Omrani, et al.. (2013). Patient with three euchromatic supernumerary marker chromosomes derived from chromosomes 1, 12, and 18: Characterization and evaluation of the aberrations. American Journal of Medical Genetics Part A. 164(3). 736–740. 3 indexed citations
9.
Gamerdinger, Ulrike, Thomas Eggermann, Regine Schubert, Gesa Schwanitz, & Martina Kreiß‐Nachtsheim. (2008). Rare interstitial deletion 9q31.2 to q33.1 de novo: Longitudinal study in a patient over a period of more than 20 years. American Journal of Medical Genetics Part A. 146A(9). 1180–1184. 10 indexed citations
10.
Eggermann, Thomas, Ulrike Gamerdinger, G Knöpfle, et al.. (2008). Mosaic Trisomy 1q Due to ade novoTranslocation in a Foetus with Early Developmental Abnormalities (Karyotype 46,XY, der(14),t(1;14)(p11;p11.2)/46,XY) Delineation of Parent and Cell Stage of Origin. International Journal of Human Genetics. 8(4). 317–323. 1 indexed citations
11.
Nestler, Ulf, et al.. (2007). Glioblastoma Simultaneously Present with Meningioma - Report of Three Cases. Central European Neurosurgery - Zentralblatt für Neurochirurgie. 68(3). 145–150. 31 indexed citations
12.
Eggermann, Thomas, Ulrike Gamerdinger, Kristin Bosse, et al.. (2005). Mosaic tetrasomy 14pter‐q13 due to a supernumerary isodicentric derivate of proximal chromosome 14q. American Journal of Medical Genetics Part A. 134A(3). 305–308. 7 indexed citations
13.
Gamerdinger, Ulrike, Kristin Bosse, Thomas Eggermann, et al.. (2005). First report of a partial trisomy 3q12-q23 de novo—FISH breakpoint determination and phenotypic characterization. European Journal of Medical Genetics. 49(3). 225–234. 4 indexed citations
14.
Lasczkowski, Gabriele, et al.. (2004). Pathogenesis of conjunctival petechiae. Forensic Science International. 147(1). 25–29. 15 indexed citations
15.
Stahl, U., Jannis Wenk, Felecia Wagener, et al.. (2004). Phosphoinositid-3-Kinase- (PI3-K) Expression. Der Pathologe. 25(1). 31–37. 2 indexed citations
16.
Gamerdinger, Ulrike, Andrea Teigler‐Schlegel, Jochen Bruch, et al.. (2003). Cryptic chromosomal aberrations leading to an AML1/ETO rearrangement are frequently caused by small insertions. Genes Chromosomes and Cancer. 36(3). 261–272. 30 indexed citations
17.
Woenckhaus, Joachim, Klaus Steger, Eva Penelo, et al.. (2002). Genomic gain of PIK3CA and increased expression of p110alpha are associated with progression of dysplasia into invasive squamous cell carcinoma. The Journal of Pathology. 198(3). 335–342. 125 indexed citations
18.
Lasczkowski, Gabriele, et al.. (2002). Visualization of Postmortem Chondrocyte Damage by Vital Staining and Confocal Laser Scanning 3D Microscopy. Journal of Forensic Sciences. 47(3). 663–666. 21 indexed citations
19.
Engels, Hartmut, et al.. (1998). Delineation of supernumerary marker chromosomes in 38 patients. American Journal of Medical Genetics. 76(4). 351–358. 49 indexed citations
20.
Eiben, B., R. Goebel, Ulrike Gamerdinger, et al.. (1992). Prenatal diagnosis of monosomy 18 and ring chromosome 18 mosaicism. Prenatal Diagnosis. 12(11). 945–950. 10 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Christine R. Bryke Breakdown of academic impact, for papers by Jacqueline R. Batanian Breakdown of academic impact, for papers by Mamoru Ozaki Breakdown of academic impact, for papers by Shunsuke Kimura Breakdown of academic impact, for papers by Hasan Acar Breakdown of academic impact, for papers by P. Mollevanger Breakdown of academic impact, for papers by Ellen Kater‐Baats Breakdown of academic impact, for papers by Javier Suela Breakdown of academic impact, for papers by Timothy J. Vyse Breakdown of academic impact, for papers by Paola Angelini
Rankless by CCL
2026