Barbara Günther

430 total citations
9 papers, 343 citations indexed

About

Barbara Günther is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Barbara Günther has authored 9 papers receiving a total of 343 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Sensory Systems and 2 papers in Genetics. Recurrent topics in Barbara Günther's work include Hearing, Cochlea, Tinnitus, Genetics (4 papers), Connexins and lens biology (4 papers) and Nicotinic Acetylcholine Receptors Study (3 papers). Barbara Günther is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (4 papers), Connexins and lens biology (4 papers) and Nicotinic Acetylcholine Receptors Study (3 papers). Barbara Günther collaborates with scholars based in Austria, Germany and Latvia. Barbara Günther's co-authors include Gerd Utermann, Andreas Janecke, Judith Löffler, Doris Nekahm-Heis, Hans‐Jürgen Menzel, Josef Smolle, Hans Christian Hennies, Olaf Rittinger, Elisabeth M. Messmer and Andreas Th. Müller and has published in prestigious journals such as Kidney International, Fertility and Sterility and Human Mutation.

In The Last Decade

Barbara Günther

8 papers receiving 335 citations

Peers

Barbara Günther
Robert A. Cucci United States
Barbara Günther
Citations per year, relative to Barbara Günther Barbara Günther (= 1×) peers Robert A. Cucci

Countries citing papers authored by Barbara Günther

Since Specialization
Citations

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

Fields of papers citing papers by Barbara Günther

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Günther

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Günther. A scholar is included among the top collaborators of Barbara Günther 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 Barbara Günther. Barbara Günther is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

9 of 9 papers shown
1.
Saisawat, Pawaree, Velibor Tasić, Virginia Vega-Warner, et al.. (2011). Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis. Kidney International. 81(2). 196–200. 65 indexed citations
2.
Obenauf, Anna C., Thomas Schwarzbraun, Martina Auer, et al.. (2010). Mapping of balanced chromosome translocation breakpoints to the basepair level from microdissected chromosomes. Journal of Cellular and Molecular Medicine. 14(8). 2078–2084. 6 indexed citations
3.
Höckner, Martina, Germar‐Michael Pinggera, Barbara Günther, et al.. (2008). Unravelling the parental origin and mechanism of formation of the 47,XY,i(X)(q10) Klinefelter karyotype variant. Fertility and Sterility. 90(5). 2009.e13–2009.e17. 14 indexed citations
4.
Haberlandt, Edda, et al.. (2006). Yellow teeth, seizures, and mental retardation: A less severe case of Kohlschütter–Tönz syndrome. American Journal of Medical Genetics Part A. 140A(3). 281–283. 15 indexed citations
5.
Janecke, Andreas, Hans Christian Hennies, Barbara Günther, et al.. (2005). GJB2 mutations in keratitis‐ichthyosis‐deafness syndrome including its fatal form. American Journal of Medical Genetics Part A. 133A(2). 128–131. 70 indexed citations
6.
Günther, Barbara, Andrea K. Steiner, Doris Nekahm-Heis, et al.. (2003). The 342-kb deletion inGJB6is not present in patients with non-syndromic hearing loss from Austria. Human Mutation. 22(2). 180–180. 35 indexed citations
7.
Janecke, Andreas, Barbara Günther, Barbara Utermann, et al.. (2002). Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria. Human Genetics. 111(2). 145–153. 62 indexed citations
8.
Löffler, Judith, et al.. (2001). Sensorineural hearing loss and the incidence of Cx26 mutations in Austria. European Journal of Human Genetics. 9(3). 226–230. 74 indexed citations
9.
Günther, Barbara, et al.. (1967). [Contribution to etiological hypothesis: amalgam and multiple sclerosis].. PubMed. 77(9). 761–76. 2 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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