J. Schmidtke

1.6k total citations
53 papers, 1.1k citations indexed

About

J. Schmidtke is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, J. Schmidtke has authored 53 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 16 papers in Genetics and 11 papers in Plant Science. Recurrent topics in J. Schmidtke's work include Chromosomal and Genetic Variations (10 papers), Cystic Fibrosis Research Advances (8 papers) and RNA and protein synthesis mechanisms (8 papers). J. Schmidtke is often cited by papers focused on Chromosomal and Genetic Variations (10 papers), Cystic Fibrosis Research Advances (8 papers) and RNA and protein synthesis mechanisms (8 papers). J. Schmidtke collaborates with scholars based in Germany, United Kingdom and Switzerland. J. Schmidtke's co-authors include Wolfgang Engel, D.N. Cooper, Michael Schmid, Jörg T. Epplen, Manfred Stuhrmann, R.K. Track, H.F. Willard, K. Kubzdela, Joel Gelernter and A. Bale and has published in prestigious journals such as Nature, Nucleic Acids Research and Journal of Clinical Investigation.

In The Last Decade

J. Schmidtke

53 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. Schmidtke Germany 19 563 423 259 192 84 53 1.1k
Peter O'Connell United States 14 808 1.4× 295 0.7× 122 0.5× 94 0.5× 49 0.6× 17 1.4k
W. Krone Germany 24 856 1.5× 467 1.1× 373 1.4× 201 1.0× 40 0.5× 72 1.7k
Melanie M. Mahtani United States 14 818 1.5× 705 1.7× 252 1.0× 68 0.4× 42 0.5× 18 1.4k
Philippe Vago France 20 422 0.7× 297 0.7× 116 0.4× 84 0.4× 101 1.2× 89 1.2k
Takahiro Nakayama Japan 16 1.0k 1.8× 182 0.4× 117 0.5× 179 0.9× 39 0.5× 34 1.4k
Peng Yeong Woon United Kingdom 14 632 1.1× 320 0.8× 159 0.6× 52 0.3× 33 0.4× 29 1.3k
Peter M. Kroisel Austria 16 935 1.7× 658 1.6× 172 0.7× 86 0.4× 109 1.3× 38 1.5k
Aı̈da Metzenberg United States 16 660 1.2× 225 0.5× 47 0.2× 105 0.5× 130 1.5× 19 1.2k
Arend Sidow United States 10 1.0k 1.8× 646 1.5× 200 0.8× 35 0.2× 27 0.3× 11 1.4k
A. Neuhäuser-Klaus Germany 22 1.2k 2.1× 449 1.1× 231 0.9× 62 0.3× 34 0.4× 61 1.6k

Countries citing papers authored by J. Schmidtke

Since Specialization
Citations

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

Fields of papers citing papers by J. Schmidtke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of J. Schmidtke. A scholar is included among the top collaborators of J. Schmidtke 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. Schmidtke. J. Schmidtke 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.
2.
Stuhrmann, Manfred, Iqbal A Bukhari, Kai Brakensiek, et al.. (2008). Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21‐q23. Clinical Genetics. 73(6). 566–572. 31 indexed citations
3.
Stuhrmann, Manfred, et al.. (2001). Familial thrombocytosis as a recessive, possibly X‐linked trait in an Arab family. British Journal of Haematology. 112(3). 616–620. 11 indexed citations
4.
Byrd, D. J., Mine Arslan‐Kirchner, Udo Vester, et al.. (2000). Renal polyamine excretion, tubular amino acid reabsorption and molecular genetics in cystinuria. Pediatric Nephrology. 14(5). 376–384. 9 indexed citations
5.
Schubert, Stephanie, et al.. (2000). Molecular evolution of the murine <i>tspy</i> genes. Cytogenetic and Genome Research. 91(1-4). 239–242. 13 indexed citations
6.
Stuhrmann, Manfred, Thilo Dörk, Matthias Frühwirth, et al.. (1997). Detection of 100% of the CFTR mutations in 63 CF families from Tyrol. Clinical Genetics. 52(4). 240–246. 18 indexed citations
7.
Will, Katrin, Jochen Reiss, Michael Dean, et al.. (1993). CFTR transcripts are undetectable in lymphocytes and respiratory epithelial cells of a CF patient homozygous for the nonsense mutation R553X.. Journal of Medical Genetics. 30(10). 833–837. 14 indexed citations
8.
Nürnberg, Peter, John D. Berard, Fred B. Bercovitch, et al.. (1993). Oligonucleotide fingerprinting of free-ranging and captive rhesus macaques from CayoSantiago: Paternity assignment and comparison of heterozygosity. Birkhäuser Basel eBooks. 67. 445–451. 9 indexed citations
9.
Handt, Oliva, André Reis, & J. Schmidtke. (1992). Ectopic transcription of the parathyroid hormone gene in lymphocytes, lymphoblastoid cells and tumour tissue. Journal of Endocrinology. 135(2). 249–256. 2 indexed citations
10.
Kidd, K.K., A. Bowcock, J. Schmidtke, et al.. (1989). Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 622-643. Cytogenetic and Genome Research. 51(1-4). 622–643. 197 indexed citations
11.
Krawczak, Michael, et al.. (1988). Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families. Human Genetics. 80(1). 78–80. 46 indexed citations
12.
Wendel, U., Ekkehard Wilichowski, J. Schmidtke, & C. Bachmann. (1988). DNA analysis of ornithine transcarbamylase deficiency. European Journal of Pediatrics. 147(4). 368–371. 2 indexed citations
13.
Schmidtke, J. & D.N. Cooper. (1988). A comprehensive list of cloned human DNA sequences. Nucleic Acids Research. 16(suppl). r403–r480. 3 indexed citations
14.
Wilichowski, Ekkehard, Michael Krawczak, E Seemanová, F. Hanefeld, & J. Schmidtke. (1987). Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markers. Human Genetics. 75(1). 32–40. 8 indexed citations
15.
Stockinger, Hannes, J. Schmidtke, Christopher J. Bostock, & Jörg T. Epplen. (1986). Human DNA sequences isolated with an immunoglobulin switch region probe: sequence, chromosomal localization, and restriction fragment length polymorphisms. Human Genetics. 73(2). 104–109. 7 indexed citations
16.
Arnemann, J, et al.. (1986). Clustered GATA repeats (Bkm sequences) on the human Y chromosome. Human Genetics. 73(4). 301–303. 29 indexed citations
17.
Epplen, Jörg T., et al.. (1982). Patterns of Cyclic AMP Phosphodiesterases in the Rat Pineal Gland:Sex Differences in Diurnal Rhythmicity. Neuroendocrinology. 34(1). 46–54. 11 indexed citations
18.
Schmidtke, J., E. Schmitt, M. Leipoldt, & Wolfgang Engel. (1979). Amount of repeated and non-repeated DNA in the genomes of closely related fish species with varying genome sizes. Comparative Biochemistry and Physiology Part B Comparative Biochemistry. 64(1). 117–120. 13 indexed citations
19.
Schmidtke, J., et al.. (1975). Regulation of cell size in fish of tetraploid origin. Nature. 254(5499). 426–427. 20 indexed citations
20.
Schmidtke, J., Niels B. Atkin, & Wolfgang Engel. (1975). Gene action in fish of tetraploid origin. II. Cellular and biochemical parameters in clupeoid and salmonoid fish. Biochemical Genetics. 13(5-6). 301–309. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Peter O'Connell Breakdown of academic impact, for papers by W. Krone Breakdown of academic impact, for papers by Melanie M. Mahtani Breakdown of academic impact, for papers by Philippe Vago Breakdown of academic impact, for papers by Takahiro Nakayama Breakdown of academic impact, for papers by Peng Yeong Woon Breakdown of academic impact, for papers by Peter M. Kroisel Breakdown of academic impact, for papers by Aı̈da Metzenberg Breakdown of academic impact, for papers by Arend Sidow Breakdown of academic impact, for papers by A. Neuhäuser-Klaus
Rankless by CCL
2026