J. Kunz

811 total citations
19 papers, 584 citations indexed

About

J. Kunz is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, J. Kunz has authored 19 papers receiving a total of 584 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 6 papers in Plant Science. Recurrent topics in J. Kunz's work include Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (4 papers) and Craniofacial Disorders and Treatments (3 papers). J. Kunz is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (4 papers) and Craniofacial Disorders and Treatments (3 papers). J. Kunz collaborates with scholars based in Germany, Switzerland and Austria. J. Kunz's co-authors include H. Hameister, G. Rettenberger, C. Klett, Ulrich Zechner, Walther Vogel, M. Schilling, Pascal O. Berberat, Helmut Friess, Murray Korc and Helmut Frieß and has published in prestigious journals such as Genomics, Journal of Medical Genetics and Journal of Neurology.

In The Last Decade

J. Kunz

19 papers receiving 556 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J. Kunz Germany	12	274	265	148	126	52	19	584
Jürgen Kunz Germany	15	511 1.9×	286 1.1×	40 0.3×	189 1.5×	53 1.0×	25	871
F. Apiou France	15	517 1.9×	245 0.9×	61 0.4×	144 1.1×	73 1.4×	31	835
S M Iguchi-Ariga Japan	9	767 2.8×	209 0.8×	68 0.5×	101 0.8×	80 1.5×	11	922
Tim L. Reudelhuber United States	13	497 1.8×	305 1.2×	44 0.3×	90 0.7×	64 1.2×	17	816
Gillian Carpenter United Kingdom	13	568 2.1×	217 0.8×	66 0.4×	87 0.7×	28 0.5×	17	706
Nancy Henderson United Kingdom	11	541 2.0×	251 0.9×	55 0.4×	59 0.5×	97 1.9×	14	825
M Ballantine United States	8	479 1.7×	158 0.6×	70 0.5×	60 0.5×	75 1.4×	8	795
N Kanda Japan	12	344 1.3×	123 0.5×	63 0.4×	89 0.7×	47 0.9×	21	628
A. de Capoa Italy	17	546 2.0×	238 0.9×	160 1.1×	53 0.4×	43 0.8×	45	732
Adrian J. McNairn United States	15	915 3.3×	119 0.4×	161 1.1×	85 0.7×	45 0.9×	19	1.1k

Countries citing papers authored by J. Kunz

Since Specialization

Citations

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

Fields of papers citing papers by J. Kunz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Kunz

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

All Works

Sort: Min cites: Since: Top N: Style:

19 of 19 papers shown

Papoulidis, Ioannis, Elisabeth Klein, Nadezda Kosyakova, et al.. (2012). Tetrasomy 9p Mosaicism Associated with a Normal Phenotype in Two Cases. Cytogenetic and Genome Research. 136(4). 237–241. 14 indexed citations

Kunz, J., Katharina Schoner, W Stein, Helga Rehder, & Bárbara Fritz. (2009). Tetrasomy 12p (Pallister-Killian syndrome): difficulties in prenatal diagnosis. Archives of Gynecology and Obstetrics. 280(6). 1049–1053. 22 indexed citations

Nowack, Rainer, P. Wachtler, J. Kunz, & Niels Rasmussen. (2009). Cranial nerve palsy in Wegener’s granulomatosis – Lessons from clinical cases. Journal of Neurology. 256(3). 299–304. 15 indexed citations

Kosan, Christian & J. Kunz. (2002). Identification and characterisation of the gene TWIST NEIGHBOR (TWISTNB) located in the microdeletion syndrome 7p21 region. Cytogenetic and Genome Research. 97(3-4). 167–170. 10 indexed citations

Ziegler, Andreas, et al.. (2001). Further evidence for linkage of low–mid frequency hearing impairment to the candidate region on chromosome 4p16.3. Clinical Genetics. 60(2). 155–160. 10 indexed citations

Kosan, Christian, et al.. (2001). Saethre-Chotzen syndrome and hyper IgE syndrome in a patient with a novel 11 bp deletion of theTWIST gene. American Journal of Medical Genetics. 104(1). 53–56. 11 indexed citations

Kühl, Nicole M., J. Kunz, & Ludger Rensing. (2000). Heat shock‐induced arrests in different cell cycle phases of rat C6‐glioma cells are attenuated in heat shock‐primed thermotolerant cells. Cell Proliferation. 33(3). 147–166. 20 indexed citations

Wilkie, Andrew O.M., Sharon W. Horsley, Robert E. Kearney, et al.. (1998). Genes in craniosynostosis. European Journal of Human Genetics. 6. 27–27. 1 indexed citations

Rivera, Horacio, et al.. (1998). Intrachromosomal triplication of distal 7p.. Journal of Medical Genetics. 35(1). 78–80. 16 indexed citations

10.

Williams, P. Gail, et al.. (1997). Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality. Clinical Genetics. 52(6). 436–441. 13 indexed citations

11.

Friess, Helmut, et al.. (1996). Pancreatic cancer: the potential clinical relevance of alterations in growth factors and their receptors. Journal of Molecular Medicine. 74(1). 35–42. 102 indexed citations

12.

Frieß, Helmut, et al.. (1996). Treatment of advanced pancreatic cancer with mistletoe: results of a pilot trial.. PubMed. 16(2). 915–20. 33 indexed citations

13.

Rettenberger, G., C. Klett, Ulrich Zechner, et al.. (1995). Visualization of the conservation of synteny between humans and pigs by heterologous chromosomal painting. Genomics. 26(2). 372–378. 223 indexed citations

14.

Wagner, Lukas, Stanislav Volik, Olga Ermolaeva, et al.. (1995). An arrayed library enriched in hncDNA corresponding to transcribed sequences of human chromosome 19: preparation and analysis. Genetic Analysis Biomolecular Engineering. 12(1). 23–31. 3 indexed citations

15.

Frieß, Helmut, M.W. Büchler, C. Beglinger, et al.. (1993). Low-Dose Octreotide Treatment Is Not Effective in Patients with Advanced Pancreatic Cancer. Pancreas. 8(5). 540–545. 47 indexed citations

16.

Kunz, J., et al.. (1991). Immunological recognition of larvalTaenia crassiceps glycolipids by sera from parasite-infected mice. Parasitology Research. 77(5). 443–447. 11 indexed citations

17.

Rhiel, Erhard, J. Kunz, & Werner Wehrmeyer. (1989). Immunocytochemical Localization of Phycoerythrin‐545 and of a Chlorophyll a/c Light Harvesting Complex inCryptomonas maculata(Cryptophyceae). Botanica Acta. 102(1). 46–53. 26 indexed citations

18.

Flügel, Rolf M., et al.. (1989). [A completely thrombosed giant aneurysm in an infant].. PubMed. 50(2). 58–60. 1 indexed citations

19.

Gehrig, Jochen, et al.. (1987). [Radiation proctocolitis following gynecologic radiotherapy: an endoscopic study].. PubMed. 117(36). 1326–32. 6 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.

Explore authors with similar magnitude of impact