M. Schürenkamp

510 citations
23 papers · 398 indexed · h-index 13

Impact in

  • Genetics top 10%
    • Forensic and Genetic Research
    • Genetic diversity and population structure
    • Genetic Associations and Epidemiology
    • Race, Genetics, and Society
    • Molecular Biology Techniques and Applications
    • Epigenetics and DNA Methylation
    • Genomics and Phylogenetic Studies
    • Identification and Quantification in Food

Papers in

    • Forensic and Genetic Research 14
    • Race, Genetics, and Society 4
    • Genetic Associations and Epidemiology 3
    • Molecular Biology Techniques and Applications 11
    • Epigenetics and DNA Methylation 2
    • RNA and protein synthesis mechanisms 2

M. Schürenkamp

23 papers receiving 384 citations

Peers

M. Schürenkamp
Comparison fields: 5 of 75
  • Genetics 312
  • Molecular Biology 269
  • Archeology 24
  • Aging 4
  • Urology 9
Replace C. Puers with:
C. Puers Germany
R. Frazier United Kingdom
P. Hoff-Olsen Norway
U. V. Borer Switzerland
Cesare Rapone Italy
A. Junge Germany
A. Krätzer Switzerland
N. Dimo-Simonin Switzerland
Anastasia Aliferi United Kingdom
V. Johnsson Finland
M. Schürenkamp relative to C. Puers Germany C. Puers's profile →
Citations per field
00.5×10×15×22×
C. Puers · 1×
Citations per year

Countries citing papers authored by M. Schürenkamp

Since Specialization
Citations

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

Fields of papers citing papers by M. Schürenkamp

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside M. Schürenkamp, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with M. Schürenkamp Line = papers co-authored together M. Schürenkamp links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 201926
2 20183
3 201728
4 20168
5 20151
6 201538
7 20149
8 200920
9 200811
10 200614
11 200224
12 200134
13 199927
14 199921
15 199819
16 199822
17 199742
18 19975
19 19964
20 199531

About M. Schürenkamp

M. Schürenkamp is a scholar working on Genetics, Molecular Biology, Endocrine and Autonomic Systems, Speech and Hearing and Cancer Research, having authored 23 papers that have together received 398 indexed citations. Recurring topics across this work include Forensic and Genetic Research (14 papers), Molecular Biology Techniques and Applications (11 papers), Race, Genetics, and Society (4 papers), Genetic Associations and Epidemiology (3 papers), Epigenetics and DNA Methylation (2 papers), Environmental DNA in Biodiversity Studies (2 papers), Cancer Genomics and Diagnostics (2 papers) and RNA and protein synthesis mechanisms (2 papers). The work is most often cited by research in Genetics (312 citations), Molecular Biology (269 citations), Archeology (24 citations), Aging (4 citations) and Urology (9 citations). M. Schürenkamp has collaborated with scholars based in Germany, Hungary and United Kingdom. Frequent co-authors include B. Brinkmann, Carsten Hohoff, Bernd Brinkmann, Heriberto Pfeiffer, Burkhard Rolf, A. Junge, Peter Wiegand, M. Kleiber, Ermanno Rossi and Marielle Vennemann. Their work appears in journals such as International Journal of Legal Medicine, Forensic Science International Genetics, Forensic Science Medicine and Pathology, Proceedings of the Royal Society B Biological Sciences and Forensic science international. Genetics supplement series.

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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