Carsten M. Pusch

2.8k total citations
76 papers, 1.7k citations indexed

About

Carsten M. Pusch is a scholar working on Molecular Biology, Genetics and Archeology. According to data from OpenAlex, Carsten M. Pusch has authored 76 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 24 papers in Genetics and 16 papers in Archeology. Recurrent topics in Carsten M. Pusch's work include Forensic and Genetic Research (14 papers), Retinal Development and Disorders (14 papers) and Forensic Anthropology and Bioarchaeology Studies (12 papers). Carsten M. Pusch is often cited by papers focused on Forensic and Genetic Research (14 papers), Retinal Development and Disorders (14 papers) and Forensic Anthropology and Bioarchaeology Studies (12 papers). Carsten M. Pusch collaborates with scholars based in Germany, United States and Italy. Carsten M. Pusch's co-authors include Nikolaus Blin, Frank Jacobi, Martina Broghammer, Michael Scholz, Bernd Wissinger, Alfred Czarnetzki, Markus Pfister, Michael Nerlich, Alfons Meindl and Raffaella Bianucci and has published in prestigious journals such as Science, Nucleic Acids Research and Nature Genetics.

In The Last Decade

Carsten M. Pusch

74 papers receiving 1.6k citations

Peers

Carsten M. Pusch

GENET

ARCHE

CMN

Colin E. Willoughby United Kingdom

Robert M. Grainger United States

A Eisenberg United States

Aida M. Andrés Spain

Jacquelyn Bond United Kingdom

Christine Jolicoeur Canada

Daniel Civello United States

Sabine Fauré France

Sigurjón A. Guðjónsson Iceland

Delphine Samson France

Colin E. Willoughby United Kingdom

Carsten M. Pusch

1.2k ×1.4

394 ×1.1

GENET

26 ×0.1

ARCHE

61 ×0.2

CMN

115 ×0.5

Citations per year, relative to Carsten M. Pusch Carsten M. Pusch (= 1×) peers Colin E. Willoughby

Countries citing papers authored by Carsten M. Pusch

Since Specialization

Citations

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

Fields of papers citing papers by Carsten M. Pusch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carsten M. Pusch

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

All Works

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20 of 20 papers shown

Czarnetzki, Alfred & Carsten M. Pusch. (2015). Identification of sarcomas in two burials of the 9th century in Western Germany. International Journal of Paleopathology. 12(3). 47–62. 2 indexed citations

Khairat, Rabab, Markus Ball, Raffaella Bianucci, et al.. (2013). First insights into the metagenome of Egyptian mummies using next-generation sequencing. Journal of Applied Genetics. 54(3). 309–325. 52 indexed citations

Metzger, Michael, et al.. (2011). Enlightening the past: Analytical proof for the use of Pistacia exudates in ancient Egyptian embalming resins. Journal of Separation Science. 34(23). 3364–3371. 14 indexed citations

Pusch, Carsten M., et al.. (2010). Epigenetic alterations by methylation of RASSF1A and DAPK1 promoter sequences in mammary carcinoma detected in extracellular tumor DNA. Cancer Genetics and Cytogenetics. 199(2). 96–100. 26 indexed citations

Pusch, Carsten M., et al.. (2008). Novel Expression Patterns for Trefoil Peptides : Presence of Tff2 and Tff3 in Rodent Cochlea. Croatica Chemica Acta. 81(1). 113–117. 3 indexed citations

Pusch, Carsten M., et al.. (2008). The lumbar spine in Neanderthals shows natural kyphosis. European Spine Journal. 17(S2). 327–330. 19 indexed citations

Yang, Tao, Markus Pfister, Nikolaus Blin, et al.. (2005). Genetic heterogeneity of deafness phenotypes linked to DFNA4. American Journal of Medical Genetics Part A. 139A(1). 9–12. 26 indexed citations

Pusch, Carsten M.. (2004). Spiking of Contemporary Human Template DNA with Ancient DNA Extracts Induces Mutations Under PCR and Generates Nonauthentic Mitochondrial Sequences. Molecular Biology and Evolution. 21(5). 957–964. 29 indexed citations

Broghammer, Martina, et al.. (2004). Reduced expression of connexin 31.1 in larynx cancer is not caused by GJB5 mutations. Cancer Letters. 214(2). 225–229. 5 indexed citations

10.

Czarnetzki, Alfred, et al.. (2004). Paleopathological examination of medieval spines with exceptional thoracic kyphosis most likely secondary to spinal tuberculosis. Journal of Neurosurgery Spine. 1(2). 238–242. 10 indexed citations

11.

Riemann‐Campe, Kathrin, Karl Sotlar, Susan Kupka, et al.. (2004). Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases. Cancer Genetics and Cytogenetics. 150(2). 128–135. 26 indexed citations

12.

Pusch, Carsten M., Birgit Meyer, Susan Kupka, et al.. (2004). Refinement of the DFNA4 locus to a 1.44�Mb region in 19q13.33. Journal of Molecular Medicine. 82(6). 398–402. 3 indexed citations

13.

Pusch, Carsten M., Martina Broghammer, & Alfred Czarnetzki. (2001). Molekulare Paläobiologie: Ancient DNA und Authentizität. Germania: Anzeiger der Römisch-Germanischen Kommission des Deutschen Archäologischen Instituts. 79(1). 121–141. 1 indexed citations

14.

Broghammer, Martina, Eberhart Zrenner, E Apfelstedt-Sylla, et al.. (2001). Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders. International Journal of Molecular Medicine. 8(1). 53–8. 1 indexed citations

15.

Kayademir, Tuncay, et al.. (1998). A novel 25 bp tandem repeat within the human trefoil peptide gene TFF2 in 21q22.3: polymorphism and mammalian evolution. European Journal of Human Genetics. 6(2). 121–128. 10 indexed citations

16.

Pusch, Carsten M., Holger Schmitt, & Nikolaus Blin. (1997). Increased cloning efficiency by cycle restriction−ligation (CRL). 2(1). 35–37. 7 indexed citations

17.

Scholz, Michael & Carsten M. Pusch. (1997). An efficient isolation method for high-quality DNA from ancient bones. 2(1). 61–64. 14 indexed citations

18.

Pusch, Carsten M. & Michael Scholz. (1997). DNA extraction from ancient human bones via enzymatic treatment. 2(1). 160–163. 7 indexed citations

19.

Müllenbach, Roman, Carsten M. Pusch, Karlheinz Holzmann, Ron F. Suijkerbuijk, & Nikolaus Blin. (1996). Distribution and linkage of repetitive clusters from the heterochromatic region of human chromosome 22. Chromosome Research. 4(4). 282–287. 2 indexed citations

20.

Pusch, Carsten M., Roman Müllenbach, Peter Gött, et al.. (1996). Cosmid-derived transcripts and sequence tags mapped to three subregions of human chromosome 22. Gene. 183(1-2). 29–33. 1 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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