Jörg Schmidtke

6.1k total citations
149 papers, 4.2k citations indexed

About

Jörg Schmidtke is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Jörg Schmidtke has authored 149 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 94 papers in Genetics, 38 papers in Molecular Biology and 24 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Jörg Schmidtke's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (30 papers), BRCA gene mutations in cancer (24 papers) and Connective tissue disorders research (16 papers). Jörg Schmidtke is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (30 papers), BRCA gene mutations in cancer (24 papers) and Connective tissue disorders research (16 papers). Jörg Schmidtke collaborates with scholars based in Germany, United Kingdom and United States. Jörg Schmidtke's co-authors include Howard J. Cooke, D.N. Cooper, Wolfgang Engel, John R. Gosden, Mine Arslan‐Kirchner, Tanja Vogel, Michael Krawczak, Barbara A. Smith, Irmgard Nippert and Kathrin Rommel and has published in prestigious journals such as Nature, Nucleic Acids Research and Blood.

In The Last Decade

Jörg Schmidtke

146 papers receiving 4.1k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Jörg Schmidtke 2.3k 1.7k 711 463 376 149 4.2k
Unnur Þorsteinsdóttir 2.1k 0.9× 3.0k 1.8× 535 0.8× 325 0.7× 196 0.5× 68 6.5k
R. Williamson 2.0k 0.9× 3.8k 2.3× 1.0k 1.5× 379 0.8× 639 1.7× 185 7.9k
Marc De Braekeleer 1.7k 0.7× 1.9k 1.1× 849 1.2× 476 1.0× 719 1.9× 235 5.6k
Joseph E. Powell 2.4k 1.0× 3.3k 2.0× 393 0.6× 214 0.5× 212 0.6× 97 6.2k
Nabeel A. Affara 3.2k 1.4× 4.2k 2.5× 461 0.6× 863 1.9× 944 2.5× 167 7.1k
Alexander Hoischen 4.0k 1.7× 3.9k 2.3× 363 0.5× 290 0.6× 115 0.3× 142 8.2k
Larry J. Shapiro 2.8k 1.2× 3.5k 2.1× 228 0.3× 565 1.2× 364 1.0× 105 5.6k
Bryan Howie 4.5k 2.0× 2.6k 1.5× 259 0.4× 415 0.9× 67 0.2× 17 7.6k
David J. Amor 2.6k 1.1× 2.6k 1.5× 218 0.3× 652 1.4× 355 0.9× 225 5.4k
Daniela Toniolo 2.4k 1.0× 5.6k 3.3× 178 0.3× 271 0.6× 391 1.0× 139 8.6k

Countries citing papers authored by Jörg Schmidtke

Since Specialization
Citations

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

Fields of papers citing papers by Jörg Schmidtke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jörg Schmidtke

This figure shows the co-authorship network connecting the top 25 collaborators of Jörg Schmidtke. A scholar is included among the top collaborators of Jörg 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 Jörg Schmidtke. Jörg 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.
Koch, Sebastian, Jörg Schmidtke, Michael Krawczak, & Amke Caliebe. (2023). Clinical utility of polygenic risk scores: a critical 2023 appraisal. Journal of Community Genetics. 14(5). 471–487. 34 indexed citations
2.
Schmidtke, Jörg, et al.. (2019). NGS-Based genetic testing for heritable cardiovascular diseases. Specific requirements for obtaining informed consent. Molecular and Cellular Probes. 45. 70–78. 1 indexed citations
3.
Schmidtke, Jörg, et al.. (2018). Rare diseases and sports: A pilot project to improve physical activity in patients with mucopolysaccharidosis. Translational Sports Medicine. 1(5). 184–190. 1 indexed citations
4.
Storf, Holger, Martin Frank, Franziska Schauer, et al.. (2016). Adopting Quality Criteria for Websites Providing Medical Information About Rare Diseases. Interactive Journal of Medical Research. 5(3). e24–e24. 14 indexed citations
5.
Schmidtke, Jörg & Kerstin Schmidt. (2013). Standardised statistical programming practices for R and SAS. EFSA Supporting Publications. 10(2). 1 indexed citations
6.
Sequeiros, Jorge, et al.. (2012). The wide variation of definitions of genetic testing in international recommendations, guidelines and reports. Journal of Community Genetics. 3(2). 113–124. 14 indexed citations
7.
Schmidtke, Jörg, et al.. (2011). Versorgungsqualität bei genetisch bedingten Erkrankungen – Sekundäranalyse humangenetischer Gutachten. Zeitschrift für Evidenz Fortbildung und Qualität im Gesundheitswesen. 106(3). 217–223. 1 indexed citations
8.
Kääriäinen, H, et al.. (2010). Genetic Screening in Europe. Public Health Genomics. 13(7-8). 524–537. 5 indexed citations
9.
Plass, Anne Marie, Marieke J.H. Baars, Martina C. Cornel, et al.. (2009). Testing the Children: Do Non-Genetic Health-Care Providers Differ in Their Decision to Advise Genetic Presymptomatic Testing on Minors? A Cross-Sectional Study in Five Countries in the European Union. Genetic Testing and Molecular Biomarkers. 13(3). 367–376. 6 indexed citations
10.
Arslan‐Kirchner, Mine, Yskert Von Kodolitsch, & Jörg Schmidtke. (2008). The Importance of Genetic Testing in the Clinical Management of Patients With Marfan Syndrome and Related Disorders. Deutsches Ärzteblatt international. 105(27). 483–91. 13 indexed citations
11.
Krawczak, Michael, Amke Caliebe, Peter J.P. Croucher, & Jörg Schmidtke. (2007). On the Testing Load Incurred by Cascade Genetic Carrier Screening for Mendelian Disorders: A Brief Report. Genetic Testing. 11(4). 417–420. 7 indexed citations
12.
Kovac, Judit, et al.. (2006). Tspy is nonfunctional in the Mongolian gerbil but functional in the Syrian hamster. Genomics. 88(1). 65–73. 4 indexed citations
13.
Schmidtke, Jörg, Brigitte Pabst, & Irmgard Nippert. (2005). DNA-based Genetic Testing Is Rising Steeply in a National Health Care System with Open Access to Services: A Survey of Genetic Test Use in Germany, 1996–2002. Genetic Testing. 9(1). 80–84. 16 indexed citations
14.
Challen, Kirsty, Hilary Harris, Claire Julian‐Reynier, et al.. (2005). Genetic education and nongenetic health professionals: Educational providers and curricula in Europe. Genetics in Medicine. 7(5). 302–310. 32 indexed citations
15.
Rasch, Dieter, et al.. (2004). The misuse of asterisks in hypothesis testing. 4 indexed citations
16.
Ensslin, Michael A., Tanja Vogel, Juan J. Calvete, et al.. (1998). Molecular Cloning and Characterization of P47, a Novel Boar Sperm-Associated Zona Pellucida-Binding Protein Homologous to a Family of Mammalian Secretory Proteins1. Biology of Reproduction. 58(4). 1057–1064. 77 indexed citations
17.
Maçek, Milan, Milan Maçek, Milan Maçek, et al.. (1991). The direct early diagnosis of cystic fibrosis by the detection of the deltaF508 CFTR gene mutation in a prematurely delivered boy. Clinical Genetics. 39(3). 219–222. 6 indexed citations
18.
Arnemann, Joachim, Georg Gradl, Jochen Casper, et al.. (1989). Characterization of rearranged Y chromosomes in human testicular tumor cell lines. Cancer Genetics and Cytogenetics. 37(2). 141–151. 8 indexed citations
19.
Schwartz, M., M Super, Jörg Schmidtke, et al.. (1988). Prenatal diagnosis of cystic fibrosis using linked DNA probes. Prenatal Diagnosis. 8(8). 619–624. 4 indexed citations
20.
Wainwright, Brandon J., Peter Scambler, Jörg Schmidtke, et al.. (1985). Localization of cystic fibrosis locus to human chromosome 7cen–q22. Nature. 318(6044). 384–385. 372 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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