Jürgen Kunze

1.1k total citations
35 papers, 588 citations indexed

About

Jürgen Kunze is a scholar working on Genetics, Molecular Biology and Language and Linguistics. According to data from OpenAlex, Jürgen Kunze has authored 35 papers receiving a total of 588 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 11 papers in Molecular Biology and 7 papers in Language and Linguistics. Recurrent topics in Jürgen Kunze's work include Linguistic research and analysis (7 papers), Linguistic Education and Pedagogy (4 papers) and Prenatal Screening and Diagnostics (4 papers). Jürgen Kunze is often cited by papers focused on Linguistic research and analysis (7 papers), Linguistic Education and Pedagogy (4 papers) and Prenatal Screening and Diagnostics (4 papers). Jürgen Kunze collaborates with scholars based in Germany, United States and Türkiye. Jürgen Kunze's co-authors include Denise Horn, Karl Sperling, Hans Knoblauch, Birgit Schechinger, Rolf‐Dieter Wegner, Stenvert L. S. Drop, Sabine Merker, André Reis, Jörg Seidel and Maki Fukami and has published in prestigious journals such as The Lancet, Hypertension and Journal of Medical Genetics.

In The Last Decade

Jürgen Kunze

29 papers receiving 560 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jürgen Kunze Germany 12 343 337 63 61 44 35 588
Maria Descartes United States 16 431 1.3× 399 1.2× 60 1.0× 94 1.5× 16 0.4× 34 720
Katherine Rojas United States 9 263 0.8× 200 0.6× 84 1.3× 51 0.8× 13 0.3× 15 424
Roel Hordijk Netherlands 15 520 1.5× 409 1.2× 100 1.6× 184 3.0× 14 0.3× 22 739
Cathy M. Tuck‐Müller United States 17 428 1.2× 515 1.5× 167 2.7× 157 2.6× 25 0.6× 37 855
C.T. Falk United States 11 547 1.6× 320 0.9× 44 0.7× 13 0.2× 35 0.8× 21 859
Ai Shintani Japan 10 136 0.4× 454 1.3× 66 1.0× 42 0.7× 11 0.3× 10 585
Chee‐Seng Ku Singapore 11 402 1.2× 295 0.9× 30 0.5× 32 0.5× 19 0.4× 14 661
Joan E. Pellegrino United States 11 215 0.6× 256 0.8× 18 0.3× 116 1.9× 24 0.5× 19 492
P Goetz Czechia 13 251 0.7× 382 1.1× 150 2.4× 47 0.8× 9 0.2× 30 629
Sara Loddo Italy 13 402 1.2× 277 0.8× 59 0.9× 123 2.0× 10 0.2× 39 639

Countries citing papers authored by Jürgen Kunze

Since Specialization
Citations

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

Fields of papers citing papers by Jürgen Kunze

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jürgen Kunze

This figure shows the co-authorship network connecting the top 25 collaborators of Jürgen Kunze. A scholar is included among the top collaborators of Jürgen Kunze 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 Jürgen Kunze. Jürgen Kunze 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.
Türkmen, Seval, Gabriele Gillessen‐Kaesbach, Peter Meinecke, et al.. (2003). Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes. European Journal of Human Genetics. 11(11). 858–865. 97 indexed citations
2.
Neumann, Luitgard M., Arpad von Moers, Jürgen Kunze, Oliver Blankenstein, & Thorsten Marquardt. (2003). Congenital disorder of glycosylation type 1a in a macrosomic 16-month-old boy with an atypical phenotype and homozygosity of the N216I mutation. European Journal of Pediatrics. 162(10). 710–713. 10 indexed citations
3.
Verheij, Joanne, Jürgen Kunze, Jan Osinga, Anthonie J. van Essen, & Robert M.W. Hofstra. (2002). ABCD syndrome is caused by a homozygous mutation in the EDNRB gene. American Journal of Medical Genetics. 108(3). 223–225. 34 indexed citations
4.
Horn, Denise, Heidemarie Neitzel, Holger Tönnies, et al.. (2002). Familial MCA/MR syndrome due to inherited submicroscopic translocation t(18;21)(q22.1q21.3) with breakpoint at the Down syndrome critical region. American Journal of Medical Genetics Part A. 117A(3). 236–244. 10 indexed citations
5.
Horn, Denise, Rudolf Happle, Heidemarie Neitzel, & Jürgen Kunze. (2002). Pigmentary mosaicism of the hyperpigmented type in two half‐brothers. American Journal of Medical Genetics. 112(1). 65–69. 11 indexed citations
6.
Guschmann, M., et al.. (2001). Mesomelic campomelia, polydactyly and Dandy–Walker cyst in siblings. Prenatal Diagnosis. 21(5). 378–382. 2 indexed citations
7.
Demuth, Ilja, Marcin W. Włodarski, Alex J. Tipping, et al.. (2000). Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9. European Journal of Human Genetics. 8(11). 861–868. 51 indexed citations
8.
Schiller, Simone, Stephanie Spranger, Birgit Schechinger, et al.. (2000). Phenotypic variation and genetic heterogeneity in Léri-Weill syndrome. European Journal of Human Genetics. 8(1). 54–62. 115 indexed citations
9.
Horn, Denise, Alice Krebsová, Jürgen Kunze, & André Reis. (2000). Homozygosity mapping in a family with microcephaly, mental retardation, and short stature to a Cohen syndrome region on 8q21.3 ‐ 8q22.1: Redefining a clinical entity. American Journal of Medical Genetics. 92(4). 285–292. 3 indexed citations
10.
Kunze, Jürgen, et al.. (1998). Eliminative parsing with graded constraints. 1. 526–526. 3 indexed citations
11.
Schuster, Herbert, Thomas F. Wienker, Hakan R. Toka, et al.. (1996). Autosomal Dominant Hypertension and Brachydactyly in a Turkish Kindred Resembles Essential Hypertension. Hypertension. 28(6). 1085–1092. 53 indexed citations
12.
Neumann, Luitgard M., Jörg Pelz, & Jürgen Kunze. (1996). A new observation of two cases of acrofacial dysostosis type Genée-Wiedemann in a family—remarks on the mode of inheritance: Report on two sibs. American Journal of Medical Genetics. 64(4). 556–562. 1 indexed citations
13.
Pelz, Jörg, et al.. (1996). Computer assisted diagnosis of malformation syndromes: An evaluation of three databases (LDDB, POSSUM, and SYNDROC). American Journal of Medical Genetics. 63(1). 257–267. 9 indexed citations
14.
Kunze, Jürgen, et al.. (1995). Autosomal‐recessive neural crest syndrome with albinism, black lock, cell migration disorder of the neurocytes of the gut, and deafness: ABCD syndrome. American Journal of Medical Genetics. 56(3). 322–326. 16 indexed citations
15.
Kunze, Jürgen, et al.. (1991). Fifth Conference of the European Chapter of the Association for Computational Linguistics. Conference of the European Chapter of the Association for Computational Linguistics. 1 indexed citations
16.
Kunze, Jürgen. (1991). Kasusrelationen und semantische Emphase. 7 indexed citations
17.
Kunze, Jürgen & John M. Opitz. (1986). The “Michelin tire baby syndrome”: An autosomal dominant trait. American Journal of Medical Genetics. 25(1). 169–169. 3 indexed citations
18.
Wegner, Rolf‐Dieter, et al.. (1981). Monosomy 10qter due to a balanced familial translocation: t(10;16)(q25.2;q24). Clinical Genetics. 19(2). 130–133. 29 indexed citations
19.
20.
Kunze, Jürgen. (1965). On syntactic synthesis.. Kybernetika. 1. 85–102. 1 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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