Susan Kupka

1.4k total citations
36 papers, 725 citations indexed

About

Susan Kupka is a scholar working on Molecular Biology, Sensory Systems and Surgery. According to data from OpenAlex, Susan Kupka has authored 36 papers receiving a total of 725 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 15 papers in Sensory Systems and 5 papers in Surgery. Recurrent topics in Susan Kupka's work include Hearing, Cochlea, Tinnitus, Genetics (15 papers), Connexins and lens biology (9 papers) and RNA regulation and disease (3 papers). Susan Kupka is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (15 papers), Connexins and lens biology (9 papers) and RNA regulation and disease (3 papers). Susan Kupka collaborates with scholars based in Germany, Hungary and United States. Susan Kupka's co-authors include Markus Pfister, Nikolaus Blin, Hans‐Peter Zenner, Tímea Tóth, István Sziklai, Birgit Haack, Hans-Peter Zenner, Ulrike Zeißler, Peter Nürnberg and Hölger Thiele and has published in prestigious journals such as The FASEB Journal, Neurobiology of Disease and Human Mutation.

In The Last Decade

Susan Kupka

36 papers receiving 716 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Susan Kupka Germany 15 350 346 143 92 79 36 725
Jo-Anne Herbrick Canada 13 146 0.4× 397 1.1× 88 0.6× 174 1.9× 65 0.8× 17 855
J. E. Veldman Netherlands 18 334 1.0× 92 0.3× 272 1.9× 141 1.5× 133 1.7× 42 711
Barbara Ploplis United States 6 231 0.7× 455 1.3× 268 1.9× 32 0.3× 35 0.4× 7 713
Oscar Diaz‐Horta United States 10 231 0.7× 235 0.7× 85 0.6× 89 1.0× 16 0.2× 13 530
Jan E. Veldman Netherlands 15 408 1.2× 95 0.3× 352 2.5× 104 1.1× 110 1.4× 27 801
Koichiro Higashi Japan 12 184 0.5× 347 1.0× 78 0.5× 22 0.2× 89 1.1× 29 596
Andrew M. Mikosz United States 9 224 0.6× 399 1.2× 30 0.2× 54 0.6× 51 0.6× 13 649
Christoph Reisser Germany 7 83 0.2× 167 0.5× 59 0.4× 64 0.7× 138 1.7× 9 441
Megan Ealy United States 15 247 0.7× 169 0.5× 75 0.5× 23 0.3× 47 0.6× 16 568
Paul Bossuyt Belgium 13 114 0.3× 440 1.3× 39 0.3× 81 0.9× 65 0.8× 15 796

Countries citing papers authored by Susan Kupka

Since Specialization
Citations

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

Fields of papers citing papers by Susan Kupka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susan Kupka

This figure shows the co-authorship network connecting the top 25 collaborators of Susan Kupka. A scholar is included among the top collaborators of Susan Kupka 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 Susan Kupka. Susan Kupka 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.
Müller, Sven, Susan Kupka, Ingmar Königsrainer, et al.. (2012). MSH2 and CXCR4 involvement in malignant VIPoma. World Journal of Surgical Oncology. 10(1). 264–264. 4 indexed citations
2.
Zieker, Derek, Frank Traub, Kay Nieselt, et al.. (2008). PGK1 a Potential Marker for Peritoneal Dissemination in Gastric Cancer. Cellular Physiology and Biochemistry. 21(5-6). 429–436. 56 indexed citations
3.
Armeanu, Sorin, Susan Kupka, Silvia Wagner, et al.. (2008). Human Precision Cut Liver Tumor Slices as a comprehensive predictive test system for the oncolytic effectiveness of measles vaccine viruses. Zeitschrift für Gastroenterologie. 46(9). 2 indexed citations
4.
Riemann‐Campe, Kathrin, et al.. (2005). Active succinate dehydrogenase (SDH) and lack of SDHD mutations in sporadic paragangliomas.. PubMed. 25(4). 2809–14. 19 indexed citations
5.
Schulte, Claudia, Urban W. Geisthoff, Andreas Lux, et al.. (2005). High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patients. Human Mutation. 25(6). 595–595. 43 indexed citations
6.
Haack, Birgit, Susan Kupka, Anna M. Siemiatkowska, et al.. (2004). Analysis of candidate genes for genotypic diagnosis in the long QT syndrome.. PubMed. 45(3). 375–81. 2 indexed citations
7.
Tóth, Tímea, Susan Kupka, Birgit Haack, et al.. (2004). GJB2mutations in patients with non-syndromic hearing loss from Northeastern Hungary. Human Mutation. 23(6). 631–632. 28 indexed citations
8.
Pusch, Carsten M., et al.. (2004). Paragangliome der Kopf-Hals-Region. HNO. 52(1). 11–17. 1 indexed citations
9.
Pusch, Carsten M., Birgit Meyer, Susan Kupka, et al.. (2004). Refinement of the DFNA4 locus to a 1.44�Mb region in 19q13.33. Journal of Molecular Medicine. 82(6). 398–402. 3 indexed citations
10.
Riemann‐Campe, Kathrin, Karl Sotlar, Susan Kupka, et al.. (2004). Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases. Cancer Genetics and Cytogenetics. 150(2). 128–135. 26 indexed citations
11.
Pfister, Markus, Hölger Thiele, Guy Van Camp, et al.. (2004). A Genotype-Phenotype Correlation with Gender-Effect for Hearing Impairment Caused by <i>TECTA</i> Mutations. Cellular Physiology and Biochemistry. 14(4-6). 369–376. 46 indexed citations
12.
Tóth, Tímea, Susan Kupka, Peter Nürnberg, et al.. (2004). Phänotypische Charakterisierung einer DFNA6-Familie mit Tieftonschwerhörigkeit. HNO. 52(2). 132–136. 1 indexed citations
13.
Tóth, Tímea, Susan Kupka, I. Sziklai, et al.. (2003). Phänotypische Charakterisierung schwerhöriger Patienten mit homozygoter 35delG-Mutation im Connexin-26-Gen. HNO. 51(5). 400–404. 2 indexed citations
14.
Kupka, Susan, Farhad Mirghomizadeh, Rainer Zimmermann, et al.. (2003). Klinische und molekulargenetische Analyse monozygoter Zwillinge mit Stapes-Gusher-Syndrom (DFN3). HNO. 51(8). 629–633. 4 indexed citations
15.
Kupka, Susan, Susanne Aberle, Birgit Haack, et al.. (2002). Frequencies ofGJB2mutations in German control individuals and patients showing sporadic non-syndromic hearing impairment. Human Mutation. 20(1). 77–78. 40 indexed citations
16.
Cryns, Kim, Markus Pfister, Ronald J. E. Pennings, et al.. (2002). Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations. Human Genetics. 110(5). 389–394. 71 indexed citations
17.
Szyfter, Witold, Markus Pfister, Krzysztof Szyfter, et al.. (2001). [An attempt to identify the most frequent genomic mutations responsible for isolated deafness in patients after cochlear implantation].. PubMed. 55(1). 79–84. 1 indexed citations
18.
Kupka, Susan, Farhad Mirghomizadeh, Tor Haug, et al.. (2000). Mutationsanalyse des Connexin26-Gens bei sporadischen Fällen mittel- bis hochgradiger Schwerhörigkeit. HNO. 48(9). 671–674. 7 indexed citations
19.
Mirghomizadeh, Farhad, Susan Kupka, & Nikolaus Blin. (1999). Assessing genetic heterogeneity of renal cell tumors.. PubMed. 19(2C). 1467–70. 1 indexed citations
20.
Kupka, Susan. (1973). [Regular supervision of pregnant women for the prevention of congenital toxoplasmosis].. PubMed. 95(32). 1122–5. 3 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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