Ines Plate

733 total citations
19 papers, 593 citations indexed

About

Ines Plate is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Ines Plate has authored 19 papers receiving a total of 593 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 13 papers in Molecular Biology and 3 papers in Clinical Biochemistry. Recurrent topics in Ines Plate's work include Forensic and Genetic Research (13 papers), Molecular Biology Techniques and Applications (5 papers) and Metabolism and Genetic Disorders (3 papers). Ines Plate is often cited by papers focused on Forensic and Genetic Research (13 papers), Molecular Biology Techniques and Applications (5 papers) and Metabolism and Genetic Disorders (3 papers). Ines Plate collaborates with scholars based in Germany, United States and Italy. Ines Plate's co-authors include R. Szibor, Sandra Hering, Jeanett Edelmann, Michael Matthias, Lutz Roewer, Danilo Deichsel, Holger Wittig, Eberhard Kuhlisch, Dieter Krause and Michael Krawczak and has published in prestigious journals such as Electrophoresis, Forensic Science International and International Journal of Oncology.

In The Last Decade

Ines Plate

19 papers receiving 576 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ines Plate Germany 12 528 438 44 26 26 19 593
A. Junge Germany 11 291 0.6× 240 0.5× 31 0.7× 36 1.4× 19 0.7× 17 367
N. Dimo-Simonin Switzerland 10 255 0.5× 213 0.5× 55 1.3× 30 1.2× 6 0.2× 25 366
M. Schürenkamp Germany 13 312 0.6× 269 0.6× 24 0.5× 24 0.9× 20 0.8× 23 398
M.C. Vide Portugal 9 274 0.5× 186 0.4× 47 1.1× 30 1.2× 17 0.7× 27 307
V. Johnsson Finland 9 353 0.7× 282 0.6× 10 0.2× 59 2.3× 15 0.6× 11 429
Carey Davis United States 11 575 1.1× 591 1.3× 57 1.3× 207 8.0× 6 0.2× 16 735
Avinash Arvind Rasalkar India 6 216 0.4× 143 0.3× 89 2.0× 6 0.2× 5 0.2× 11 373
Diego Montiel González Netherlands 9 178 0.3× 172 0.4× 60 1.4× 17 0.7× 6 0.2× 13 289
B.V. Ravi Prasad India 7 250 0.5× 162 0.4× 57 1.3× 4 0.2× 72 2.8× 11 385
Donata Luiselli Italy 7 272 0.5× 84 0.2× 89 2.0× 5 0.2× 13 0.5× 7 389

Countries citing papers authored by Ines Plate

Since Specialization
Citations

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

Fields of papers citing papers by Ines Plate

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ines Plate

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

All Works

19 of 19 papers shown
1.
Hering, Sandra, et al.. (2008). The STR cluster DXS10148–DXS8378–DXS10135 provides a powerful tool for X-chromosomal haplotyping at Xp22. International Journal of Legal Medicine. 122(6). 489–492. 48 indexed citations
2.
Szibor, R., et al.. (2006). Forensic mass screening using mtDNA. International Journal of Legal Medicine. 120(6). 372–376. 21 indexed citations
3.
Szibor, R., et al.. (2006). Mitochondrial D-loop (CA) n repeat length heteroplasmy: frequency in a German population sample and inheritance studies in two pedigrees. International Journal of Legal Medicine. 121(3). 207–213. 14 indexed citations
4.
Szibor, R., Sandra Hering, Eberhard Kuhlisch, et al.. (2005). Haplotyping of STR cluster DXS6801–DXS6809–DXS6789 on Xq21 provides a powerful tool for kinship testing. International Journal of Legal Medicine. 119(6). 363–369. 84 indexed citations
5.
Hering, Sandra, Eberhard Kuhlisch, Jeanett Edelmann, et al.. (2004). DXS10011: studies on structure, allele distribution in three populations and genetic linkage to further q-telomeric chromosome X markers. International Journal of Legal Medicine. 118(6). 313–319. 24 indexed citations
6.
Edelmann, Jeanett, et al.. (2003). Validation of the X-chromosomal STR DXS6809. International Journal of Legal Medicine. 117(4). 241–244. 22 indexed citations
7.
Szibor, R., Jeanett Edelmann, Sandra Hering, et al.. (2003). Cell line DNA typing in forensic genetics—the necessity of reliable standards. Forensic Science International. 138(1-3). 37–43. 91 indexed citations
8.
Szibor, R., et al.. (2003). Identification of the minor component of a mixed stain by using mismatch primer-induced restriction sites in amplified mtDNA. International Journal of Legal Medicine. 117(3). 160–164. 6 indexed citations
9.
Szibor, R., et al.. (2003). Chromosome X haplotyping in deficiency paternity testing principles and case report. International Congress Series. 1239. 815–820. 8 indexed citations
10.
Edelmann, Jeanett, Danilo Deichsel, Sandra Hering, Ines Plate, & R. Szibor. (2002). Sequence variation and allele nomenclature for the X-linked STRs DXS9895, DXS8378, DXS7132, DXS6800, DXS7133, GATA172D05, DXS7423 and DXS8377. Forensic Science International. 129(2). 99–103. 72 indexed citations
11.
Edelmann, Jeanett, Sandra Hering, Michael Matthias, et al.. (2001). Announcement of population data 16 X-chromosome STR loci frequency data from a German population. 11 indexed citations
12.
Edelman, J., Sandra Hering, R. Lessig, et al.. (2001). 16 X-chromosone STR Loci frquency data. Forensic Science International. 124(2-3). 215–218. 88 indexed citations
13.
Szibor, R., Michael Matthias, Ines Plate, & Dieter Krause. (2000). Efficiency of forensic mtDNA analysis. Forensic Science International. 113(1-3). 71–78. 21 indexed citations
14.
Szibor, R., et al.. (2000). Population Data on the X Chromosome Short Tandem Repeat Locus HumHPRTB in Two Regions of Germany. Journal of Forensic Sciences. 45(1). 14669J–14669J. 36 indexed citations
15.
Kirches, Elmar, Stefan Vielhaber, Michaela Warich-Kirches, et al.. (1999). Mitochondrial tRNA<sup>Cys</sup> Mutation A5823G in a Patient with Motor Neuron Disease and Temporal Lobe Epilepsy. Pathobiology. 67(4). 214–218. 5 indexed citations
16.
Schneider-Stock, R, et al.. (1999). No microsatellite instability, but frequent LOH in liposarcomas.. International Journal of Oncology. 14(4). 721–6. 5 indexed citations
17.
Szibor, R., et al.. (1998). Population genetic data of the STR HumD3S1358 in two regions of Germany. International Journal of Legal Medicine. 111(3). 160–161. 5 indexed citations
18.
Szibor, R., Ines Plate, N. Beck, et al.. (1998). Correspondence. Journal of Forensic Sciences. 43(2). 445–449. 1 indexed citations
19.
Szibor, R., et al.. (1997). Mitochondrial D‐loop 3′ (CA)n repeat polymorphism: Optimization of analysis and population data. Electrophoresis. 18(15). 2857–2860. 31 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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