J. Schmidtke

3.0k total citations
33 papers, 455 citations indexed

About

J. Schmidtke is a scholar working on Genetics, Molecular Biology and Ecology. According to data from OpenAlex, J. Schmidtke has authored 33 papers receiving a total of 455 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 8 papers in Molecular Biology and 3 papers in Ecology. Recurrent topics in J. Schmidtke's work include Genomics and Rare Diseases (4 papers), Molecular Biology Techniques and Applications (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). J. Schmidtke is often cited by papers focused on Genomics and Rare Diseases (4 papers), Molecular Biology Techniques and Applications (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). J. Schmidtke collaborates with scholars based in Germany, United Kingdom and Netherlands. J. Schmidtke's co-authors include Ségolène Aymé, D.N. Cooper, K.K. Kidd, P. Pearson, A. Bowcock, Willard A. Van Engel, M. Chipperfield, M. Tolley, B. Maidak and J. Hewitt and has published in prestigious journals such as Nucleic Acids Research, Human Genetics and Forensic Science International.

In The Last Decade

J. Schmidtke

31 papers receiving 439 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 11 242 192 65 38 36 33 455
H. Xiao United States 12 286 1.2× 364 1.9× 35 0.5× 60 1.6× 51 1.4× 25 619
Martha Kalff-Suske Germany 10 159 0.7× 312 1.6× 27 0.4× 51 1.3× 33 0.9× 15 475
R. Williamson United Kingdom 12 270 1.1× 341 1.8× 99 1.5× 21 0.6× 23 0.6× 27 703
Leah Sabacan United States 10 205 0.8× 276 1.4× 44 0.7× 37 1.0× 34 0.9× 17 480
Giulia Arrigo Italy 12 240 1.0× 339 1.8× 49 0.8× 28 0.7× 18 0.5× 21 594
Bernd Auber Germany 13 223 0.9× 194 1.0× 47 0.7× 41 1.1× 40 1.1× 48 492
K.K. Kidd United States 13 335 1.4× 392 2.0× 37 0.6× 66 1.7× 58 1.6× 37 730
Glen R. Monroe Netherlands 12 313 1.3× 216 1.1× 65 1.0× 35 0.9× 56 1.6× 20 524
Edmond G. Lemire Canada 14 202 0.8× 240 1.3× 142 2.2× 38 1.0× 26 0.7× 42 616
Hans Matsson Sweden 11 255 1.1× 387 2.0× 31 0.5× 41 1.1× 23 0.6× 15 610

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.
Eiben, B., et al.. (2025). Age-specific uptake of non-invasive prenatal tests (NIPT) in Germany: a decision theory-based analysis. Journal of Community Genetics. 16(6). 769–774.
2.
Schmidtke, J., et al.. (2014). Konzepte zur Mitteilung genetischer Zusatzbefunde in der medizinischen Diagnostik und Forschung. Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz. 58(2). 166–173. 1 indexed citations
3.
Klintschar, Michael, Udo Bilkenroth, Mine Arslan‐Kirchner, J. Schmidtke, & D Stiller. (2008). Marfan syndrome: clinical consequences resulting from a medicolegal autopsy of a case of sudden death due to aortic rupture. International Journal of Legal Medicine. 123(1). 55–58. 22 indexed citations
4.
Aymé, Ségolène & J. Schmidtke. (2007). Networking for rare diseases: a necessity for Europe. Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz. 50(12). 1477–1483. 82 indexed citations
5.
Schmidtke, J., et al.. (2006). Education in Medical Genetics for Physicians: Germany. Public Health Genomics. 9(4). 235–239. 10 indexed citations
6.
Dörk, Thilo, et al.. (1997). A frequent polymorphism of the gene mutated in ataxia telangiectasia. Molecular and Cellular Probes. 11(1). 71–73. 6 indexed citations
7.
Nippert, Irmgard, et al.. (1997). Genetic Services in Germany. European Journal of Human Genetics. 5(Suppl. 2). 81–88. 3 indexed citations
8.
Krawczak, Michael, Jochen Hampe, J. Hundrieser, et al.. (1993). Paternity testing with oligonucleotide multilocus probe (CAC)5/(GTG)5: A multicenter study. Forensic Science International. 59(2). 101–117. 9 indexed citations
9.
Cooper, D.N. & J. Schmidtke. (1992). Molecular Genetic Approaches to the Analysis and Diagnosis of Human Inherited Disease: An Overview. Annals of Medicine. 24(1). 29–42. 14 indexed citations
10.
Cooper, D.N. & J. Schmidtke. (1991). Diagnosis of genetic disease using recombinant DNA. Third edition. Human Genetics. 87(5). 307–34. 17 indexed citations
11.
Williamson, R., A. Bowcock, K.K. Kidd, et al.. (1991). Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 24 of 27). Cytogenetic and Genome Research. 58(3-4). 1790–1800. 1 indexed citations
12.
Williamson, R., A. Bowcock, K.K. Kidd, et al.. (1991). Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 16 of 27). Cytogenetic and Genome Research. 58(3-4). 1685–1705. 1 indexed citations
13.
Williamson, R., A. Bowcock, K.K. Kidd, et al.. (1990). Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms (Part 1 of 14). Cytogenetic and Genome Research. 55(1-4). 457–472. 49 indexed citations
14.
Valle, Denise, et al.. (1989). Genetics and biochemistry of variant human phenotypes. ORCA Online Research @Cardiff (Cardiff University). 5 indexed citations
15.
Schmidtke, J. & D.N. Cooper. (1989). A comprehensive list of cloned human DNA sequences. Nucleic Acids Research. 17(suppl). r173–r281. 2 indexed citations
16.
Cooper, D.N. & J. Schmidtke. (1989). Diagnosis of genetic disease using recombinant DNA. Second edition. Human Genetics. 83(4). 307–334. 7 indexed citations
17.
Arnemann, J, et al.. (1989). DNA fingerprinting for paternity and maternity in group O Cayo Santiago-derived rhesus monkeys at the German Primate Center: results of a pilot study.. PubMed. 8(1). 181–4. 10 indexed citations
18.
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. 922–947. Cytogenetic and Genome Research. 51(1-4). 922–947. 1 indexed citations
19.
Kidd, K.K., A. Bowcock, P. Pearson, et al.. (1988). Report of the committee on human gene mapping by recombinant DNA techniques (Part 1 of 6). Cytogenetic and Genome Research. 49(1-3). 132–145. 11 indexed citations
20.
Ogilvie, Donald, B P Wordsworth, L. Priestley, et al.. (1987). Segregation of all four major fibrillar collagen genes in the Marfan syndrome.. Europe PMC (PubMed Central). 41(6). 1071–82. 34 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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