Andreas Dufke

4.7k total citations
60 papers, 1.4k citations indexed

About

Andreas Dufke is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Andreas Dufke has authored 60 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Genetics, 28 papers in Molecular Biology and 27 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Andreas Dufke's work include Genomic variations and chromosomal abnormalities (28 papers), Prenatal Screening and Diagnostics (24 papers) and Chromosomal and Genetic Variations (15 papers). Andreas Dufke is often cited by papers focused on Genomic variations and chromosomal abnormalities (28 papers), Prenatal Screening and Diagnostics (24 papers) and Chromosomal and Genetic Variations (15 papers). Andreas Dufke collaborates with scholars based in Germany, United States and France. Andreas Dufke's co-authors include H. Enders, Thomas Liehr, Thomas Eggermann, Michael Bonin, Ute Grasshoff, Olaf Rieß, Ulrike A. Mau‐Holzmann, Heike Starke, Karl Oliver Kagan and Dagmar Wieczorek and has published in prestigious journals such as SHILAP Revista de lepidopterología, Bioinformatics and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Andreas Dufke

57 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andreas Dufke Germany 22 865 695 351 310 109 60 1.4k
Holger Tönnies Germany 23 833 1.0× 927 1.3× 179 0.5× 221 0.7× 86 0.8× 55 1.6k
Evica Rajcan‐Separovic Canada 24 770 0.9× 775 1.1× 386 1.1× 178 0.6× 71 0.7× 58 1.6k
Jayne Y. Hehir‐Kwa Netherlands 24 1.1k 1.3× 854 1.2× 378 1.1× 221 0.7× 108 1.0× 53 1.9k
Udo Trautmann Germany 23 1.1k 1.2× 930 1.3× 328 0.9× 331 1.1× 50 0.5× 65 1.7k
Sharon W. Horsley United Kingdom 19 1.3k 1.5× 882 1.3× 367 1.0× 436 1.4× 98 0.9× 30 1.8k
Erica Andersen United States 16 773 0.9× 612 0.9× 340 1.0× 85 0.3× 159 1.5× 28 1.5k
Marguerite Prieur France 22 740 0.9× 789 1.1× 171 0.5× 233 0.8× 73 0.7× 33 1.5k
Alma Kuechler Germany 19 722 0.8× 649 0.9× 238 0.7× 194 0.6× 66 0.6× 46 1.2k
Paolo Simi Italy 22 571 0.7× 633 0.9× 138 0.4× 108 0.3× 131 1.2× 82 1.4k
Sung‐Hae Kang United States 20 925 1.1× 737 1.1× 348 1.0× 180 0.6× 60 0.6× 30 1.4k

Countries citing papers authored by Andreas Dufke

Since Specialization
Citations

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

Fields of papers citing papers by Andreas Dufke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andreas Dufke

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas Dufke. A scholar is included among the top collaborators of Andreas Dufke 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 Andreas Dufke. Andreas Dufke 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.
Rieß, Olaf, Marc Sturm, German Demidov, et al.. (2024). Genomes in clinical care. npj Genomic Medicine. 9(1). 20–20. 11 indexed citations
2.
3.
Dufke, Andreas, Thomas Eggermann, Karl Oliver Kagan, Markus Hoopmann, & Miriam Elbracht. (2023). Prenatal testing for Imprinting Disorders: A clinical perspective. Prenatal Diagnosis. 43(8). 983–992. 4 indexed citations
4.
Singer, Sylke, Marc Sturm, German Demidov, et al.. (2021). New euchromatic variant dup(11)(p15.3p15.1) transmitted through two generations defined by low coverage whole genome sequencing. American Journal of Medical Genetics Part A. 185(10). 3053–3056. 1 indexed citations
5.
Kagan, Karl Oliver, Markus Hoopmann, Natalia Prodan, et al.. (2020). First Trimester Screening for Common Trisomies and Microdeletion 22q11.2 Syndrome Using Cell-Free DNA: A Prospective Clinical Study. Fetal Diagnosis and Therapy. 47(11). 841–852. 18 indexed citations
6.
Park, Joohyun, Karin Schäferhoff, Luigi Janiri, et al.. (2019). Novel HIVEP2 Variants in Patients with Intellectual Disability. Molecular Syndromology. 10(4). 195–201. 7 indexed citations
7.
Dufke, Andreas. (2018). S2k-Leitlinie Humangenetische Diagnostik und Genetische Beratung. Medizinische Genetik. 30(4). 5 indexed citations
8.
Schroeder, Christopher, Arif B. Ekici, Ute Moog, et al.. (2014). Genome-wide UPD screening in patients with intellectual disability. European Journal of Human Genetics. 22(10). 1233–1235. 4 indexed citations
9.
Dufke, Andreas, et al.. (2012). Mirror-Image Asymmetry in Monozygotic Twins with Kabuki Syndrome. Molecular Syndromology. 3(2). 94–97. 6 indexed citations
10.
Tzschach, Andreas, Ute Grasshoff, Karin Schäferhoff, et al.. (2012). Interstitial 9q34.11–q34.13 deletion in a patient with severe intellectual disability, hydrocephalus, and cleft lip/palate. American Journal of Medical Genetics Part A. 158A(7). 1709–1712. 6 indexed citations
11.
Chen, Wei, Vera M. Kalscheuer, Andreas Tzschach, et al.. (2008). Mapping translocation breakpoints by next-generation sequencing. Genome Research. 18(7). 1143–1149. 102 indexed citations
12.
Kuçi, Selim, Zyrafete Kuçi, Susanne Schmid, et al.. (2008). Efficient in vitro generation of adult multipotent cells from mobilized peripheral blood CD133+ cells. Cell Proliferation. 41(1). 12–27. 22 indexed citations
13.
Dufke, Andreas, Sylke Singer, Ulrike A. Mau‐Holzmann, et al.. (2006). De novostructural chromosomal imbalances: molecular cytogenetic characterization of partial trisomies. Cytogenetic and Genome Research. 114(3-4). 342–350. 11 indexed citations
14.
Beschorner, Rudi, Manfred Wehrmann, Michael Bonin, et al.. (2006). Extradural ependymal tumor with myxopapillary and ependymoblastic differentiation in a case of Schinzel–Giedion syndrome. Acta Neuropathologica. 113(3). 339–346. 30 indexed citations
15.
Dufke, Andreas, Sven Poths, Ulrike A. Mau‐Holzmann, et al.. (2005). A rapid microarray based whole genome analysis for detection of uniparental disomy. Human Mutation. 26(2). 153–159. 44 indexed citations
16.
Dufke, Andreas & Olaf Rieß. (2004). Genomisches Imprinting - Einfluß durch IVF und ICSI?. 1(1). 28–32. 1 indexed citations
17.
Grasshoff, Ute, Sylke Singer, Thomas Liehr, et al.. (2003). A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q24→1q22 and partial monosomy 4q27→q28. Cytogenetic and Genome Research. 103(1-2). 17–23. 26 indexed citations
18.
Rauch, R., Anita Rauch, A. Koch, et al.. (2002). Cervical origin of the subclavian artery as a specific marker for monosomy 22q11. The American Journal of Cardiology. 89(4). 481–484. 12 indexed citations
19.
Binder, Gerhard, Thomas Eggermann, H. Enders, Michael B. Ranke, & Andreas Dufke. (2001). Tall stature, gonadal dysgenesis, and stigmata of Turner’s syndrome caused by a structurally altered X chromosome. The Journal of Pediatrics. 138(2). 285–287. 19 indexed citations
20.
Dufke, Andreas, et al.. (2001). Unusual chromosomal mosaicism as a cause of mental retardation and congenital malformations in a familial reciprocal translocation carrier, t(17;22)(q24.2;q11.23). Cytogenetic and Genome Research. 93(3-4). 168–170. 22 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 Holger Tönnies Breakdown of academic impact, for papers by Evica Rajcan‐Separovic Breakdown of academic impact, for papers by Jayne Y. Hehir‐Kwa Breakdown of academic impact, for papers by Udo Trautmann Breakdown of academic impact, for papers by Sharon W. Horsley Breakdown of academic impact, for papers by Erica Andersen Breakdown of academic impact, for papers by Marguerite Prieur Breakdown of academic impact, for papers by Alma Kuechler Breakdown of academic impact, for papers by Paolo Simi Breakdown of academic impact, for papers by Sung‐Hae Kang
Rankless by CCL
2026