A. Junge

483 total citations
17 papers, 367 citations indexed

About

A. Junge is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, A. Junge has authored 17 papers receiving a total of 367 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 9 papers in Molecular Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in A. Junge's work include Forensic and Genetic Research (9 papers), Molecular Biology Techniques and Applications (4 papers) and Mitochondrial Function and Pathology (3 papers). A. Junge is often cited by papers focused on Forensic and Genetic Research (9 papers), Molecular Biology Techniques and Applications (4 papers) and Mitochondrial Function and Pathology (3 papers). A. Junge collaborates with scholars based in Germany, France and Netherlands. A. Junge's co-authors include B. Brinkmann, Burkhard Madea, E. Meyer, Peter Wiegand, M. Schürenkamp, Burkhard Rolf, Anne Baasner, Claudia Schäfer, T. Lederer and B Madea and has published in prestigious journals such as Human Mutation, Human Genetics and Forensic Science International.

In The Last Decade

A. Junge

17 papers receiving 340 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. Junge Germany 11 291 240 36 31 19 17 367
M.C. Vide Portugal 9 274 0.9× 186 0.8× 30 0.8× 47 1.5× 17 0.9× 27 307
M. Schürenkamp Germany 13 312 1.1× 269 1.1× 24 0.7× 24 0.8× 20 1.1× 23 398
V. Johnsson Finland 9 353 1.2× 282 1.2× 59 1.6× 10 0.3× 15 0.8× 11 429
Jennifer A. McElhoe United States 10 299 1.0× 407 1.7× 104 2.9× 19 0.6× 6 0.3× 18 488
B.M. Dupuy Norway 10 290 1.0× 206 0.9× 24 0.7× 22 0.7× 25 1.3× 15 350
Julia Andersen United Kingdom 7 243 0.8× 201 0.8× 46 1.3× 16 0.5× 19 1.0× 10 301
Alexis Hernández Spain 6 233 0.8× 151 0.6× 37 1.0× 37 1.2× 21 1.1× 9 310
Diego Montiel González Netherlands 9 178 0.6× 172 0.7× 17 0.5× 60 1.9× 6 0.3× 13 289
B. Eriksen Denmark 9 214 0.7× 176 0.7× 38 1.1× 10 0.3× 13 0.7× 17 267
Katie L. Swango United States 9 154 0.5× 262 1.1× 102 2.8× 15 0.5× 4 0.2× 10 406

Countries citing papers authored by A. Junge

Since Specialization
Citations

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

Fields of papers citing papers by A. Junge

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Junge

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

All Works

17 of 17 papers shown
1.
Madea, Burkhard, et al.. (2011). STRs, mini STRs and SNPs – A comparative study for typing degraded DNA. Legal Medicine. 13(2). 68–74. 37 indexed citations
2.
Junge, A., R. Dettmeyer, & Burkhard Madea. (2008). Identification of Biological Samples in a Case of Contamination of a Cytological Slide Preparation*. Journal of Forensic Sciences. 53(3). 739–741. 3 indexed citations
3.
Junge, A., B. Brinkmann, Rolf Fimmers, & Burkhard Madea. (2005). Mutations or exclusion: an unusual case in paternity testing. International Journal of Legal Medicine. 120(6). 360–363. 18 indexed citations
4.
Junge, A., et al.. (2003). Validation of the multiplex kit genRES MPX-2 for forensic casework analysis. International Journal of Legal Medicine. 117(6). 317–325. 27 indexed citations
5.
Klein, Rachel Herndon, et al.. (2003). A very long ACTBP2 (SE33) allele. International Journal of Legal Medicine. 117(4). 235–236. 10 indexed citations
6.
Junge, A., et al.. (2002). Successful DNA Typing of a Urine Sample in a Doping Control Case Using Human Mitochondrial DNA Analysis. Journal of Forensic Sciences. 47(5). 1–3. 22 indexed citations
7.
Junge, A., et al.. (2001). Genetic variation and population genetic data of the short tandem repeat locus D8S320. Forensic Science International. 119(1). 11–16. 1 indexed citations
8.
Lutz, Sabine, Holger Wittig, Hans‐Joachim Weisser, et al.. (2000). Is it possible to differentiate mtDNA by means of HVIII in samples that cannot be distinguished by sequencing the HVI and HVII regions?. Forensic Science International. 113(1-3). 97–101. 54 indexed citations
9.
Junge, A., A. Baasner, R. Dettmeyer, & Burkhard Madea. (1999). Pränatale Paternitätsbestimmung mittels PCR-VNTR-Polymorphismen. Rechtsmedizin. 9(5). 193–196. 2 indexed citations
10.
Junge, A. & Burkhard Madea. (1999). Population studies of the Y-chromosome specific polymorphisms DYS19, DYS389 I+II, DYS390 and DYS393 in a Western German population (Bonn area). Forensic Science International. 101(3). 195–201. 5 indexed citations
11.
Baasner, Anne, Claudia Schäfer, A. Junge, & Burkhard Madea. (1998). Polymorphic sites in human mitochondrial DNA control region sequences: population data and maternal inheritance. Forensic Science International. 98(3). 169–178. 40 indexed citations
12.
Brinkmann, B., A. Junge, E. Meyer, & Peter Wiegand. (1998). Population genetic diversity in relation to microsatellite heterogeneity. Human Mutation. 11(2). 135–144. 50 indexed citations
13.
Junge, A. & Burkhard Madea. (1998). Validation studies and characterization of variant alleles at the short tandem repeat locus D12S391. International Journal of Legal Medicine. 112(1). 67–69. 8 indexed citations
14.
Rolf, Burkhard, M. Schürenkamp, A. Junge, & B. Brinkmann. (1997). Sequence polymorphism at the tetranucleotide repeat of the human beta-actin related pseudogene H-beta-Ac-psi-2 (ACTBP2) locus. International Journal of Legal Medicine. 110(2). 69–72. 42 indexed citations
15.
Brinkmann, B., E. Meyer, & A. Junge. (1996). Complex mutational events at the HumD21S11 locus. Human Genetics. 98(1). 60–64. 32 indexed citations
16.
Piccinini, A., et al.. (1995). Short tandem repeat (STR) system HumD21S11: Population genetic study on an Italian population. International Journal of Legal Medicine. 108(3). 165–166. 4 indexed citations
17.
Junge, A. & W. Werner. (1989). Investigations on interactions of phosphorus compounds in partially acidulated phosphate rock and fertilizer effectiveness. Nutrient Cycling in Agroecosystems. 20(3). 129–134. 12 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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