J. Kunze

1.0k total citations
40 papers, 577 citations indexed

About

J. Kunze is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, J. Kunze has authored 40 papers receiving a total of 577 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 18 papers in Genetics and 7 papers in Surgery. Recurrent topics in J. Kunze's work include Genomic variations and chromosomal abnormalities (6 papers), Congenital limb and hand anomalies (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). J. Kunze is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Congenital limb and hand anomalies (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). J. Kunze collaborates with scholars based in Germany, Japan and United States. J. Kunze's co-authors include Karl Sperling, M Tolksdorf, H. Riehm, T. Klemm, H. ‐R. Wiedemann, T Strachan, E Seemanová, Valerie Newton, F. Hanefeld and Simone M. Sauter and has published in prestigious journals such as Human Molecular Genetics, Human Mutation and Human Genetics.

In The Last Decade

J. Kunze

37 papers receiving 553 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J. Kunze Germany	14	328	226	72	61	60	40	577
Joëlle Augé France	8	353 1.1×	232 1.0×	46 0.6×	49 0.8×	73 1.2×	9	583
Martine Doco‐Fenzy France	15	349 1.1×	302 1.3×	59 0.8×	42 0.7×	47 0.8×	29	690
Angelo Iulianella Canada	17	557 1.7×	281 1.2×	53 0.7×	70 1.1×	58 1.0×	29	754
Virginia C. Thurston United States	12	297 0.9×	224 1.0×	27 0.4×	56 0.9×	34 0.6×	17	599
Huw Dorkins United Kingdom	14	309 0.9×	356 1.6×	96 1.3×	30 0.5×	54 0.9×	27	646
Véronica Cusin France	12	443 1.4×	309 1.4×	34 0.5×	91 1.5×	28 0.5×	13	721
Shehla Mohammed United Kingdom	12	497 1.5×	248 1.1×	92 1.3×	61 1.0×	57 0.9×	25	680
Nisha Patel Saudi Arabia	17	428 1.3×	267 1.2×	60 0.8×	52 0.9×	69 1.1×	39	727
Jo-Anne Herbrick Canada	13	397 1.2×	197 0.9×	106 1.5×	17 0.3×	47 0.8×	17	855
Carol A. Crowe United States	17	582 1.8×	318 1.4×	32 0.4×	53 0.9×	100 1.7×	28	904

Countries citing papers authored by J. Kunze

Since Specialization

Citations

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

Fields of papers citing papers by J. Kunze

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

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20 of 20 papers shown

Schaller, Jörg, et al.. (2009). Kutaner maligner peripherer Nervenscheidentumor bei Neurofibromatose Typ 1. Der Hautarzt. 60(10). 830–833. 1 indexed citations

Schaller, Jörg, et al.. (2009). Juvenile hyaline Fibromatose. Der Hautarzt. 60(9). 740–742. 1 indexed citations

Zerres, Klaus, Jan Senderek, Sabine Rudnik‐Schöneborn, et al.. (2004). New options for prenatal diagnosis in autosomal recessive polycystic kidney disease by mutation analysis of the PKHD1 gene. Clinical Genetics. 66(1). 53–57. 25 indexed citations

Sauter, Simone M., Wolfgang Engel, Luitgard M. Neumann, J. Kunze, & Jürgen Neesen. (2003). Novel mutations in theAtlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to theSPG3A locus. Human Mutation. 23(1). 98–98. 46 indexed citations

Becker, Rolf, J. Kunze, Denise Horn, et al.. (2002). Autosomal recessive type of Adams–Oliver syndrome: prenatal diagnosis. Ultrasound in Obstetrics and Gynecology. 20(5). 506–510. 15 indexed citations

Mostofsky, Stewart H., J. Kunze, Laurie E. Cutting, Howard M. Lederman, & Martha B. Denckla. (2000). Judgment of Duration in Individuals With Ataxia-Telangiectasia. Developmental Neuropsychology. 17(1). 63–74. 30 indexed citations

Tyler, Kenneth L., Nanette Sarioglu, & J. Kunze. (1999). Five familial cases of opsismodysplasia substantiate the hypothesis of autosomal recessive inheritance. American Journal of Medical Genetics. 83(1). 47–52. 13 indexed citations

Horn, David M., et al.. (1997). Extreme microcephaly, severe growth and mental retardation, flexion contractures, and ichthyotic skin in two brothers: a new syndrome or mild form of Neu-Laxova syndrome?. Clinical Dysmorphology. 6(4). 323–328. 10 indexed citations

Gieseler, Frank, et al.. (1997). Topoisomerase Activities in Undifferentiated Acute Myeloblastic Leukemias and Monocytic Differentiated Leukemias. Recent results in cancer research. 143. 321–327. 1 indexed citations

10.

Gieseler, Frank, Axel Glasmacher, H. Wandt, et al.. (1996). Topoisomerase II activities in AML and their correlation with cellular sensitivity to anthracyclines and epipodophyllotoxines.. PubMed. 10(7). 1177–80. 27 indexed citations

11.

Kunze, J., et al.. (1993). Kohlschütter Syndrome: Syndrome of Epilepsy - Dementia - Amelogenesis Imperfecta. Neuropediatrics. 24(6). 337–338. 13 indexed citations

12.

Kunze, J., et al.. (1992). Polysyndaktylie mit Brachymetacarpie (Typ Bonola). Klinische Pädiatrie. 204(1). 43–47. 2 indexed citations

13.

Wegner, R.‐D., Marc J. Metzger, F. Hanefeld, et al.. (1988). AT‐related disorder. Clinical Genetics. 33(1). 20–32. 56 indexed citations

14.

Kunze, J., et al.. (1985). De Barsy syndrome?an autosomal recessive, progeroid syndrome. European Journal of Pediatrics. 144(4). 348–354. 22 indexed citations

15.

Kunze, J. & T. Klemm. (1980). Mesomelic dysplasia, type langer?A homozygous state for dyschondrosteosis. European Journal of Pediatrics. 134(3). 269–272. 24 indexed citations

16.

Kunze, J.. (1980). NEUROLOGICAL DISORDERS IN PATIENTS WITH CHROMOSOMAL ANOMALIES. Neuropediatrics. 11(3). 203–249. 9 indexed citations

17.

Kunze, J., K Heyne, & H. ‐R. Wiedemann. (1979). Diaphragmatic hernia in a female newborn with focal dermal hypoplasia and marked asymmetric malformations (Goltz-Gorlin Syndrome). European Journal of Pediatrics. 131(3). 213–218. 19 indexed citations

18.

Kunze, J., M Tolksdorf, & H. ‐R. Wiedemann. (1975). Cat Eye-Syndrom. Human Genetics. 26(4). 11 indexed citations

19.

Kunze, J., H. Doose, & M Tolksdorf. (1975). Dysplasie-Epilepsie-Syndrom bei Ringchromosom 21. Neuropediatrics. 6(4). 398–402. 5 indexed citations

20.

Kunze, J. & M Tolksdorf. (1974). [Indentification of chromosomal polymorphisms and some aberrations identified by new cytogenetical methods (author's transl)].. PubMed. 117(1). 29–46. 3 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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