Karin Kirschhofer

607 total citations
11 papers, 475 citations indexed

About

Karin Kirschhofer is a scholar working on Molecular Biology, Sensory Systems and Endocrine and Autonomic Systems. According to data from OpenAlex, Karin Kirschhofer has authored 11 papers receiving a total of 475 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Sensory Systems and 5 papers in Endocrine and Autonomic Systems. Recurrent topics in Karin Kirschhofer's work include Hearing, Cochlea, Tinnitus, Genetics (9 papers), Connexins and lens biology (6 papers) and Neuroscience of respiration and sleep (5 papers). Karin Kirschhofer is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (9 papers), Connexins and lens biology (6 papers) and Neuroscience of respiration and sleep (5 papers). Karin Kirschhofer collaborates with scholars based in Austria, United States and Netherlands. Karin Kirschhofer's co-authors include F. Wachtler, Klemens Frei, Wolf‐Dieter Baumgartner, Trevor Lucas, Klara Weipoltshammer, Isabelle Schatteman, David C. Hughes, Kristien Verhoeven, Peter Van Hauwe and Paul Coucke and has published in prestigious journals such as Nature Genetics, Developmental Biology and The Laryngoscope.

In The Last Decade

Karin Kirschhofer

11 papers receiving 465 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Karin Kirschhofer Austria	10	382	277	164	104	85	11	475
Xiao Mei Ouyang United States	10	414 1.1×	353 1.3×	143 0.9×	72 0.7×	46 0.5×	13	557
Edi Lúcia Sartorato Brazil	15	422 1.1×	377 1.4×	156 1.0×	109 1.0×	89 1.0×	64	689
Elie El‐Zir Lebanon	5	402 1.1×	274 1.0×	142 0.9×	144 1.4×	33 0.4×	6	552
C. R. Srikumari Srisailapathy India	12	598 1.6×	482 1.7×	204 1.2×	133 1.3×	117 1.4×	34	757
Ibis Menéndez United States	11	590 1.5×	487 1.8×	173 1.1×	131 1.3×	124 1.5×	20	776
James W. Askew United States	6	485 1.3×	434 1.6×	141 0.9×	96 0.9×	153 1.8×	11	593
S. M. Slapnick United States	12	420 1.1×	220 0.8×	120 0.7×	111 1.1×	41 0.5×	16	606
Peter Van Hauwe Belgium	12	611 1.6×	356 1.3×	317 1.9×	137 1.3×	76 0.9×	18	787
Steve D.M. Brown United Kingdom	7	316 0.8×	354 1.3×	106 0.6×	63 0.6×	25 0.3×	8	522
Sigrid Wayne United States	11	364 1.0×	344 1.2×	115 0.7×	74 0.7×	28 0.3×	19	543

Countries citing papers authored by Karin Kirschhofer

Since Specialization

Citations

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

Fields of papers citing papers by Karin Kirschhofer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karin Kirschhofer

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

All Works

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11 of 11 papers shown

Lucas, Trevor, et al.. (2007). Relevance of the A1555G Mutation in the 12S rRNA Gene for Hearing Impairment in Austria. Otology & Neurotology. 28(7). 884–886. 8 indexed citations

Lucas, Trevor, Klara Weipoltshammer, Wolf‐Dieter Baumgartner, et al.. (2007). High Incidence of GJB2 Mutations During Screening of Newborns for Hearing Loss in Austria. Ear and Hearing. 28(3). 298–301. 15 indexed citations

Frei, Klemens, Trevor Lucas, Károly Szuhai, et al.. (2005). GJB2 Mutations in Hearing Impairment: Identification of a Broad Clinical Spectrum for Improved Genetic Counseling. The Laryngoscope. 115(3). 461–465. 21 indexed citations

Frei, Klemens, et al.. (2004). Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern Austria. Hearing Research. 196(1-2). 115–118. 23 indexed citations

Frei, Klemens, et al.. (2004). Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in Austria. Hearing Research. 194(1-2). 81–86. 12 indexed citations

Frei, Klemens, Trevor Lucas, Christian Schöfer, et al.. (2003). A Novel Connexin 26 Mutation Associated with Autosomal Recessive Sensorineural Deafness. Audiology and Neurotology. 9(1). 47–50. 14 indexed citations

Frei, Klemens, Károly Szuhai, Trevor Lucas, et al.. (2002). Connexin 26 mutations in cases of sensorineural deafness in eastern Austria. European Journal of Human Genetics. 10(7). 427–432. 63 indexed citations

Kirschhofer, Karin, Judith B. Kenyon, Peter Franz, et al.. (1998). Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family. Cytogenetic and Genome Research. 82(1-2). 126–130. 33 indexed citations

Verhoeven, Kristien, Karin Kirschhofer, P. Kevin Legan, et al.. (1998). Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment. Nature Genetics. 19(1). 60–62. 253 indexed citations

10.

Kirschhofer, Karin, Miloš Grim, Bodo Christ, & F. Wachtler. (1994). Emergence of Myogenic and Endothelial Cell Lineages in Avian Embryos. Developmental Biology. 163(1). 270–278. 18 indexed citations

11.

Christ, Bodo, et al.. (1991). Differentation of endothelial cells in avian embryos does not depend on gastrulation. Acta Histochemica. 91(2). 193–199. 15 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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