Markus Pfister

4.8k total citations
85 papers, 2.0k citations indexed

About

Markus Pfister is a scholar working on Sensory Systems, Molecular Biology and Neurology. According to data from OpenAlex, Markus Pfister has authored 85 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Sensory Systems, 38 papers in Molecular Biology and 18 papers in Neurology. Recurrent topics in Markus Pfister's work include Hearing, Cochlea, Tinnitus, Genetics (48 papers), Vestibular and auditory disorders (16 papers) and Connexins and lens biology (14 papers). Markus Pfister is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (48 papers), Vestibular and auditory disorders (16 papers) and Connexins and lens biology (14 papers). Markus Pfister collaborates with scholars based in Germany, United States and Hungary. Markus Pfister's co-authors include Nikolaus Blin, Susan Kupka, Marlies Knipper, H. P. Zenner, Hans‐Peter Zenner, Carsten M. Pusch, Ulrike Zimmermann, Richard J. Smith, Guy Van Camp and Peter Ruth and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and Journal of Neuroscience.

In The Last Decade

Markus Pfister

84 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Markus Pfister Germany 27 1.1k 842 429 335 272 85 2.0k
Anand N. Mhatre United States 24 916 0.8× 866 1.0× 327 0.8× 242 0.7× 266 1.0× 46 1.8k
Kunihiro Fukushima Japan 28 824 0.7× 1.1k 1.3× 335 0.8× 381 1.1× 362 1.3× 121 2.3k
Michel Leibovici France 20 1.3k 1.2× 1.8k 2.1× 400 0.9× 351 1.0× 184 0.7× 25 2.9k
Rick A. Friedman United States 25 876 0.8× 661 0.8× 431 1.0× 236 0.7× 228 0.8× 53 1.7k
Nahid G. Robertson United States 22 1.1k 1.0× 616 0.7× 726 1.7× 242 0.7× 238 0.9× 31 1.7k
Miguel A. Moreno‐Pelayo Spain 19 1.2k 1.1× 1.4k 1.6× 384 0.9× 302 0.9× 164 0.6× 59 2.3k
Salvatore Melchionda Italy 22 1.6k 1.4× 1.5k 1.8× 478 1.1× 350 1.0× 235 0.9× 41 2.3k
Pu Dai China 28 1.6k 1.4× 1.3k 1.5× 745 1.7× 348 1.0× 533 2.0× 202 2.5k
Ronna Hertzano United States 27 1.2k 1.1× 739 0.9× 290 0.7× 418 1.2× 177 0.7× 57 2.0k
Carla Nishimura United States 24 1.0k 0.9× 828 1.0× 402 0.9× 246 0.7× 355 1.3× 33 2.3k

Countries citing papers authored by Markus Pfister

Since Specialization
Citations

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

Fields of papers citing papers by Markus Pfister

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Markus Pfister

This figure shows the co-authorship network connecting the top 25 collaborators of Markus Pfister. A scholar is included among the top collaborators of Markus Pfister 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 Markus Pfister. Markus Pfister 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.
Budde, Birgit, Janine Altmüller, Susanne Motameny, et al.. (2020). Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss. Clinical Genetics. 98(1). 32–42. 24 indexed citations
2.
Panuccio, Giuseppe, Giovanni Torsello, Markus Pfister, et al.. (2016). Computer-aided endovascular aortic repair using fully automated two- and three-dimensional fusion imaging. Journal of Vascular Surgery. 64(6). 1587–1594.e1. 11 indexed citations
3.
Ealy, Megan, Nicole C. Meyer, Isabelle Schrauwen, et al.. (2014). Rare Variants in BMP2 and BMP4 Found in Otosclerosis Patients Reduce Smad Signaling. Otology & Neurotology. 35(3). 395–400. 10 indexed citations
4.
Franz, Christoph, Ulrike Zimmermann, Sze Chim Lee, et al.. (2013). Autonomous functions of murine thyroid hormone receptor TRα and TRβ in cochlear hair cells. Molecular and Cellular Endocrinology. 382(1). 26–37. 19 indexed citations
5.
Brandt, Niels, Christoph Franz, Peter Ruth, et al.. (2012). Ergic2, a Brain Specific Interacting Partner of Otoferlin. Cellular Physiology and Biochemistry. 29(5-6). 941–948. 7 indexed citations
6.
Winter, Harald, Lukas Rüttiger, Marcus Müller, et al.. (2009). Deafness in TRβ Mutants Is Caused by Malformation of the Tectorial Membrane. Journal of Neuroscience. 29(8). 2581–2587. 27 indexed citations
7.
Schrauwen, Isabelle, Megan Ealy, Erik Fransén, et al.. (2009). Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations. Human Genetics. 127(2). 155–162. 24 indexed citations
8.
Zenner, H. P., Markus Pfister, & Niels Birbaumer. (2006). Tinnitus Sensitization. Otology & Neurotology. 27(8). 1054–1063. 57 indexed citations
9.
Yang, Tao, Markus Pfister, Nikolaus Blin, et al.. (2005). Genetic heterogeneity of deafness phenotypes linked to DFNA4. American Journal of Medical Genetics Part A. 139A(1). 9–12. 26 indexed citations
10.
Palmada, Mònica, et al.. (2005). Loss of function mutations of the GJB2 gene detected in patients with DFNB1-associated hearing impairment. Neurobiology of Disease. 22(1). 112–118. 53 indexed citations
11.
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
12.
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
13.
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
14.
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
15.
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
16.
Pfister, Markus. (2002). Molekulargenetische Aspekte in der HNO-Heilkunde. HNO. 50(9). 791–793. 1 indexed citations
17.
Lin, Doris, Jayne A. Goldstein, Anand N. Mhatre, et al.. (2001). Assessment of denaturing high-performance liquid chromatography (DHPLC) in screening for mutations in connexin 26 (GJB2). Human Mutation. 18(1). 42–51. 41 indexed citations
18.
Pfister, Markus & Anil K. Lalwani. (2000). DFN4: Non-Syndromic Autosomal Dominant X-Linked Sensorineural Hearing Impairment. Advances in oto-rhino-laryngology. 56. 196–199. 1 indexed citations
19.
Pfister, Markus, H. Maier, Anthony W. Gummer, & Serena Preyer. (1997). In-vivo-Cochleoskopie durch das runde Fenster. HNO. 45(4). 216–221. 2 indexed citations
20.
Hemmert, Werner, et al.. (1994). Frequency response of mature guinea-pig outer hair cells to stereociliary displacement. Hearing Research. 77(1-2). 116–124. 12 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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