Iris Köpschall

1.6k total citations
20 papers, 1.3k citations indexed

About

Iris Köpschall is a scholar working on Sensory Systems, Neurology and Molecular Biology. According to data from OpenAlex, Iris Köpschall has authored 20 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Sensory Systems, 8 papers in Neurology and 6 papers in Molecular Biology. Recurrent topics in Iris Köpschall's work include Hearing, Cochlea, Tinnitus, Genetics (20 papers), Vestibular and auditory disorders (8 papers) and Hearing Loss and Rehabilitation (4 papers). Iris Köpschall is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (20 papers), Vestibular and auditory disorders (8 papers) and Hearing Loss and Rehabilitation (4 papers). Iris Köpschall collaborates with scholars based in Germany, Spain and United Kingdom. Iris Köpschall's co-authors include Karin Rohbock, Ulrike Zimmermann, Marlies Knipper, Hans‐Peter Zenner, Lukas Rüttiger, Justin Tan, Thomas Schimmang, Wibke Singer, Harald Winter and Mark Praetorius and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Neuroscience.

In The Last Decade

Iris Köpschall

20 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Iris Köpschall Germany	17	1.0k	432	383	330	259	20	1.3k
Karin Rohbock Germany	23	1.3k 1.3×	619 1.4×	501 1.3×	427 1.3×	351 1.4×	29	1.7k
J.K. Brunso-Bechtold United States	17	397 0.4×	365 0.8×	230 0.6×	367 1.1×	617 2.4×	28	1.3k
Anne E. Luebke United States	21	651 0.6×	414 1.0×	397 1.0×	460 1.4×	265 1.0×	47	1.6k
Dwayne D. Simmons United States	21	934 0.9×	370 0.9×	261 0.7×	403 1.2×	296 1.1×	48	1.2k
Saïda Hadjab Sweden	14	348 0.3×	194 0.4×	117 0.3×	365 1.1×	193 0.7×	21	942
Michiko Ikeda Japan	21	273 0.3×	193 0.4×	673 1.8×	215 0.7×	575 2.2×	52	1.6k
A L Dahl United States	9	407 0.4×	252 0.6×	351 0.9×	236 0.7×	446 1.7×	10	874
Setsuko Suemune Japan	19	226 0.2×	187 0.4×	177 0.5×	293 0.9×	730 2.8×	30	1.5k
Brahim Tighilet France	27	720 0.7×	255 0.6×	1.1k 2.9×	182 0.6×	207 0.8×	66	1.6k
Robert L. Gulley United States	22	613 0.6×	271 0.6×	252 0.7×	495 1.5×	589 2.3×	32	1.3k

Countries citing papers authored by Iris Köpschall

Since Specialization

Citations

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

Fields of papers citing papers by Iris Köpschall

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Iris Köpschall

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

Zuccotti, Annalisa, Sze Chim Lee, Wibke Singer, et al.. (2013). L-type CaV1.2 deletion in the cochlea but not in the brainstem reduces noise vulnerability: implication for CaV1.2-mediated control of cochlear BDNF expression. Frontiers in Molecular Neuroscience. 6. 20–20. 13 indexed citations

Singer, Wibke, Annalisa Zuccotti, Mirko Jaumann, et al.. (2012). Noise-Induced Inner Hair Cell Ribbon Loss Disturbs Central Arc Mobilization: A Novel Molecular Paradigm for Understanding Tinnitus. Molecular Neurobiology. 47(1). 261–279. 98 indexed citations

Zuccotti, Annalisa, Stephanie Kuhn, C. Franz, et al.. (2012). Lack of Brain-Derived Neurotrophic Factor Hampers Inner Hair Cell Synapse Physiology, But Protects against Noise-Induced Hearing Loss. Journal of Neuroscience. 32(25). 8545–8553. 68 indexed citations

Panford-Walsh, Rama, Wibke Singer, Lukas Rüttiger, et al.. (2008). Midazolam Reverses Salicylate-Induced Changes in Brain-Derived Neurotrophic Factor and Arg3.1 Expression: Implications for Tinnitus Perception and Auditory Plasticity. Molecular Pharmacology. 74(3). 595–604. 34 indexed citations

Singer, Wibke, Rama Panford-Walsh, Dirk Watermann, et al.. (2008). Salicylate Alters the Expression of Calcium Response Transcription Factor 1 in the Cochlea: Implications for Brain-Derived Neurotrophic Factor Transcriptional Regulation. Molecular Pharmacology. 73(4). 1085–1091. 19 indexed citations

Tan, Justin, Lukas Rüttiger, Rama Panford-Walsh, et al.. (2007). Tinnitus behavior and hearing function correlate with the reciprocal expression patterns of BDNF and Arg3.1/arc in auditory neurons following acoustic trauma. Neuroscience. 145(2). 715–726. 90 indexed citations

Rüttiger, Lukas, Rama Panford-Walsh, Thomas Schimmang, et al.. (2006). BDNF mRNA expression and protein localization are changed in age-related hearing loss. Neurobiology of Aging. 28(4). 586–601. 40 indexed citations

Winter, Harald, Claudia Braig, Ulrike Zimmermann, et al.. (2006). Thyroid hormone receptors TRα1 and TRβ differentially regulate gene expression ofKcnq4and prestin during final differentiation of outer hair cells. Journal of Cell Science. 119(14). 2975–2984. 65 indexed citations

Rüttiger, Lukas, Matthias Sausbier, Ulrike Zimmermann, et al.. (2004). Deletion of the Ca²+-activated potassium (BK) α-subunit but not the BKβ1-subunit leads to progressive hearing loss. Proceedings of the National Academy of Sciences. 101(35). 12922–12927. 163 indexed citations

10.

Schimmang, Thomas, Justin Tan, Ulrike Zimmermann, et al.. (2003). Lack of Bdnf and TrkB signalling in the postnatal cochlea leads to a spatial reshaping of innervation along the tonotopic axis and hearing loss. Development. 130(19). 4741–4750. 114 indexed citations

11.

Weber, Thomas, Ulrike Zimmermann, Harald Winter, et al.. (2002). Thyroid hormone is a critical determinant for the regulation of the cochlear motor protein prestin. Proceedings of the National Academy of Sciences. 99(5). 2901–2906. 91 indexed citations

12.

Knipper, Marlies, Guy P. Richardson, Andreas F. Mack, et al.. (2001). Thyroid Hormone-deficient Period Prior to the Onset of Hearing Is Associated with Reduced Levels of β-Tectorin Protein in the Tectorial Membrane. Journal of Biological Chemistry. 276(42). 39046–39052. 53 indexed citations

13.

Zimmermann, Ulrike, et al.. (2000). Molecular characterization of anion exchangers in the cochlea. Molecular and Cellular Biochemistry. 205(1-2). 25–37. 8 indexed citations

14.

Knipper, Marlies, H. Maier, Mark Praetorius, et al.. (2000). Thyroid Hormone Deficiency Before the Onset of Hearing Causes Irreversible Damage to Peripheral and Central Auditory Systems. Journal of Neurophysiology. 83(5). 3101–3112. 152 indexed citations

15.

Knipper, Marlies, J. Lautermann, H. Maier, et al.. (1999). Distinct thyroid hormone‐dependent expression of trkB and p75NGFR in nonneuronal cells during the critical TH‐dependent period of the cochlea. Journal of Neurobiology. 38(3). 338–356. 4 indexed citations

16.

Knipper, Marlies, Christine E. Bandtlow, Iris Köpschall, et al.. (1998). Thyroid hormone affects Schwann cell and oligodendrocyte gene expression at the glial transition zone of the VIIIth nerve prior to cochlea function. Development. 125(18). 3709–3718. 113 indexed citations

17.

Knipper, Marlies, Iris Köpschall, Karin Rohbock, et al.. (1996). Transient expression of NMDA receptors during rearrangement of AMPA-receptor-expressing fibers in the developing inner ear. Cell and Tissue Research. 287(1). 23–41. 62 indexed citations

18.

Knipper, Marlies, Ulrike Zimmermann, Karin Rohbock, Iris Köpschall, & Hans‐Peter Zenner. (1996). Expression of neurotrophin receptor trkB in rat cochlear hair cells at time of rearrangement of innervation. Cell and Tissue Research. 283(3). 339–353. 43 indexed citations

19.

Zimmermann, Ulrike, et al.. (1995). Synaptophysin and Gap-43 proteins in efferent fibers of the inner ear during postnatal development. Developmental Brain Research. 89(1). 73–86. 50 indexed citations

20.

Knipper, Marlies, et al.. (1995). Immunological identification of candidate proteins involved in regulating active shape changes of outer hair cells. Hearing Research. 86(1-2). 100–110. 26 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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