Sebastian Eck

3.4k total citations
23 papers, 1.0k citations indexed

About

Sebastian Eck is a scholar working on Genetics, Cancer Research and Molecular Biology. According to data from OpenAlex, Sebastian Eck has authored 23 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 11 papers in Cancer Research and 9 papers in Molecular Biology. Recurrent topics in Sebastian Eck's work include Cancer Genomics and Diagnostics (10 papers), Genomics and Rare Diseases (8 papers) and Genetic factors in colorectal cancer (4 papers). Sebastian Eck is often cited by papers focused on Cancer Genomics and Diagnostics (10 papers), Genomics and Rare Diseases (8 papers) and Genetic factors in colorectal cancer (4 papers). Sebastian Eck collaborates with scholars based in Germany, Austria and United States. Sebastian Eck's co-authors include Tim M. Strom, Anna Benet‐Pagès, Hans Scheffer, Marjan M. Weiss, Erika Souche, Helger G. Yntema, Mariëlle Alders, Egbert Bakker, Thomas Meitinger and Gert Matthijs and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Sebastian Eck

21 papers receiving 976 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sebastian Eck Germany 12 448 366 168 119 91 23 1.0k
Irina R. Tikhonova United States 3 526 1.2× 721 2.0× 235 1.4× 56 0.5× 100 1.1× 3 1.3k
Jayne Y. Hehir‐Kwa Netherlands 24 1.1k 2.5× 854 2.3× 217 1.3× 66 0.6× 108 1.2× 53 1.9k
Robert Steen United States 7 565 1.3× 488 1.3× 120 0.7× 80 0.7× 76 0.8× 10 1.1k
Lifeng Tian United States 15 366 0.8× 474 1.3× 146 0.9× 45 0.4× 50 0.5× 47 900
Peggy D. Robertson United States 9 855 1.9× 946 2.6× 272 1.6× 88 0.7× 143 1.6× 12 1.7k
John Pappas United States 17 309 0.7× 296 0.8× 47 0.3× 114 1.0× 42 0.5× 54 885
Yulan Lu China 19 314 0.7× 527 1.4× 170 1.0× 49 0.4× 44 0.5× 83 1.2k
Carlo Marcelis Netherlands 25 433 1.0× 757 2.1× 79 0.5× 57 0.5× 31 0.3× 67 1.6k
Emanuele Agolini Italy 16 327 0.7× 479 1.3× 46 0.3× 73 0.6× 61 0.7× 82 989
Abdelhamid Barakat Morocco 23 491 1.1× 774 2.1× 110 0.7× 58 0.5× 35 0.4× 132 1.6k

Countries citing papers authored by Sebastian Eck

Since Specialization
Citations

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

Fields of papers citing papers by Sebastian Eck

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sebastian Eck

This figure shows the co-authorship network connecting the top 25 collaborators of Sebastian Eck. A scholar is included among the top collaborators of Sebastian Eck 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 Sebastian Eck. Sebastian Eck 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.
Kraft, Florian, Anna Benet‐Pagès, Daniel Berner, et al.. (2023). Quality assurance within the context of genome diagnostics (a german perspective). Medizinische Genetik. 35(2). 91–104. 1 indexed citations
2.
Eck, Sebastian, et al.. (2021). Wie SchülerInnen über Gott denken. SHILAP Revista de lepidopterología.
3.
Dincer, Yasemin, Julian Schulz, Monika Cohen, et al.. (2018). Multiple Integration and Data Annotation Study (MIDAS): improving next-generation sequencing data analysis by genotype-phenotype correlations. LaboratoriumsMedizin. 42(1-2). 1–8. 2 indexed citations
4.
Eck, Sebastian. (2018). Challenges in data storage and data management in a clinical diagnostic setting. LaboratoriumsMedizin. 42(6). 219–224. 2 indexed citations
5.
Weinmaier, Thomas, Jonathan Hoser, Sebastian Eck, et al.. (2015). Genomic factors related to tissue tropism in Chlamydia pneumoniae infection. BMC Genomics. 16(1). 268–268. 11 indexed citations
6.
Matthijs, Gert, Erika Souche, Mariëlle Alders, et al.. (2015). Guidelines for diagnostic next-generation sequencing. European Journal of Human Genetics. 24(1). 2–5. 337 indexed citations
7.
Matthijs, Gert, Mariëlle Alders, Peter Bauer, et al.. (2014). EuroGentest guidelines for diagnostic next generation sequencing. European Journal of Human Genetics. 22. 566–566. 3 indexed citations
8.
Stögmann, Elisabeth, Eva M. Reinthaler, Salwa El Tawil, et al.. (2013). Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. Brain. 136(4). 1155–1160. 51 indexed citations
9.
Jansen, Sandra, Bernhard Aigner, Hubert Pausch, et al.. (2013). Assessment of the genomic variation in a cattle population by re-sequencing of key animals at low to medium coverage. BMC Genomics. 14(1). 446–446. 54 indexed citations
10.
Grumbt, Barbara, Sebastian Eck, Tanja Hinrichsen, & Kaimo Hirv. (2013). Diagnostic Applications of Next Generation Sequencing in Immunogenetics and Molecular Oncology. Transfusion Medicine and Hemotherapy. 40(3). 196–206. 20 indexed citations
11.
Schulte, Eva C., Darina Czamara, Daniel C. Ellwanger, et al.. (2013). Rare Variants in PLXNA4 and Parkinson’s Disease. PLoS ONE. 8(11). e79145–e79145. 15 indexed citations
12.
Rothbauer, Ulrich, et al.. (2013). c-Jun/c-Fos heterodimers regulate cellular genes via a newly identified class of methylated DNA sequence motifs. Nucleic Acids Research. 42(5). 3059–3072. 62 indexed citations
13.
Sabrautzki, Sibylle, Isabel Rubio‐Aliaga, Wolfgang Hans, et al.. (2012). New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis. Mammalian Genome. 23(7-8). 416–430. 26 indexed citations
14.
Eck, Sebastian, Anna Benet‐Pagès, Philipp A. Greif, et al.. (2012). Diagnostic applications of next generation sequencing: working towards quality standards/Diagnostische Anwendung von Next Generation Sequencing: Auf dem Weg zu Qualitätsstandards. LaboratoriumsMedizin. 36(4). 227–239. 5 indexed citations
15.
Jamra, Rami Abou, Annick Raas‐Rothschild, Sebastian Eck, et al.. (2011). Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature. The American Journal of Human Genetics. 88(6). 788–795. 167 indexed citations
16.
Greif, Philipp A., Sebastian Eck, Nikola P. Konstandin, et al.. (2011). Identification of recurring tumor-specific somatic mutations in acute myeloid leukemia by transcriptome sequencing. Leukemia. 25(5). 821–827. 44 indexed citations
17.
Kalla, Markus, Christine Göbel, Ulrich Rothbauer, et al.. (2010). CpG-Methylation Regulates a Class of Epstein-Barr Virus Promoters. PLoS Pathogens. 6(9). e1001114–e1001114. 91 indexed citations
18.
Greif, Philipp A., Sebastian Eck, Nikola P. Konstandin, et al.. (2010). Identification of Recurring Tumor-Specific Somatic Mutations In Acute Myeloid Leukemia by Transcriptome Sequencing.. Blood. 116(21). 1059–1059. 2 indexed citations
19.
Eck, Sebastian, Anna Benet‐Pagès, Krzysztof Flisikowski, et al.. (2009). Whole genome sequencing of a single Bos taurusanimal for single nucleotide polymorphism discovery. Genome biology. 10(8). R82–R82. 93 indexed citations
20.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Irina R. Tikhonova Breakdown of academic impact, for papers by Jayne Y. Hehir‐Kwa Breakdown of academic impact, for papers by Robert Steen Breakdown of academic impact, for papers by Lifeng Tian Breakdown of academic impact, for papers by Peggy D. Robertson Breakdown of academic impact, for papers by John Pappas Breakdown of academic impact, for papers by Yulan Lu Breakdown of academic impact, for papers by Carlo Marcelis Breakdown of academic impact, for papers by Emanuele Agolini Breakdown of academic impact, for papers by Abdelhamid Barakat
Rankless by CCL
2026