E. Schleiermacher

737 total citations
38 papers, 514 citations indexed

About

E. Schleiermacher is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, E. Schleiermacher has authored 38 papers receiving a total of 514 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Plant Science. Recurrent topics in E. Schleiermacher's work include Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (6 papers) and Carcinogens and Genotoxicity Assessment (5 papers). E. Schleiermacher is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (6 papers) and Carcinogens and Genotoxicity Assessment (5 papers). E. Schleiermacher collaborates with scholars based in Germany, Thailand and United States. E. Schleiermacher's co-authors include Almut Nebel, F. Vogel, I. Anton‐Lamprecht, Uli Schmidt, V. Lenhard, R Mertelsmann, Trevor Smith, T. M. Schroeder, F. Herrmann and Harry Scherthan and has published in prestigious journals such as The Journal of Experimental Medicine, Journal of Clinical Oncology and Human Reproduction.

In The Last Decade

E. Schleiermacher

38 papers receiving 462 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. Schleiermacher Germany 15 198 161 134 108 84 38 514
Anita Mattsson Sweden 14 243 1.2× 132 0.8× 23 0.2× 55 0.5× 74 0.9× 26 558
Thomas Walsh Ireland 15 214 1.1× 70 0.4× 65 0.5× 52 0.5× 102 1.2× 26 490
Barbara D′haene Belgium 9 410 2.1× 186 1.2× 100 0.7× 196 1.8× 28 0.3× 11 670
Winfried Hofmann Germany 12 202 1.0× 74 0.5× 47 0.4× 41 0.4× 24 0.3× 51 447
Chongjian Chen China 17 739 3.7× 265 1.6× 214 1.6× 206 1.9× 97 1.2× 31 1.0k
Norio Miharu Japan 15 159 0.8× 292 1.8× 122 0.9× 36 0.3× 459 5.5× 27 717
Bisharah L. Libbus United States 11 178 0.9× 83 0.5× 40 0.3× 72 0.7× 20 0.2× 20 426
Jennifer Sze Man Mak Hong Kong 13 426 2.2× 168 1.0× 41 0.3× 20 0.2× 82 1.0× 20 936
Koichi Ushizawa Japan 17 267 1.3× 247 1.5× 15 0.1× 91 0.8× 66 0.8× 31 702
Travis Drucker United States 8 194 1.0× 123 0.8× 60 0.4× 135 1.3× 12 0.1× 10 523

Countries citing papers authored by E. Schleiermacher

Since Specialization
Citations

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

Fields of papers citing papers by E. Schleiermacher

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. Schleiermacher

This figure shows the co-authorship network connecting the top 25 collaborators of E. Schleiermacher. A scholar is included among the top collaborators of E. Schleiermacher 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 E. Schleiermacher. E. Schleiermacher 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.
Eggermann, Thomas, Hartmut Engels, Markus M. Nöthen, et al.. (1996). Tetrasomy 18p de novo: Identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing. Human Genetics. 97(5). 568–572. 17 indexed citations
2.
3.
Eggermann, Thomas, Markus M. Nöthen, Jutta Müller‐Navia, et al.. (1996). Tetrasomy 18p de novo: identification by FISH with conventional and microdissection probes and analysis of parental origin and formation by short sequence repeat typing. Human Genetics. 97(5). 568–572. 2 indexed citations
4.
Nebel, Almut, et al.. (1995). Complete and precise characterization of marker chromosomes by application of microdissection in prenatal diagnosis. Human Genetics. 96(6). 661–667. 44 indexed citations
5.
Schleiermacher, E., et al.. (1993). Direct detection of repetitive, whole chromosome paint and telomere DNA probes by immunogold electron microscopy. Chromosome Research. 1(1). 45–51. 15 indexed citations
6.
Herrmann, F., et al.. (1992). Elevated circulating levels of tumor necrosis factor predict unresponsiveness to treatment with interferon alfa-2b in chronic myelogenous leukemia.. Journal of Clinical Oncology. 10(4). 631–634. 23 indexed citations
7.
Klein, H, Michael Lübbert, Wolfgang Oster, et al.. (1990). Synthesis of granulocyte colony-stimulating factor and its requirement for terminal divisions in chronic myelogenous leukemia.. The Journal of Experimental Medicine. 171(5). 1785–1790. 19 indexed citations
8.
9.
Notghi, Arman, Ursula Nestle, Pierre Brissot, et al.. (1990). Chromosomal aberrations in patients with primary biliary cirrhosis. Human Genetics. 85(5). 546–50. 5 indexed citations
10.
Anton‐Lamprecht, I., E. Schleiermacher, & M. Wolf. (1988). Autosomal recessive anhidrotic ectodermal dysplasia: report of a case and discrimination of diagnostic features.. PubMed. 24(2). 183–95. 8 indexed citations
11.
12.
Schmidt, W., et al.. (1982). Ultrasonographic diagnoses of major lymphatic system abnormalities prior to 20 weeks of pregnancy. European Journal of Obstetrics & Gynecology and Reproductive Biology. 14(3). 163–170. 1 indexed citations
13.
Sch�fer, Dieter, et al.. (1981). High resolution analysis and differential condensation in RBA-banded human chromosomes. Human Genetics. 59(3). 187–93. 17 indexed citations
14.
Schleiermacher, E., et al.. (1978). The HLA system and leprosy in Thailand. Human Genetics. 42(2). 201–213. 28 indexed citations
15.
Schleiermacher, E., et al.. (1974). Brother and sister with trisomy 10p: A new syndrome. Human Genetics. 23(3). 163–72. 34 indexed citations
16.
Schleiermacher, E., et al.. (1973). Action of mitomycin C on mouse spermatogonia. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 19(1). 99–108. 28 indexed citations
17.
Vogel, F., et al.. (1971). Chemisch-induzierte Mutationen bei S�uger und Mensch. Die Naturwissenschaften. 58(3). 131–141. 8 indexed citations
18.
Schleiermacher, E., et al.. (1969). The effects of cytoxan on the chromosomes of mouse bone marrow. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 8(3). 623–628. 31 indexed citations
19.
Schleiermacher, E., et al.. (1967). A constant chromosome aberration in two children with acute myeloic leukaemia. Human Genetics. 5(1). 80–82. 6 indexed citations
20.
Schleiermacher, E.. (1966). �ber den Einflu� von Trenimon und Endoxan auf die Meiose der m�nnlichen Maus. Human Genetics. 3(2). 134–155. 38 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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